Child Health Research Centre, University of Queensland, Brisbane, Queensland, Australia.
Institute for Molecular Bioscience, University of Queensland, Brisbane, Queensland, Australia.
Neuroendocrinology. 2023;113(10):1059-1075. doi: 10.1159/000533413. Epub 2023 Aug 4.
Sex steroid hormone fluctuations may underlie both reproductive disorders and sex differences 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).
Using UK Biobank and FinnGen data, genome-wide association meta-analyses were conducted for nine reproductive disorders, and genetic correlation between disorders was 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.
Excellent model fit existed between a latent factor underlying five reproductive disorders (χ2 (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 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.
A common genetic factor, correlated with depression, underlies risk of reproductive disorders, with implications for aetiology and treatment. Genetic variation in ESR1 is associated with reproductive disorders and depression, highlighting the importance of oestrogen signalling for both reproductive and mental health.
性激素波动可能是生殖障碍和终生抑郁症患病率性别差异的基础。先前的研究报告称,生殖障碍与抑郁症之间以及生殖障碍之间存在高共病性。本研究旨在评估生殖障碍的多变量遗传结构及其在共同遗传因素上的负荷,并探讨该潜在因素是否与女性抑郁症(包括围产期抑郁症[PND])具有共同的遗传结构。
使用英国生物库和芬兰基因数据,对 9 种生殖障碍进行了全基因组关联荟萃分析,并估计了障碍之间的遗传相关性。基因组结构方程模型确定了潜在的遗传因素,该因素可解释障碍之间显著的遗传相关性。鉴定出与潜在因素和抑郁均显著相关的 SNP。
存在一个潜在因素,该因素可解释 5 种生殖障碍(χ2(5)= 6.4;AIC = 26.4;CFI = 1.00;SRMR = 0.03),具有很高的标准化负荷,其中月经过多(0.96,SE = 0.05);卵巢囊肿(0.94,SE = 0.05);子宫内膜异位症(0.83,SE = 0.05);绝经症状(0.77,SE = 0.10);和子宫肌瘤(0.65,SE = 0.05)。该潜在因素与 PND(rG = 0.37,SE = 0.15,p = 1.4e-03)、仅女性抑郁症(rG = 0.48,SE = 0.06,p = 7.2e-11)和男性和女性抑郁症(MD)(rG = 0.35,SE = 0.03,p = 1.8e-30)均具有遗传相关性,其主要基因座与 FSHB/ARL14EP(rs11031006;p = 9.1e-33)相关。与潜在因素显著相关的 ESR1 内含子中的 SNP 也与 PND、女性抑郁症和 MD 相关。
与抑郁相关的共同遗传因素是生殖障碍风险的基础,这对病因和治疗具有重要意义。ESR1 的遗传变异与生殖障碍和抑郁症相关,突出了雌激素信号在生殖和心理健康中的重要性。