Unravelling the genetic causality of immunoglobulin G N-glycans in ischemic stroke

• Published in: Glycoconjugate journal Vol. 40; no. 4; pp. 413 - 420
• Main Authors: Wang, Biyan, Gao, Lei, Zhang, Jie, Meng, Xiaoni, Xu, Xizhu, Hou, Haifeng, Xing, Weijia, Wang, Wei, Wang, Youxin
• Format: Journal Article
• Language: English
• Published: New York Springer US 01.08.2023; Springer Nature B.V
• Subjects: Bayes Theorem; Bayesian analysis; Biochemistry; Biomedical and Life Sciences; Causality; Genome-Wide Association Study; Glycosylation; Humans; Immunoglobulin G; Immunoglobulin G - genetics; Immunoglobulins; Ischemia; Ischemic Stroke; Life Sciences; Liquid chromatography; Mendelian Randomization Analysis; N-glycans; Pathology; Polysaccharides; Polysaccharides - genetics; Population genetics; Risk factors; Sensitivity analysis; Stroke; Ischemic stroke; N-glycans; Mendelian randomization; Causality; Immunoglobulin G
• ISSN: 0282-0080; 1573-4986; 1573-4986
• DOI: 10.1007/s10719-023-10127-6

Background: Evidence suggests that immunoglobulin G (IgG) N-glycosylation is associated with ischemic stroke (IS). However, the causality of IgG N-glycosylation for IS remains unknown. Methods: Two-sample Mendelian randomization (MR) analyses were performed to investigate the potential causal effects of genetically determined IgG N-glycans on IS using publicly available summarized genetic data from East Asian and European populations. Genetic instruments were used as proxies for IgG N-glycan traits. IgG N-glycans were analysed using ultra-performance liquid chromatography. Four complementary MR methods were performed, including the inverse variance weighted method (IVW), MR‒Egger, weighted median and penalized weighted median. Furthermore, to further test the robustness of the results, MR based on Bayesian model averaging (MR-BMA) was then applied to select and prioritize IgG N-glycan traits as risk factors for IS. Results: After correcting for multiple testing, in two-sample MR analyses, genetically predicted IgG N-glycans were unrelated to IS in both East Asian and European populations, and the results remained consistent and robust in the sensitivity analysis. Moreover, MR-BMA also showed consistent results in both East Asian and European populations. Conclusions: Contrary to observational studies, the study did not provide enough genetic evidence to support the causal associations of genetically predicted IgG N-glycan traits and IS, suggesting that N-glycosylation of IgG might not directly involve in the pathogenesis of IS.