Evidence map›Paper›PMID 40699496›Full record

ArticleSarcoidosis, vasculitis, and diffuse lung diseases : official journal of WASOG2025

Homocysteine and risk of interstitial lung disease: A mendelian randomization approach to causal inference.

Shimin Li, Xiaochen Hu, Xin Hu, Hang Liu, Shanshan Meng

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Article in Sarcoidosis, vasculitis, and diffuse lung diseases : official journal of WASOG, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

5 authors.

Shimin LiPulmonary and Critical Care Medicine, The First Affiliated Hospital of Harbin Medical University , Harbin, Heilongjiang.
Xiaochen HuPulmonary and Critical Care Medicine, The First Affiliated Hospital of Harbin Medical University , Harbin, Heilongjiang.
Xin HuPulmonary and Critical Care Medicine, The First Affiliated Hospital of Harbin Medical University , Harbin, Heilongjiang.
Hang LiuPulmonary and Critical Care Medicine, The First Affiliated Hospital of Harbin Medical University , Harbin, Heilongjiang.
Shanshan MengPulmonary and Critical Care Medicine, The First Affiliated Hospital of Harbin Medical University , Harbin, Heilongjiang.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimHomocysteine (Hcy) has been implicated in inflammatory, oxidative stress (OS), and endoplasmic reticulum (ER) stress mechanisms, which are hypothesized to contribute to the pathogenesis of interstitial lung disease (ILD). Given the paucity of evidence regarding Hcy's role in ILD, a two-sample Mendelian randomization study was performed to investigate the causal association between Hcy and ILD.

methodsWe sourced data for total plasma Hcy from genome-wide association studies (GWAS) involving 44,147 European individuals. Data for ILD, idiopathic pulmonary fibrosis (IPF), IPF-related respiratory insufficiency, and systemic autoimmune disease-associated IPF were derived from the FinnGen consortium. To evaluate the causal association of reduced total plasma Hcy with ILD and related conditions, a range of Mendelian randomization (MR) analytical techniques were utilized to analyze the data. The results are reported as odds ratios (ORs) with corresponding 95% confidence intervals (CIs). We conducted sensitivity analyses through leave-one-out procedures and Radial MR plots.

resultsOur IVW estimates suggested that total plasma Hcy had a potential causal association with IPF (OR=0.649, 95%CI: 0.495-0.851), indicating that along with total plasma Hcy depressed 1 µmol/L, odds of IPF decreased 0.351. Although it seemed that decreased total plasma Hcy level is associated with lower odds of IPF-related respiratory insufficiency (OR=0.672, 95%CI: 0.489-0.924), due to the existence of horizontal pleiotropy, this causal association was not robust. In addition, MR leave-one-out and Radial MR sensitivity analyses showed there is no outlier among the selected IVs that could affect the potential causal relationship between Hcy and IPF.

conclusionsThe levels of total plasma Hcy may bear a significant association with the risk of developing IPF, a specific form of ILD. However, to definitively establish a causal relationship between elevated Hcy levels and the pathogenesis of ILD, additional well-controlled, prospective studies are indispensable.

Identifiers

PMID40699496
PMCPMC12242866

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