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Genetic Predisposition for Negative Affect Predicts Mental Health Burden During the COVID-19 Pandemic

Overview
Specialties Neurology
Psychiatry
Date 2024 Apr 8
PMID 38587666
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Abstract

The coronavirus disease 2019 (COVID-19) pandemic was accompanied by an increase in mental health challenges including depression, stress, loneliness, and anxiety. Common genetic variants can contribute to the risk for psychiatric disorders and may present a risk factor in times of crises. However, it is unclear to what extent polygenic risk played a role in the mental health response to the COVID-19 pandemic. In this study, we investigate whether polygenic scores (PGSs) for mental health-related traits can distinguish between four resilience-vulnerability trajectories identified during the COVID-19 pandemic and associated lockdowns in 2020/21. We used multinomial regression in a genotyped subsample (n = 1316) of the CovSocial project. The most resilient trajectory characterized by the lowest mental health burden and the highest recovery rates served as the reference group. Compared to this most resilient trajectory, a higher value on the PGS for the well-being spectrum decreased the odds for individuals to be in one of the more vulnerable trajectories (adjusted R-square = 0.3%). Conversely, a higher value on the PGS for neuroticism increased the odds for individuals to be in one of the more vulnerable trajectories (adjusted R-square = 0.2%). Latent change in mental health burden extracted from the resilience-vulnerability trajectories was not associated with any PGS. Although our findings support an influence of PGS on mental health during COVID-19, the small added explained variance suggests limited utility of such genetic markers for the identification of vulnerable individuals in the general population.

References
1.
Abdellaoui A, Verweij K . Dissecting polygenic signals from genome-wide association studies on human behaviour. Nat Hum Behav. 2021; 5(6):686-694. DOI: 10.1038/s41562-021-01110-y. View

2.
Iob E, Ajnakina O, Steptoe A . The interactive association of adverse childhood experiences and polygenic susceptibility with depressive symptoms and chronic inflammation in older adults: a prospective cohort study. Psychol Med. 2023; 53(4):1426-1436. DOI: 10.1017/S0033291721003007. View

3.
Musliner K, Andersen K, Agerbo E, Albinana C, Vilhjalmsson B, Rajagopal V . Polygenic liability, stressful life events and risk for secondary-treated depression in early life: a nationwide register-based case-cohort study. Psychol Med. 2021; 53(1):217-226. DOI: 10.1017/S0033291721001410. View

4.
Nievergelt C, Maihofer A, Klengel T, Atkinson E, Chen C, Choi K . International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci. Nat Commun. 2019; 10(1):4558. PMC: 6783435. DOI: 10.1038/s41467-019-12576-w. View

5.
Lewis C, Vassos E . Polygenic risk scores: from research tools to clinical instruments. Genome Med. 2020; 12(1):44. PMC: 7236300. DOI: 10.1186/s13073-020-00742-5. View