Frontiers in Nutrition (Oct 2024)

A Mendelian randomization analysis of inflammatory skin disease risk due to mineral deficiencies

  • Ronghui Wu,
  • Ronghui Wu,
  • Hao Tian,
  • Tianqi Zhao,
  • Yangyang Tian,
  • Xianhua Jin,
  • Mingji Zhu

DOI
https://doi.org/10.3389/fnut.2024.1404117
Journal volume & issue
Vol. 11

Abstract

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BackgroundMineral deficiencies, such as iron (Fe), zinc (Zn), and selenium (Se), play crucial roles in inflammation and immune responses and are linked to chronic inflammatory skin diseases. This study used genome-wide association study (GWAS) data and Mendelian randomization (MR) to investigate the genetic causality among serum levels of five minerals (Fe, Cu, Zn, Se, Ca), three iron metabolism indicators (TSAT, TIBC, ferritin), and three chronic inflammatory skin diseases [psoriasis (PS), atopic dermatitis (AD), acne vulgaris (AV)].MethodsTwo-sample MR analyses using the “TwoSample MR” package in R were conducted with aggregate outcome data from the FinnGen database. The inverse-variance-weighted (IVW) method was applied to assess causal relationships between mineral levels and disease outcomes. Robustness was examined via heterogeneity and pleiotropy tests.ResultsIVW analysis showed significant association between blood transferrin saturation (TSAT) and PS (p = 0.004, OR = 1.18). Serum Zn and Se levels showed inverse correlation with AD (p = 0.039, OR = 0.92). However, due to limited SNPs, robustness was reduced.ConclusionTSAT is genetically linked to PS, highlighting iron homeostasis in disease development. Zn and Se intake may reduce AD risk.

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