Associations between polygenic risk scores for cardiometabolic phenotypes and adolescent depression and body dissatisfaction

被引:1
作者
Ekberg, Krista M. [1 ]
Michelini, Giorgia [2 ]
Schneider, Kristin L. [1 ]
Docherty, Anna R. [3 ]
Shabalin, Andrey A. [3 ]
Perlman, Greg [4 ]
Kotov, Roman [4 ]
Klein, Daniel N. [5 ]
Waszczuk, Monika A. [1 ]
机构
[1] Rosalind Franklin Univ Med & Sci, Dept Psychol, N Chicago, IL 60064 USA
[2] Queen Mary Univ London, Dept Biol & Expt Psychol, London, England
[3] Univ Utah, Dept Psychiat, Salt Lake City, UT USA
[4] SUNY Stony Brook, Dept Psychiat, Stony Brook, NY USA
[5] SUNY Stony Brook, Dept Psychol, Stony Brook, NY USA
关键词
TYPE-2; DIABETES-MELLITUS; MASS INDEX; PHYSICAL-ACTIVITY; WEIGHT STATUS; SYMPTOMS; OBESITY; PREVALENCE; CHILDREN; YOUTH; CHILDHOOD;
D O I
10.1038/s41390-024-03323-z
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background: Adolescents with elevated body mass index (BMI) are at an increased risk for depression and body dissatisfaction. Type 2 diabetes (T2D) is an established risk factor for depression. However, shared genetic risk between cardiometabolic conditions and mental health outcomes remains understudied in youth. Methods: The current study examined associations between polygenic risk scores (PRS) for BMI and T2D, and symptoms of depression and body dissatisfaction, in a sample of 827 community adolescents (M-age = 13.63, SDage = 1.01; 76% girls). BMI, depressive symptoms, and body dissatisfaction were assessed using validated self-report questionnaires. Results: BMI-PRS was associated with phenotypic BMI (beta = 0.24, p < 0.001) and body dissatisfaction (beta = 0.17, p < 0.001), but not with depressive symptoms. The association between BMI-PRS and body dissatisfaction was significantly mediated by BMI (indirect effect = 0.10, CI [0.07-0.13]). T2D-PRS was not associated with depression or body dissatisfaction. Conclusions: The results suggest phenotypic BMI may largely explain the association between genetic risk for elevated BMI and body dissatisfaction in adolescents. Further research on age-specific genetic effects is needed, as summary statistics from adult discovery samples may have limited utility in youth.
引用
收藏
页码:1853 / 1860
页数:8
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