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Serotonergic multilocus genetic variation moderates the association between interpersonal relationship and adolescent depressive symptoms.
Zeng, Zihao; Peng, Liyi; Liu, Shuangjin; Yang, Qin; Wang, Hongcai; He, Zhen; Hu, Yiqiu.
Afiliación
  • Zeng Z; School of Educational Science, Hunan Normal University, Changsha 410081, China; Department of Clinical Psychology, Vrije Universiteit Amsterdam, Van der Boechorststraat 7, 1081 BT Amsterdam, the Netherlands.
  • Peng L; School of Educational Science, Hunan Normal University, Changsha 410081, China.
  • Liu S; School of Educational Science, Hunan Normal University, Changsha 410081, China.
  • Yang Q; School of Educational Science, Hunan Normal University, Changsha 410081, China.
  • Wang H; School of Educational Science, Hunan Normal University, Changsha 410081, China.
  • He Z; School of Educational Science, Hunan Normal University, Changsha 410081, China.
  • Hu Y; School of Educational Science, Hunan Normal University, Changsha 410081, China; Research Center for Mental Health Education of Hunan Province, Changsha 410100, China; Cognition and Human Behavior Key Laboratory of Hunan Province, Changsha 410081, China; Center for Mind-Brain Science, Hunan Normal Un
J Affect Disord ; 340: 616-625, 2023 11 01.
Article en En | MEDLINE | ID: mdl-37597782
ABSTRACT

BACKGROUND:

Research suggests that genetic variants linked to serotonin functioning moderate the association between environmental stressors and depressive symptoms, but examining gene-environment interactions with single polymorphisms limits power.

METHODS:

A multilocus genetic profile score (MGPS) approach to measuring serotonergic multilocus genetic variation and examined interactions with interpersonal relationship, insomnia with depressive symptoms as outcomes in an adolescent sample (average age = 14.15 ± 0.63 years since first measurement; range 13 to 15).

RESULTS:

(1) interpersonal relationship predicted adolescent depressive symptoms; (2) insomnia mediated the effect of interpersonal relationships on adolescent depressive symptoms; (3) the THP2 gene rs4570625 polymorphism G allele was a key risk factor for depressive symptom, and the MGPS moderated the effects of teacher-student relationship and insomnia on adolescent depressive symptom. Specifically, as the MGPS increased, the effects of insomnia on adolescent depressive symptom were enhanced; further, when the MGPS score increased, the effect of teacher-student relationship on depression showed a similar phenomenon with an increased slope and enhanced prediction; and (4) the results of sensitivity analysis showed that multilocus genetic interaction with the environment had a better explanatory power and stability for depression than single polymorphism studies.

CONCLUSION:

MGPS provides substantial power to examine gene-environmental interactions linked to affective outcomes among adolescents.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Depresión / Trastornos del Inicio y del Mantenimiento del Sueño Tipo de estudio: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Humans Idioma: En Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Depresión / Trastornos del Inicio y del Mantenimiento del Sueño Tipo de estudio: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Humans Idioma: En Año: 2023 Tipo del documento: Article