Rheumatology (Oxford, England) · 2026
Loneliness, traditional risk factor control, genetic predisposition, and development of musculoskeletal disorders.
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Ma Xiaofeng, Song Xin, Zou Yanqiu, Zhang Di, Yang Bin, Lei Bowen, Zhou Jinyu, Zhao Xunying, Xiang Rong, Qu Yang, Zheng Sirui, Yu Ting, Han Tao, Zhong Yangdan, Xia Maoyao, Fan Mengyu, Jiang Xia, Zhang Ben
Аннотация
OBJECTIVES: The objectives of this study were to investigate prospective associations of loneliness and social isolation with musculoskeletal (MSK) disorder risk, to evaluate their relative importance relative to that of traditional risk factors, and assess interactions with genetic predispositions.
METHODS: We analysed data from 315 197 UK Biobank participants. Loneliness and social isolation were assessed through self-reported questionnaires. The primary outcome was the incidence of any MSK disorder, with secondary outcomes comprising five specific MSK conditions of high burden [osteoarthritis, gout, rheumatoid arthritis, low back pain, and neck pain]. Cox regressions were performed to examine the associations between loneliness, social isolation, traditional risk factor control, polygenic risk score, and risk of overall and specific MSK disorders.
RESULTS: During a median follow-up of 13.3 years, 79 689 MSK cases were documented. Loneliness [hazard ratio (HR) = 1.14, 95% CI = 1.11-1.17] was associated with an increased risk of overall MSK disorders, whereas social isolation was associated with a modestly lower risk of MSK disorders (HR = 0.96, 95% CI = 0.94-0.99). Loneliness ranked higher in relative strength than most of the traditional risk factors. Significant interactions (on both additive and multiplicative scales) between loneliness and traditional risk factor control were observed. When stratified by genetic risk, loneliness was consistently associated with an increased risk of overall MSK disorders across strata. Joint analysis indicated the absence of loneliness to offset the genetic risk of overall MSK disorders. When extending to five specific conditions, largely consistent patterns of results were observed.
CONCLUSION: Loneliness is associated with increased MSK disorder risk, shows an interaction with the degree of risk factor control, and its absence may modify genetic predisposition. These findings support targeting loneliness to reduce the burden of MSK disorders.
METHODS: We analysed data from 315 197 UK Biobank participants. Loneliness and social isolation were assessed through self-reported questionnaires. The primary outcome was the incidence of any MSK disorder, with secondary outcomes comprising five specific MSK conditions of high burden [osteoarthritis, gout, rheumatoid arthritis, low back pain, and neck pain]. Cox regressions were performed to examine the associations between loneliness, social isolation, traditional risk factor control, polygenic risk score, and risk of overall and specific MSK disorders.
RESULTS: During a median follow-up of 13.3 years, 79 689 MSK cases were documented. Loneliness [hazard ratio (HR) = 1.14, 95% CI = 1.11-1.17] was associated with an increased risk of overall MSK disorders, whereas social isolation was associated with a modestly lower risk of MSK disorders (HR = 0.96, 95% CI = 0.94-0.99). Loneliness ranked higher in relative strength than most of the traditional risk factors. Significant interactions (on both additive and multiplicative scales) between loneliness and traditional risk factor control were observed. When stratified by genetic risk, loneliness was consistently associated with an increased risk of overall MSK disorders across strata. Joint analysis indicated the absence of loneliness to offset the genetic risk of overall MSK disorders. When extending to five specific conditions, largely consistent patterns of results were observed.
CONCLUSION: Loneliness is associated with increased MSK disorder risk, shows an interaction with the degree of risk factor control, and its absence may modify genetic predisposition. These findings support targeting loneliness to reduce the burden of MSK disorders.