Department of Twin Research and Genetic Epidemiology, School of Life Course Sciences, King's College London, London, United Kingdom.
Laboratory of Theoretical and Applied Functional Genomics, Novosibirsk State University, Novosibirsk, Russia.
Pain. 2021 Apr 1;162(4):1176-1187. doi: 10.1097/j.pain.0000000000002100.
Sex differences for chronic back pain (cBP) have been reported, with females usually exhibiting greater morbidity, severity, and poorer response to treatment. Genetic factors acting in an age-specific manner have been implicated but never comprehensively explored. We performed sex- and age-stratified genome-wide association study and single nucleotide polymorphism-by-sex interaction analysis for cBP defined as "Back pain for 3+ months" in 202,077 males and 237,754 females of European ancestry from UK Biobank. Two and 7 nonoverlapping genome-wide significant loci were identified for males and females, respectively. A male-specific locus on chromosome 10 near SPOCK2 gene was replicated in 4 independent cohorts. Four loci demonstrated single nucleotide polymorphism-by-sex interaction, although none of them were formally replicated. Single nucleotide polymorphism-explained heritability was higher in females (0.079 vs 0.067, P = 0.006). There was a high, although not complete, genetic correlation between the sexes (r = 0.838 ± 0.041, different from 1 with P = 7.8E-05). Genetic correlation between the sexes for cBP decreased with age (0.858 ± 0.049 in younger people vs 0.544 ± 0.157 in older people; P = 4.3E-05). There was a stronger genetic correlation of cBP with self-reported diagnosis of intervertebral disk degeneration in males than in females (0.889 vs 0.638; P = 3.7E-06). Thus, the genetic component of cBP in the UK Biobank exhibits a mild sex- and age-dependency. This provides an insight into the possible causes of sex- and age-specificity in epidemiology and pathophysiology of cBP and chronic pain at other anatomical sites.
慢性背痛(cBP)的性别差异已有报道,女性通常表现出更高的发病率、严重程度和对治疗的反应较差。年龄特异性作用的遗传因素已被涉及,但从未得到全面探讨。我们对 202077 名欧洲血统的男性和 237754 名女性进行了按性别和年龄分层的全基因组关联研究和单核苷酸多态性与性别相互作用分析,这些人被定义为“背痛持续 3 个月以上”。分别在男性和女性中确定了 2 个和 7 个非重叠的全基因组显著位点。在染色体 10 上靠近 SPOCK2 基因的一个男性特异性位点在 4 个独立队列中得到了复制。有 4 个位点表现出单核苷酸多态性与性别相互作用,但没有一个得到正式复制。女性的单核苷酸多态性解释的遗传率更高(0.079 对 0.067,P=0.006)。虽然不完全相同,但两性之间存在高度遗传相关性(r=0.838±0.041,与 1 不同,P=7.8E-05)。cBP 的性别间遗传相关性随着年龄的增长而降低(年轻人中为 0.858±0.049,老年人中为 0.544±0.157;P=4.3E-05)。在男性中,cBP 与自我报告的椎间盘退行性病变诊断的遗传相关性强于女性(0.889 对 0.638;P=3.7E-06)。因此,英国生物银行中 cBP 的遗传成分表现出轻微的性别和年龄依赖性。这为 cBP 及其他解剖部位的慢性疼痛在流行病学和病理生理学中的性别和年龄特异性的可能原因提供了深入了解。