Kendler Kenneth S, Ohlsson Henrik, Neale Michael, van Loo Hanna, Rosmalen Judith G M, Sundquist Jan, Sundquist Kristina
Virginia Institute for Psychiatric and Behavioral Genetics, Virginia Commonwealth University, Richmond, VA, USA.
Department of Psychiatry, Virginia Commonwealth University, RichmondVA, USA.
Psychol Med. 2025 Apr 28;55:e125. doi: 10.1017/S0033291725000923.
Functional Somatic Disorders (FSD) and Internalizing Psychiatric Disorders (IPD) are frequently comorbid and likely share familial/genetic risk factors.
We performed a Common Factor Multivariate Analysis of 2 FSDs, Fibromyalgia (FM) and Irritable Bowel Syndrome (IBS), and two IPDs, Major Depression (MD) and Anxiety Disorders (AD), in five kinds of Swedish female-female relative pairs: monozygotic (n = 8,052) dizygotic (n = 7216), full siblings (n = 712,762), half-siblings reared together (n = 23,623), and half-siblings reared apart (n = 53,873). Model fitting was by full information maximum likelihood using OpenMx.
The best-fit model included genetic, shared environmental, and unique environmental factors. The common factor, 50% heritable with a small shared environmental effect, loaded more strongly on the two IPDs (0.80) than the 2 FSDs (0.40). Disorder-specific genetic effects were larger for the 2 FSDs (0.30) than the 2 IPDs (0.03). Estimated genetic correlations were high for MD and AD (+0.91), moderate between IBS and IPDs (+0.62), and intermediate between FM and MD (+0.54), FM and AD (+0.28), and FM and IBS (+0.38). Shared environmental influences on all disorders were present but small.
In women, FSDs and IPDs shared a moderate proportion of their genetic risk factors, greater for IBS than for FM. However, the genetic sharing between IBS and FM was less than between MD and AD, suggesting that FSDs do not form a highly genetically coherent group of disorders. The shared environment made a modest contribution to the familial aggregation of FSDs and IPDs.
功能性躯体疾病(FSD)和内化性精神障碍(IPD)常合并存在,且可能共享家族/遗传风险因素。
我们对两种FSD(纤维肌痛症(FM)和肠易激综合征(IBS))以及两种IPD(重度抑郁症(MD)和焦虑症(AD))进行了共同因素多变量分析,研究对象为五种瑞典女性亲属对:同卵双胞胎(n = 8052)、异卵双胞胎(n = 7216)、全同胞姐妹(n = 712762)、共同抚养的半同胞姐妹(n = 23623)以及分开抚养的半同胞姐妹(n = 53873)。使用OpenMx通过全信息最大似然法进行模型拟合。
最佳拟合模型包括遗传因素、共享环境因素和独特环境因素。共同因素约50%可遗传,共享环境效应较小,在两种IPD(约0.80)上的负荷比两种FSD(0.40)更强。特定疾病的遗传效应在两种FSD(约0.30)上比两种IPD(约0.03)更大。MD和AD之间的估计遗传相关性较高(+0.91),IBS与IPD之间为中度(+0.62),FM与MD之间(+0.54)、FM与AD之间(+0.28)以及FM与IBS之间(+0.38)为中等程度。共享环境对所有疾病都有影响,但较小。
在女性中,FSD和IPD共享一定比例的遗传风险因素,IBS比FM更多。然而,IBS和FM之间的遗传共享低于MD和AD之间,这表明FSD并非高度遗传一致的疾病组。共享环境对FSD和IPD的家族聚集有适度贡献。