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Hormone and reproductive factors and risk of systemic lupus erythematosus: a Mendelian randomized study. | LitMetric

Hormone and reproductive factors and risk of systemic lupus erythematosus: a Mendelian randomized study.

Immunol Res

Key Laboratory of Chinese Medicine Rheumatology of Zhejiang Province, School of Basic Medical Sciences, Zhejiang Chinese Medical University, Hangzhou, 310053, China.

Published: August 2024

AI Article Synopsis

  • Systemic lupus erythematosus (SLE) is an autoimmune disease influenced by hormonal and reproductive factors, although the exact causal relationships are uncertain.
  • A Mendelian randomization study used genetic variants linked to hormonal factors to explore their effects on SLE risk, employing various analytical methods to ensure robustness.
  • The study found a significant association between higher levels of circulating follistatin and increased SLE risk, indicating potential pathways for targeted treatment approaches.

Article Abstract

Systemic lupus erythematosus (SLE) is an autoimmune and inflammatory disease with a risk associated with hormonal and reproductive factors. However, the potential causal effects between these factors and SLE remain unclear. A two-sample Mendelian randomization study was conducted using the published summary data from the genome-wide association study database. Five independent genetic variants associated with hormonal and reproductive factors were selected as instrumental variables: age at menarche, age at natural menopause, estradiol, testosterone, and follistatin. To estimate the causal relationship between these exposure factors and disease outcome, we employed the inverse-variance weighted, weighted median, and MR-Egger methods. In addition, we carried out multiple sensitivity analyses to validate model assumptions. Inverse variance weighted showed that there was a causal association between circulating follistatin and SLE risk (OR = 1.38, 95% CI 1.03 to 1.86, P = 0.033). However, no evidence was found that correlation between AAM (OR = 1.04, 95% CI 0.77 to 1.40, P = 0.798), ANM (OR = 0.99, 95% CI 0.92 to 1.06, P = 0.721), E2 (OR = 1.40, 95% CI 0.14 to 13.56, P = 0.772), T (OR = 1.25, 95% CI 0.70 to 2.28, P = 0.459), and SLE risk. Our study revealed that elevated circulating follistatin associates with an increased risk of SLE. This finding suggests that the regulatory signals mediated by circulating follistatin may provide a potential mechanism relevant to the treatment of SLE.

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Source
http://dx.doi.org/10.1007/s12026-024-09470-zDOI Listing

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