Aberdeen Pain Research Collaboration, University of Aberdeen, UK.
Eur J Pain. 2012 Aug;16(7):1053-63. doi: 10.1002/j.1532-2149.2011.00095.x. Epub 2012 Jan 26.
Chronic pain is pathological, persisting beyond normal tissue healing time. Previous work has suggested ∼50% variation in chronic pain development is heritable. No data are currently available on the heritability of pain categorized using the Chronic Pain Grade (CPG). Furthermore, few existing studies have accounted for potential confounders that may themselves be under genetic control or indeed 'heritable' non-genetic traits. This study aimed to determine the relative contributions of genetic, measured and shared environmental and lifestyle factors to chronic pain. Chronic pain status was determined and CPG measured in participants from Generation Scotland: the Scottish Family Health Study, a large cohort of well-characterized, extended families from throughout Scotland, UK. Heritability estimates (h (2) ) for 'any chronic pain' and 'severe' chronic pain (CPG 3 or 4) were generated using SOLAR software, with and without adjustment for shared household effects and measured covariates age, body mass index, gender, household income, occupation and physical activity. Data were available for 7644 individuals in 2195 extended families. Without adjustment, h (2) for 'any chronic pain' was 29% [standard errors (SE) 6%; p < 0.001], and for 'severe' chronic pain was 44% (SE 3%; p <0.001). After adjustment, 'any chronic pain' h(2) = 16% (SE 7%; p = 0.02) and 'severe' chronic pain h(2) = 30% (SE 13%; p = 0.007). Co-heritability of both traits was 11% (SE 76%). This study supports the use of chronic pain as a phenotype in genetic studies, with adequate correction for confounders to specifically identify genetic risk factors for chronic pain.
慢性疼痛是病理性的,持续时间超过正常组织愈合时间。以前的研究表明,慢性疼痛发展的变异约有 50%是遗传的。目前尚无使用慢性疼痛分级(CPG)对疼痛进行分类的遗传率数据。此外,很少有现有研究考虑到可能本身受遗传控制或实际上是“遗传”非遗传特征的潜在混杂因素。本研究旨在确定遗传、测量和共享环境及生活方式因素对慢性疼痛的相对贡献。慢性疼痛状况由苏格兰家族健康研究(Generation Scotland:苏格兰家庭健康研究)的参与者确定,该研究是一个来自英国苏格兰各地的大型、特征良好的扩展家庭队列。使用 SOLAR 软件生成“任何慢性疼痛”和“严重”慢性疼痛(CPG 3 或 4)的遗传率估计值(h (2) ),并分别调整共享家庭效应和测量协变量年龄、体重指数、性别、家庭收入、职业和体力活动。2195 个扩展家庭中有 7644 人提供了数据。未经调整时,“任何慢性疼痛”的 h (2) 为 29%[标准误差(SE)为 6%;p<0.001],“严重”慢性疼痛的 h (2) 为 44%(SE 为 3%;p<0.001)。调整后,“任何慢性疼痛”的 h (2) 为 16%(SE 为 7%;p=0.02),“严重”慢性疼痛的 h (2) 为 30%(SE 为 13%;p=0.007)。两种特征的共同遗传率为 11%(SE 为 76%)。本研究支持将慢性疼痛作为遗传研究中的表型使用,并对混杂因素进行充分校正,以专门确定慢性疼痛的遗传风险因素。