Vassend Olav, Røysamb Espen, Nielsen Christopher Sivert, Czajkowski Nikolai Olavi
Department of Psychology, University of Oslo.
Norwegian Institute of Public Health.
Health Psychol. 2017 Aug;36(8):729-739. doi: 10.1037/hea0000484. Epub 2017 Mar 13.
Musculoskeletal (MS) complaints are reported commonly, but the extent to which such complaints reflect the severity of site-specific pathology or a more generalized susceptibility to feel pain/discomfort is uncertain. Both site-specific and more widespread MS conditions have been shown to be linked to anxiety and depression, but the nature of this relationship is poorly understood. In the present study the role of neuroticism as a shared risk factor that may possibly explain the co-occurrence between anxiety-depression and MS complaints was investigated.
The sample consisted of 746 monozygotic and 770 dizygotic twins in the age group of 50-65 years (M = 57.11, SD = 4.5). Using Cholesky modeling, genetic and environmental influences on neuroticism, anxiety-depression and MS symptoms, and the associations among these phenotypes were determined.
A single factor accounted for about 50% of the overall variance in MS symptom reporting. The best-fitting biometric model included sex-specific additive genetic and individual-specific environmental effects. All 3 phenotypes were strongly influenced by genetic factors, heritability (h2) = 0.41-0.56. Furthermore, while there was a considerable overlap in genetic risk factors among the 3 phenotypes, a substantial proportion of the genetic risk shared between MS complaints and anxiety-depression was independent of neuroticism.
Evidence for a common underlying susceptibility to report MS symptoms, genetically linked to both neuroticism and anxiety-depression symptoms, was found. (PsycINFO Database Record
肌肉骨骼(MS)方面的不适主诉很常见,但这些主诉在多大程度上反映特定部位病理的严重程度或对疼痛/不适更普遍的易感性尚不确定。特定部位和更广泛的MS病症都已被证明与焦虑和抑郁有关,但这种关系的本质却知之甚少。在本研究中,调查了神经质作为一个共同风险因素的作用,它可能解释焦虑抑郁与MS不适主诉之间的共现情况。
样本包括746对同卵双胞胎和770对异卵双胞胎,年龄在50 - 65岁之间(M = 57.11,SD = 4.5)。使用Cholesky模型,确定了遗传和环境对神经质、焦虑抑郁和MS症状的影响,以及这些表型之间的关联。
一个单一因素约占MS症状报告总体方差的50%。最佳拟合生物测量模型包括性别特异性加性遗传和个体特异性环境效应。所有这三种表型都受到遗传因素的强烈影响,遗传率(h2)= 0.41 - 0.56。此外,虽然这三种表型之间的遗传风险因素有相当大的重叠,但MS不适主诉与焦虑抑郁之间共享的很大一部分遗传风险独立于神经质。
发现了一种共同的潜在易感性证据,即报告MS症状,这在基因上与神经质和焦虑抑郁症状都有关联。(PsycINFO数据库记录