Association between genetically predicted leukocyte telomere length and non-scarring alopecia: A two-sample Mendelian randomization study

Yicheng Li; Shuting Yang; Minjun Liao; Zijun Zheng; Mengyao Li; Xuerong Wei; Mengqian Liu; Lei Yang

doi:10.3389/fimmu.2022.1072573

Association between genetically predicted leukocyte telomere length and non-scarring alopecia: A two-sample Mendelian randomization study

Front Immunol. 2023 Jan 30:13:1072573. doi: 10.3389/fimmu.2022.1072573. eCollection 2022.

Authors

Yicheng Li¹, Shuting Yang², Minjun Liao³, Zijun Zheng¹, Mengyao Li¹, Xuerong Wei¹, Mengqian Liu¹, Lei Yang¹

Affiliations

¹ Department of Burns, Nanfang Hospital, Southern Medical University, Guangzhou, China.
² National Clinical Research Center for Metabolic Diseases, Key Laboratory of Diabetes Immunology (Central South University), Ministry of Education, and Department of Metabolism and Endocrinology, The Second Xiangya Hospital of Central South University, Changsha, Hunan, China.
³ Guangdong Provincial Key Laboratory of Gastroenterology, Department of Gastroenterology and Hepatology Unit, Nanfang Hospital, Southern Medical University, Guangzhou, China.

Abstract

Background: The most commonly acknowledged non-scarring alopecia are androgenetic alopecia (AGA) and alopecia areata (AA). Previous studies have revealed various risk factors associated with alopecia. However, the relationship between leukocyte telomere length (LTL) and non-scarring alopecia remains unclear.

Methods: A two-sample Mendelian randomization (MR) analysis was performed to evaluate the causality between genetically predicted LTL and the risk of non-scarring alopecia. MR analyses were performed using the inverse variance-weighted (IVW) method and complemented with other MR methods.

Results: The summary statistics of the genome-wide association studies (GWAS) for AGA and AA were obtained from the FinnGen biobank, which included 119,185 and 211,428 individuals, respectively. A total of 126 single nucleotide polymorphisms (SNPs) with genome-wide significance were selected as the instrumental variables for LTL. The MR analyses suggested a causal relationship between LTL and AGA, and the risk of AGA increased by 3.19 times as the genetically predicted LTL was shortened by one standard deviation in log transformed form under the IVW method (OR = 4.19, 95% CI = 1.20-14.61, p = 0.024). The other MR methods also demonstrated a similar trend of the effect of LTL on AGA. There was no causal relationship between LTL and AA (p > 0.05). Sensitivity analyses further demonstrated that the current results were less likely to be affected by confounders and bias.

Conclusion: Our results suggested a potential causal relationship between LTL and AGA, and shortened LTL was associated with an increased risk of AGA.

Keywords: Mendelian randomization; alopecia areata; androgenetic alopecia; leukocyte telomere length; non-scarring alopecia.

Publication types

Research Support, Non-U.S. Gov't

MeSH terms

Alopecia Areata*
Genome-Wide Association Study*
Humans
Leukocytes
Mendelian Randomization Analysis
Telomere / genetics

Supplementary concepts

Diffuse alopecia

Grants and funding

This work was supported by the Science and Technology Innovation Project of Guangdong Province (no. 2018KJYZ005), the Natural Science Foundation of Guangdong Province (no. 2020A151501107), the Natural Science Foundation of Tibet Autonomous Region (no. XZ2017ZR-ZY021), and the Guangdong Province Key Field R&D Programme Project (no. 2020B1111150001).