Frontiers in Nutrition (Dec 2024)

Effect of micronutrients on the risk of Graves’ disease: a Mendelian randomization study

  • Fangsen Chen,
  • Fangsen Chen,
  • Rongliang Qiu,
  • Zhiqing Lin,
  • Junhan Chen,
  • Peitian Liu,
  • Yanling Huang,
  • Yanling Huang

DOI
https://doi.org/10.3389/fnut.2024.1432420
Journal volume & issue
Vol. 11

Abstract

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BackgroundMicronutrient research on Graves’ disease (GD) is limited and controversial. Therefore, in order to explore possible correlations between genetically predicted amounts of six micronutrients [Copper (Cu), Iron (Ir), Zinc (Zn), Calcium (Ca), Vitamin C (VC), and Vitamin D (VD)] and GD risk, we carried out Mendelian randomization research (MR).MethodsWe conducted an MR analysis using genome-wide association studies (GWAS) from people of European ancestry and aggregated information from UK Biobank to provide insight into the relationships between micronutrients and GD. The causal link between exposure and outcome was tested using three different techniques: Inverse Variance Weighted (IVW), MR-Egger, and Weighted Median Estimator (WME). The heterogeneity of outcomes was also assessed using Cochran’s Q statistic, and pleiotropy was assessed by MR-Egger intercept, MR-PRESSO.ResultsIVW analyses showed evidence of no significant effect of genetically predicted micronutrient concentrations on GD, except for Cu. (Cu: OR = 1.183, p = 0.025; Ir: OR = 1.031, p = 0.794; Zn: OR = 1.072, p = 0.426; Ca: OR = 1.040, p = 0.679; VC: OR = 1.011, p = 0.491; VD: OR = 0.902, p = 0.436). Significant heterogeneity was observed in Ca and VD (Ca: Q = 264.2, p = 0.002; VD: Q = 141.42, p = 0.047). The MR-Egger intercept method identified horizontal pleiotropy between serum Ca levels and GD (MR-Egger intercept = −0.010, p = 0.030), with no similar findings for other micronutrients.ConclusionMR analysis showed a possible causal relationship between the genetically predicted concentration of Cu and the risk of GD, whereas the genetically predicted concentrations of Ir, Zn, Ca, VC, and VD may not be causally related to the risk of GD.

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