Gastroesophageal reflux disease increases predisposition to severe COVID-19: Insights from integrated Mendelian randomization and genetic analysis

被引:0
作者
Pan, Jingjing [1 ,2 ]
Li, Jianhua [1 ,2 ]
机构
[1] Zhejiang Prov Ctr Dis Control & Prevent, Dept Microbiol, Hangzhou, Peoples R China
[2] Zhejiang Key Lab Publ Hlth Detect & Pathogenesis R, Hangzhou, Peoples R China
关键词
colocalization analysis; COVID-19; gastroesophageal reflux disease; Mendelian randomization; molecular pathway analysis; shared genomic loci; RISK;
D O I
10.1111/ahg.12584
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
ObjectiveThis study aims to investigate the potential causal relationship, shared genomic loci, as well as potential molecular pathways and tissue-specific expression patterns between gastroesophageal reflux disease (GERD) and the risk of hospitalized/severe 2019 coronavirus disease (COVID-19).MethodsWe employed linkage disequilibrium score regression and bidirectional Mendelian randomization (MR) analysis to explore potential genetic associations between GERD (N = 602,604) and hospitalized COVID-19 (N = 2095,324) as well as severe COVID-19 (N = 1086,211). Additionally, shared genomic loci were extracted from common pivotal regions, further confirmed through corresponding colocalization analyses. GERD-driven molecular pathway network was constructed using extensive literature data mining to understand the molecular-level impacts of GERD on COVID-19.ResultsOur results revealed a significant positive genetic correlation between GERD and both hospitalized (rg = 0.418) and severe COVID-19 (rg = 0.314). Furthermore, the MR analysis demonstrated a unidirectional causal effect of genetic predisposition to GERD on COVID-19 outcomes, including hospitalized COVID-19 (odds ratio [OR]: 1.33, 95% confidence interval [CI]: 1.27-1.44, p = 9.17e - 12) and severe COVID-19 (OR: 1.27, 95% CI: 1.18-1.37, p = 1.20e - 05). Additionally, GERD and both COVID-19 conditions shared one genomic locus with lead-SNPs rs1011407 and rs1123573, corresponding to the transcription factor BCL11A. Colocalization analysis further demonstrated a significant positive correlation between genome-wide association study and expression quantitative trait locus (eQTL) abnormalities, including rs1011407 (eQTL_p = 2.35e - 07) and rs1123573 (eQTL_p = 2.74e - 05). Molecular pathway analysis indicated that GERD might promote the progression of COVID-19 by inducting immune-activated and inflammation-related pathways.ConclusionThese findings confirm that genetically determined GERD may increase the susceptibility to hospitalized/severe COVID-19. The shared genetic loci and the potential molecular pathways offer valuable insights into causal connections between GERD and COVID-19.
引用
收藏
页码:54 / 65
页数:12
相关论文
共 45 条
  • [31] Gastroesophageal reflux disease-associated esophagitis induces endogenous cytokine production leading to motor abnormalities
    Rieder, Florian
    Cheng, Ling
    Harnett, Karen M.
    Chak, Amitabh
    Cooper, Gregory S.
    Isenberg, Gerard
    Ray, Monica
    Katz, Jeffry A.
    Catanzaro, Andrew
    O'Shea, Robert
    Post, Anthony B.
    Wong, Richard
    Sivak, Michael V.
    McCormick, Thomas
    Phillips, Manijeh
    West, Gail A.
    Willis, Joseph E.
    Biancani, Piero
    Fiocchi, Claudio
    [J]. GASTROENTEROLOGY, 2007, 132 (01) : 154 - 165
  • [32] Genetic polymorphisms of ACE1, ACE2, and TMPRSS2 associated with COVID-19 severity: A systematic review with meta-analysis
    Saengsiwaritt, Wacharapol
    Jittikoon, Jiraphun
    Chaikledkaew, Usa
    Udomsinprasert, Wanvisa
    [J]. REVIEWS IN MEDICAL VIROLOGY, 2022, 32 (04)
  • [33] Contributions of human ACE2 and TMPRSS2 in determining host-pathogen interaction of COVID-19
    Senapati, Sabyasachi
    Banerjee, Pratibha
    Bhagavatula, Sandilya
    Kushwaha, Prem Prakash
    Kumar, Shashank
    [J]. JOURNAL OF GENETICS, 2021, 100 (01)
  • [34] Cytoscape: A software environment for integrated models of biomolecular interaction networks
    Shannon, P
    Markiel, A
    Ozier, O
    Baliga, NS
    Wang, JT
    Ramage, D
    Amin, N
    Schwikowski, B
    Ideker, T
    [J]. GENOME RESEARCH, 2003, 13 (11) : 2498 - 2504
  • [35] Szklarczyk D, 2019, NUCLEIC ACIDS RES, V47, pD607, DOI [10.1093/nar/gky1131, 10.1093/nar/gkac1000]
  • [36] Insights to SARS-CoV-2 life cycle, pathophysiology, and rationalized treatments that target COVID-19 clinical complications
    Trougakos, Ioannis P.
    Stamatelopoulos, Kimon
    Terpos, Evangelos
    Tsitsilonis, Ourania E.
    Aivalioti, Evmorfia
    Paraskevis, Dimitrios
    Kastritis, Efstathios
    Pavlakis, George N.
    Dimopoulos, Meletios A.
    [J]. JOURNAL OF BIOMEDICAL SCIENCE, 2021, 28 (01)
  • [37] Self-medication in hospitalized patients with COVID-19: A cross-sectional study in northern Peru
    Vasquez-Elera, Luis E.
    Failoc-Rojas, Virgilio E.
    Martinez-Rivera, Raisa N.
    Morocho-Alburqueque, Noelia
    Temoche-Rivas, Mario S.
    Valladares-Garrido, Mario J.
    [J]. GERMS, 2022, 12 (01): : 46 - 53
  • [38] Detection of widespread horizontal pleiotropy in causal relationships inferred from Mendelian randomization between complex traits and diseases
    Verbanck, Marie
    Chen, Chia-Yen
    Neale, Benjamin
    Do, Ron
    [J]. NATURE GENETICS, 2018, 50 (05) : 693 - +
  • [39] A simple new approach to variable selection in regression, with application to genetic fine mapping
    Wang, Gao
    Sarkar, Abhishek
    Carbonetto, Peter
    Stephens, Matthew
    [J]. JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 2020, 82 (05) : 1273 - 1300
  • [40] Functional mapping and annotation of genetic associations with FUMA
    Watanabe, Kyoko
    Taskesen, Erdogan
    van Bochoven, Arjen
    Posthuma, Danielle
    [J]. NATURE COMMUNICATIONS, 2017, 8