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Review
. 2016 Jan;41(1):142-62.
doi: 10.1038/npp.2015.294. Epub 2015 Sep 22.

Differential Susceptibility of the Developing Brain to Contextual Adversity and Stress

Affiliations
Review

Differential Susceptibility of the Developing Brain to Contextual Adversity and Stress

W Thomas Boyce. Neuropsychopharmacology. 2016 Jan.

Abstract

A swiftly growing volume of literature, comprising both human and animal studies and employing both observational and experimental designs, has documented striking individual differences in neurobiological sensitivities to environmental circumstances within subgroups of study samples. This differential susceptibility to social and physical environments operates bidirectionally, in both adverse and beneficial contexts, and results in a minority subpopulation with remarkably poor or unusually positive trajectories of health and development, contingent upon the character of environmental conditions. Differences in contextual susceptibility appear to emerge in early development, as the interactive and adaptive product of genetic and environmental attributes. This paper surveys what is currently known of the mechanisms or mediators of differential susceptibility, at the levels of temperament and behavior, physiological systems, brain circuitry and neuronal function, and genetic and epigenetic variation. It concludes with the assertion that differential susceptibility is inherently grounded within processes of biological moderation, the complexities of which are at present only partially understood.

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Figures

Figure 1
Figure 1
An ‘archeology' of mechanisms for differential susceptibility to social conditions.
Figure 2
Figure 2
Receptive vocabulary scores by socioeconomic status in the National Longitudinal Study of Children and Youth (Willms, 2002).
Figure 3
Figure 3
Cumulative results from studies of adversity × reactivity interactions predicting developmental and health outcomes. The figure is a stylized representation of the general form of interaction effects found in multiple studies over 20 years of research.
Figure 4
Figure 4
Observed parental support × sympathetic reactivity interactions predicting timing and tempo of pubertal development (Ellis et al, 2011b).
Figure 5
Figure 5
Endotoxin load and CD14 genotype interactions predicting probability of atopic sensitization (from Guerra and Martinez, 2008).
Figure 6
Figure 6
A differential susceptibility model: early environments (E1) and individual genetic variation (G) shape DS in an early conditional adaptation; later environments (E2) and biological susceptibility (DS) determine developmental and health outcomes (O) in biology × context interactions. Such interactions and their triadic linkages to intermediate- and longer-term outcomes are thus arguably both the originating source and the functional mechanism of DS.

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