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Causal associations between obstructive sleep apnea and COVID-19: A bidirectional Mendelian randomization study

BACKGROUNDS: The COVID-19 pandemic has caused significant impact on human health. Whether obstructive sleep apnea (OSA) increases the risk of COVID-19 remains unclear. We sought to clarify this issue using two-sample Mendelian randomization (TSMR) analysis in large cohorts. METHODS: Bidirectional tw...

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Detalles Bibliográficos
Autores principales: Gao, Xiang, Wei, Tao, Wang, Huijun, Sui, Rongcui, Liao, Jianhong, Sun, Dance, Han, Demin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier B.V. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9557138/
https://www.ncbi.nlm.nih.gov/pubmed/36334498
http://dx.doi.org/10.1016/j.sleep.2022.09.013
Descripción
Sumario:BACKGROUNDS: The COVID-19 pandemic has caused significant impact on human health. Whether obstructive sleep apnea (OSA) increases the risk of COVID-19 remains unclear. We sought to clarify this issue using two-sample Mendelian randomization (TSMR) analysis in large cohorts. METHODS: Bidirectional two-sample Mendelian randomization (MR) was used to evaluate the potential causality between OSA and COVID-19 by selecting single-nucleotide polymorphisms (SNPs) as instrumental variables (IVs) from genome-wide association studies (GWAS). The inverse-variance weighted (IVW) method was selected as the main approach for data analysis to estimate the possible causal effects. Alternative methods such as MR-Egger, the MR pleiotropy residual sum and outlier (MR-PRESSO), and leave-one-out analysis methods were implemented as sensitivity analysis approaches to ensure the robustness of the results. RESULTS: All forward MR analyses consistently indicated the absence of a causal relationship between OSA and any COVID-19 phenotype. In the reverse MR analysis, the IVW mode demonstrated that severe respiratory confirmed COVID-19 was correlated with a 4.9% higher risk of OSA (OR, 1.049; 95%CI, 1.018–1.081; P = 0.002), consistent in MR-PRESSO (OR = 1.049, 95%CI 1.018–1.081, P = 0.004), weighted median (OR = 1.048, 95%CI 1.003–1.095, P = 0.035), and MR-Egger (OR = 1.083, 95%CI 1.012–1.190, P = 0.041) methods. CONCLUSIONS: There is no significant evidence supporting a causal association between OSA and any COVID phenotype, while we identified potential evidence for a causal effect of severe COVID-19 on an increased risk of OSA.