Chen Lingxiao, Ferreira Manuela L, Nassar Natasha, Preen David B, Hopper John L, Li Shuai, Bui Minh, Beckenkamp Paula R, Shi Baoyi, Arden Nigel K, Ferreira Paulo H
Faculty of Medicine and Health, Institute of Bone and Joint Research, The Kolling Institute, Northern Clinical School, University of Sydney, Sydney, NSW 2064, Australia.
Faculty of Medicine and Health, Children's Hospital Westmead Clinical School, University of Sydney, Sydney, Australia.
EClinicalMedicine. 2021 Nov 14;42:101202. doi: 10.1016/j.eclinm.2021.101202. eCollection 2021 Dec.
We aimed to quantify the association between chronic musculoskeletal pain and all-cause mortality, and to investigate the extent to which this association is mediated by physical activity, smoking status, alcohol consumption, and opioid use.
For this population-based cohort study, we used data from UK Biobank, UK between baseline visit (2006-2010) to 18th December 2020. We assessed the associations between chronic musculoskeletal pain and all-cause mortality using a Cox proportional hazards model. We performed causal mediation analyses to examine the proportion of the association between chronic musculoskeletal pain and all-cause mortality.
Of the 384,367 included participants, a total of 187,269 participants reported chronic musculoskeletal pain. Higher number of pain sites was associated with increased risk of all-cause mortality compared to having no pain (e.g., four sites vs no site of pain, Hazard Ratio [HR] 1.46, 95% Confidence Interval [CI] 1.35 to 1.57). The multiple mediator analyses showed that the mediating proportions of all four mediators ranged from 53.4% to 122.6%: among participants with two or more pain sites, the effect estimate reduced substantially, for example, HR reduced from 1.25 (95% CI: 1.21 to 1.30; two pain sites) to 1.07 (95% CI: 1.01 to 1.11; two pain sites).
We found that higher number of pain sites was associated with increased risk of all-cause mortality compared to having no pain, and at least half of the association of chronic musculoskeletal pain with increased all-cause mortality may be accounted for by four mediators.
Twins Research Australia.
我们旨在量化慢性肌肉骨骼疼痛与全因死亡率之间的关联,并研究这种关联在多大程度上由身体活动、吸烟状况、饮酒量和阿片类药物使用所介导。
在这项基于人群的队列研究中,我们使用了英国生物银行(UK Biobank)从基线访视(2006 - 2010年)至2020年12月18日期间来自英国的数据。我们使用Cox比例风险模型评估慢性肌肉骨骼疼痛与全因死亡率之间的关联。我们进行了因果中介分析,以检验慢性肌肉骨骼疼痛与全因死亡率之间关联的比例。
在纳入的384,367名参与者中,共有187,269名参与者报告有慢性肌肉骨骼疼痛。与无疼痛相比,疼痛部位数量较多与全因死亡率风险增加相关(例如,四个疼痛部位与无疼痛部位相比,风险比[HR]为1.46,95%置信区间[CI]为1.35至1.57)。多重中介分析表明,所有四种中介因素的中介比例范围为53.4%至122.6%:在有两个或更多疼痛部位的参与者中,效应估计值大幅降低,例如,HR从1.25(95%CI:1.21至1.30;两个疼痛部位)降至1.07(95%CI:1.01至1.11;两个疼痛部位)。
我们发现,与无疼痛相比,疼痛部位数量较多与全因死亡率风险增加相关,并且慢性肌肉骨骼疼痛与全因死亡率增加之间至少一半的关联可能由四种中介因素所解释。
澳大利亚双胞胎研究组织。