Author:
Bolton Kelly L.,Koh Youngil,Foote Michael B.,Im Hogune,Jee Justin,Sun Choong Hyun,Safonov Anton,Ptashkin Ryan,Moon Joon Ho,Lee Ji Yeon,Jung Jongtak,Kang Chang Kyung,Song Kyoung-Ho,Choe Pyeong Gyun,Park Wan Beom,Kim Hong Bin,Oh Myoung-don,Song Han,Kim Sugyeong,Patel Minal,Derkach Andriy,Gedvilaite Erika,Tkachuk Kaitlyn A.,Braunstein Lior Z.,Gao Teng,Papaemmanuil Elli,Babady N. Esther,Pessin Melissa S.,Kamboj Mini,Diaz Luis A.,Ladanyi Marc,Rauh Michael J.,Natarajan Pradeep,Machiela Mitchell J.,Awadalla Philip,Joseph Vijai,Offit Kenneth,Norton Larry,Berger Michael F,Levine Ross L,Kim Eu Suk,Kim Nam Joong,Zehir Ahmet
Abstract
ABSTRACTAcquired 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.1–4 These adverse sequelae may be mediated by altered inflammatory profiles observed in patients with CH.2,5,6 A pro-inflammatory immunologic profile is also associated with worse outcomes of certain infections, including SARS-CoV-2 and its associated disease Covid-19.7,8 Whether CH predisposes to severe Covid-19 or other infections is unknown. Among 515 individuals with Covid-19 from Memorial Sloan Kettering (MSK) and the Korean Clonal Hematopoiesis (KoCH) consortia, we found that CH was associated with severe Covid-19 outcomes (OR=1.9, 95%=1.2-2.9, p=0.01). We further explored the relationship between CH and risk of other infections in 14,211 solid tumor patients at MSK. CH was significantly associated with risk of Clostridium Difficile (HR=2.0, 95% CI: 1.2-3.3, p=6×10−3) and Streptococcus/Enterococcus infections (HR=1.5, 95% CI=1.1-2.1, p=5×10−3). These findings suggest a relationship between CH and risk of severe infections that warrants further investigation.
Publisher
Cold Spring Harbor Laboratory