TY - JOUR
T1 - A MUC5B Gene Polymorphism, rs35705950-T, Confers Protective Effects Against COVID-19 Hospitalization but Not Severe Disease or Mortality
AU - Million Veteran Program COVID-19 Science Initiative
AU - Verma, Anurag
AU - Minnier, Jessica
AU - Wan, Emily S.
AU - Huffman, Jennifer E.
AU - Gao, Lina
AU - Joseph, Jacob
AU - Ho, Yuk Lam
AU - Wu, Wen Chih
AU - Cho, Kelly
AU - Gorman, Bryan R.
AU - Rajeevan, Nallakkandi
AU - Pyarajan, Saiju
AU - Garcon, Helene
AU - Meigs, James B.
AU - Sun, Yan V.
AU - Reaven, Peter D.
AU - McGeary, John E.
AU - Suzuki, Ayako
AU - Gelernter, Joel
AU - Lynch, Julie A.
AU - Petersen, Jeffrey M.
AU - Zekavat, Seyedeh Maryam
AU - Natarajan, Pradeep
AU - Dalal, Sharvari
AU - Jhala, Darshana N.
AU - Arjomandi, Mehrdad
AU - Gatsby, Elise
AU - Lynch, Kristine E.
AU - Bonomo, Robert A.
AU - Freiberg, Matthew
AU - Pathak, Gita A.
AU - Zhou, Jin J.
AU - Donskey, Curtis J.
AU - Madduri, Ravi K.
AU - Wells, Quinn S.
AU - Huang, Rose D.L.
AU - Polimanti, Renato
AU - Chang, Kyong Mi
AU - Liao, Katherine P.
AU - Tsao, Philip S.
AU - Wilson, Peter W.F.
AU - Hung, Adriana M.
AU - O’Donnell, Christopher J.
AU - Gaziano, John M.
AU - Hauger, Richard L.
AU - Iyengar, Sudha K.
AU - Luoh, Shiuh Wen
N1 - Publisher Copyright:
Copyright © 2022 by the American Thoracic Society.
PY - 2022/11/15
Y1 - 2022/11/15
N2 - 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 3 1023) and joint meta-analyses with the HGI (Ncases = 13,320; Ncontrols = 1,508,841; OR, 0.90 [0.86–0.95]; P = 8.99 3 1025). 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.
AB - 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 3 1023) and joint meta-analyses with the HGI (Ncases = 13,320; Ncontrols = 1,508,841; OR, 0.90 [0.86–0.95]; P = 8.99 3 1025). 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.
KW - coronavirus disease 2019
KW - electronic health records
KW - genetic association
KW - idiopathic pulmonary fibrosis
KW - severe acute respiratory syndrome coronavirus 2
UR - http://www.scopus.com/inward/record.url?scp=85142400476&partnerID=8YFLogxK
U2 - 10.1164/RCCM.202109-2166OC
DO - 10.1164/RCCM.202109-2166OC
M3 - Article
C2 - 35771531
AN - SCOPUS:85142400476
SN - 1073-449X
VL - 206
SP - 1220
EP - 1229
JO - American Journal of Respiratory and Critical Care Medicine
JF - American Journal of Respiratory and Critical Care Medicine
IS - 10
ER -