Causal effect of vitamin D on myasthenia gravis: a two-sample Mendelian randomization study

Observational studies suggest that vitamin D supplementation may be effective in preventing myasthenia gravis (MG). However, the causal relationship between circulating vitamin D levels and MG remains unclear. This study aimed to examine the genetic causality of circulating vitamin D and MG using da...

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Veröffentlicht in:Frontiers in nutrition (Lausanne) 2023-07, Vol.10, p.1171830-1171830
Hauptverfasser: Fan, Yidan, Huang, Huaiying, Chen, Xiangda, Chen, Yuexuan, Zeng, Xiashi, Lin, Fenwei, Chen, Xu
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Sprache:eng
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Zusammenfassung:Observational studies suggest that vitamin D supplementation may be effective in preventing myasthenia gravis (MG). However, the causal relationship between circulating vitamin D levels and MG remains unclear. This study aimed to examine the genetic causality of circulating vitamin D and MG using data from large population-based genome-wide association studies (GWAS). SNPs (single nucleotide polymorphisms) strongly associated with exposure were selected. Two-sample Mendelian Randomization (MR) was performed with inverse variance weighting (IVW), MR-Egger (Mendelian randomization-Egger), weight median and MR-PRESSO (Mendelian randomization pleiotropy residual sum and outlier) methods. Heterogeneity was tested via IVW and MR-Egger. Pleiotropy was tested using MR-Egger intercept test and MR-PRESSO method. MR-PRESSO was also used to detect outliers. Leave-one-out analysis was used to identify SNPs with potential effect. Reverse MR analysis was also performed. In IVW, circulating vitamin D levels had no causal effect on MG [OR = 0.91 (0.67-1.22),  = 0.532] and MG had no causal effect on circulating vitamin D [OR = 1.01 (099-1.02),  = 0.663]. No heterogeneity or pleiotropy was observed (  > 0.05). Other MR methods also agreed with IVW results. This study provides the causal relationship between genetically predicted circulating vitamin D levels and MG and provides new insights into the genetics of MG.
ISSN:2296-861X
2296-861X
DOI:10.3389/fnut.2023.1171830