A common genetic factor underlies genetic risk for gynaecological and reproductive disorders and is correlated with risk to depression

被引:3
|
作者
Kiewa, Jacqueline [1 ,2 ,8 ]
Mortlock, Sally [2 ]
Meltzer-Brody, Samantha [3 ]
Middeldorp, Christel [1 ,4 ,5 ,6 ,7 ]
Wray, Naomi R. [2 ]
Byrne, Enda M. [1 ]
机构
[1] Univ Queensland, Child Hlth Res Ctr, Brisbane 4101, Australia
[2] Univ Queensland, Inst Mol Biosci, Brisbane 4072, Australia
[3] Univ N Carolina, Dept Psychiat, 2759, Chapel Hill, NC USA
[4] Childrens Hlth Queensland Hosp & Hlth Serv, Child & Youth Mental Hlth Serv, Brisbane, Australia
[5] Univ Amsterdam, Amsterdam Univ Med Ctr, Dept Child & Adolescent Psychiat & Psychol, Amsterdam, Netherlands
[6] Arkin Inst Mental Hlth, Dept Youth & Family, Dept Res, Amsterdam, Netherlands
[7] Acad Ctr Child & Adolescent Psychiat, Levvel, Amsterdam, Netherlands
[8] Univ Queensland, Inst Mol Bioscience, Carmody Rd, St Lucia, Qld 4051, Australia
基金
澳大利亚国家健康与医学研究理事会; 英国医学研究理事会;
关键词
ESTROGEN-RECEPTOR-ALPHA; DNA-DAMAGE; ENDOMETRIOSIS; ASSOCIATION; ADENOMYOSIS; MUTATIONS; VARIANTS; INSIGHTS; UPDATE; P53;
D O I
10.1159/000533413
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IntroductionSex steroid hormone fluctuations may underlie both reproductive disorders and sex difference in lifetime depression prevalence. Previous studies report high comorbidity among reproductive disorders and between reproductive disorders and depression. This study sought to assess the multivariate genetic architecture of reproductive disorders and their loading onto a common genetic factor, and investigated whether this latent factor shares a common genetic architecture with female depression, including perinatal depression (PND).MethodUsing UK Biobank and FinnGen data, genome-wide association meta-analyses were conducted for nine reproductive disorders, and genetic correlation between disorders estimated. Genomic Structural Equation Modelling identified a latent genetic factor underlying disorders, accounting for their significant genetic correlations. SNPs significantly associated with both latent factor and depression were identified. ResultsExcellent model fit existed between a latent factor underlying five reproductive disorders (2 (5)=6.4; AIC=26.4; CFI=1.00; SRMR=0.03) with high standardised loadings for menorrhagia (0.96, SE=0.05); ovarian cysts (0.94, SE=0.05); endometriosis (0.83, SE=0.05); menopausal symptoms (0.77, SE=0.10); and uterine fibroids (0.65, SE=0.05). This latent factor was genetically correlated with perinatal depression (PND) (rG = 0.37, SE=0.15, P=1.4e-03), depression in females only (rG=0.48, SE=0.06, P=7.2e-11) and depression in both males and females (MD) (rG=0.35, SE=0.03, P=1.8e-30), with its top locus associated with FSHB/ARL14EP (rs11031006; P=9.1e-33). SNPs intronic to ESR1, significantly associated with the latent factor, were also associated with PND, female depression, and MD. Discussion/ConclusionA common genetic factor, correlated with depression, underlies risk to reproductive disorders, with implications for etiology and treatment. Genetic variation in ESR1 is associated with reproductive disorders and depression, highlighting the importance of estrogen signalling to both reproductive and mental health.
引用
收藏
页码:1059 / 1075
页数:17
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