Associations of polygenic risks, depression, and obesity-related traits in Taiwan Biobank

被引:7
|
作者
Liao, Shu-Fen [1 ,2 ]
Su, Chun-Yun [3 ]
Su, Mei-Hsin [4 ]
Chen, Cheng-Yun [3 ]
Chen, Chia-Yen [5 ,6 ]
Lin, Yen-Feng [7 ]
Pan, Yi-Jiun [8 ]
Hsiao, Po-Chang [9 ]
Chen, Pei-Chun [3 ]
Huang, Yen-Tsung [10 ]
Wu, Chi-Shin [11 ]
Wang, Shi-Heng [3 ,4 ,12 ]
机构
[1] Taipei Med Univ, Wan Fang Hosp, Dept Med Res, Taipei, Taiwan
[2] Taipei Med Univ, Coll Publ Hlth, Sch Publ Hlth, Taipei, Taiwan
[3] China Med Univ, Coll Publ Hlth, Dept Publ Hlth, Taichung, Taiwan
[4] China Med Univ, Coll Publ Hlth, Dept Occupat Safety & Hlth, Taichung, Taiwan
[5] Biogen, Cambridge, MA USA
[6] Broad Inst MIT & Harvard, Stanley Ctr Psychiat Res, Cambridge, MA USA
[7] Natl Hlth Res Inst, Ctr Neuropsychiat Res, Miaoli, Taiwan
[8] China Med Univ, Coll Med, Sch Med, Taichung, Taiwan
[9] Natl Taiwan Univ, Coll Publ Hlth, Taipei, Taiwan
[10] Inst Stat Sci, Acad Sinica, Taipei, Taiwan
[11] Natl Hlth Res Inst, Natl Ctr Geriatr & Welf Res, Miaoli, Taiwan
[12] China Med Univ, Coll Publ Hlth, 100,Sec 1 Jingmao Rd, Taichung 100, Taiwan
关键词
Polygenic liability; Comorbidity; Shared genetic etiology; Genetic correlation; Depression; Obesity; BODY-MASS INDEX; GENETIC EPIDEMIOLOGY; MAJOR DEPRESSION; FTO GENE; STRATIFICATION; HEALTH;
D O I
10.1016/j.jad.2022.09.149
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: The comorbidity of obesity and major depressive disorder (MDD) may be attributable to a bidi-rectional relationship and shared genetic influence. We aimed to examine the polygenic associations between obesity and MDD and to characterize their corresponding impacts on the obesity mechanism.Methods: Genome-wide genotyping was available in 106,604 unrelated individuals from Taiwan Biobank. Polygenic risk score (PRS) for body mass index (BMI) and MDD was derived to evaluate their effects on obesity -related traits. Stratified analyses were performed for the modified effect of depression on the polygenic associations.Results: The MDD PRS was positively associated with waistline (beta in per SD increase in PRS = 0.12), hipline (beta = 0.08), waist-hip ratio (WHR) (beta = 0.05), body fat rate (beta = 0.08), BMI (beta = 0.05), overweight (OR = 1.02 for BMI >= 25), and obesity (OR = 1.05 for BMI >= 30). For the synergism between depression and BMI PRS, the presence of active depression symptoms defined by the PHQ-4 (p for interaction < 0.05 for waistline, WHR, and BMI) was more salient than lifetime MDD. Limitations: Limitations include recall bias for MDD due to a retrospective self-reporting questionnaire, a low response rate of the PHQ-4 for evaluating active psychological symptoms, and limited generalizability to non -Taiwanese ancestries.Conclusions: The shared genetic etiology of obesity and depression was demonstrated. The amplified effect of BMI polygenic effect on obesity for individuals with active depressive symptoms was also characterized. The study may be helpful for designing public health interventions to reduce the disease burden caused by obesity and depression.
引用
收藏
页码:397 / 403
页数:7
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