The Effect of Body Fat Distribution on Systemic Sclerosis

Author:

Villanueva-Martin GonzaloORCID,Acosta-Herrera Marialbert,Kerick MartinORCID,López-Isac ElenaORCID,Simeón Carmen P.ORCID,Callejas José L.,Assassi Shervin,Beretta LorenzoORCID,SSc Group International,(ASIG) Australian Scleroderma Interest Group,Allanore Yannick,Proudman Susanna M.,Nikpour Mandana,Fonseca Carmen,Denton Christopher P.,Radstake Timothy R. D. J.,Mayes Maureen D.ORCID,Jiang Xia,Martin JavierORCID,Bossini-Castillo LaraORCID

Abstract

Obesity contributes to a chronic proinflammatory state, which is a known risk factor to develop immune-mediated diseases. However, its role in systemic sclerosis (SSc) remains to be elucidated. Therefore, we conducted a two-sample mendelian randomization (2SMR) study to analyze the effect of three body fat distribution parameters in SSc. As instrumental variables, we used the allele effects described for single nucleotide polymorphisms (SNPs) in different genome-wide association studies (GWAS) for SSc, body mass index (BMI), waist-to-hip ratio (WHR) and WHR adjusted for BMI (WHRadjBMI). We performed local (pHESS) and genome-wide (LDSC) genetic correlation analyses between each of the traits and SSc and we applied several Mendelian randomization (MR) methods (i.e., random effects inverse-variance weight, MR-Egger regression, MR pleiotropy residual sum and outlier method and a multivariable model). Our results show no genetic correlation or causal relationship between any of these traits and SSc. Nevertheless, we observed a negative causal association between WHRadjBMI and SSc, which might be due to the effect of gastrointestinal complications suffered by the majority of SSc patients. In conclusion, reverse causality might be an especially difficult confounding factor to define the effect of obesity in the onset of SSc.

Publisher

MDPI AG

Subject

General Medicine

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