Genetic influences on the neural and physiological bases of acute threat: A research domain criteria (RDoC) perspective.

Am J Med Genet B Neuropsychiatr Genet
Authors
Keywords
Abstract

The NIMH Research Domain Criteria (RDoC) initiative aims to describe key dimensional constructs underlying mental function across multiple units of analysis-from genes to observable behaviors-in order to better understand psychopathology. The acute threat ("fear") construct of the RDoC Negative Valence System has been studied extensively from a translational perspective, and is highly pertinent to numerous psychiatric conditions, including anxiety and trauma-related disorders. We examined genetic contributions to the construct of acute threat at two units of analysis within the RDoC framework: (1) neural circuits and (2) physiology. Specifically, we focused on genetic influences on activation patterns of frontolimbic neural circuitry and on startle, skin conductance, and heart rate responses. Research on the heritability of activation in threat-related frontolimbic neural circuitry is lacking, but physiological indicators of acute threat have been found to be moderately heritable (35-50%). Genetic studies of the neural circuitry and physiology of acute threat have almost exclusively relied on the candidate gene method and, as in the broader psychiatric genetics literature, most findings have failed to replicate. The most robust support has been demonstrated for associations between variation in the serotonin transporter (SLC6A4) and catechol-O-methyltransferase (COMT) genes with threat-related neural activation and physiological responses. However, unbiased genome-wide approaches using very large samples are needed for gene discovery, and these can be accomplished with collaborative consortium-based research efforts, such as those of the Psychiatric Genomics Consortium (PGC) and Enhancing Neuro Imaging Genetics through Meta-Analysis (ENIGMA) Consortium.

Year of Publication
2016
Journal
Am J Med Genet B Neuropsychiatr Genet
Volume
171B
Issue
1
Pages
44-64
Date Published
2016 Jan
ISSN
1552-485X
URL
DOI
10.1002/ajmg.b.32384
PubMed ID
26377804
PubMed Central ID
PMC4715467
Links
Grant list
F32 MH102890 / MH / NIMH NIH HHS / United States
R21 MH098212 / MH / NIMH NIH HHS / United States