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A MUC5B Gene Polymorphism, rs35705950-T, Confers Protective Effects Against COVID-19 Hospitalization but Not Severe Disease or Mortality.
Verma, Anurag; Minnier, Jessica; Wan, Emily S; Huffman, Jennifer E; Gao, Lina; Joseph, Jacob; Ho, Yuk-Lam; Wu, Wen-Chih; Cho, Kelly; Gorman, Bryan R; Rajeevan, Nallakkandi; Pyarajan, Saiju; Garcon, Helene; Meigs, James B; Sun, Yan V; Reaven, Peter D; McGeary, John E; Suzuki, Ayako; Gelernter, Joel; Lynch, Julie A; Petersen, Jeffrey M; Zekavat, Seyedeh Maryam; Natarajan, Pradeep; Dalal, Sharvari; Jhala, Darshana N; Arjomandi, Mehrdad; Gatsby, Elise; Lynch, Kristine E; Bonomo, Robert A; Freiberg, Matthew; Pathak, Gita A; Zhou, Jin J; Donskey, Curtis J; Madduri, Ravi K; Wells, Quinn S; Huang, Rose D L; Polimanti, Renato; Chang, Kyong-Mi; Liao, Katherine P; Tsao, Philip S; Wilson, Peter W F; Hung, Adriana M; O'Donnell, Christopher J; Gaziano, John M; Hauger, Richard L; Iyengar, Sudha K; Luoh, Shiuh-Wen.
  • Verma A; Corporal Michael J. Crescenz VA Medical Center, Philadelphia, Pennsylvania.
  • Minnier J; Department of Medicine, Perelman School of Medicine, and.
  • Wan ES; OHSU-PSU School of Public Health and.
  • Huffman JE; Knight Cancer Institute, Oregon Health & Science University, Portland, Oregon.
  • Gao L; VA Portland Health Care System, Portland, Oregon.
  • Joseph J; Department of Medicine, Pulmonary, Critical Care, Sleep, and Allergy Section.
  • Ho YL; Channing Division of Network Medicine and.
  • Wu WC; MAVERIC.
  • Cho K; Knight Cancer Institute, Oregon Health & Science University, Portland, Oregon.
  • Gorman BR; VA Portland Health Care System, Portland, Oregon.
  • Rajeevan N; Department of Medicine.
  • Pyarajan S; Medicine, Cardiovascular, Brigham & Women's Hospital, Boston, Massachusetts.
  • Garcon H; MAVERIC.
  • Meigs JB; Department of Medicine, Cardiology, Providence VA Healthcare System, Providence, Rhode Island.
  • Sun YV; Alpert Medical School & School of Public Health, Brown University, Providence, Rhode Island.
  • Reaven PD; MAVERIC.
  • McGeary JE; Medicine, Aging, Brigham & Women's Hospital and.
  • Suzuki A; MAVERIC.
  • Gelernter J; Yale Center for Medical Informatics.
  • Lynch JA; Clinical Epidemiology Research Center (CERC).
  • Petersen JM; MAVERIC.
  • Zekavat SM; Department of Medicine, Harvard Medical School, Boston, Massachusetts.
  • Natarajan P; MAVERIC.
  • Dalal S; Medicine, General Internal Medicine and.
  • Jhala DN; Epidemiology, School of Public Health and.
  • Arjomandi M; Atlanta VA Healthcare System, Decatur, Georgia.
  • Gatsby E; Department of Medicine, Phoenix VA Healthcare System, Phoenix, Arizona.
  • Lynch KE; College of Medicine, University of Arizona, Phoenix, Arizona.
  • Bonomo RA; Department of Psychiatry and Human Behavior, Providence VA Medical Center, Providence, Rhode Island.
  • Freiberg M; Department of Psychiatry and Human Behavior, Brown University Medical School, Providence, Rhode Island.
  • Pathak GA; Department of Medicine, Gastroenterology, Durham VA Medical Center, Durham, North Carolina.
  • Zhou JJ; Department of Medicine, Gastroenterology, Duke University, Durham, North Carolina.
  • Donskey CJ; Division of Human Genetics, Department of Psychiatry, and.
  • Madduri RK; VA Connecticut Healthcare System, West Haven, Connecticut.
  • Wells QS; VA Informatics & Computing Infrastructure (VINCI), VA Salt Lake City Healthcare System, Salt Lake City, Utah.
  • Huang RDL; Department of Medicine and.
  • Polimanti R; Corporal Michael J. Crescenz VA Medical Center, Philadelphia, Pennsylvania.
  • Chang KM; Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Liao KP; Computational Biology & Bioinformatics, Yale University School of Medicine, New Haven, Connecticut.
  • Tsao PS; Program in Medical and Population Genetics, Cardiovascular Disease Initiative, Broad Institute of Harvard and MIT, Cambridge, Massachusetts.
  • Wilson PWF; Department of Medicine, Harvard Medical School, Boston, Massachusetts.
  • Hung AM; Cardiovascular Research Center, Massachusetts General Hospital, Boston, Massachusetts.
  • O'Donnell CJ; Program in Medical and Population Genetics, Cardiovascular Disease Initiative, Broad Institute of Harvard and MIT, Cambridge, Massachusetts.
  • Gaziano JM; Corporal Michael J. Crescenz VA Medical Center, Philadelphia, Pennsylvania.
  • Hauger RL; Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Iyengar SK; Corporal Michael J. Crescenz VA Medical Center, Philadelphia, Pennsylvania.
  • Luoh SW; Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Am J Respir Crit Care Med ; 206(10): 1220-1229, 2022 Nov 15.
Article in English | MEDLINE | ID: covidwho-2138355
ABSTRACT
Rationale A common MUC5B gene polymorphism, rs35705950-T, is associated with idiopathic pulmonary fibrosis (IPF), but its role in severe acute respiratory syndrome coronavirus 2 infection and disease severity is unclear.

Objectives:

To assess whether rs35705950-T confers differential risk for clinical outcomes associated with coronavirus disease (COVID-19) infection among participants in the Million Veteran Program (MVP).

Methods:

The MUC5B rs35705950-T allele was directly genotyped among MVP participants; clinical events and comorbidities were extracted from the electronic health records. Associations between the incidence or severity of COVID-19 and rs35705950-T were analyzed within each ancestry group in the MVP followed by transancestry meta-analysis. Replication and joint meta-analysis were conducted using summary statistics from the COVID-19 Host Genetics Initiative (HGI). Sensitivity analyses with adjustment for additional covariates (body mass index, Charlson comorbidity index, smoking, asbestosis, rheumatoid arthritis with interstitial lung disease, and IPF) and associations with post-COVID-19 pneumonia were performed in MVP subjects. Measurements and Main

Results:

The rs35705950-T allele was associated with fewer COVID-19 hospitalizations in transancestry meta-analyses within the MVP (Ncases = 4,325; Ncontrols = 507,640; OR = 0.89 [0.82-0.97]; P = 6.86 × 10-3) and joint meta-analyses with the HGI (Ncases = 13,320; Ncontrols = 1,508,841; OR, 0.90 [0.86-0.95]; P = 8.99 × 10-5). The rs35705950-T allele was not associated with reduced COVID-19 positivity in transancestry meta-analysis within the MVP (Ncases = 19,168/Ncontrols = 492,854; OR, 0.98 [0.95-1.01]; P = 0.06) but was nominally significant (P < 0.05) in the joint meta-analysis with the HGI (Ncases = 44,820; Ncontrols = 1,775,827; OR, 0.97 [0.95-1.00]; P = 0.03). Associations were not observed with severe outcomes or mortality. Among individuals of European ancestry in the MVP, rs35705950-T was associated with fewer post-COVID-19 pneumonia events (OR, 0.82 [0.72-0.93]; P = 0.001).

Conclusions:

The MUC5B variant rs35705950-T may confer protection in COVID-19 hospitalizations.
Subject(s)
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Idiopathic Pulmonary Fibrosis / COVID-19 Type of study: Experimental Studies / Observational study / Prognostic study / Reviews Topics: Long Covid / Variants Limits: Humans Language: English Journal: Am J Respir Crit Care Med Journal subject: Critical Care Year: 2022 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Idiopathic Pulmonary Fibrosis / COVID-19 Type of study: Experimental Studies / Observational study / Prognostic study / Reviews Topics: Long Covid / Variants Limits: Humans Language: English Journal: Am J Respir Crit Care Med Journal subject: Critical Care Year: 2022 Document Type: Article