IF 2.6 4区 医学 Q1 NUTRITION & DIETETICS
Qiang He, Jinning Zhang, Huaiyang Liu, Yu Jin, Yao Liu, Yong Sun, Jianing Liu
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引用次数: 0

摘要

背景:肥胖与盂肱关节骨性关节炎(GJO)之间的关系尚不清楚,其代谢机制也不清楚。本研究通过腰高比(WHtR)调查了中心性肥胖与GJO发病率之间的前瞻性关联,并研究了甘油三酯(TG)是否介导了这种关系。方法:我们分析了2006年至2014年期间32,881名英国生物银行参与者的数据,中位随访时间为8.85年(IQR: 7.15-10.75)。使用Cox比例风险模型和因果中介分析来估计WHtR和TG对GJO风险的直接和间接影响,调整了人口统计学、社会经济、生活方式和合并症变量。结果:基线时的WHtR和TG水平均与较高的GJO风险显著相关(p p = 0.038),与BMI无关。同样,高TG组的参与者比低TG组的参与者风险增加1.46倍(AHR = 1.46, 95% CI: 1.06-2.02, p = 0.022)。这些关联在年龄、性别、体力活动、工作强度和BMI的亚组中是一致的。中介分析表明,TG解释了21.9%的WHtR-GJO关联。中介效应在年轻人、女性和不运动的个体中更强,但在BMI正常或体力负荷低的个体中不显著。结论:WHtR测量的中心性肥胖是GJO的独立危险因素。甘油三酯部分介导了这种关联,提示脂质毒性可能参与了GJO的代谢发病机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Association Between Central Obesity and Glenohumeral Joint Osteoarthritis and the Potential Mediating Role of Serum Triglycerides.

Background: The relationship between obesity and glenohumeral joint osteoarthritis (GJO) remains unclear, and the metabolic mechanisms involved are not well understood. This study investigated the prospective association between central obesity, assessed by waist-to-height ratio (WHtR), and GJO incidence, and examined whether triglycerides (TG) mediate this relationship.

Methods: We analyzed data from 32,881 UK Biobank participants enrolled between 2006 and 2014, with a median follow-up of 8.85 years (IQR: 7.15-10.75). Cox proportional hazards models and causal mediation analysis were used to estimate the direct and indirect effects of WHtR and TG on GJO risk, adjusting for demographic, socioeconomic, lifestyle, and comorbidity variables.

Results: Both WHtR and TG levels at baseline were significantly associated with higher GJO risk (p < 0.05). Compared to individuals with normal WHtR, those with severe central obesity had a 1.52-fold higher GJO risk (AHR = 1.52, 95% CI: 1.02-2.27, p = 0.038), independent of BMI. Similarly, participants in the highest TG tertile had a 1.46-fold increased risk compared to the lowest tertile (AHR = 1.46, 95% CI: 1.06-2.02, p = 0.022). These associations were consistent across subgroups by age, sex, physical activity, work intensity, and BMI. Mediation analysis showed that TG explained 21.9% of the WHtR-GJO association. The mediating effect was stronger in younger adults, women, and physically inactive individuals, but not significant in those with normal BMI or low physical workload.

Conclusions: Central obesity, as measured by WHtR, is an independent risk factor for GJO. TG partially mediates this association, suggesting that lipid toxicity may contribute to the metabolic pathogenesis of GJO.

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