Clonal hematopoiesis is associated with risk of severe Covid-19

Kelly L. Bolton(Washington University in St. Louis), Youngil Koh(Seoul National University Hospital), Michael B. Foote(Memorial Sloan Kettering Cancer Center), Hogune Im(Genome and Company (South Korea)), Justin Jee(Memorial Sloan Kettering Cancer Center), Choong Hyun Sun(Genome and Company (South Korea)), Anton Safonov(Memorial Sloan Kettering Cancer Center), Ryan Ptashkin(Memorial Sloan Kettering Cancer Center), Joon Ho Moon(Kyungpook National University Hospital), Ji Yeon Lee(National Medical Center), Jongtak Jung(Seoul National University Bundang Hospital), Chang Kyung Kang(Seoul National University Hospital), Kyoung‐Ho Song(Seoul National University Bundang Hospital), Pyoeng Gyun Choe(Seoul National University Hospital), Wan Beom Park(Seoul National University Hospital), Hong Bin Kim(Seoul National University Bundang Hospital), Myoung‐don Oh(Seoul National University Hospital), Han Song(Genome and Company (South Korea)), Sugyeong Kim(Genome and Company (South Korea)), Minal Patel(Memorial Sloan Kettering Cancer Center), Andriy Derkach(Memorial Sloan Kettering Cancer Center), Erika Gedvilaite(Memorial Sloan Kettering Cancer Center), Kaitlyn Tkachuk(Memorial Sloan Kettering Cancer Center), Brian J. Wiley(Washington University in St. Louis), Ireaneus C. Chan(Washington University in St. Louis), Lior Z. Braunstein(Memorial Sloan Kettering Cancer Center), Teng Gao(Memorial Sloan Kettering Cancer Center), Elli Papaemmanuil(Memorial Sloan Kettering Cancer Center), N. Esther Babady(Memorial Sloan Kettering Cancer Center), Melissa S. Pessin(Memorial Sloan Kettering Cancer Center), Mini Kamboj(Memorial Sloan Kettering Cancer Center), Luis A. Díaz(Memorial Sloan Kettering Cancer Center), Marc Ladanyi(Memorial Sloan Kettering Cancer Center), Michael J. Rauh(Queen's University), Pradeep Natarajan(Brigham and Women's Hospital), Mitchell J. Machiela(National Cancer Institute), Philip Awadalla(Ontario Institute for Cancer Research), Joseph Vijai(Memorial Sloan Kettering Cancer Center), Kenneth Offit(Memorial Sloan Kettering Cancer Center), Larry Norton(Memorial Sloan Kettering Cancer Center), Michael F. Berger(Memorial Sloan Kettering Cancer Center), Ross L. Levine(Memorial Sloan Kettering Cancer Center), Eu Suk Kim(Seoul National University Bundang Hospital), Nam Joong Kim(Seoul National University Hospital), Ahmet Zehir(Memorial Sloan Kettering Cancer Center)
Nature Communications
October 13, 2021
Cited by 140Open Access
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Abstract

Abstract Acquired somatic mutations in hematopoietic stem and progenitor cells (clonal hematopoiesis or CH) are associated with advanced age, increased risk of cardiovascular and malignant diseases, and decreased overall survival. These adverse sequelae may be mediated by altered inflammatory profiles observed in patients with CH. A pro-inflammatory immunologic profile is also associated with worse outcomes of certain infections, including SARS-CoV-2 and its associated disease Covid-19. Whether CH predisposes to severe Covid-19 or other infections is unknown. Among 525 individuals with Covid-19 from Memorial Sloan Kettering (MSK) and the Korean Clonal Hematopoiesis (KoCH) consortia, we show that CH is associated with severe Covid-19 outcomes (OR = 1.85, 95%=1.15–2.99, p = 0.01), in particular CH characterized by non-cancer driver mutations (OR = 2.01, 95% CI = 1.15–3.50, p = 0.01). We further explore the relationship between CH and risk of other infections in 14,211 solid tumor patients at MSK. CH is significantly associated with risk of Clostridium Difficile (HR = 2.01, 95% CI: 1.22–3.30, p = 6×10 −3 ) and Streptococcus/Enterococcus infections (HR = 1.56, 95% CI = 1.15–2.13, p = 5×10 −3 ). These findings suggest a relationship between CH and risk of severe infections that warrants further investigation.


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