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The Challenge of Social Genomics: A Commentary on “Social Genomics and the Life Course: Opportunities and Challenges for Multilevel Population Research”

Jason Schnittker

The preceding chapter by Michael J. Shanahan provides an excellent review of social genomics as it relates to health. In my comments, I would like to entertain the challenges embedded in the perspective. The chapter is comprehensive and forward-looking, but the implications of social genomics for research on socioeconomic status (SES) and health are mixed. On the one hand, the chapter is, in many respects, aspirational, with Shanahan outlining three stages for moving the debate forward from where the field is now. The positive tone is entirely appropriate given the very high upside of social genomics: In principle, social genomics will circumvent the silos created by disciplines, encourage a robust multilevel approach, and allow population scientists to explain health-related phenomena rather than merely describe them. No less important is the possibility of new discoveries, which the framework has, in my opinion, already delivered on (including in Shanahan’s excellent empirical work). On the other hand, despite expanding on several fronts simultaneously, social genomics as Shanahan articulates it does not put the influences it catalogues on the same conceptual plane. The chapter is more detailed, specific, and directive with respect to the genomic aspects of social genomics than with the social aspects. Furthermore, as a matter of emphasis, some influences are elevated above others. Some of the topics Shanahan encourages more research on can (and should) be explored fruitfully without considering genetic transcription, inflammatory processes, or other aspects of social genomics. It is worth thinking seriously about what direction aging research will move should it fully embrace a social genomic agenda.



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13 The Challenge of Social Genomics: A Commentary on “Social Genomics and the Life Course: Opportunities and Challenges for Multilevel Population Research” Jason Schnittker The preceding chapter by Michael J. Shanahan provides an excellent review of social genomics as it relates to health. In my comments, I would like to entertain the challenges embedded in the perspective. The chapter is comprehensive and forward-looking, but the implications of social genom- ics for research on socioeconomic status (SES) and health are mixed. On the one hand, the chapter is, in many respects, aspirational, with Shanahan outlining three stages for moving the debate forward from where the field is now. The positive tone is entirely appropriate given the very high upside of social genomics: In principle, social genomics will circumvent the silos created by disciplines, encourage a robust multilevel approach, and al- low population scientists to explain health-related phenomena rather than merely describe them. No less important is the possibility of new discover- ies, which the framework has, in my opinion, already delivered on (includ- ing in Shanahan’s excellent empirical work). On the other hand, despite expanding on several fronts simultaneously, social genomics as Shanahan articulates it does not put the influences it catalogues on the same concep- tual plane. The chapter is more detailed, specific, and directive with respect to the genomic aspects of social genomics than with the social aspects. Furthermore, as a matter of emphasis, some influences are elevated above others. Some of the topics Shanahan encourages more research on can (and should) be explored fruitfully without considering genetic transcription, inflammatory processes, or other aspects of social genomics. It is worth thinking seriously about what direction aging research will move should it fully embrace a social genomic agenda. 277

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278 NEW DIRECTIONS IN THE SOCIOLOGY OF AGING In Shanahan’s chapter, the appeal of social genomics is cast in terms of identifying mechanisms and strengthening causal effects, which, early in his chapter, Shanahan describes as the “major payoff” for population research. He emphasizes the potential evolution of the literature in noting that after transcriptional activity is established, scientists can begin to understand how social experiences affect health. These ideas have a great deal of reso- nance as long as social scientists are unable to identify how social factors get under the skin, as the argument goes. Strong claims regarding causality cannot be made, especially in the context of nonexperimental data (Taylor, Repetti, and Seeman, 1997). Causality is also crucial for prevention and intervention, as Shanahan notes in the conclusion of his chapter. There is a distinction between identifying effects and providing ex- planations. There can be a strong sense of the former without the latter, regardless of the level of a putative effect. Effective intervention can occur before an understanding of what connects an actionable “lever” with an outcome. There are many examples of such levers, and they are arrayed across multiple levels of analysis. Doctors used aspirin, for example, long before they understood how it worked, and, of course, the effects of aspirin were no less real when they were poorly conceptualized. (Digitalis provides another example.) The same logic applies to causes further upstream. Social scientists recognize that SES, the focus of Shanahan’s chapter, has causal effects on health even without being able to explain all of those effects in their entirety. To be sure, the absence of a chained mechanistic explanation might be unsatisfying from some perspectives. Furthermore, the fact that intervention can take place with incomplete knowledge does not mean researchers should not try to find mechanisms—they can and should seek mechanisms. Yet there are risks to demanding a full account that proceeds from the macro to the micro or to thinking that social effects are weak or superficial in absence of a complete biological explanation. For one, the provisionality Shanahan identifies with respect to causal inference in the social sciences applies as much to biological processes as social ones, resulting in uncertainty at all levels. Shanahan points to the widespread use of nonexperimental survey data in population research, but nonexperimental data are used in social genomics as well and there, too, this usage has serious implications. The observational methods employed for studying gene-environment interactions, for example, are often con- taminated by gene-gene interactions, undermining confidence regarding the main effects of genes (Conley and Rauscher, 2010). Furthermore, at least in the social sciences, methods suitable for disambiguating correlation and causation (e.g., the use of compulsory education laws to identify the effects of education on mortality) are often ill suited for illuminating mechanisms. More generally, the goals of social scientific explanation can diverge in meaningful ways from those of biological explanation. Along these lines,

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THE CHALLENGE OF SOCIAL GENOMICS 279 Shanahan notes that social genomic research demonstrates the relevance of SES for gene transcription, but a full explanation of the relationship between SES and health requires rigorous explanation both up and down the line. As Shanahan notes, this research reveals little regarding what it is about SES that matters, often relying on single indicators. The same is true at other junctures in the chain of connections between SES and health. Chronic stress and the activation of the sympathetic nervous system pro- vides one potential mechanism linking SES to transcription processes and ultimately to health (as established in the case of HIV-1). However, appeal- ing to stress merely invites further speculation regarding why and how SES is related to chronic stress. This issue is further complicated by the apparent resilience of those of low SES. Shanahan notes this, but scholars understand very little about the topic and, on its own, it is worthy of focused atten- tion. Some of these gaps and complications likely explain why interactions between genes and features of SES otherwise united in their relationship to “resources” are occasionally inconsistent even in their direction (e.g., Pescosolido et al., 2008). In short, there is much to be done simply in terms of characterizing the environment. Shanahan is sensitive to these issues and concludes his chapter by dis- cussing several topics for future research, including how possibly to refine measures of social risk factors, the specificity of causes and effects, and the value of comparative studies. It is notable, however, that these discussions become increasingly speculative, and Shanahan has fewer empirical ex- amples the further he moves away from influences that lie beneath the skin. The point is not that these influences are less relevant. As Shanahan argues, research should explore, for example, the effects of the welfare state, the network of correlations among stressors, and self-regulation processes. Yet studying how these influences are related to health does not require the collection of gene expression data, biomarkers, or neuroimaging, and it is not necessary to wait until such data are produced to investigate them further. These influences also probably implicate far more than stress or other biological processes that inform much of the transcription research. Understanding the role of the political economy in health, for example, will require more than an understanding of transcription. Indeed, insisting on collecting transcription-relevant data as a matter of emphasis may, in some instances, lead investigations astray. One risk in demanding a biological mechanism lies in prematurely foreclosing on a generative sense of uncertainty, especially when mediating pathways are dynamic. Shanahan provides some illustrative specific examples of media- tion. For instance, he reviews how SES may be linked to HIV-1 progres- sion through activation of the sympathetic nervous system and, in turn, HIV’s transcription and replication. Yet, in general, SES is linked to health through a variety of proximate mechanisms that change over time and,

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280 NEW DIRECTIONS IN THE SOCIOLOGY OF AGING therefore, the link will involve different biological pathways at different times. The relationship between SES and cholesterol, for instance, switched direction with the introduction of statins (Chang and Lauderdale, 2009). In this case, the identification of a mediating mechanism does not settle the debate regarding causality any more than the use of statins ensures the elimination of the association between SES and heart disease. Provisionality, in this sense, is part of the effect itself, not a reflection of scientific naiveté. A related complication concerns the scope of social genomics as it applies to the literature on SES and health. The perspective Shanahan ar- ticulates is capacious, implicating multilevel processes in an integrated life course framework. But when it comes to the specific results of the studies he reviews, much of it is quite focused. For example, Shanahan focuses much of his attention on gene-environment interactions—how do social factors affect gene transcription—which he identifies as the core agenda of social genomics. This work has immediate appeal to social scientists (e.g., Caspi et al., 2003). Among other things, studies of this sort move the literature away from simply gene or environment questions to gene and environment questions. Yet focusing on interactions can constrain the scientific imagi- nation nearly as much as focusing on main effects. It also leaves scientists ill prepared to take the null hypothesis (no interaction) seriously, which is increasingly required given the state of the gene-environment literature. The literature also suffers from well-known replication problems, with interac- tions significant in one study often insignificant in another (e.g., Risch et al., 2009). Shanahan ultimately emphasizes the relatively robust patterns found in research on transcription processes and, in turn, inflammatory processes. But if this is the area with the most scientific confidence, then the relevance of social genomics for SES and health is suddenly smaller than it once seemed. The set of disease outcomes related to SES exceeds the set related to the inflammatory response. If stress has a prominent transcriptional fingerprint, as Shanahan notes, SES has an enormous mortality footprint. Lest researchers disregard genes or environments altogether, motivating in- teraction effects should perhaps take a back-seat to motivating main effects. Surely genes are worth exploring even if social processes have little bearing on how they are expressed, just as social processes are worth exploring even if they sometimes operate independently of genetic transcription or inflammation. Beyond these concerns are some risks to organizing a debate according to the concept of levels, at least as the idea is usually articulated. In any multilevel investigation, some levels emerge as more important than others, even if the goal is to shed light on many different influences. Furthermore, the idea of a level implies a boundary, and, despite the ecumenical nature of social genomics, some of these boundaries are becoming sharper, not softer.

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THE CHALLENGE OF SOCIAL GENOMICS 281 It is possible to be sensitive to all the relevant influences, without attempt- ing to reduce an outcome to a narrow set of risk factors. A notable feature of the current multilevel approach, for example, is a split between those moving toward higher levels of analysis, such as those interested in differ- ent policy settings and political economies, and those moving toward more micro-level processing, such as biomarkers, neurons, and genes. Shanahan encourages movement in both directions and effectively reviews both arms of the literature. Yet it is important to be mindful of the vast meso-level in between. This may be where much of the action is, and, indeed, much of the research Shanahan reviews would seem to push in a meso direction. Shanahan highlights, for example, the role of a sense of threat or height- ened vigilance in mediating the link between social stress and transcription profiles. He further highlights, by way of review, the role of changes in corticolimbic circuitry in linking stress to vigilance. In this way, he links SES to stress to neurons to cognition to health, consistent with his mediational focus. Psychological influences provide a crucial link in this chain, but it is useful to pause with every link and, thus, to dwell on the independent relevance of psychological influences, apart from any role they may play in explaining the relationship between SES and health. For one, heightened vigilance is not entirely a reflection of SES. Fur- thermore, important psychological influences can be measured in survey instruments without also collecting biological samples. (In Shanahan’s framework, the primary purpose of Stage Three is to collect biological and genetic data in more representative samples in order to confirm results from earlier stages.) It is important, for example, to study the relationship between social context and sense of threat whether or not the relation- ship reflects the corticolimbic system. A counterargument, articulated by Shanahan, is that social genomic research illuminates the importance of psychology and, therefore, that the study of genes is a useful tool for the discovery and refinement of social mechanisms. But if social genomics is fundamentally about illuminating mediational pathways, it would do just as well to remind social scientists that the mind is important as to remind them that genes are important, and the former can be considered without the latter. Indeed, the literature risks misplaced specificity by focusing on genetic transcription, and, in the process of further reduction over consecu- tive stages, risks overlooking other important influences. Regardless of the route that leads researchers to psychological influences, it is important to give them their full conceptual due, and a tight focus on transcription pro- cesses might prevent this. In the formidable sweep of Shanahan’s chapter, an emphasis on psy- chological factors might appear modest. It might even appear regressive. There is no mistaking the cutting-edge allure of genetic transcription and the inflammatory response. It is also impressive how many social scientists,

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282 NEW DIRECTIONS IN THE SOCIOLOGY OF AGING like Shanahan, have developed expertise in fields other than their own. Yet an appreciation of human psychology alone addresses many of the themes discussed in Shanahan’s chapter, including scientific integration, causality, contingency, and multilevel integration. Psychology is concerned with how the environment is internalized, and, in this sense, psychological factors are no less “under the skin” than genes. The scope of psychological influences is also appropriate to the task of explaining socioeconomic differences in health insofar as they are related to multiple health outcomes through many different pathways. Furthermore, the reluctance of some disciplines to integrate genomics is very closely related to the reluctance of the same disciplines to integrate psychology: In both cases, social scientists fear explaining behavior in terms of individual attributes rather than social structures, or in terms of disposi- tions rather than constraints. Yet the empirical foundation of psychology is strong, long-standing, and sophisticated in ways that are not dissimilar to the foundation of social genomics. Decades of research reveal that psycho- logical factors are crucial to behavior and intersect with the environment in interesting ways (Ross and Nisbett, 1991). Psychological factors motivate behavior and therefore can link environments to action. They are also cen- tral to how the social environment is created, construed, and remembered, and therefore can speak to person-environment interactions. The high de- gree of contingency within social genomics—an especially appealing aspect of the field—is echoed throughout contemporary personality psychology (Mischel, 2004). If population research wishes to traverse levels while progressing “inward” in some fashion, psychology provides an excellent avenue. And if the challenge of integration rests as much with psychology as genes, the challenge is no less great. References Caspi, A., Sugden, K., Moffitt, T.E., Taylor, A., Craig, I.W., Harrington, H., et al. (2003). Influence of life stress on depression: Moderation by a polymorphism in the 5-HTT gene. Science, 301, 386-389. Chang, V.W., and Lauderdale, D.S. (2009). Fundamental cause theory, technological innova- tion, and health disparities: The case of cholesterol in the era of statins. Journal of Health and Social Behavior, 50, 245-260. Conley, D., and Rauscher, E. (2010). Genetic Interactions with Prenatal Social Environment: Effects on Academic and Behavioral Outcomes. Cambridge, MA: National Bureau of Economic Research. Mischel, W. (2004). Toward an integrative science of the person. Annual Review of Psychol- ogy, 55, 1-22. Pescosolido, B.A., Perry, B.J., Long, J.S., Martin, J.K., Nurnberger, J.I.J., and Hesselbrock, V. (2008). Under the influence of genetics: How transdisciplinarity leads us to rethink social pathways to illness. American Journal of Sociology, 114, S171-S201.

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THE CHALLENGE OF SOCIAL GENOMICS 283 Risch, N., Herrell, R., Lehner, T., Liang, K.-Y., Eaves, L., Hoh, J., et al. (2009). Interaction between the serotonin transporter gene (5-HTTLPR), stressful life events, and risk of depression. Journal of the American Medical Association, 301, 2,462-2,471. Ross, L., and Nisbett, R.E. (1991). The Person and the Situation: Perspectives of Social Psy- chology. New York: McGraw-Hill. Taylor, S.E., Repetti, R.L., and Seeman, T. (1997). Health psychology: What is an unhealthy environment and how does it get under the skin? Annual Review of Psychology, 48(1), 411-447.