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

Ronghui Wu; Hao Tian; Tianqi Zhao; Yangyang Tian; Xianhua Jin; Mingji Zhu

doi:10.3389/fnut.2024.1404117

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

Front Nutr. 2024 Oct 14:11:1404117. doi: 10.3389/fnut.2024.1404117. eCollection 2024.

Authors

Ronghui Wu^{1

2}, Hao Tian³, Tianqi Zhao¹, Yangyang Tian¹, Xianhua Jin¹, Mingji Zhu¹

Affiliations

¹ Department of Dermatology, China-Japan Union Hospital of Jilin University, Changchun, China.
² Department of Dermatology, Chinese People's Liberation Army General Hospital, Beijing, China.
³ Department of Orthopedics, China-Japan Union Hospital of Jilin University, Changchun, China.

Abstract

Background: Mineral 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)].

Methods: Two-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.

Results: IVW 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.

Conclusion: TSAT is genetically linked to PS, highlighting iron homeostasis in disease development. Zn and Se intake may reduce AD risk.

Keywords: Mendelian randomization; acne vulgaris; atopic dermatitis; iron metabolism; mineral; psoriasis.

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This research was funded by the Science and Technology Department of Jilin Province, China (grant number: 20220204004YY).