Causal relationships of metabolites with allergic diseases: a trans-ethnic Mendelian randomization study

被引:5
|
作者
Tu, Junhao [1 ,2 ]
Wen, Jinyang [3 ]
Luo, Qing [1 ]
Li, Xin [4 ]
Wang, Deyun [2 ]
Ye, Jing [1 ,4 ,5 ,6 ]
机构
[1] Nanchang Univ, Affiliated Hosp 1, Jiangxi Med Coll, Dept Otorhinolaryngol Head & Neck Surg, Nanchang, Jiangxi, Peoples R China
[2] Natl Univ Singapore, Natl Univ Hlth Syst, Yong Loo Lin Sch Med, Dept Otolaryngol, Singapore, Singapore
[3] Huazhong Univ Sci & Technol, Tongji Hosp, Tongji Med Coll, Dept Radiol, Wuhan, Hubei, Peoples R China
[4] Jiangxi Med Acad Nutr & Hlth Management, Nanchang, Jiangxi, Peoples R China
[5] Nanchang Univ, Affiliated Hosp 1, Jiangxi Med Coll, Dept Allergy, Nanchang, Jiangxi, Peoples R China
[6] Nanchang Univ, Affiliated Hosp 1, Inst Otorhinolaryngol, Jiangxi Med Coll, Nanchang, Jiangxi, Peoples R China
关键词
Allergic diseases; Allergic rhinitis; Asthma; Metabolites; Mendelian randomization; TRYPTOPHAN;
D O I
10.1186/s12931-024-02720-6
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
BackgroundAllergic diseases exert a considerable impact on global health, thus necessitating investigations into their etiology and pathophysiology for devising effective prevention and treatment strategies. This study employs a Mendelian randomization (MR) analysis and meta-analysis to identify metabolite targets potentially associated with allergic diseases.MethodsA two-sample MR analysis was conducted to explore potential causal relationships between circulating and urinary metabolites and allergic diseases. Exposures were derived from a genome-wide association study (GWAS) of 486 circulating metabolites and a GWAS of 55 targeted urinary metabolites. Outcome data for allergic diseases, including atopic dermatitis (AD), allergic rhinitis (AR), and asthma, were obtained from the FinnGen biobank in Europe (cohort 1) and the Biobank Japan in Asia (cohort 2). MR results from both cohorts were combined using a meta-analysis.ResultsMR analysis identified 50 circulating metabolites and 6 urinary metabolites in cohort 1 and 54 circulating metabolites and 2 urinary metabolites in cohort 2 as potentially causally related to allergic diseases. A meta-analysis of the MR results revealed stearoylcarnitine (OR 8.654; 95% CI 4.399-17.025; P = 4.06E-10) and 1-arachidonoylglycerophosphoinositol (OR 2.178; 95% CI 1.388-3.419; P = 7.15E-04) as the most reliable causal circulating metabolites for asthma and AR, respectively. Further, histidine (OR 0.734; 95% CI: 0.594-0.907; P = 0.004), tyrosine (OR 0.601; 95% CI: 0.380-0.952; P = 0.030), and alanine (OR 0.280; 95% CI: 0.125-0.628; P = 0.002) emerged as urinary metabolites with the greatest protective effects against asthma, AD, and AR, respectively.ConclusionsImbalances in numerous circulating and urinary metabolites may be implicated in the development and progression of allergic diseases. These findings have significant implications for the development of targeted strategies for the prevention and treatment of allergic diseases.
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页数:13
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