Clinical Research Centre, Southern Medical University, Guangzhou, China; Department of Orthopedics, General Hospital of Southern Theater Command of PLA, Guangzhou, China.
Clinical Research Centre, Southern Medical University, Guangzhou, China.
Lancet Glob Health. 2023 Mar;11 Suppl 1:S2. doi: 10.1016/S2214-109X(23)00087-6.
Large adulthood body size was associated with increased risk of osteoarthritis. We aimed to examine the association between body size trajectories from childhood to adulthood and potential interactions with genetic susceptibility on osteoarthritis risk.
We included participants from the UK Biobank aged 38-73 years in 2006-10. Childhood body size information was collected by questionnaire. Adulthood BMI was assessed and transformed into three categories (<25 kg/m for normal, 25-29·9 kg/m for overweight, and >30 kg/m for obesity). A Cox proportional hazards regression model was applied to assess the association between body size trajectories and osteoarthritis incidence. Osteoarthritis-related polygenic risk score (PRS) was constructed to evaluate its interactions with body size trajectories on osteoarthritis risk.
For the 466 292 participants included, we identified nine body size trajectories [thinner to normal (11·6%), overweight (17·2%), or obesity (26·9%); average to normal (11·8%), overweight (16·2%), or obesity (23·7%); and plumper to normal (12·3%), overweight (16·2%), or obesity (23·6%)]. Compared with individuals in the average-to-normal group, all other trajectory groups had higher risks of osteoarthritis, after adjustment for demographic, social-economic and lifestyle covariates (hazard ratios [HRs] 1·05-2·41; all p<0·01). Among them, thinner-to-obesity (HR 2·41; 95% CI 2·23-2·49) had the most prominent association with increased osteoarthritis risk. A high PRS was significantly associated with an increased risk of osteoarthritis (1·14; 1·11-1·16), whereas no interaction between childhood-to-adulthood body size trajectories and PRS on osteoarthritis risks was observed. The population attributable fraction suggested that body size towards normal in adulthood could eliminate osteoarthritis cases by 18·67% for thinner-to-overweight to 38·74% for plumper-to-obesity.
Average-to-normal body size seems to be the healthiest childhood-to-adulthood trajectory for osteoarthritis risk, whereas a trajectory of increased body size from thinner to obesity has the highest risk for osteoarthritis. These associations are independent of osteoarthritis genetic susceptibility.
The National Natural Science Foundation of China (32000925) and Guangzhou Science and Technology Program (202002030481).
成年人的体型较大与骨关节炎风险增加有关。我们旨在研究从儿童期到成年期的体型轨迹与骨关节炎风险之间的关系,并探讨其与遗传易感性的潜在相互作用。
我们纳入了 2006-2010 年参加英国生物银行研究、年龄在 38-73 岁的参与者。通过问卷调查收集儿童期的体型信息。评估成年期 BMI,并将其转换为三个类别(<25kg/m2 为正常、25-29.9kg/m2 为超重和>30kg/m2 为肥胖)。应用 Cox 比例风险回归模型评估体型轨迹与骨关节炎发病之间的关联。构建骨关节炎相关多基因风险评分(PRS),以评估其与体型轨迹对骨关节炎风险的相互作用。
在纳入的 466292 名参与者中,我们确定了 9 种体型轨迹[从瘦到正常(11.6%)、超重(17.2%)或肥胖(26.9%);从平均到正常(11.8%)、超重(16.2%)或肥胖(23.7%);从胖到正常(12.3%)、超重(16.2%)或肥胖(23.6%)]。与平均到正常组相比,所有其他轨迹组的骨关节炎发病风险均较高,调整人口统计学、社会经济和生活方式因素后(危险比[HR]1.05-2.41;均<0.01)。其中,从瘦到肥胖(HR 2.41;95%CI 2.23-2.49)与骨关节炎风险增加的相关性最显著。高 PRS 与骨关节炎风险增加显著相关(1.14;1.11-1.16),而儿童期到成年期的体型轨迹与 PRS 对骨关节炎风险之间未见交互作用。人群归因分数表明,成年时向正常体型发展可使从瘦到超重的骨关节炎病例减少 18.67%,从胖到肥胖的骨关节炎病例减少 38.74%。
平均到正常的体型似乎是儿童期到成年期骨关节炎风险最健康的体型轨迹,而从瘦到肥胖的体型增加轨迹与骨关节炎的风险最高。这些关联独立于骨关节炎的遗传易感性。
国家自然科学基金(32000925)和广州市科技计划项目(202002030481)。