Causal Association Between 12 Micronutrients and Common Chronic Respiratory Diseases: A Bidirectional Two-Sample Mendelian Randomization Study.

IF 1.4 4区 生物学 Q4 GENETICS & HEREDITY
Genetics research Pub Date : 2025-05-28 eCollection Date: 2025-01-01 DOI:10.1155/genr/7575005
Tingting Zhu, Xiuyun Chen, Qing Wang, Fang Li, Junjun Yang, Xinyu Zhu, Jingmei Wang, Jixiang Bo
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引用次数: 0

Abstract

Background: This study aims to investigate the causal relationships between 12 micronutrients and common chronic respiratory diseases, revealing whether these nutrients play a causative role in either preventing or exacerbating these conditions. Methods: We employed a bidirectional two-sample Mendelian randomization (MR) approach to explore the causal relationships between micronutrients and chronic respiratory diseases. Data were sourced from the IEU GWAS database, with micronutrients serving as exposure variables and chronic respiratory diseases as outcome variables for causal assessment. This was followed by reverse MR analysis, where the steps were reversed. Analytical methods included inverse-variance weighting (IVW), MR-Egger regression, and the weighted median method to correct for potential pleiotropy and reverse causality. Cochran's Q test and the MR-PRESSO method were used for pleiotropy tests to ensure robustness and reliability of the results. Results: The MR analysis revealed that the genetically predicted calcium is a protective factor for asthma (OR = 0.99, 95% CI 0.984-0.995, p < 0.01), vitamin B12 is a risk factor for asthma (OR = 1.015, 95% CI 1.005-1.024, p < 0.01), and vitamin E is a protective factor for idiopathic pulmonary fibrosis (IPF) (OR = 0.952, 95% CI 0.916-0.989, p=0.012). In the reverse MR analysis, asthma showed a potential causal relationship with calcium levels (OR = 0.829, 95% CI 0.704-0.976, p=0.025), while pneumoconiosis showed a potential risk causal relationship with calcium levels (OR = 1.003, 95% CI 1.002-1.004, p < 0.010). Additionally, pneumoconiosis was found to have a potential protective causal relationship with vitamin E levels (OR = 0.999, 95% CI 0.999-1.000, p=0.034), and sarcoidosis was found to have a potential protective causal relationship with vitamin B12 levels (OR = 0.989, 95% CI 0.979-1.000, p=0.044). Conclusion: This study shows significant causal associations among calcium, vitamin B12, and vitamin E with chronic respiratory diseases. There is a bidirectional protective causal relationship between calcium and asthma, suggesting that increasing calcium intake may reduce the risk of asthma. However, the causal relationships among other vitamins, minerals, and chronic respiratory diseases remain inconclusive, necessitating further research to validate these findings' robustness and generalizability.

12种微量营养素与常见慢性呼吸道疾病的因果关系:一项双向双样本孟德尔随机研究。
背景:本研究旨在探讨12种微量营养素与常见慢性呼吸系统疾病之间的因果关系,揭示这些营养素是否在预防或加重这些疾病中起因果作用。方法:采用双向双样本孟德尔随机化(MR)方法,探讨微量营养素与慢性呼吸系统疾病之间的因果关系。数据来自IEU GWAS数据库,微量营养素作为暴露变量,慢性呼吸道疾病作为因果评估的结果变量。接下来是反向核磁共振分析,步骤颠倒过来。分析方法包括反方差加权(IVW)、MR-Egger回归和加权中位数法,以校正潜在的多效性和反向因果关系。采用Cochran’s Q检验和MR-PRESSO法进行多效性检验,以确保结果的稳健性和可靠性。结果:MR分析显示,基因预测的钙是哮喘的保护因素(OR = 0.99, 95% CI 0.984 ~ 0.995, p < 0.01),维生素B12是哮喘的危险因素(OR = 1.015, 95% CI 1.005 ~ 1.024, p < 0.01),维生素E是特发性肺纤维化(IPF)的保护因素(OR = 0.952, 95% CI 0.916 ~ 0.989, p=0.012)。在反向MR分析中,哮喘与钙水平存在潜在的因果关系(OR = 0.829, 95% CI 0.704-0.976, p=0.025),尘肺与钙水平存在潜在的风险因果关系(OR = 1.003, 95% CI 1.002-1.004, p < 0.010)。此外,尘肺病与维生素E水平存在潜在的保护性因果关系(OR = 0.999, 95% CI 0.999-1.000, p=0.034),结节病与维生素B12水平存在潜在的保护性因果关系(OR = 0.989, 95% CI 0.979-1.000, p=0.044)。结论:本研究显示钙、维生素B12和维生素E与慢性呼吸道疾病之间存在显著的因果关系。钙与哮喘之间存在双向保护性因果关系,提示增加钙摄入量可降低哮喘风险。然而,其他维生素、矿物质和慢性呼吸系统疾病之间的因果关系仍不确定,需要进一步的研究来验证这些发现的稳健性和普遍性。
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来源期刊
Genetics research
Genetics research 生物-遗传学
自引率
6.70%
发文量
74
审稿时长
>12 weeks
期刊介绍: Genetics Research is a key forum for original research on all aspects of human and animal genetics, reporting key findings on genomes, genes, mutations and molecular interactions, extending out to developmental, evolutionary, and population genetics as well as ethical, legal and social aspects. Our aim is to lead to a better understanding of genetic processes in health and disease. The journal focuses on the use of new technologies, such as next generation sequencing together with bioinformatics analysis, to produce increasingly detailed views of how genes function in tissues and how these genes perform, individually or collectively, in normal development and disease aetiology. The journal publishes original work, review articles, short papers, computational studies, and novel methods and techniques in research covering humans and well-established genetic organisms. Key subject areas include medical genetics, genomics, human evolutionary and population genetics, bioinformatics, genetics of complex traits, molecular and developmental genetics, Evo-Devo, quantitative and statistical genetics, behavioural genetics and environmental genetics. The breadth and quality of research make the journal an invaluable resource for medical geneticists, molecular biologists, bioinformaticians and researchers involved in genetic basis of diseases, evolutionary and developmental studies.
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