The persuasion network is modulated by drug-use risk and predicts anti-drug message effectiveness

Richard Huskey, J Michael Mangus, Benjamin O Turner, René Weber, Richard Huskey, J Michael Mangus, Benjamin O Turner, René Weber

Abstract

While a persuasion network has been proposed, little is known about how network connections between brain regions contribute to attitude change. Two possible mechanisms have been advanced. One hypothesis predicts that attitude change results from increased connectivity between structures implicated in affective and executive processing in response to increases in argument strength. A second functional perspective suggests that highly arousing messages reduce connectivity between structures implicated in the encoding of sensory information, which disrupts message processing and thereby inhibits attitude change. However, persuasion is a multi-determined construct that results from both message features and audience characteristics. Therefore, persuasive messages should lead to specific functional connectivity patterns among a priori defined structures within the persuasion network. The present study exposed 28 subjects to anti-drug public service announcements where arousal, argument strength, and subject drug-use risk were systematically varied. Psychophysiological interaction analyses provide support for the affective-executive hypothesis but not for the encoding-disruption hypothesis. Secondary analyses show that video-level connectivity patterns among structures within the persuasion network predict audience responses in independent samples (one college-aged, one nationally representative). We propose that persuasion neuroscience research is best advanced by considering network-level effects while accounting for interactions between message features and target audience characteristics.

Keywords: elaboration likelihood model; fMRI; functional connectivity; persuasion; public service announcements.

© The Author (2017). Published by Oxford University Press.

Figures

Fig. 1.
Fig. 1.
Psychophysiological interaction results when seeding from the medial prefrontal cortex. The figure shows the AS x PHYS > Scrambled Control x PHYS contrast for (A) high-risk and (B) low-risk subjects. Results are cluster corrected for multiple comparisons with the cluster defining threshold set at Z = 2.3 and a cluster extent threshold of P  < 0.05. The red circle represents the seed ROI.
Fig. 2.
Fig. 2.
Psychophysiological interaction results when seeding from the middle frontal gyrus. The figure shows the AS x PHYS > Scrambled Control x PHYS contrast for (A) high-risk and (B) low-risk subjects. Results are cluster corrected for multiple comparisons with the cluster defining threshold set at Z = 2.3 and a cluster extent threshold of P <0.05. Note: No activations survived thresholding for high-risk subjects. The red circle represents the seed ROI.
Fig. 3.
Fig. 3.
Psychophysiological interaction results when seeding from the inferior lateral occipital cortex. The figure shows the MSV x PHYS > Scrambled Control x PHYS contrast for (A) high-risk and (B) low-risk subjects. Results are cluster corrected for multiple comparisons with the cluster defining threshold set at Z = 2.3 and a cluster extent threshold of P <0.05. The red circle represents the seed ROI.
Fig. 4.
Fig. 4.
Network-as-predictor results for high-risk subjects. A stepwise regression model was constructed where self-reported pMSV, pAS, and their interaction was entered in the first step and MFG-SPL connectivity parameter estimates (PEs) were entered in the second step. This analysis shows the unique contribution of self-report and network-connectivity PEs to overall prediction accuracy of perceived message effectiveness in two independent samples (IS1 and IS2). Results are not shown for the low-risk group as the inclusion of network-connectivity PEs did not significantly improve prediction accuracies.

References

    1. Abraham A., Pedregosa F., Eickenberg M., et al. (2014). Machine learning for neuroimaging with scikit-learn. Frontiers in Neuroinformatics, 8, 14.
    1. Bartra O., McGuire J.T., Kable J.W. (2013). The valuation system: a coordinate-based meta-analysis of BOLD fMRI experiments examining neural correlates of subjective value. NeuroImage, 76, 412–27.
    1. Bassett D.S., Gazzaniga M.S. (2011). Understanding complexity in the human brain. Trends in Cognitive Sciences, 15 (5),200–9.
    1. Bassett D.S., Sporns O. (2017). Network neuroscience. Nature Neuroscience, 20 (3), 353–64.
    1. Beckmann C.F., Smith S.M. (2004). Probabilistic independent component analysis for functional magnetic resonance imaging. IEEE Transactions on Medical Imaging, 23 (2), 137–52.
    1. Berkman E.T., Falk E.B. (2013). Beyond brain mapping: using neural measures to predict real-world outcomes. Current Directions in Psychological Science, 22(1), 45–50.
    1. Berkman E.T., Falk E.B., Lieberman M.D. (2011). In the trenches of real-world self-control: neural correlates of breaking the link between craving and smoking. Psychological Science, 22(4),498–506.
    1. Bigsby E., Cappella J.N., Seitz H.H. (2013). Efficiently and effectively evaluating public service announcements: additional evidence for the utility of perceived effectiveness. Communication Monographs, 80(1), 1–23.
    1. Botvinick M.M., Huffstetler S., McGuire J.T. (2009). Effort discounting in human nucleus accumbens. Cognitive, Affective, & Behavioral Neuroscience, 9(1), 16–27.
    1. Braver T.S., Krug M.K., Chiew K.S., et al. (2014). Mechanisms of motivation-cognition interaction: Challenges and opportunities. Cognitive, Affective & Behavioral Neuroscience, 14(2), 443–72.
    1. Bullmore E., Sporns O. (2012). The economy of brain network organization. Nature Reviews Neuroscience, 13(5), 336–49.
    1. Cappella J.N., Yzer M.C., Fishbein M. (2003). Using beliefs about positive and negative consequences as the basis for designing message interventions for lowering risky behavior In: Romer D. editors. Reducing Adolescent Risk: Toward an Integrated Approach, pp. 210–220. Thousand Oaks, CA: Sage Publications.
    1. Chua H.F., Liberzon I., Welsh R.C., Strecher V.J. (2009). Neural correlates of message tailoring and self-relatedness in smoking cessation programming. Biological Psychiatry, 65(2), 165–8.
    1. Cohen J., Cohen P., West S.G., Aiken L.S. (2003). Applied Multiple Regression/Correlation Analysis for the Behavioral Sciences, 3rd edn.Mahwah, NJ: Lawrence Erlbaum Associates.
    1. Cooper N., Bassett D.S., Falk E.B. (2017). Coherent activity between brain regions that code for value is linked to the malleability of human behavior. Scientific Reports, 7(43250), 4325..
    1. Dillard J.P., Shen L., Vail R.G. (2007a). Does perceived message effectiveness cause persuasion or vice versa? 17 consistent answers. Human Communication Research, 33(4), 467–88.
    1. Dillard J.P., Weber K.M., Vail R.G. (2007b). The relationship between the perceived and actual effectiveness of persuasive messages: a meta-analysis with implications for formative campaign research. Journal of Communication, 57(4), 613–31.
    1. Dinh-Williams L., Mendrek A., Dumais A., Bourque J., Potvin S. (2014). Executive-affective connectivity in smokers viewing anti-smoking images: an fMRI study. Psychiatry Research: Neuroimaging, 224(3), 262–8.
    1. Do K.T., Galván A. (2015). FDA cigarette warning labels lower craving and elicit frontoinsular activation in adolescent smokers. Social Cognitive and Affective Neuroscience 10 (11),1484–96.
    1. Do K.T., Galván A. (2016). Neural sensitivity to smoking stimuli is associated with cigarette craving in adolescent smokers. Journal of Adolescent Health, 58(2), 186–94.
    1. Falk E.B., Berkman E.T., Lieberman M.D. (2012). From neural responses to population behavior: neural focus group predicts population-level media effects. Psychological Science, 23(5), 439–45.
    1. Falk E.B., Berkman E.T., Mann T., Harrison B., Lieberman M.D. (2010). Predicting persuasion-induced behavior change from the brain. Journal of Neuroscience, 30(25), 8421–4.
    1. Falk E.B., Berkman E.T., Whalen D., Lieberman M.D. (2011). Neural activity during health messaging predicts reductions in smoking above and beyond self-report. Health Psychology, 30(2), 177–85.
    1. Falk E.B., Cascio C.N., Coronel J.C. (2015). Neural prediction of communication-relevant outcomes. Communication Methods and Measures, 9(1–2), 30–54.
    1. Falk E.B., O’Donnell M.B., Tompson S., et al. (2016). Functional brain imaging predicts public health campaign success. Social Cognitive and Affective Neuroscience, 11(2), 204–14.
    1. Falk E. B., Rameson L., Berkman E. T.. et al. (2009). The neural correlates of persuasion: A common network across cultures and media. Journal of Cognitive Neuroscience, 22(11), 2447–2459.
    1. Falk E.B., Rameson L., Berkman E.T., et al. (2010). The neural correlates of persuasion: a common network across cultures and media. Journal of Cognitive Neuroscience, 22(11), 2447–59.
    1. Falk E.B., Scholz C. (2018). Persuasion, influence and value: perspectives from communication and social neuroscience. Annual Review of Psychology, 69(1), doi: 10.1146/annurev-psych-122216-011821.
    1. Friston K.J. (1994). Functional and effective connectivity in neuroimaging: a synthesis. Human Brain Mapping, 2(1–2), 56–78.
    1. Friston K.J. (2011). Functional and effective connectivity: a review. Brain Connectivity, 1(1), 13–36.
    1. Friston K.J., Buechel C., Fink G.R., Morris J., Rolls E., Dolan R.J. (1997). Psychophysiological and modulatory interactions in neuroimaging. NeuroImage, 6(3), 218–29.
    1. Glasser M.F., Coalson T.S., Robinson E.C., et al. (2016). A multi-modal parcellation of human cerebral cortex. Nature, 7615(563), 171–8.
    1. Imhof M.A., Schmalzle R., Renner B., Schupp H.T. (2017). How real-life health messages engage our brains: shared processing of effective anti-alcohol videos. Social Cognitive and Affective Neuroscience, 12(7), 1188–96.
    1. Kang Y., Cappella J.N., Fishbein M. (2006). The attentional mechanism of message sensation value: interaction between message sensation value and argument quality on message effectiveness. Communication Monographs, 73(4), 351–78.
    1. Kaye S.-A., White M.J., Lewis I. (2016). The use of neurocognitive methods in assessing health communication messages: a systematic review. Journal of Health Psychology, 22(12), 1534–55.
    1. Kool W., McGuire J.T., Wang G.J., Botvinick M.M., Brosnan S.F. (2013). Neural and behavioral evidence for an intrinsic cost of self-control. PLoS ONE, 8(8), 72626.
    1. Lang A. (2006). Using the limited capacity model of motivated mediated message processing to design effective cancer communication messages. Journal of Communication, 56(1), S57–80.
    1. McLaren D.G., Ries M.L., Xu G., Johnson S.C. (2012). A generalized form of context-dependent psychophysiological interactions (gPPI): a comparison to standard approaches. NeuroImage, 61(4), 1277–86.
    1. Noar S.M., Benac C.N., Harris M.S. (2007). Does tailoring matter? Meta-analytic review of tailored print health behavior change interventions. Psychological Bulletin, 133(4), 673–93.
    1. O’Doherty J., Dayan P., Schultz J., Deichmann R., Friston K., Dolan R.J. (2004). Dissociable roles of ventral and dorsal striatum in instrumental conditioning. Science, 304(5669), 452–4.
    1. O’Reilly J.X., Woolrich M.W., Behrens T.E.J., Smith S.M., Johansen-Berg H. (2012). Tools of the trade: psychophysiological interactions and functional connectivity. Social Cognitive and Affective Neuroscience, 7(5), 604–9.
    1. Pegors T.K., Tompson S., O’Donnell M.B., Falk E.B. (2017). Predicting behavior change from persuasive messages using neural representational similarity and social network analyses. NeuroImage, 157, 118–28.
    1. Petersen S.E., Sporns O. (2015). Brain networks and cognitive architectures. Neuron, 88(1), 207–19.
    1. Petty R.E., Cacioppo J.T. (1986). The elaboration likelihood model of persuasion In: Berkowitz L., editor, Advances in Experimental Social Psychology (v19 ed., pp. 123–205). New York, NY: Academic Press.
    1. Poldrack R.A., Farah M.J. (2015). Progress and challenges in probing the human brain. Nature 526(7573), 371–9.
    1. Ramsay I.S., Yzer M.C., Luciana M., Vohs K.D., Macdonald A.W.I. (2013). Affective and executive network processing associated with persuasive antidrug messages. Journal of Cognitive Neuroscience, 25(7), 1136–47.
    1. Rogers E.M. (1994). A History of Communication Study: A Biographical Approach. New York, NY: The Free Press.
    1. Rubinov M., Sporns O. (2010). Complex network measures of brain connectivity: uses and interpretations. NeuroImage, 52(3), 1059–69.
    1. Seelig D., Wang A.-L., Jaganathan K., Loughead J.W., Blady S.J., Childress A.R., Romer D. (2014). Low message sensation health promotion videos are better remembered and activate areas of the brain associated with memory encoding. PLoS One, 9(11), e113256..
    1. Sizemore A.E., Bassett D.S. (inpress). Dynamic graph metrics: Tutorial, toolbox, and tale. NeuroImage, doi: 10.1016/j.neuroimage.2017.06.081.
    1. Slater M.D., Rouner D. (2002). Entertainment-education and elaboration likelihood: understanding the processing of narrative persuasion. Communication Theory, 12(2), 173–91.
    1. Tottenham N., Galván A. (2016). Stress and the adolescent brain: amygdala-prefrontal cortex circuitry and ventral striatum as developmental targets. Neuroscience and Biobehavioral Reviews, 70, 217–27.
    1. Vezich I.S., Falk E.B., Lieberman M.D. (2016). Persuasion neuroscience: new potential to test dual-process theories In: Harmon-Jones E., Inzlicht M., editors. Social Neuroscience: Biological Approaches to Social Psychology, 1st edn., pp. 34–58, New York, NY: Routledge.
    1. Vezich I.S., Katzman P.L., Ames D.L., Falk E.B., Lieberman M.D. (2016). Modulating the neural bases of persuasion: why/how, gain/loss, and users/non-users. Social Cognitive and Affective Neuroscience, 12(2), 283–97.
    1. Wang Z., Vang M., Lookadoo K., Tchernev J.M., Cooper C. (2014). Engaging high-sensation seekers: the dynamic interplay of sensation seeking, message visual-auditory complexity and arousing content. Journal of Communication, 5(1), 101–24.
    1. Weber R., Eden A., Huskey R., Mangus J.M., Falk E. (2015). Bridging media psychology and cognitive neuroscience: challenges and opportunities. Journal of Media Psychology, 27(3), 146–56.
    1. Weber R., Huskey R., Mangus J.M.. et al. (2014). Neural predictors of message effectiveness during counterarguing in anti-drug campaigns. Communication Monographs, 82(1), 4–30.
    1. Weber R., Huskey R., Mangus J.M., Westcott-Baker A., Turner B.O. (2015). Neural predictors of message effectiveness during counterarguing in anti-drug campaigns. Communication Monographs, 82(1), 4–30.
    1. Weber R., Mangus J.M., Huskey R. (2015). Brain imaging in communication research: a practical guide to understanding and evaluating fMRI studies. Communication Methods and Measures, 9(1-2), 5–29.
    1. Weber R., Westcott-Baker A., Anderson G.L. (2013). A multilevel analysis of antimarijuana public service announcement effectiveness. Communication Monographs, 80(3), 302–30.
    1. Wilson S.M., Molnar-Szakacs I., Iacoboni M. (2008). Beyond superior temporal cortex: intersubject correlations in narrative speech comprehension. Cerebral Cortex, 18(1), 230–42.
    1. Woolrich M.W., Behrens T.E.J., Beckmann C.F., Jenkinson M., Smith S.M. (2004). Multilevel linear modelling for FMRI group analysis using Bayesian inference. NeuroImage, 21(4), 1732–47.
    1. Worsley K.J. (2001). Statistical analysis of activation images In: Jezzard P., Matthews P.M., Smith S.M., editors. Functional Mri: An Introduction to Methods (pp. 251–270). Oxford, United Kingdom: Oxford University Press.
    1. Yarkoni T., Poldrack R.A., Nichols T.E., Van Essen D.C., Wager T.D. (2011). Large-scale automated synthesis of human functional neuroimaging data. Nature Methods, 8(8), 665–70.
    1. Yeshurun Y., Swanson S., Simony E., et al. (2017). Same story, different story: the neural representation of interpretive frameworks. Psychological Science, 28(3), 307–19.
    1. Zhao X., Strasser A., Cappella J.N., Lerman C., Fishbein M. (2011). A measure of perceived argument strength: reliability and validity. Communication Methods and Measures, 5(1), 48–75.

Source: PubMed

Подписаться