Wojczynski Mary K, North Kari E, Pedersen Nancy L, Sullivan Patrick F
Department of Biostatistics, Section on Statistical Genetics, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Am J Gastroenterol. 2007 Oct;102(10):2220-9. doi: 10.1111/j.1572-0241.2007.01479.x.
Among individuals who satisfy diagnostic criteria for both major depressive disorder (MDD) and irritable bowel syndrome (IBS), little is known about the role of familial tendency and environmental influences in disease susceptibility. Therefore, we aimed to examine if there is a genetic component to the co-occurrence of MDD and IBS in participants from the population-based Swedish Twin Registry.
We implemented a nested case-control analysis and a co-twin control analysis. IBS cases were ascertained using an adapted version of the Rome II criteria and MDD cases were assessed using a shortened version of the Computerized International Diagnostic Interview. The case-control analysis included individuals with complete covariate information (N = 29,616), and adjusted for twin pair, 3-yr age band, and sex. The co-twin control analysis considered 288 twin pairs discordant for IBS. Odds ratios (OR) and 95% confidence intervals (CI) were estimated using generalized estimating equations for the case-control analysis and conditional logistic regression for the co-twin control analysis.
In all analyses, comorbid disorders of chronic widespread pain, chronic fatigue-like illness, and MDD were more common in IBS cases than controls. In the case-control analysis, individuals with IBS had an increased odds of MDD (OR 2.7, 95% CI 2.3-3.2). In the co-twin analysis, the association was similar (OR 2.2, 95% CI 1.5-3.3) when both MZ and DZ twins were used, and larger among only MZ twins (OR 3.2, 95% CI 1.7-6.1).
From this analysis, we found no evidence that genetic and family environmental factors explain the association between MDD and IBS. Rather, one of these disorders appears to be part of the disease-causing sequence of events, or biologic disease pathway, for the other disorder. However, it was not possible to evaluate the timing of onset between MDD and IBS in this study.
在符合重度抑郁症(MDD)和肠易激综合征(IBS)诊断标准的个体中,关于家族倾向和环境影响在疾病易感性中的作用知之甚少。因此,我们旨在研究基于人群的瑞典双胞胎登记处的参与者中,MDD和IBS共病是否存在遗传因素。
我们进行了巢式病例对照分析和同卵双胞胎对照分析。IBS病例通过采用改编版的罗马II标准确定,MDD病例使用简化版的计算机化国际诊断访谈进行评估。病例对照分析纳入了具有完整协变量信息的个体(N = 29,616),并对双胞胎对、3岁年龄组和性别进行了调整。同卵双胞胎对照分析考虑了288对IBS不一致的双胞胎对。使用广义估计方程对病例对照分析估计比值比(OR)和95%置信区间(CI),使用条件逻辑回归对同卵双胞胎对照分析进行估计。
在所有分析中,慢性广泛性疼痛、慢性疲劳样疾病和MDD的共病在IBS病例中比对照组更常见。在病例对照分析中,IBS个体患MDD的几率增加(OR 2.7,95% CI 2.3 - 3.2)。在同卵双胞胎分析中,使用同卵双胞胎(MZ)和异卵双胞胎(DZ)时关联相似(OR 2.2,95% CI 1.5 - 3.3),仅在同卵双胞胎中关联更大(OR 3.2,95% CI 1.7 - 6.1)。
通过该分析,我们没有发现遗传和家庭环境因素可解释MDD和IBS之间关联的证据。相反,这些疾病中的一种似乎是另一种疾病致病事件序列或生物学疾病途径的一部分。然而,本研究中无法评估MDD和IBS发病时间先后顺序。