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Circulating Interleukins and Risk of Multiple Sclerosis: A Mendelian Randomization Study

Hui Lü, Pengfei Wu, Wan Zhang, Xiaoyao Liao

2021Frontiers in Immunology38 citationsDOIOpen Access PDF

Abstract

Background Previous research have implicated critical roles of systemic inflammation in the development of Multiple Sclerosis (MS). But the causal relationship between interleukins (ILs) and MS has not been fully elucidated. Objective In this study, we applied Mendelian randomization (MR) approaches to address the causal associations between genetically determined circulating levels of ILs and the risk of MS. Methods Genetic instruments for circulating IL-1 receptor antagonist (IL-1Ra), IL-2 receptor α subunit (IL-2Rα), IL-6, IL-16, IL-17, and IL-18 were obtained from recently published genome-wide association studies (GWAS). Summary-level data for MS were obtained from the International Multiple Sclerosis Genetics Consortium. MR analyses were performed using the R software (version 3.6.1, The R Foundation) and the TwoSampleMR package. Results Genetic predisposition to higher circulating levels of IL-2Rα were significantly associated with MS risk. The odds ratio (OR) was 1.22 (95% confidence interval [CI], 1.12–1.32; p < 0.001) per one standard deviation increase in circulating IL-2Rα levels. There was a suggestive association of circulating IL-1Ra with MS risk (OR, 0.94; 95% CI, 0.88–0.99; p = 0.027). The other ILs were not associated with the outcome. Conclusion Our results indicated that circulating IL-2Rα was causally associated with risk of MS.

Topics & Concepts

Mendelian randomizationOdds ratioMultiple sclerosisMedicineGenome-wide association studyConfidence intervalGenetic associationImmunologyInternal medicineInterleukin 1 receptor antagonistInterleukinOncologyReceptor antagonistReceptorSingle-nucleotide polymorphismGeneticsGenotypeCytokineBiologyAntagonistGeneGenetic variantsInflammasome and immune disordersMultiple Sclerosis Research StudiesPsoriasis: Treatment and Pathogenesis