Yang Yuanhao, Zhao Huiying, Heath Andrew C, Madden Pamela A F, Martin Nicholas G, Nyholt Dale R
Statistical and Genomic Epidemiology Laboratory,Institute of Health and Biomedical Innovation,Queensland University of Technology,Brisbane,Queensland,Australia.
Department of Psychiatry,Washington University School of Medicine,St. Louis,MO,USA.
Twin Res Hum Genet. 2016 Aug;19(4):341-50. doi: 10.1017/thg.2016.46. Epub 2016 Jun 15.
Migraine frequently co-occurs with depression. Using a large sample of Australian twin pairs, we aimed to characterize the extent to which shared genetic factors underlie these two disorders. Migraine was classified using three diagnostic measures, including self-reported migraine, the ID migraine™ screening tool, or migraine without aura (MO) and migraine with aura (MA) based on International Headache Society (IHS) diagnostic criteria. Major depressive disorder (MDD) and minor depressive disorder (MiDD) were classified using the Diagnostic and Statistical Manual of Mental Disorders (DSM) criteria. Univariate and bivariate twin models, with and without sex-limitation, were constructed to estimate the univariate and bivariate variance components and genetic correlation for migraine and depression. The univariate heritability of broad migraine (self-reported, ID migraine, or IHS MO/MA) and broad depression (MiDD or MDD) was estimated at 56% (95% confidence interval [CI]: 53-60%) and 42% (95% CI: 37-46%), respectively. A significant additive genetic correlation (r G = 0.36, 95% CI: 0.29-0.43) and bivariate heritability (h 2 = 5.5%, 95% CI: 3.6-7.8%) was observed between broad migraine and depression using the bivariate Cholesky model. Notably, both the bivariate h 2 (13.3%, 95% CI: 7.0-24.5%) and r G (0.51, 95% CI: 0.37-0.69) estimates significantly increased when analyzing the more narrow clinically accepted diagnoses of IHS MO/MA and MDD. Our results indicate that for both broad and narrow definitions, the observed comorbidity between migraine and depression can be explained almost entirely by shared underlying genetically determined disease mechanisms.
偏头痛常与抑郁症同时出现。我们以大量澳大利亚双胞胎对为样本,旨在确定这两种疾病在多大程度上由共同的遗传因素所致。偏头痛通过三种诊断方法进行分类,包括自我报告的偏头痛、ID偏头痛™筛查工具,或根据国际头痛协会(IHS)诊断标准划分的无先兆偏头痛(MO)和有先兆偏头痛(MA)。重度抑郁症(MDD)和轻度抑郁症(MiDD)根据《精神疾病诊断与统计手册》(DSM)标准进行分类。构建了有或无性别限制的单变量和双变量双胞胎模型,以估计偏头痛和抑郁症的单变量和双变量方差成分以及遗传相关性。宽泛型偏头痛(自我报告、ID偏头痛或IHS MO/MA)和宽泛型抑郁症(MiDD或MDD)的单变量遗传率分别估计为56%(95%置信区间[CI]:53 - 60%)和42%(95% CI:37 - 46%)。使用双变量Cholesky模型观察到宽泛型偏头痛和抑郁症之间存在显著的加性遗传相关性(rG = 0.36,95% CI:0.29 - 0.43)和双变量遗传率(h2 = 5.5%,95% CI:3.6 - 7.8%)。值得注意的是,在分析IHS MO/MA和MDD这一更狭义的临床公认诊断时,双变量h2(13.3%,95% CI:7.0 - 24.5%)和rG(0.51,95% CI:0.37 - 0.69)的估计值均显著增加。我们的结果表明,无论对于宽泛定义还是狭义定义,偏头痛和抑郁症之间观察到的共病现象几乎完全可以由共同的潜在遗传决定的疾病机制来解释。