Ding Lilu, Dai Ruoqi, Jin Dian, Li Zhanyi, Qian Jing, Zhu Jiahao, Miao Jingyou, Zhang Hui, Wang Jing, Xu Yan, Li Yingjun
Department of Epidemiology and Health Statistics, School of Public Health, Hangzhou Medical College, 481 Binwen Road, Hangzhou, 310053, China.
Zhejiang Provincial Center for Disease Control and Prevention, 3399 Binsheng Road, Hangzhou, 310051, China.
Arch Public Health. 2025 Jul 2;83(1):174. doi: 10.1186/s13690-025-01670-9.
Osteoarthritis (OA), a leading cause of disability worldwide, is increasingly recognized for its systemic impact. Despite its prevalence, the age-dependent effects of OA remain underexplored, particularly regarding its association with comorbidities across the life course.
Using the UK Biobank (78,825 incident OA cases; 301,071 age-/sex-matched controls; age range: 40-86 years) and the CHARLS cohort (China, 5,735 participants, age range: 45-92 years), we employed Cox models with age as the time scale to estimate hazard ratios (HRs) for OA-associated comorbidities, including bone diseases, metabolic disorders, and mental health conditions, stratified by age at diagnosis. Analyses adjusted for sociodemographic factors and population-attributable fractions (PAFs) were calculated to quantify preventable burdens.
OA was associated with significantly increased risks across multiple comorbidities. All comorbidities exhibited an age-dependent gradient: relative risks were highest in younger individuals and declined with age, while absolute risks increased due to OA's higher prevalence in older populations. For example, HRs for metabolic disorders declined from 2.55 (95% CI: 2.36-2.76) in those aged 40-49 to 1.77 (95% CI: 1.74-1.81) in those aged ≥ 70. Validation in CHARLS confirmed these patterns.
The systemic effects of OA vary substantially by age at onset. Younger individuals face elevated proportional risks likely shaped by behavioral, occupational, and structural factors, while older adults bear a larger absolute burden. These findings underscore the need for age-sensitive strategies to reduce long-term health consequences of OA and promote healthy aging.
骨关节炎(OA)是全球致残的主要原因,其对全身的影响日益受到关注。尽管OA患病率很高,但年龄对OA的影响仍未得到充分研究,尤其是在其与一生中合并症的关联方面。
我们使用英国生物银行(78825例新发OA病例;301071例年龄/性别匹配的对照;年龄范围:40 - 86岁)和中国健康与养老追踪调查(CHARLS)队列(中国,5735名参与者,年龄范围:45 - 92岁),采用以年龄为时间尺度的Cox模型来估计OA相关合并症的风险比(HRs),这些合并症包括骨病、代谢紊乱和心理健康状况,并按诊断时的年龄进行分层。分析对社会人口学因素进行了调整,并计算了人群归因分数(PAFs)以量化可预防的负担。
OA与多种合并症的风险显著增加相关。所有合并症都呈现出年龄依赖性梯度:相对风险在较年轻个体中最高,并随年龄下降,而绝对风险因OA在老年人群中患病率较高而增加。例如,代谢紊乱的HRs从40 - 49岁人群中的2.55(95%置信区间:2.36 - 2.76)降至70岁及以上人群中的1.77(95%置信区间:1.74 - 1.81)。CHARLS队列中的验证证实了这些模式。
OA的全身影响因发病年龄而异。较年轻个体面临比例风险升高,这可能受到行为、职业和结构因素的影响,而老年人承担着更大的绝对负担。这些发现强调了需要采取对年龄敏感的策略,以减少OA对长期健康的影响并促进健康老龄化。