Potentially causal association between immunoglobulin G N-glycans and cardiometabolic diseases: Bidirectional two-sample Mendelian randomization study

被引:0
作者
Meng, Xiaoni [1 ,2 ,3 ]
Liu, Di [4 ]
Cao, Meiling [3 ]
Wang, Wei [3 ,5 ]
Wang, Youxin [3 ,6 ]
机构
[1] Capital Med Univ, Beijing Inst Resp Med, Dept Clin Epidemiol, Beijing 100020, Peoples R China
[2] Capital Med Univ, Beijing Chao Yang Hosp, Beijing 100020, Peoples R China
[3] Capital Med Univ, Sch Publ Hlth, Beijing Key Lab Clin Epidemiol, 10 Youanmen, Beijing 100069, Peoples R China
[4] Chinese Acad Sci, Shenzhen Inst Adv Technol, Shenzhen 518055, Peoples R China
[5] Edith Cowan Univ, Ctr Precis Hlth, Perth, WA 6027, Australia
[6] North China Univ Sci & Technol, Sch Publ Hlth, Tangshan 063210, Peoples R China
基金
中国国家自然科学基金;
关键词
Cardiometabolic disease; Mendelian randomization study; Immunoglobulin G N-glycosylation; CORONARY-HEART-DISEASE; C-REACTIVE PROTEIN; DIABETES-MELLITUS; RISK; GLYCOSYLATION; LOCI; FIBRINOGEN; IDENTIFICATION; INFLAMMATION; COMPLEMENT;
D O I
10.1016/j.ijbiomac.2024.135125
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: Observational studies support that altered immunoglobulin G (IgG) N-glycosylation and inflammatory factors are associated with cardiometabolic diseases (CMDs); nevertheless, the causality between them remains unclear. Methods: Two-sample Mendelian randomization (MR) analyses were conducted to systematically investigate the bidirectional causality between IgG N-glycans and nine CMDs in both East Asians and Europeans. Results: In the forward MR analysis, the univariable MR analysis presented suggestive causality of 14 and eight genetically instrumented IgG N-glycans with CMDs in East Asians and Europeans, respectively; the multivariable MR analysis showed that ten and 11 pairs of glycan-CMD associations were identified in East Asian and European populations, respectively. In the reverse MR analysis, based on East Asians and Europeans, the univariable MR analysis presented suggestive causality of seven and 12 genetically instrumented CMDs with IgG N-glycans, respectively; the multivariable MR analysis presented that six and five CMD-glycan causality were found in East Asian and Europeans, respectively. Conclusions: The comprehensive MR analyses provide suggestive evidence of bidirectional causality between IgG N-glycans and CMDs. This work helps to understand the molecular mechanism of the occurrence/progression of CMDs, optimize existing and develop new strategies to prevent CMDs, and contribute to the early identification of high-risk groups of CMDs.
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页数:13
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