Neuroticism/Negative Emotionality Is Associated with Increased Reactivity to Uncertain Threat in the Bed Nucleus of the Stria Terminalis, Not the Amygdala

Author:

Grogans Shannon E.,Hur Juyoen,Barstead Matthew G.,Anderson Allegra S.,Islam Samiha,Kim Hyung Cho,Kuhn Manuel,Tillman Rachael M.,Fox Andrew S.ORCID,Smith Jason F.,DeYoung Kathryn A.,Shackman Alexander J.ORCID

Abstract

Neuroticism/negative emotionality (N/NE)—the tendency to experience anxiety, fear, and other negative emotions—is a fundamental dimension of temperament with profound consequences for health, wealth, and well-being. Elevated N/NE is associated with a panoply of adverse outcomes, from reduced socioeconomic attainment to psychiatric illness. Animal research suggests that N/NE reflects heightened reactivity to uncertain threat in the bed nucleus of the stria terminalis (BST) and central nucleus of the amygdala (Ce), but the relevance of these discoveries to humans has remained unclear. Here we used a novel combination of psychometric, psychophysiological, and neuroimaging approaches to test this hypothesis in an ethnoracially diverse, sex-balanced sample of 220 emerging adults selectively recruited to encompass a broad spectrum of N/NE. Cross-validated robust-regression analyses demonstrated that N/NE is preferentially associated with heightened BST activation during the uncertain anticipation of a genuinely distressing threat (aversive multimodal stimulation), whereas N/NE was unrelated to BST activation during certain-threat anticipation, Ce activation during either type of threat anticipation, or BST/Ce reactivity to threat-related faces. It is often assumed that different threat paradigms are interchangeable assays of individual differences in brain function, yet this has rarely been tested. Our results revealed negligible associations between BST/Ce reactivity to the anticipation of threat and the presentation of threat-related faces, indicating that the two tasks are nonfungible. These observations provide a framework for conceptualizing emotional traits and disorders; for guiding the design and interpretation of biobank and other neuroimaging studies of psychiatric risk, disease, and treatment; and for refining mechanistic research.

Funder

HHS | NIH | National Institute on Alcohol Abuse and Alcoholism

HHS | NIH | National Institute on Drug Abuse

HHS | NIH | National Institute of Mental Health

HHS | NIH | NIH Office of the Director

National Research Foundation of Korea

Yonsei Signature Research Cluster Program

UC | UCD | California National Primate Research Center

UC | UCD | UC Davis

University of Maryland

Publisher

Society for Neuroscience

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