Fan Rui, Zhang Zhihan, Huang Qinlian, Liu Linqi, Que Wenjun, Lu Dan, Jing Sisi, Gan Yaoqi, Liu Shiyi, Xiao Fei
Department of Neurology, Chongqing Key Laboratory of Neurology, The First Affiliated Hospital of Chongqing Medical University, No.1 Youyi Road, Yuzhong District, Chongqing, 400016, China.
Department of Blood Transfusion, The First Affiliated Hospital of Chongqing Medical University, Yuzhong District, No.1 Youyi Road, Chongqing, China.
Clin Rheumatol. 2025 Apr 14. doi: 10.1007/s10067-025-07426-8.
To detect the association between regional adiposity distribution and the incidence of seven autoimmune diseases (ADs) in UK Biobank cohort and Mendelian randomization (MR) analyses.
We used Cox models to evaluate the associations between seven adiposity distribution measures and seven ADs (systemic lupus erythematosus [SLE], seropositive rheumatoid arthritis [PRA], psoriasis [PSO], multiple sclerosis [MS], myasthenia gravis [MG], Crohn's disease [CD] and ulcerative colitis [UC]) in cohort studies. In the MR analyses, we used the inverse variance-weighted MR method to estimate causal effects between adiposity distribution and obesity-related ADs in the cohort.
In the cohort study, PSO, MG, CD, and female UC were associated with almost all types of adiposity distribution; PRA and male UC were associated with central adiposity distribution; SLE and MS were found to be not associated with any types of obesity. Almost all adiposity distribution were certified in MR as an exposure to PSO, MG and PRA.
Adiposity, despite its distribution, are associated with an increased risk of PSO and MG, and central adiposity distribution is robustly associated with the increased risk of PRA, indicating that lifestyle interventions aimed at obesity contribute to preventing ADs. Key Points • Body mass index (BMI) was a risk factor for several autoimmune diseases, such as systemic lupus erythematosus (SLE), rheumatoid arthritis (RA), psoriasis (PSO), multiple sclerosis (MS) and inflammatory bowel disease (IBD). However, obesity as a heterogeneous and complex condition and that regional fat mass has obviously differential contributions to the development of obesity-related diseases. • We revealed that all types of adiposity distribution, whether general, central or peripheral, were associated with an increased risk of psoriasis and myasthenia gravis, and central adiposity distribution was robustly associated with the increased risk of seropositive rheumatoid arthritis. • Our findings indicated that lifestyle interventions aimed at individuals with obesity might contribute to preventing autoimmune diseases.
在英国生物银行队列中检测局部肥胖分布与七种自身免疫性疾病(AD)发病率之间的关联,并进行孟德尔随机化(MR)分析。
在队列研究中,我们使用Cox模型评估七种肥胖分布指标与七种AD(系统性红斑狼疮[SLE]、血清阳性类风湿关节炎[PRA]、银屑病[PSO]、多发性硬化症[MS]、重症肌无力[MG]、克罗恩病[CD]和溃疡性结肠炎[UC])之间的关联。在MR分析中,我们使用逆方差加权MR方法来估计队列中肥胖分布与肥胖相关AD之间的因果效应。
在队列研究中,PSO、MG、CD和女性UC与几乎所有类型的肥胖分布相关;PRA和男性UC与中心性肥胖分布相关;SLE和MS与任何类型的肥胖均无关联。几乎所有肥胖分布在MR分析中均被证实是PSO、MG和PRA的暴露因素。
无论肥胖分布如何,肥胖都与PSO和MG风险增加相关,中心性肥胖分布与PRA风险增加密切相关,这表明针对肥胖的生活方式干预有助于预防AD。要点 • 体重指数(BMI)是几种自身免疫性疾病的危险因素,如系统性红斑狼疮(SLE)、类风湿关节炎(RA)、银屑病(PSO)、多发性硬化症(MS)和炎症性肠病(IBD)。然而,肥胖是一种异质性和复杂性疾病,局部脂肪量对肥胖相关疾病的发展有明显不同的影响。 • 我们发现,所有类型的肥胖分布,无论是全身性、中心性还是外周性,都与银屑病和重症肌无力风险增加相关,中心性肥胖分布与血清阳性类风湿关节炎风险增加密切相关。 • 我们的研究结果表明,针对肥胖个体的生活方式干预可能有助于预防自身免疫性疾病。