Evidence of a Causal Relationship Between Body Mass Index and Immune-Mediated and Inflammatory Skin Diseases and Biomarkers: A Mendelian Randomization Study.

IF 1.9 4区 医学 Q3 DERMATOLOGY Clinical, Cosmetic and Investigational Dermatology Pub Date : 2024-11-23 eCollection Date: 2024-01-01 DOI:10.2147/CCID.S496066
Zhaoyi Li, Yibin Zhao
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Abstract

Aim: Increasing observational studies are revealing a positive correlation between body mass index (BMI) and the risk of Immune-mediated and Inflammatory Skin Diseases (IMID), however the causal relationship is not yet definite.

Objective: The aim of the study was to conduct a two-sample Mendelian randomization (TSMR) to explore the potential causality between BMI, and IMID and biomarkers.

Methods: The summary statistics for BMI (n = 322,154), at genome-wide significant level, were derived from the Genetic Investigation of Anthropometric Traits consortium (GIANT). The outcome data for IMID (Psoriasis, vitiligo, Atopic dermatitis (AD), acne, Bullous diseases, Dermatitis herpetiformis, Systemic lupus erythematosus (SLE), Alopecia Areata (AA), Hidradenitis suppurativa (HS) and Systemic sclerosis), and biomarkers were obtained from genome-wide association studies (GWAS). The TSMR analyses were performed in four methods, including inverse variance weighted (IVW) method, MR-Egger regression, the weighted median estimator (WME) and simple mode.

Results: The IVW analysis showed that the per standard deviation (SD) increase in BMI increased a 57% risk of psoriasis. We also observed the suggestive evidence of a causal relationship between BMI and AD and HS. This analysis did not support causality of Vitiligo, Acne, Bullous pemphigoid, Dermatitis herpetiformis, SLE, AA and Systemic sclerosis. The higher risk of BMI may be explained by higher levels of Triglycerides, C-reactive protein (CRP), Interleukin 6, Erythrocyte sedimentation rate (ESR) and Neutrophil count. The high-density lipoprotein (HDL) has an inverse relationship with BMI. No influences were defined for Total cholesterol, low-density lipoprotein (LDL), Rheumatoid factor (RF), Basophil count and Eosinophil count.

Conclusion: Our two-sample MR analysis proved the causal evidence for the associations between BMI and IMID, including psoriasis, AD and HS, which might be related to the elevated expression of biomarkers, including Triglycerides, CRP, Interleukin 6, ESR and neutrophil count.

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身体质量指数与免疫性和炎症性皮肤病及生物标志物之间因果关系的证据:孟德尔随机研究》。
目的:越来越多的观察性研究显示,体重指数(BMI)与免疫介导和炎症性皮肤病(IMID)的患病风险呈正相关,但其因果关系尚不明确:本研究旨在采用双样本孟德尔随机法(TSMR)探讨 BMI 与 IMID 和生物标志物之间的潜在因果关系:全基因组显著水平的 BMI(n = 322 154)汇总统计数据来自人体测量特征遗传调查联盟(GIANT)。IMID(银屑病、白癜风、特应性皮炎(AD)、痤疮、牛皮癣、疱疹性皮炎、系统性红斑狼疮(SLE)、脱发(AA)、化脓性扁桃体炎(HS)和系统性硬化症)和生物标志物的结果数据来自全基因组关联研究(GWAS)。TSMR 分析采用了四种方法,包括反方差加权法(IVW)、MR-Egger 回归法、加权中位数估计法(WME)和简单模式:IVW分析显示,体重指数每增加一个标准差(SD),患银屑病的风险就会增加57%。我们还观察到 BMI 与 AD 和 HS 之间存在因果关系的提示性证据。这项分析并不支持白癜风、痤疮、大疱性类天疱疮、疱疹性皮炎、系统性红斑狼疮、AA 和系统性硬化症之间的因果关系。甘油三酯、C 反应蛋白(CRP)、白细胞介素 6、红细胞沉降率(ESR)和中性粒细胞计数水平较高,这可能是 BMI 风险较高的原因。高密度脂蛋白(HDL)与体重指数呈反比关系。总胆固醇、低密度脂蛋白(LDL)、类风湿因子(RF)、嗜碱性粒细胞计数和嗜酸性粒细胞计数均无影响:我们的双样本 MR 分析证明了 BMI 与 IMID(包括银屑病、AD 和 HS)之间的因果关系,这可能与甘油三酯、CRP、白细胞介素 6、血沉和嗜中性粒细胞计数等生物标志物的表达升高有关。
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来源期刊
CiteScore
2.80
自引率
4.30%
发文量
353
审稿时长
16 weeks
期刊介绍: Clinical, Cosmetic and Investigational Dermatology is an international, peer-reviewed, open access journal that focuses on the latest clinical and experimental research in all aspects of skin disease and cosmetic interventions. Normal and pathological processes in skin development and aging, their modification and treatment, as well as basic research into histology of dermal and dermal structures that provide clinical insights and potential treatment options are key topics for the journal. Patient satisfaction, preference, quality of life, compliance, persistence and their role in developing new management options to optimize outcomes for target conditions constitute major areas of interest. The journal is characterized by the rapid reporting of clinical studies, reviews and original research in skin research and skin care. All areas of dermatology will be covered; contributions will be welcomed from all clinicians and basic science researchers globally.
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