Genetic associations with resilience to potentially traumatic events and vantage sensitivity to social support.

Candidate gene association study Differential susceptibility model Potentially traumatic events Resilience Social support

Journal

Archives of psychiatric nursing
ISSN: 1532-8228
Titre abrégé: Arch Psychiatr Nurs
Pays: United States
ID NLM: 8708534

Informations de publication

Date de publication:
10 2022
Historique:
received: 13 09 2021
revised: 30 05 2022
accepted: 03 07 2022
entrez: 5 9 2022
pubmed: 6 9 2022
medline: 9 9 2022
Statut: ppublish

Résumé

Stress responses and mental health outcomes greatly vary when individuals are exposed to potentially traumatic events (PTEs). The Differential Susceptibility Model (DSM) (Pluess, 2015) suggests individual differences in stress responses are influenced by gene-environment interactions, with genes conferring reactivity. While individuals can be resilient (or vulnerable) to PTEs, they can also have vantage sensitivity (or resistance) to social support. This study examined whether selected genotypes moderated the effect of PTEs and social support on mental health. This cross-sectional candidate gene study included 450 college students (M age = 20.4, 79.3 % women) who provided buccal cells for genotyping and completed measures of psychosocial variables. DNA was genotyped for 12 genetic variants. Hierarchical regression revealed that the Mental Health Inventory (MHI) was associated with the Trauma History Questionnaire (THQ), rs1800795 in IL-6, and THQ × rs1800795 [R Findings partially support the DSM that the G/G genotype of rs1800795 in IL-6 is associated with resilience to PTEs, and the Met/Met genotype of rs4680 in COMT is associated with vantage sensitivity to social support. Limitations include cross-sectional design, limited PTE measurement, small convenience sample, and noncorrection for multiple significance test. Clinicians need to view resilience holistically and understand resilience is associated with psychosocial and genetic factors.

Identifiants

pubmed: 36064238
pii: S0883-9417(22)00085-1
doi: 10.1016/j.apnu.2022.07.013
pii:
doi:

Substances chimiques

Interleukin-6 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

147-157

Informations de copyright

Copyright © 2022 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest None.

Auteurs

Kosuke Niitsu (K)

School of Nursing & Health Studies, University of Washington Bothell, Mailing Address: 17927 113th Ave NE, Bothell, WA 98011, USA. Electronic address: kniitsu@uw.edu.

Julia F Houfek (JF)

University of Nebraska Medical Center, Omaha, NE, USA.

Michael J Rice (MJ)

University of Colorado Anschutz Medical Campus, Aurora, CO, USA.

Scott F Stoltenberg (SF)

University of Nebraska-Lincoln, Lincoln, NE, USA.

Kevin Kupzyk (K)

University of Nebraska Medical Center, Omaha, NE, USA.

Cecilia Barron (C)

University of Nebraska Medical Center, Omaha, NE, USA.

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Classifications MeSH