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Affective wellbeing moderates the association between polygenic risk score for neuroticism and change in neuroticism

INTRODUCTION: Neuroticism has societal, mental and physical health relevance, with an etiology involving genetic predisposition, psychological influence, and their interaction. OBJECTIVES: To understand whether the association between polygenic risk score for neuroticism (PRS-N) and neuroticism is m...

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Detalles Bibliográficos
Autores principales: Bahbouhová, J., Cade, M. V., De Sadeleer, A. T., Dibbets, C., Herrmann, L.-Q., Hovens, P. O. F., Jakson, B. M., Reising, R. C., Menne-Lothmann, C., Decoster, J., van Winkel, R., Collip, D., Delespaul, P., De Hert, M., Derom, C., Thiery, E., Jacobs, N., Wichers, M., van Os, J., Rutten, B. P. F., Gülöksüz, S., Klingenberg, B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10596326/
http://dx.doi.org/10.1192/j.eurpsy.2023.422
Descripción
Sumario:INTRODUCTION: Neuroticism has societal, mental and physical health relevance, with an etiology involving genetic predisposition, psychological influence, and their interaction. OBJECTIVES: To understand whether the association between polygenic risk score for neuroticism (PRS-N) and neuroticism is moderated by affective well-being. METHODS: Data were derived from TwinssCan, a general population twin cohort (age range=15-35 years, 478 monozygotic twins). Self-report questionnaires were used to measure well-being and neuroticism. PRS-N was trained from the Genetics of Personality Consortium (GPC) and United Kingdom Biobank (UKB). Multilevel mixed-effects models were used to test baseline and changes in well-being and neuroticism. RESULTS: Baseline wellbeing and neuroticism were associated (β=-1.35, p<0.001). PRSs-N were associated with baseline neuroticism (lowest p-value: 0.008 in GPC, 0.01 in UKB). In interaction models (PRS x wellbeing), GPC PRS-N (β=0.38, p=0.04) and UKB PRS-N (β=0.81, p<0.001) had significant interactions. PRSs-N were associated with changes in neuroticism (lowest p-value: 0.03 in GPC, 0.3 in UKB). Furthermore, changes in wellbeing and neuroticism were associated (β =-0.66, p<0.001). In interaction models (PRS x change in wellbeing), only UKB PRS-N had a significant interaction (β=0.80, p<0.001). CONCLUSIONS: Interaction between polygenic risk, wellbeing and neuroticism, were observed regarding baselines measures and change over time. Depending on the analysis step, the direction of the effect changed. DISCLOSURE OF INTEREST: None Declared