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Association between COVID‐19 and myasthenia gravis (MG): A genetic correlation and Mendelian randomization study

BACKGROUND: Observational studies have suggested an association between coronavirus disease 2019 (COVID‐19) and myasthenia gravis (MG). Here, we aimed to estimate the genetic correlation and causal relationship between COVID‐19 susceptibility, hospitalization, severity, and MG phenotypes using linka...

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Autores principales: Sun, Dongren, Tu, Liangdan, Wang, Xiaofei, Du, Qin, Wang, Rui, Shi, Ziyan, Chen, Hongxi, Zhou, Hongyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10636397/
https://www.ncbi.nlm.nih.gov/pubmed/37638499
http://dx.doi.org/10.1002/brb3.3239
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author Sun, Dongren
Tu, Liangdan
Wang, Xiaofei
Du, Qin
Wang, Rui
Shi, Ziyan
Chen, Hongxi
Zhou, Hongyu
author_facet Sun, Dongren
Tu, Liangdan
Wang, Xiaofei
Du, Qin
Wang, Rui
Shi, Ziyan
Chen, Hongxi
Zhou, Hongyu
author_sort Sun, Dongren
collection PubMed
description BACKGROUND: Observational studies have suggested an association between coronavirus disease 2019 (COVID‐19) and myasthenia gravis (MG). Here, we aimed to estimate the genetic correlation and causal relationship between COVID‐19 susceptibility, hospitalization, severity, and MG phenotypes using linkage disequilibrium score regression (LDSC) and Mendelian randomization (MR) approach. METHODS: Summary statistics of COVID‐19 susceptibility, hospitalization, and severity were used as instrumental variables for exposure traits. Large‐scale genome‐wide association study (GWAS) data for MG were used as outcome traits. The inverse variance weighted approach was used for the main MR analysis, complemented by MR‐Egger, weighted median, simple mode, and weighted mode methods. Sensitivity analysis was implemented using Cochran's Q test, MR‐PRESSO method, and MR‐Egger intercept test. RESULTS: LDSC analysis did not reveal any genetic correlation among COVID‐19 susceptibility, hospitalization, severity, and MG phenotypes, including MG, early‐onset MG, and late‐onset MG (p > .05). Our MR analysis did not provide evidence supporting a causal effect of COVID‐19 susceptibility, hospitalization, or severity on MG phenotypes (p > .05). Extensive sensitivity analysis strengthened the robustness and consistency of the MR estimates. CONCLUSION: Our study did not find evidence of a genetic correlation or causal relationship among COVID‐19 susceptibility, hospitalization, severity, and MG. Future studies with more GWAS data are needed to evaluate the association between COVID‐19 phenotypes and MG and its subgroups.
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spelling pubmed-106363972023-11-15 Association between COVID‐19 and myasthenia gravis (MG): A genetic correlation and Mendelian randomization study Sun, Dongren Tu, Liangdan Wang, Xiaofei Du, Qin Wang, Rui Shi, Ziyan Chen, Hongxi Zhou, Hongyu Brain Behav Brief Report BACKGROUND: Observational studies have suggested an association between coronavirus disease 2019 (COVID‐19) and myasthenia gravis (MG). Here, we aimed to estimate the genetic correlation and causal relationship between COVID‐19 susceptibility, hospitalization, severity, and MG phenotypes using linkage disequilibrium score regression (LDSC) and Mendelian randomization (MR) approach. METHODS: Summary statistics of COVID‐19 susceptibility, hospitalization, and severity were used as instrumental variables for exposure traits. Large‐scale genome‐wide association study (GWAS) data for MG were used as outcome traits. The inverse variance weighted approach was used for the main MR analysis, complemented by MR‐Egger, weighted median, simple mode, and weighted mode methods. Sensitivity analysis was implemented using Cochran's Q test, MR‐PRESSO method, and MR‐Egger intercept test. RESULTS: LDSC analysis did not reveal any genetic correlation among COVID‐19 susceptibility, hospitalization, severity, and MG phenotypes, including MG, early‐onset MG, and late‐onset MG (p > .05). Our MR analysis did not provide evidence supporting a causal effect of COVID‐19 susceptibility, hospitalization, or severity on MG phenotypes (p > .05). Extensive sensitivity analysis strengthened the robustness and consistency of the MR estimates. CONCLUSION: Our study did not find evidence of a genetic correlation or causal relationship among COVID‐19 susceptibility, hospitalization, severity, and MG. Future studies with more GWAS data are needed to evaluate the association between COVID‐19 phenotypes and MG and its subgroups. John Wiley and Sons Inc. 2023-08-28 /pmc/articles/PMC10636397/ /pubmed/37638499 http://dx.doi.org/10.1002/brb3.3239 Text en © 2023 The Authors. Brain and Behavior published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Brief Report
Sun, Dongren
Tu, Liangdan
Wang, Xiaofei
Du, Qin
Wang, Rui
Shi, Ziyan
Chen, Hongxi
Zhou, Hongyu
Association between COVID‐19 and myasthenia gravis (MG): A genetic correlation and Mendelian randomization study
title Association between COVID‐19 and myasthenia gravis (MG): A genetic correlation and Mendelian randomization study
title_full Association between COVID‐19 and myasthenia gravis (MG): A genetic correlation and Mendelian randomization study
title_fullStr Association between COVID‐19 and myasthenia gravis (MG): A genetic correlation and Mendelian randomization study
title_full_unstemmed Association between COVID‐19 and myasthenia gravis (MG): A genetic correlation and Mendelian randomization study
title_short Association between COVID‐19 and myasthenia gravis (MG): A genetic correlation and Mendelian randomization study
title_sort association between covid‐19 and myasthenia gravis (mg): a genetic correlation and mendelian randomization study
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10636397/
https://www.ncbi.nlm.nih.gov/pubmed/37638499
http://dx.doi.org/10.1002/brb3.3239
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