Susceptibility to peer influence in adolescents: Associations between psychophysiology and behavior
Zachary M. Meehan
Julie A. Hubbard
Christina C. Moore
Fanny Mlawer
SimpleOriginal

Summary

This adolescent study examined the link between heart activity and how peers influenced their behavior. Increased heart rate while observed by peers was linked to more prosocial behavior. The study shows the body responds to peers.

Susceptibility to peer influence in adolescents: Associations between psychophysiology and behavior

Keywords Antisocial; Peer influence; Prosocial; Psychophysiology; Susceptibility

Abstract

The current study investigated in-the-moment links between adolescents’ autonomic nervous system activity and susceptibility to three types of peer influence (indirect, direct, continuing) on two types of behavior (antisocial, prosocial). The sample included 144 racially ethnically diverse adolescents (46% male, 53% female, 1% other; Mage = 16.02 years). We assessed susceptibility to peer influence behaviorally using the Public Goods Game (PGG) while measuring adolescents’ mean heart rate (MHR) and pre-ejection period (PEP). Three key findings emerged from bivariate dual latent change score modeling: (1) adolescents whose MHR increased more as they transitioned from playing the PGG alone (pre-influence) to playing while simply observed by peers (indirect influence) displayed more prosocial behavior; (2) adolescents whose PEP activity increased more (greater PEP activity = shorter PEP latency) as they transitioned from indirect influence to being encouraged by peers to engage in antisocial behavior (direct influence) engaged in more antisocial behavior; and (3) adolescents whose PEP activity decreased less as they transitioned from direct influence on prosocial behavior to playing the PGG alone again (continuing influence) displayed more continuing prosocial behavior (marginal effect). The discussion focuses on the role of psychophysiology in understanding adolescents’ susceptibility to peer influence.

As adolescents spend more time together, peers’ influence over one another increases (Steinberg & Lerner, 2004). Peer influence is not inherently negative and is, in fact, critical to healthy development (Allen & Antonishak, 2008). At the same time, it increases the risk of developing maladaptive behaviors (e.g., delinquency; Müller & Minger, 2013). For this reason, it is essential to understand the processes that lead some teens to be more susceptible to peer influence than others. The goal of the current study was to investigate in-the-moment relations between autonomic nervous system (ANS) activity and susceptibility to peer influence.

Peer influence

Although peer influence is often conceptualized as harmful, teens influence one another to engage in various behaviors. Of course, these actions include antisocial behaviors such as lying, stealing, and cheating (Calkins & Keane, 2009). At the same time, peers also influence each other to engage in prosocial behaviors such as helping, sharing, and cooperating (Dirks et al., 2018). Finally, teens encourage peers to engage in risky behaviors such as substance use which are not clearly categorized as prosocial or antisocial (Prinstein & Dodge, 2008).

Another important distinction is the degree of peer involvement in peer influence. We typically imagine peers influencing one another through the explicit encouragement of specific behaviors, a process termed direct influence. However, the mere presence of peers is enough to alter adolescent behavior, a phenomenon labeled indirect influence. In addition, even when teens are no longer in the presence of peers who directly influenced them, they may continue to engage in the behaviors that peers encouraged, a construct we call continuing influence.

Extant research uses inconsistent terminology when referring to types of peer influence; thus, it is important to clarify how our nomenclature maps onto existing work. Direct influence has elsewhere been termed peer feedback (van Hoorn et al., 2014, 2016), peer contagion (Cohen & Prinstein, 2006), exposure to social norms (Prinstein et al., 2011), and exposure to peer groups (Gardner & Steinberg, 2005). Likewise, indirect influence has been termed social evaluation (Somerville, 2013) or the presence of peer spectators (van Hoorn et al., 2014, 2016) or peer observers (Silva et al., 2016). The phenomenon of continuing influence has rarely been directly studied in the literature and, thus, is not referred to explicitly.

Experimental studies have documented teens’ susceptibility to direct, indirect, and continuing peer influence on antisocial and risky behaviors. van Hoorn and colleagues (2014) demonstrated that adolescents display more antisocial behavior when encouraged to do so by peers, and Cohen and Prinstein (2006) found this same direct influence effect on both antisocial and risky behaviors. Teens also engage in more antisocial and risky behaviors simply when in the presence of peers compared to when they are alone, although this effect is typically weaker than the direct influence effect (Gardner & Steinberg, 2005; Reynolds et al., 2014; Silva et al., 2016). Finally, the effects of direct influence on antisocial and risky behaviors continue even when peers are no longer present, although this continuing effect is less than the preceding effect of direct influence (Cohen & Prinstein, 2006; Prinstein et al., 2011; van Hoorn et al., 2014).

There is also experimental support for adolescents’ susceptibility to direct and continuing peer influence on prosocial behaviors. Teens display more prosocial behavior when directly encouraged by peers to do so (van Hoorn et al., 2014) or when they learn that peers intend to engage in these behaviors themselves (ChoukasBradley et al., 2015; Foulkes et al., 2018). Moreover, peer influence on prosocial behavior continues when peers are no longer present, although again, this effect often is weaker than the preceding effect of direct influence (Choukas-Bradley et al., 2015; Frey & Meier, 2004; van Hoorn et al., 2014). To our knowledge, only two studies have investigated indirect influence on prosocial behavior, and the findings differed. Whereas van Hoorn and colleagues (2016) showed that teens’ prosocial behavior increased when simply in the presence of peers, van Hoorn and colleagues (2014) failed to find this effect.

With some exceptions, most investigations cited above compared two types of influence on one type of behavior. In the current study, we assessed three types of peer influence (indirect, direct, continuing) on two forms of behavior (antisocial, prosocial). In this way, we aimed to advance our understanding of the differential effects of indirect, direct, and continuing influence on both antisocial and prosocial behavior.

Susceptibility to peer influence

Adolescents are especially likely to conform to peers’ expectations. In an investigation by Gardner and Steinberg (2005), adolescents engaged in equal amounts of risk-taking as adults when they were alone. However, adolescents but not adults increased their risk-taking in the presence of peers. This study exemplifies the literature demonstrating that adolescents can make wise choices as well as adults (e.g., Reyna & Panagiotopoulos, 2020), but are more likely to fail to use these skills when in the presence of peers (Albert et al., 2013).

Although teens are typically more susceptible to peer influence than adults (Steinberg & Monahan, 2007), some adolescents are more susceptible than others. Müller and Minger (2013) reviewed 66 studies of factors predicting susceptibility to peer influence on antisocial behavior. They concluded that the strongest and most reliable predictor was age, with those in early and middle adolescence being most susceptible.

Albert and Steinberg (2011) proposed a theory to explain adolescents’ unique susceptibility to peer influence. They postulated that the adolescent brain is in a phase of development in which peers are particularly likely to activate a reward-sensitive motivational state (Cauffman et al., 2010). In the presence of peers, adolescents are especially likely to choose short-term gratification over long-term safety/benefit, because the simple presence of peers primes them to focus on immediate rewards. Although this framework focuses on antisocial and risky behaviors, the same rewardsalient priming effect occurs around prosocial behaviors as well (e.g., Kwak & Huettel, 2016; van Hoorn et al., 2014, 2016).

Albert and Steinberg (2011) also theorized that heightened emotional arousal or blunted emotion regulation might increase adolescents’ susceptibility to peer influence, a theory backed by empirical support (Chein et al., 2011; Cohen et al., 2016). Adolescents, more so than children or adults, show heightened emotional arousal (Somerville et al., 2013) and reduced emotion regulation (Perino et al., 2016; Somerville et al., 2011) when simply in the presence of peers. Furthermore, Gardner and colleagues (2008) found that individual differences in adolescents’ emotion regulation corresponded to their susceptibility to peer influence on risky behaviors.

Indeed, in their recent review of neurobiological studies of adolescents’ susceptibility to peer influence, Do and colleagues (2020) highlighted neural markers of both social reward processing and emotional arousal/dysregulation. They speculated that individual differences in both domains play an important role in differential susceptibility to peer influence, and they summarized investigations providing empirical support for this speculation (e.g., Chein et al., 2011; Pfeifer et al., 2011; Somerville et al., 2013; Welborn et al., 2016).

Notably absent from both reviews (Do et al., 2020; Müller & Minger, 2013) were investigations of psychophysiological factors predicting susceptibility to peer influence. However, prominent researchers have touted the promise of psychophysiology as an explanation for adolescent social behavior (e.g., Murray-Close, 2012a, 2012b; Prinstein & Giletta, 2020). In the current study, we examine physiological predictors of susceptibility to peer influence, and to the best of our knowledge, this is the first study to do so. Based on Albert and Steinberg’s (2011) theorizing on the role of both emotional arousal and reward sensitivity in adolescents’ susceptibility to peer influence, as well as Do and colleagues (2020) review of the role of neural markers of these constructs in the context of peer influence specifically, we chose physiological indices linked to emotional arousal and reward sensitivity. More broadly, the current study fits nicely within the theoretical framework of biological sensitivity to context (Ellis & Boyce, 2008), in that we investigate whether psychophysiology can help us understand which adolescents are especially likely to change their behavior in response to peer influence.

Psychophysiology and susceptibility to peer influence

Composed of the sympathetic (SNS) and parasympathetic nervous systems (PNS), the ANS is the most-studied physiological system in the peer literature (Murray-Close, 2012a). The SNS is responsible for excitatory functions (e.g., fight or flight), whereas the PNS is responsible for inhibitory and restorative functions (e.g., rest and restore; Murray-Close, 2012a).

The cardiovascular system is an excellent target for ANS study because multiple physiological measures can be derived from its output using electrocardiography (ECG) to record electrical signals of the heart and impedance cardiography (ICG) to record changes in blood volume. Perhaps the most recognizable metric of ECG is mean heart rate (MHR). MHR indexes either SNS activity (Anderson & Adolphs, 2014) or PNS activity (Thayer & Lane, 2000), depending upon the use of the vagal brake as assessed through respiratory sinus arrhythmia (RSA; Porges, 2001). However, when MHR increases following stressful and/or excitatory events such as peer influence, this physiological change may illustrate a normative emotional response (Stroud et al., 2009), serve as a reliable proxy of energy expenditure (Halsey et al., 2019), and suggest ANS activation driven by emotional arousal or dysregulation (Anderson & Adolphs, 2014). In fact, Wascher recently explicitly stated that increased MHR is considered a measure of emotional arousal in the context of evolutionary biology (Wascher, 2021).

A second cardiac metric is pre-ejection period (PEP), a measure of cardiac contractility requiring both ECG and ICG. PEP is the moment between the depolarization of the left ventricle and when the cardiac valves close. PEP may be uniquely suited as an indicator of reward sensitivity (Beauchaine et al., 2013). Brenner and colleagues (2005) examined whether PEP, RSA, or heart rate reactivity best assessed reward responsivity and found PEP to be the most psychometrically strong metric. Additional studies have validated PEP as an index of reward sensitivity in social situations in particular (Brinkmann & Franzen, 2017; Franzen et al., 2019).

The current study

The goal of the current study was to examine ANS activity as a predictor of adolescents’ susceptibility to peer influence. Strengths of the study include: (1) the study of susceptibility to three types of peer influence (indirect, direct, continuing), (2) the investigation of peer influence on two types of behavior (prosocial, antisocial), and (3) the use of two metrics of ANS activity (MHR, PEP). We hypothesized that adolescents who experienced greater ANS activity during peer influence would be more susceptible across all three types of peer influence on both types of behavior across both ANS activity indices.

An additional strength is the measurement of ANS activity at the same moment that adolescents experience peer influence and respond behaviorally. Most investigations assess youths’ physiology in a different context than the behavior it is hypothesized to predict (see Murray-Close, 2012b for a review). Some studies simply assess baseline physiology and use it to predict social behavior (e.g., Crozier et al., 2008). Other investigations do assess physiology in a social context but use it to predict behavior as reported by the youth themselves or their parents, teachers, or peers (e.g., Hubbard et al., 2002). However, with few exceptions (e.g., Moore et al., 2018), researchers have not measured physiology and the behavior it is hypothesized to predict at the same moment. In the current study, we assessed both ANS activity and behavioral responses to peer influence at the same moment in time. Moreover, we analyzed their co-occurrence using bivariate latent change score modeling (Kievit et al., 2018), with a particular focus on the covariation of latent change scores indexing ANS activity and behavioral responding to peer influence (referred to as the “path of primary interest” in the Results).

A final strength of the study was the inclusion of both baseline measures of ANS activity and a self-report measure of emotion regulation as covariates in analyses. This approach allowed us to investigate whether state-like ANS activity predicted in-themoment behavioral responses to peer influence over and above trait-like differences in emotional and physiological functioning. These covariates were particularly important in establishing that potential in-the-moment links between physiology and behavior were not simply the result of underlying individual differences in emotional or physiological functioning, but rather, that ANS activity in response to peer influence in fact served as a unique driver of behavior in that very moment.

Method

Overview

As part of a larger project involving a two-hour laboratory visit, 144 participants completed an experimental task assessing susceptibility to peer influence as we measured their ANS activity. In addition, adolescents reported on their ability to regulate emotions, and parents reported on family demographics. At the end of the visit, the experimenter debriefed adolescents (including an explanation of the deception described below), answered questions, and compensated adolescents and parents for their participation with $20 and $10, respectively.

Participants

Original cohort

During 2013–2014, we recruited participants from 74 4th- and 5thgrade classrooms in 9 schools in a mid-Atlantic state. We sent parental permission forms home with 1,910 children; 62% of children received parental consent, provided child assent, and completed data collection (N = 1191). Parents of 988 children agreed to be re-contacted for future studies.

Current cohort

From June 2019 to February 2020, we recruited a subsample of the original cohort through mail, email, and phone for additional data collection in 10th or 11th grade. We contacted all participants with up-to-date contact information, and we recruited all participants whose parents consented and who assented. Initial mail or email contacts were followed by a phone call, during which we thoroughly explained procedures to parents, including the fact that adolescents would be deceived.

The current cohort included 145 adolescents (46% male, 53% female, and 1% other) with an average age of 16.02 years (SD = 0.63). However, one participant ended the lab visit before the assessment of susceptibility to peer influence could be completed, resulting in an effective sample size of 144. This sample’s racial/ethnic breakdown was 65% European American, 12% African American, 10% Latino American, 7% Asian American, and 6% mixed race or ethnicity. Parents reported annual household income as less than $20,000 (3%), $20,000–$50,000 (16%), $50,000–100,000 (22%), $100,000–$150,000 (22%), and greater than $150,000 (36%).

We compared the 145 participants in the current cohort to the remaining 1044 participants in the original cohort on 4th or 5th grade variables, including demographics, peer victimization (teacher-, self-, and peer-report), peer rejection (teacher- and peer-report), and depressive and anxious symptoms (teacherand self-report). Participants in the current cohort (64%) were more likely to be European American than youth who participated in the original study but not the current study (50%), χ2 (1) = 10.07, p = .002.

Procedures and measures

Self-reported emotion regulation

Adolescents completed the Emotion Regulation Questionnaire (ERQ; Gullone & Taffe, 2012). A sample item was “I control my feelings about things by changing the way I think about them,” and adolescents responded on a scale from 1 = Strongly Disagree to 5 = Strongly Agree. The measure possesses strong construct and convergent validity (Gullone & Taffe, 2012). We averaged ratings across the ten items, with higher scores reflecting greater emotion regulation, and labeled this variable Emotion Regulation. Cronbach’s alpha was .69. Unfortunately, our data set did not include an analogous trait-like self-report measure of reward processing.

Susceptibility to peer influence

Adolescents completed a four-minute computerized version of the Public Goods Game (PGG) adapted from the protocol used by van Hoorn and colleagues (2014, 2016). The experimenter explained the rules using standardized instructions, visual aids, and comprehension checks. Adolescents believed they were one of four online players, all participating from different universities; in truth, the other three players were virtual. In each of 30 rounds, players received five tokens worth 3 cents each and decided how many to keep versus donate to a “public goods pot.” During each round, all tokens donated to the pot were doubled in value, then distributed equally. During the game, participants were unaware of how many tokens other players donated or how many tokens they received after each round. However, at the end of the game, the experimenter told all participants that they had earned $5.

The best strategy to optimize individual gain was to keep all tokens, whereas the best strategy to optimize the group’s gain was to donate all tokens. For this reason, we conceptualized keeping tokens as antisocial behavior and donating tokens as prosocial behavior. The experimenter conveyed this concept to participants through instructions (i.e., “The best way for you to make money is to keep your tokens” versus “The best way for you and the other players to make money is to donate your tokens”).

The game was divided into four blocks. The first five rounds, labeled the Pre-Influence Block, were used to establish adolescents’ baseline rate of donating/keeping tokens.

The next ten rounds were labeled the Indirect Influence Block and were used to assess whether adolescents changed their donating/keeping behavior when simply observed by peers. In these rounds, adolescents believed that five additional same-age peers also participating from other universities were online and observing, although in truth, these “observer peers” were also virtual. To reinforce this belief, photos of the observer peers (selected from a database of morphed adolescent faces) appeared on the screen throughout this block, although photos of the player peers were not on the screen.

The next ten rounds were labeled the Direct Influence Block and were used to assess whether adolescents changed their behavior when directly encouraged to do so by peers. In each round, the same five virtual peers who observed in the previous block now provided either positive feedback (thumbs-up icon below their photo) or no feedback (no icon) about adolescents’ behavior. In a between-subjects design, participants were randomly assigned to either a condition in which peers encouraged the prosocial behavior of donating tokens (N = 78) or the antisocial behavior of keeping tokens (N = 66); of note, random assignment resulted in a somewhat uneven distribution of participants across conditions. In the Prosocial Condition, the more tokens adolescents donated, the more thumbs-up icons they received, whereas in the Antisocial Condition, the more tokens they kept, the more thumbs-up icons they received. Participants in the Prosocial Condition received five thumbs-up icons for donating five tokens, four or five icons for donating four tokens, three or four icons for donating three tokens, two or three icons for donating two tokens, one or two icons for donating one token, and no icons for donating zero tokens. These specifications were reversed for the Antisocial Condition.

The final five rounds were labeled the Continuing Influence Block and were used to assess the extent to which adolescents returned to their baseline donating/keeping behavior versus demonstrated continuation of peer influence once peers left. In these rounds, the peers’ photos disappeared from the screen, indicating that they had gone offline. Before the game began, the experimenter explained and assessed adolescents’ comprehension of the presence (through their photos) and influence (through thumbs-up icons) of the observer peers.

We averaged the number of tokens participants donated across the rounds of each block, resulting in variables labeled Token Donation Pre-Influence, Token Donation Indirect Influence, Token Donation Direct Influence, and Token Donation Continuing Influence.

The PGG was originally developed to study group cooperative behavior (Ledyard, 1995) and did not include a peer influence manipulation. High token donation has been validated as a form of prosocial behavior through positive associations with selfreports of altruism and trust as well as behavioral measures of charitable giving (Banerjee et al., 2021; Galizzi & NavarroMartinez, 2019; Laury & Taylor, 2008). To our knowledge, no published studies have linked low token donation to antisocial behavior; however, in the larger data set for this project, token donation was negatively associated with self-reports of conduct problems, r(144) = −.18, p = .03, and callous-unemotional traits, r(144) = −.21, p = .01. The PGG has since been adapted by van Hoorn and colleagues (2014, 2016) as a lab-based simulation of peer influence through the inclusion of observers who either simply watch participants’ token donation or actively encourage participants to either donate or keep their tokens. These researchers found that both simple observation by peers and direct encouragement by peers to donate tokens increased token donation, whereas direct encouragement by peers to keep tokens decreased token donation.

We made two adaptations to the PGG as administered by van Hoorn and colleagues (2014). First, we sequenced the blocks so that the Indirect Influence Block preceded the Direct Influence Block, whereas van Hoorn used the reverse order. Second, in the Direct Influence Block, we randomized participants to one of two conditions (Antisocial and Prosocial), whereas van Hoorn and colleagues added a third condition (no influence), which we did not include because of its redundancy with the Indirect Influence Block.

After the game, adolescents rated the extent to which the peers liked it if they kept tokens or donated tokens, each on a scale from 1 = not at all to 5 = very much. Adolescents in the Antisocial Condition (mean = 4.50) rated peers as liking token keeping more than adolescents in the Prosocial Condition (mean = 1.78), F(1,143) = 207.12, p < .001. In contrast, adolescents in the Prosocial Condition (mean = 4.46) rated peers as liking token donation more than adolescents in the Antisocial Condition (mean = 2.77), F(1,143) = 71.22, p < .001.

ANS activity

We recorded and analyzed MHR and PEP using the MindWare Mobile Cardio system and software. To measure MHR, we placed ECG electrodes in a standard lead two configuration: one above the right clavicle, one below the left rib cage, and one below the right rib cage. To measure PEP, we collected ICG using four additional ECG electrodes: two on the chest (one above the jugular notch and one below the xiphoid process) and two on the back (one 1.5” above the jugular notch and another 1.5” lower than the xiphoid process). The ICG signal is generated by passing a current between the two electrodes on the back and sensing the resulting voltage with the electrodes on the chest, which is modulated by the volume of blood in the chest. A small box attached to the sensor leads wirelessly transmitted adolescents’ physiological recordings to a computer in the next room. After sensor placement, participants spent five minutes watching a neutral nature video to habituate to the sensors.

We sampled ECG and ICG data at a rate of 500 Hz and applied a muscle-nose band-pass filter with a low cutoff of 0.5 Hz and a high cutoff of 45 Hz. If we observed electrical interference noise in the ECG data, we applied a notch filter at 60 Hz. We quantified MHR as the average heart rate, and we quantified PEP as the average of the latency from the beginning of the ventricular depolarization (ECG Q peak) to the time the aortic valve opens and blood is ejected out of the left ventricle and into the aorta (B peak of the first-order derivative of ICG signals; dZ/dt; Sherwood et al., 1990). We detected the B peak using the maximum slope method. A single graduate assistant examined and removed artifacts within each interval for all participants.

Immediately before completing the PGG, participants completed a three-minute baseline assessment, during which time they sat quietly and relaxed. The duration of the PGG blocks varied due to the number of trials in each block, with the Pre-Influence and Continuing Influence Blocks lasting 30 seconds and the Indirect Influence and Direct Influence Blocks lasting 90 seconds. For both MHR and PEP, we averaged scores across the 30-second intervals of the baseline period (six intervals) or each block of the PGG (one or three intervals), and for variables with multiple intervals, we further averaged across intervals. A 30-second interval is sufficient to assess both MHR (Kobayashi, 2013) and PEP (Kortekaas et al., 2018; Sherwood et al., 1990).

These calculations resulted in ten variables assessing ANS activity labeled MHR (PEP) Baseline, MHR (PEP) Pre-Influence, MHR (PEP) Indirect Influence, MHR (PEP) Direct Influence, and MHR (PEP) Continuing Influence. Because shorter PEP latency indexes greater ANS arousal, to ease interpretation, we multiplied PEP scores by −1 so that higher scores represent greater ANS activity across both MHR and PEP. Throughout the remainder of the paper, we refer to “PEP activity” rather than “PEP scores,” with more activity meaning shorter PEP latency and less activity meaning longer PEP latency.

Missing data

The sample size for each measure of PEP and MHR ranged from 128 (89% of 144) to 134 (93%) and from 139 (97%) to 143 (99%), respectively. Missing data for ANS activity resulted from sensor placement errors, technical software issues, and physiological artifacts.

Results

Preliminary analyses

Descriptive statistics are presented in Table 1 and bivariate correlations in Table 2. We assessed gender and race/ethnicity as potential covariates using analyses of variance (ANOVA) with demographic variables predicting study variables. Although no differences in race/ethnicity emerged, females (M = 81.68) had higher MHR Baseline than males (M = 77.50), F (1,140) = 4.59, p = .03, and females (M = 81.32) had higher MHR Direct Influence than males (M = 77.06), F (1,137) = 4.41, p = .04. Thus, gender was included as a covariate in primary analyses.

Block × condition ANOVA for Token Donation

Next, we conducted a two-way ANOVA to examine whether Token Donation differed across the within-subjects Blocks (PreInfluence, Indirect Influence, Direct Influence, and Continuing Influence) and between-subjects Conditions (Antisocial and Prosocial) of the PGG. Main effects for Block, F (3,140) = 7.09, p < .001, and Condition, F (1,142) = 5.60, p = .02, were qualified by a significant interaction, F (3, 140) = 20.42, p < .001. Post hoc comparisons using a Bonferroni correction for the Block main effect suggested that adolescents significantly increased their Token Donation from the Pre-Influence Block (M = 1.84) to the Indirect Influence Block (M = 2.05), suggesting that adolescents donated more tokens when observed by peers than when alone. We report this Block difference for the full sample because the between-subjects experimental manipulation (Antisocial vs. Prosocial) had not yet occurred.

Simple effects for Condition per Block suggested that adolescents in the Antisocial Condition did not differ from those in the Prosocial Condition on token donation in the Pre-Influence Block (Mantisocial = 1.81; Mprosocial = 1.87), F (1, 142) = .09, p = .77, or the Indirect Influence Block (Mantisocial = 2.00; Mprosocial = 2.10), F (1, 142) = .24, p = .63. However, adolescents in the Prosocial Condition donated more tokens than adolescents in the Antisocial Condition in both the Direct Influence Block (Mantisocial = 1.65; Mprosocial = 2.50), F (1, 142) = 15.64, p < .001, and the Continuing Influence Block (Mantisocial = 1.53; Mprosocial = 2.44), F (1, 142) = 15.44, p < .001. Thus, adolescents did not differ in their Token Donation before peer encouragement; however, adolescents in the Prosocial Condition donated more tokens than those in the Antisocial Condition thereafter, including when they were once again alone.

Simple effects for Block per Condition suggested that adolescents differed across Blocks in their Token Donation in both the Antisocial Condition, F (3, 63) = 12.33, p < .001, and Prosocial Condition, F (3, 75) = 18.73, p < .001. Post hoc comparisons suggested three significant differences between Blocks for the Antisocial Condition. Adolescents donated fewer tokens in the Direct Influence Block (M = 1.65) and the Continuing Influence Block (M = 1.53) than the Indirect Influence Block (M = 2.00); they also donated more tokens in the Pre-Influence Block (M = 1.81) than the Continuing Influence Block. Thus, when peers encouraged adolescents to keep their tokens, they decreased their donation below the level that they displayed when simply observed by peers, and they maintained this lower level of donation once peers were no longer observing them. Five significant differences between Blocks emerged for the Prosocial Condition. Adolescents donated more tokens in the Indirect Influence Block (M = 2.10), the Direct Influence Block (M = 2.50), and the Continuing Influence Block (M = 2.44) than the Pre-Influence Block (M = 1.87); they also donated fewer tokens in the Indirect Influence Block than the Direct Influence Block or the Continuing Influence Block. Thus, adolescents in the Prosocial Condition increased their Token Donation when they were observed by peers, they further increased their donation when peers encouraged them to do so, and they maintained this higher level of donation once peers were no longer observing them (see Figure 1).

Screenshot 2025-05-21 at 22.06.51

Figure 1. Token Donation differences by Block and Condition. Note. Error bars represent the 95% confidence interval. Different subscripts a, b, and c denote differences between Blocks within a Condition. Different subscripts x and y denote differences between Conditions within a Block.

Primary analyses

We used bivariate dual latent change score modeling (Kievit et al., 2018) to assess relations between adolescents’ susceptibility to peer influence and ANS activity across the Blocks and Conditions of the PGG. We created six models, with each model including one transition between PGG Blocks (Pre-Influence to Indirect Influence, Indirect Influence to Direct Influence, and Direct Influence to Continuing Influence) and one measure of ANS activity (MHR and PEP). We defined the first block as the first time point (T1) and the second block as the second time point (T2) for each transition. We chose to examine these three transitions discretely because of our interest in the psychophysiology underlying each distinct type of peer influence (indirect, direct, continuing). Each model was created using MPlus version 8 with maximum likelihood estimating with robust standard errors to account for skew and missing data (Muthén & Muthén, 1998–2017).

Latent change scores are conceptualized as the function of autoregressive and residual components. We created two latent change scores in each model, Change in Token Donation and Change in ANS Activity. We set the autoregressive path for each latent change score from T2 to T1 indicators to one and the T2 indicator variance to zero. We set the T2 indicators with a loading fixed to one to account for residual variance. We allowed the T1 indicators to covary with their respective latent change scores. These parameter constraints allow the latent change scores to separate true score changes from measurement error. We regressed each of the two latent change scores onto each of the two T1 variables, resulting in four cross-lagged pathways. Finally, we covaried the T1 variables and the latent change scores (see Figure 2).

Screenshot 2025-04-20 at 10.14.30Screenshot 2025-04-20 at 10.15.07Screenshot 2025-04-20 at 10.16.00

In each of the six models, the path of primary interest was path ρ, the covariation between Change in Token Donation and Change in ANS Activity. This path represents the real-time link between ANS activity and behavioral responding to peer influence. The model structure provides a rigorous test of this covariation, in that it takes into account the covariation of T1 ANS Activity and T1 Token Donation (path Φ), the prediction of Change in ANS Activity from T1 Token Donation (path γ1), and the prediction of Change in Token Donation from T1 ANS Activity (path γ2; Kievit et al., 2018). When significant effects emerged in either the MHR or PEP model for a transition, we tested whether the path of primary interest ρ differed between ANS indices in these two models (Paternoster et al., 1998). We included three covariates in each model: gender, Emotion Regulation, and MHR (PEP) Baseline when predicting that ANS variable.

For the second and third transitions, we modeled both the Antisocial and Prosocial Conditions and examined differences between them. We first compared a model in which all paths were constrained to be equal across Conditions to an unconstrained model (a model in which all paths were free to vary). If the χ2 difference tests revealed that the models were significantly or marginally different, we then released the path of primary interest. If a second χ2 difference test comparing a model in which all paths except the path of primary interest were constrained to be equal across Conditions to an unconstrained model resulted in equivalent models, we concluded that differences in path ρ could explain discrepancies between Conditions.

Below, we provide tables of results for models and Conditions when the path of primary interest ρ was significant (Tables 3–5). See Supplementary Tables 1–5 for the remaining models and Conditions in which the path of primary interest ρwas not significant.

Transition from Pre-Influence to Indirect Influence

The MHR [χ2 (11) = 6.80, p = .81; CFI = 1.00; TLI = 1.00; SRMR = .04; RMSEA = .00] and PEP [(χ2 (11) = 16.16, p = .14; CFI = .99; TLI = .98; SRMR = .09; RMSEA = .06] models both had excellent fit. However, path ρ was only significant for the MHR model. In that model, the Token Donation Latent Change Score was positively related to the MHR Latent Change Score (estimate = .19, p = .02), suggesting that the more adolescents’ MHR increased as they transitioned from playing the PGG alone to being observed by peers, the greater their increase in token donation across this transition (see Table 3). For the PEP model, the relation between the Token Donation Latent Change Score and the PEP Latent Change Score was not significant (estimate = −.11, p = .17). Path ρ differed between the MHR and PEP models (z = 2.65, p = .008).

Susceptibility to peer influence

We began by examining whether adolescents demonstrated susceptibility to peer influence while playing the PGG. Participants displayed all three types of influence across both types of behaviors. They donated more tokens when observed by peers than when alone (indirect influence effect), they donated more tokens (prosocial behavior) or fewer tokens (antisocial behavior) based on peers’ differential encouragement (direct influence effect), and they continued to be influenced by peers’ encouragement (both prosocial and antisocial) once peers were no longer present (continuing influence). These findings demonstrate the power of peer influence in adolescents’ lives, especially given the contrived nature of the PGG. This robust evidence of susceptibility to peer influence in participants’ behavior provided a firm foundation upon which to examine whether this susceptibility was related to ANS activity.

Psychophysiology and susceptibility to peer influence

Two assumptions of Albert and Steinberg’s (2011) model of adolescent susceptibility to peer influence provide a framework for interpreting our findings. First, adolescents demonstrate a unique propensity toward affective reactivity to social stimuli (Somerville, 2013), evidenced by stress responses in multiple bodily systems (e.g., Stroud et al., 2009). Second, adolescents display a unique difficulty with cognitive control, particularly when faced with the opportunity for social reward (Somerville et al., 2011). In combination, these two tendencies “prime” adolescents toward an emotional mindset and reward-sensitive motivation state when in the presence of peers. In the following sections, we discuss in-themoment links between ANS activity and susceptibility to peer influence at each transition of the PGG in terms of this theory.

Transition from Pre-Influence to Indirect Influence

The more adolescents’ heart rates increased as they transitioned from playing the PGG alone to being observed by peers, the greater their increase in token donation. In other studies, increases in MHR indicate emotional arousal (Anderson & Adolphs, 2014; Wascher, 2021), particularly in the presence of peers (Stroud et al., 2009), and endocrinological studies suggest that adolescents more so than children release stress hormones when observed by peers (Gunnar et al., 2009; Stroud et al., 2009). During this indirect influence, participants were likely trying to determine peers’ expectations for their behavior. Neuroimaging studies support this contention, with adolescents displaying heightened activity in brain regions implicated in mentalizing (van Hoorn et al., 2016) and social perspective-taking (Van den Bos et al., 2011) when in the presence of peers. Thus, the simple presence of peers may prime adolescents to mount an emotional, physiological, endocrinological, and neurobiological response to mobilize efforts to match peers’ expectations.

Table 3. Model of Mean Heart Rate with Token Donation for the transition from Pre-Influence to Indirect Influence

Screenshot 2025-05-21 at 22.18.54

Note. Estimates are standardized. Pre-I = Pre-Influence Block; II = Indirect Influence Block; MHR = Mean Heart Rate. The notation following each coefficient name refers to the corresponding pathway in Figure 2.

Table 4. Model of Pre-Ejection Period with Token Donation in the Antisocial Condition for the transition from Indirect Influence to Direct Influence

Screenshot 2025-05-21 at 22.15.32

Note. Estimates are standardized. II = Indirect Influence Block; DI = Direct Influence Block; PEP = Pre-Ejection Period. The notation following each coefficient name refers to the corresponding pathway in Figure 2.

Table 5. Model of Pre-Ejection Period with Token Donation in the Prosocial Condition for the transition from Direct Influence to Continuing Influence

Screenshot 2025-05-21 at 22.21.23

Note. Estimates are standardized. DI = Direct Influence Block; CI = Continuing Influence Block; PEP = Pre-Ejection Period. The notation following each coefficient name refers to the corresponding pathway in Figure 2.

Transition from Indirect Influence to Direct Influence

For adolescents encouraged by peers to keep their tokens, a positive relation emerged between PEP activity and this antisocial behavior as they transitioned from indirect to direct influence (recall that PEP variables are reverse-scored, such that greater PEP activity indicates shorter PEP latency). In other studies, PEP has been uniquely associated with reward sensitivity (Brenner et al., 2005), especially when social rewards are explicit (Brinkmann & Franzen, 2017).

The differential finding for antisocial versus prosocial behavior suggests that adolescents may require more effort to comply with antisocial than prosocial peer encouragement. The display of peerencouraged antisocial behavior may also result from a breakdown in behavioral regulation and impulse control (Somerville et al., 2011) that does not apply to prosocial behavior, as prosocial behavior is socially sanctioned. PEP activity during direct peer influence on antisocial behavior may also capture the physiological underpinnings of neurobiological susceptibility to peer influence inherent in documented maturational imbalances between competing brain systems (Chein et al., 2011; Cohen et al., 2016).

Transition from Direct Influence to Continuing Influence

The less adolescents’ PEP activity decreased as they transitioned from being directly encouraged to engage in the prosocial behavior of donating tokens to being alone, the less their token donation decreased (marginal effect). Theorists speculate that adolescents may view themselves as the target of social evaluation even when they are alone, a phenomenon termed the imaginary audience (Somerville, 2013). This imaginary audience may have mitigated the return of both physiology and behavior to baseline levels for adolescents in the prosocial condition, especially if teens found conforming to the expectations of this imaginary audience socially rewarding.

The differential finding for prosocial versus antisocial behavior suggests that teens exert more effort to comply with prosocial than antisocial peer expectations in their peers’ absence. When peers leave, acting in one’s own self-interest may be effortless, whereas acting in others’ interests may require some effort.

Alternative interpretations of physiological indices

We relied heavily on Albert and Steinberg’s (2011) theory to select the constructs of emotional arousal and reward sensitivity as the focus of our study of adolescents’ susceptibility to peer influence. We considered Do and colleagues’ (2020) review of neural markers of susceptibility to peer influence as justification for this selection, given their explicit focus on neural markers of both constructs. Furthermore, our choice of MHR and PEP as indices of emotional arousal and reward processing, respectively, was solidly based in empirical literature (Anderson & Adolphs, 2014; Beauchaine et al., 2013; Brenner et al., 2005; Brinkmann & Franzen, 2017; Franzen et al., 2019; Halsey et al., 2019; Stroud et al., 2009; Wascher, 2021). For these reasons, throughout the preceding Discussion, we have interpreted our findings in this vein. However, physiological variables and psychological constructs do not share a one-to-one correspondence, and it is important to note other possible interpretations of our findings.

Beyond emotional arousal, researchers have interpreted MHR more specifically as a marker of stress (e.g., Von Dawans et al., 2011; Vrijkotte et al., 2000) or excitement (Drachen et al., 2010; Mitkidis et al., 2015; Wulfert et al., 2005). In the current study, increases in heart rate were linked to increases in token donation when adolescents transitioned from being alone to being observed by peers. Although we interpreted this MHR increase as a sign of emotional arousal, adolescents may have experienced peers’ presence more specifically as stressful, exciting, or some combination of these emotions. Future researchers may want to incorporate selfratings of emotion into procedures such as ours to gain a clearer view of adolescents’ emotional experience when in the presence of peers, as well as how this experience may help identify those adolescents most susceptible to indirect peer influence.

Similarly, some researchers consider PEP to be an index of emotional reactivity (Evans et al., 2016; Seddon et al., 2020) rather than reward sensitivity. However, whereas alternative interpretations of MHR findings in our study seem distinctly possible, the link between PEP and reward sensitivity appears more robust, particularly in contexts of social evaluation, for three reasons. First, Beauchaine and colleagues (2012, 2013) used a four-step process to argue elegantly and forcefully for PEP as a marker of reward sensitivity and not emotional reactivity. Second, several rigorous studies have validated PEP as uniquely linked to reward sensitivity (Beauchaine et al., 2013; Franzen et al., 2019), particularly in social situations (Brinkmann & Frankzen, 2017). Finally, and of note, those scholars who consider PEP to index of emotional reactivity often measure PEP in the context of social evaluation and reward. For all of these reasons, we consider the explanation of PEP as an index of reward sensitivity to be most likely.

Limitations and future directions

An important limitation of the current study is that participants’ token donation and keeping behavior during the PGG may index something other than susceptibility to peer influence. Specifically, participants may have interpreted observer peers’ encouragement of token donation or keeping as an indication of normative behavior in this context. If that is the case, then participants may have donated or kept tokens not because peers encouraged them to do so, but because this understanding of normative behavior may have increased their belief that other players would do the same. The PGG is a prisoner’s dilemma, in which players gain the most if everyone cooperates, but players lose the most if they cooperate when others do not. Thus, participants may have donated or kept tokens not because of peer influence but because of a desire to earn the most money possible, or they may have acted in response to both peer influence and a desire to earn money. For this reason, future researchers should assess behavioral susceptibility to peer influence using approaches that do not involve the prisoner’s dilemma.

Furthermore, the ecological validity of token donation as a prosocial behavior and token keeping as an antisocial behavior is limited, in spite of positive associations between token donation and both altruism and charitable giving (Banerjee et al., 2021; Galizzi & Navarro-Martinez, 2019; Laury & Taylor, 2008) and negative associations between token donation and both conduct problems and callous-unemotional traits (larger data set for the current project). Furthermore, assessing both prosocial and antisocial behavior using the same measure (number of tokens donated/kept) ignores the fact that these two behaviors are not simply opposite ends of one continuum, although they are quite strongly negatively correlated across many studies (e.g., Carlo et al., 2014; Hardy et al., 2015; Hastings et al., 2000) and interventions that promote prosocial behavior often result in reductions in antisocial behavior (e.g., Vliek et al., 2014). Even so, individuals may display either high or low levels of both prosocial and antisocial behavior. Unfortunately, our measurement approach does not allow for this possibility; by using token donation as an assessment of both behaviors, the two constructs are inherently dependent, with participants who display high levels of one necessarily displaying low levels of the other. For these reasons, we encourage future researchers to develop new means of measuring susceptibility to peer influence that not only more closely mimic the behaviors important to teens but that also allow prosocial and antisocial behavior to be assessed as separate constructs.

Beyond these two primary concerns, our study was marked by three additional limitations. First, we did not examine RSA as a physiological correlate of susceptibility to peer influence. Given that RSA indexes emotion regulation, and given that emotional arousal is linked to susceptibility to peer influence (Albert & Steinberg, 2011; Somerville, 2013), the inclusion of RSA would advance our understanding of the role of psychophysiology in adolescents’ susceptibility to peer influence. However, such an approach will require behavioral measures of susceptibility that last considerably longer than the blocks of the PGG, given that RSA require minutes and not seconds to capture (Shaffer et al., 2020). Second, we assessed susceptibility to peer influence on prosocial and antisocial behaviors, but not risky behaviors. We encourage researchers to utilize procedures suitable for the measurement of susceptibility to peer influence on risky behaviors in future studies of psychophysiology and peer influence. Finally, our sample was limited to adolescents. It will be important for future research to investigate links between psychophysiology and susceptibility to peer influence across the developmental spectrum from childhood to adulthood.

Conclusions

In the present study, we used bivariate dual latent change score modeling to examine the links between ANS activity (MHR, PEP) and two forms of behavior (prosocial, antisocial) under three types of peer influence (indirect, direct, continuing). Findings suggested that adolescents who experienced greater MHR activity during indirect influence engaged in more prosocial behavior, adolescents who experienced greater PEP activity during direct influence on antisocial behavior displayed more of that behavior, and adolescents who sustained greater PEP activity during continuing influence maintained greater engagement in prosocial behavior. To our knowledge, this is the first study of the physiological correlates of susceptibility to peer influence, and one of only a handful of studies to investigate in-the-moment associations between psychophysiology and youth behavior of any type. However, we look forward to seeing more investigations in this promising line of research in the future.

Abstract

The current study investigated in-the-moment links between adolescents’ autonomic nervous system activity and susceptibility to three types of peer influence (indirect, direct, continuing) on two types of behavior (antisocial, prosocial). The sample included 144 racially ethnically diverse adolescents (46% male, 53% female, 1% other; Mage = 16.02 years). We assessed susceptibility to peer influence behaviorally using the Public Goods Game (PGG) while measuring adolescents’ mean heart rate (MHR) and pre-ejection period (PEP). Three key findings emerged from bivariate dual latent change score modeling: (1) adolescents whose MHR increased more as they transitioned from playing the PGG alone (pre-influence) to playing while simply observed by peers (indirect influence) displayed more prosocial behavior; (2) adolescents whose PEP activity increased more (greater PEP activity = shorter PEP latency) as they transitioned from indirect influence to being encouraged by peers to engage in antisocial behavior (direct influence) engaged in more antisocial behavior; and (3) adolescents whose PEP activity decreased less as they transitioned from direct influence on prosocial behavior to playing the PGG alone again (continuing influence) displayed more continuing prosocial behavior (marginal effect). The discussion focuses on the role of psychophysiology in understanding adolescents’ susceptibility to peer influence.

Summary

Adolescent peer influence, while crucial for development, also elevates the risk of maladaptive behaviors. This study investigated the real-time relationship between autonomic nervous system (ANS) activity and susceptibility to peer influence in adolescents. The research examined three types of peer influence (indirect, direct, continuing) on prosocial and antisocial behaviors, utilizing mean heart rate (MHR) and pre-ejection period (PEP) as ANS activity indices.

Peer Influence

Peer influence encompasses a spectrum of behavioral impacts, including antisocial (lying, stealing), prosocial (helping, sharing), and risky behaviors (substance use). The influence can be direct (explicit encouragement), indirect (mere presence of peers), or continuing (persistence of behavior even after peer interaction ceases). Existing research lacks consistent terminology, with various terms used to describe these influence types.

Susceptibility to Peer Influence

Adolescents exhibit heightened susceptibility to peer influence compared to adults, particularly during early and middle adolescence. This susceptibility stems from neurobiological developmental stages where peer presence activates reward-sensitive motivational states, prioritizing short-term gratification over long-term consequences. Heightened emotional arousal and reduced emotion regulation further contribute to this increased susceptibility. While prior research explored psychological and neural factors, psychophysiological predictors remained largely unexplored. This study addresses this gap by examining physiological indices of emotional arousal and reward sensitivity.

Psychophysiology and Susceptibility to Peer Influence

The ANS, comprising the sympathetic and parasympathetic nervous systems, provides valuable physiological indicators. Cardiovascular measures, such as MHR and PEP (derived from electrocardiography and impedance cardiography), were employed. MHR reflects ANS activity, potentially indicating emotional arousal, while PEP, indexing cardiac contractility, serves as an indicator of reward sensitivity.

The Current Study

This study investigated ANS activity as a predictor of adolescent susceptibility to peer influence, focusing on three influence types and two behavioral forms. A key strength is the simultaneous measurement of ANS activity and behavioral responses, using bivariate latent change score modeling to analyze co-occurrence. Baseline ANS activity and emotion regulation were included as covariates to isolate in-the-moment effects.

Method

The study used a longitudinal design, recruiting adolescents from a larger cohort and assessing their susceptibility to peer influence through a modified Public Goods Game (PGG). Physiological data (MHR, PEP) and self-reported emotion regulation were collected. The PGG involved manipulation of peer influence (indirect, direct, continuing) and behavioral outcomes (prosocial, antisocial token donation).

Results

Analyses revealed significant effects of peer influence on token donation across the PGG blocks. Bivariate dual latent change score modeling demonstrated significant associations between ANS activity and susceptibility to peer influence. Specifically, increased MHR during indirect influence correlated with increased prosocial behavior, while greater PEP activity during direct influence on antisocial behavior predicted increased antisocial behavior. Sustained PEP activity during continuing influence corresponded to maintained prosocial behavior.

Discussion

Findings align with theories positing heightened emotional reactivity and reward sensitivity in adolescents' response to peer influence. Increased MHR during indirect influence suggests an emotional response to peer observation, potentially driven by efforts to conform to perceived social expectations. PEP activity, linked to reward sensitivity, reflects the potential for enhanced reward response in both prosocial and antisocial scenarios. Differential effects for prosocial and antisocial behaviors highlight the complexities of adolescent responses to peer influence, potentially reflecting varying effort levels to conform to societal expectations.

Limitations and Future Directions

Limitations include the PGG's potential interpretation as reflecting normative behavior rather than pure peer influence and the inherent dependence of prosocial and antisocial behavior measures. Future research should employ alternative behavioral paradigms, including measurements of risky behaviors, utilize more ecologically valid prosocial and antisocial behavior measures, incorporate RSA and study a wider age range.

Conclusions

The study provides novel insights into the psychophysiological underpinnings of adolescent susceptibility to peer influence, demonstrating real-time associations between ANS activity and behavioral responses. Further research in this area is encouraged to extend these findings.

Abstract

The current study investigated in-the-moment links between adolescents’ autonomic nervous system activity and susceptibility to three types of peer influence (indirect, direct, continuing) on two types of behavior (antisocial, prosocial). The sample included 144 racially ethnically diverse adolescents (46% male, 53% female, 1% other; Mage = 16.02 years). We assessed susceptibility to peer influence behaviorally using the Public Goods Game (PGG) while measuring adolescents’ mean heart rate (MHR) and pre-ejection period (PEP). Three key findings emerged from bivariate dual latent change score modeling: (1) adolescents whose MHR increased more as they transitioned from playing the PGG alone (pre-influence) to playing while simply observed by peers (indirect influence) displayed more prosocial behavior; (2) adolescents whose PEP activity increased more (greater PEP activity = shorter PEP latency) as they transitioned from indirect influence to being encouraged by peers to engage in antisocial behavior (direct influence) engaged in more antisocial behavior; and (3) adolescents whose PEP activity decreased less as they transitioned from direct influence on prosocial behavior to playing the PGG alone again (continuing influence) displayed more continuing prosocial behavior (marginal effect). The discussion focuses on the role of psychophysiology in understanding adolescents’ susceptibility to peer influence.

Summary

This study investigated the relationship between autonomic nervous system (ANS) activity and susceptibility to peer influence in adolescents. It examined three types of peer influence (indirect, direct, continuing) on both prosocial and antisocial behaviors, using mean heart rate (MHR) and pre-ejection period (PEP) as ANS activity indices. The study hypothesized that greater ANS activity during peer influence would predict greater susceptibility across all three influence types and both behavior types.

Peer Influence

Peer influence significantly impacts adolescent behavior, encompassing antisocial (lying, stealing), prosocial (helping, sharing), and risky behaviors (substance use). The study distinguished between direct influence (explicit encouragement), indirect influence (mere presence of peers), and continuing influence (persisting behavior after peer interaction). The researchers clarified their terminology in relation to existing literature, noting inconsistencies in the field.

Susceptibility to Peer Influence

Adolescents demonstrate heightened susceptibility to peer influence compared to adults, particularly during early and middle adolescence. This susceptibility stems from the developing adolescent brain's reward-sensitive motivational state, making them prioritize immediate gratification over long-term consequences in the presence of peers. Heightened emotional arousal and reduced emotion regulation further amplify this susceptibility. Prior research has emphasized neural markers of social reward processing and emotional dysregulation in explaining individual differences in susceptibility. This study uniquely explored psychophysiological factors as potential predictors.

Psychophysiology and Susceptibility to Peer Influence

The ANS, comprising the sympathetic and parasympathetic nervous systems, was investigated through cardiovascular measures. MHR, reflecting either SNS or PNS activity depending on vagal brake assessment, was used as an index of emotional arousal. PEP, a measure of cardiac contractility, served as an indicator of reward sensitivity. The study aimed to assess whether these physiological indices could predict susceptibility to peer influence, advancing the understanding of biological sensitivity to context.

The Current Study

This study's strengths included its examination of three peer influence types and two behavior types, along with the use of both MHR and PEP. The simultaneous measurement of ANS activity and behavioral responses during peer influence is a key methodological advantage. The inclusion of baseline ANS activity and self-reported emotion regulation as covariates controlled for individual differences.

Method

The study used a subsample (N=144) from a larger longitudinal project, involving adolescents (mean age 16.02) completing a peer influence task while their ANS activity was measured. Self-reported emotion regulation and parental demographic information were also collected. A computerized Public Goods Game (PGG) was adapted to assess susceptibility to peer influence, manipulated through indirect (peer observation), direct (peer feedback), and continuing (post-interaction) conditions. MHR and PEP were recorded using ECG and ICG, respectively, with baseline measures also obtained.

Results

Analyses revealed significant effects of peer influence on token donation (prosocial/antisocial behavior). Bivariate dual latent change score modeling examined relationships between ANS activity and susceptibility to peer influence across PGG transitions. Results indicated that increased MHR during indirect influence correlated with increased prosocial behavior; increased PEP during direct antisocial influence correlated with increased antisocial behavior; and sustained PEP during continuing prosocial influence correlated with maintained prosocial behavior.

Discussion

The findings support Albert and Steinberg's model of adolescent susceptibility to peer influence, highlighting emotional arousal (MHR) and reward sensitivity (PEP) as key factors. The results are discussed in relation to existing research on adolescents' affective reactivity, cognitive control, and the role of imagined audiences. Alternative interpretations of physiological indices are also considered.

Limitations and Future Directions

Limitations include the potential interpretation of PGG behavior as reflecting normative behavior rather than peer influence, and the limited ecological validity of token donation/keeping as prosocial/antisocial behavior. Other limitations included the exclusion of RSA, focus on prosocial and antisocial behaviors (excluding risky behaviors), and the adolescent-only sample. Future research directions are suggested.

Conclusions

The study provided novel insights into the physiological underpinnings of adolescent susceptibility to peer influence. The findings contribute to a growing body of research emphasizing the importance of psychophysiological factors in understanding adolescent social behavior.

Abstract

The current study investigated in-the-moment links between adolescents’ autonomic nervous system activity and susceptibility to three types of peer influence (indirect, direct, continuing) on two types of behavior (antisocial, prosocial). The sample included 144 racially ethnically diverse adolescents (46% male, 53% female, 1% other; Mage = 16.02 years). We assessed susceptibility to peer influence behaviorally using the Public Goods Game (PGG) while measuring adolescents’ mean heart rate (MHR) and pre-ejection period (PEP). Three key findings emerged from bivariate dual latent change score modeling: (1) adolescents whose MHR increased more as they transitioned from playing the PGG alone (pre-influence) to playing while simply observed by peers (indirect influence) displayed more prosocial behavior; (2) adolescents whose PEP activity increased more (greater PEP activity = shorter PEP latency) as they transitioned from indirect influence to being encouraged by peers to engage in antisocial behavior (direct influence) engaged in more antisocial behavior; and (3) adolescents whose PEP activity decreased less as they transitioned from direct influence on prosocial behavior to playing the PGG alone again (continuing influence) displayed more continuing prosocial behavior (marginal effect). The discussion focuses on the role of psychophysiology in understanding adolescents’ susceptibility to peer influence.

Summary

This study investigated the relationship between a teenager's autonomic nervous system (ANS) activity and their susceptibility to peer influence. Researchers examined how ANS activity predicted responses to three types of peer influence (indirect, direct, continuing) on both prosocial and antisocial behaviors. The study used heart rate (MHR) and pre-ejection period (PEP) as measures of ANS activity.

Peer Influence

Peer influence affects teens' behavior in various ways. It can lead to both positive (prosocial) and negative (antisocial) actions, as well as risky behaviors. Influence can be direct (explicit encouragement), indirect (mere presence of peers), or continuing (lasting effects even after peer interaction ends). Previous research used inconsistent terms for these types of influence.

Susceptibility to Peer Influence

Teenagers are particularly susceptible to peer pressure, especially during early and middle adolescence. This heightened susceptibility is linked to brain development, where the reward system is especially sensitive to peer influence, leading to a focus on immediate gratification. Increased emotional arousal and less effective emotion regulation also contribute to this vulnerability. Previous research has focused on neural factors, while this study explored psychophysiological aspects.

Psychophysiology and Susceptibility to Peer Influence

The ANS, comprising the sympathetic and parasympathetic nervous systems, plays a key role. MHR, reflecting either sympathetic or parasympathetic activity depending on context, can indicate emotional arousal. PEP, a measure of cardiac contractility, is linked to reward sensitivity. The study hypothesized that higher ANS activity during peer influence would predict greater susceptibility to that influence.

The Current Study

This study's strengths included examining three types of peer influence and two types of behavior, using two ANS activity measures, and measuring ANS activity and behavior simultaneously. Using baseline ANS activity and self-reported emotion regulation as covariates helped isolate the effects of in-the-moment ANS activity.

Method

144 high school students (ages 15-16) participated in a lab study involving a modified Public Goods Game (PGG) that measured peer influence. ANS activity (MHR and PEP) was measured using the MindWare Mobile Cardio system. Students also completed the Emotion Regulation Questionnaire (ERQ). The PGG involved four blocks: pre-influence, indirect influence (peer observation), direct influence (peer feedback), and continuing influence (post-peer interaction).

Results

Analysis showed significant effects of peer influence on token donation (prosocial behavior). Indirect influence increased donation, direct influence increased prosocial donation and decreased antisocial (keeping tokens) behavior. Continuing influence persisted even without peers present. Bivariate dual latent change score modeling revealed that higher MHR increases during indirect influence corresponded with greater increases in token donation. Higher PEP activity during direct antisocial influence related to more antisocial behavior, and sustained PEP activity during continuing prosocial influence was linked to continued prosocial behavior.

Discussion

The findings support the idea that emotional arousal (MHR) and reward sensitivity (PEP) contribute to susceptibility to peer influence. Increases in heart rate during indirect influence reflect a heightened response to peer observation, while PEP's relation to antisocial and prosocial behaviors shows how reward sensitivity influences choices in the presence and absence of peers.

Limitations and Future Directions

Limitations included the potential interpretation of PGG behavior as responding to norms rather than peer influence, and the use of token donation/keeping as a measure of both prosocial and antisocial behavior. Future research should use alternative behavioral measures, separately assess prosocial and antisocial behavior, and include RSA and a wider age range. Despite these limitations, this study offers valuable insights into the psychophysiological mechanisms underlying adolescent susceptibility to peer influence.

Conclusions

The study demonstrated a link between ANS activity and adolescent susceptibility to peer influence, highlighting the roles of emotional arousal and reward sensitivity. This novel research opens up new avenues for understanding the interplay between physiology and peer influence during adolescence.

Abstract

The current study investigated in-the-moment links between adolescents’ autonomic nervous system activity and susceptibility to three types of peer influence (indirect, direct, continuing) on two types of behavior (antisocial, prosocial). The sample included 144 racially ethnically diverse adolescents (46% male, 53% female, 1% other; Mage = 16.02 years). We assessed susceptibility to peer influence behaviorally using the Public Goods Game (PGG) while measuring adolescents’ mean heart rate (MHR) and pre-ejection period (PEP). Three key findings emerged from bivariate dual latent change score modeling: (1) adolescents whose MHR increased more as they transitioned from playing the PGG alone (pre-influence) to playing while simply observed by peers (indirect influence) displayed more prosocial behavior; (2) adolescents whose PEP activity increased more (greater PEP activity = shorter PEP latency) as they transitioned from indirect influence to being encouraged by peers to engage in antisocial behavior (direct influence) engaged in more antisocial behavior; and (3) adolescents whose PEP activity decreased less as they transitioned from direct influence on prosocial behavior to playing the PGG alone again (continuing influence) displayed more continuing prosocial behavior (marginal effect). The discussion focuses on the role of psychophysiology in understanding adolescents’ susceptibility to peer influence.

Summary

This study looked at how teens' bodies react when they're around their friends and how that affects their behavior. It used a game where teens earned money by either keeping it or sharing it with others. Sometimes, they were watched by "friends" online, sometimes the friends gave them thumbs up to encourage sharing or keeping, and sometimes they played alone after having friends online. The study measured their heart rate and another body signal to see how their bodies reacted. The results showed that how their bodies responded was linked to whether they shared or kept their money, depending on if friends were watching or encouraging them.

Peer Influence

Teens affect each other's actions – both good and bad. Friends might encourage lying, stealing, or cheating (bad), but also helping, sharing, or working together (good). They can also push each other to do risky things like trying drugs. Even just being around friends can change how a teen acts, whether or not the friends are telling them what to do. This effect can last even after the friends are gone.

Susceptibility to Peer Influence

Teens are really influenced by what their friends think. They often do risky things with friends that they wouldn't do alone. Younger teens are usually more easily influenced than older teens. A teen's brain is still developing, so they might choose instant fun over thinking about the long-term consequences, especially if their friends are around. Strong feelings or trouble controlling emotions can also make it easier to follow the crowd.

Psychophysiology and Susceptibility to Peer Influence

The study measured teens' heart rate and another body signal that shows how their body is reacting. Changes in heart rate can show excitement or stress. The other signal is linked to how much teens want rewards. These body signals showed a link to how teens acted in the game depending on whether they were alone, watched, or encouraged by friends.

The Current Study

This study examined how teens' heart rate and another body signal predicted how they reacted to friends' influence. It had many strengths: it looked at how teens responded when friends were watching, encouraging, and even after they were gone; it studied both good and bad behaviors; and it measured two different body signals. It also measured these body signals at the exact same time as the teens' actions in the game. The study also took into account how well teens could control their feelings and their usual body signals.

Method

One hundred forty-four teens played a computer game where they could keep or share money. While playing, the researchers measured their heart rate and another body signal to see how their bodies reacted. The teens also answered questions about how well they controlled their emotions.

Results

Teens shared money more when being watched by friends than when alone. When friends encouraged sharing, they shared more; and when friends encouraged keeping, they shared less. This continued even after the “friends” were no longer in the game. How their heart rate changed when being watched by "friends" was linked to how much they shared. The other body signal showed a link to sharing or not sharing, depending on whether friends were encouraging bad behavior or not, and whether they were still around or not.

Highlights