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Genetics of smoking and risk of clonal hematopoiesis.
Levin, Michael G; Nakao, Tetsushi; Zekavat, Seyedeh M; Koyama, Satoshi; Bick, Alexander G; Niroula, Abhishek; Ebert, Benjamin; Damrauer, Scott M; Natarajan, Pradeep.
Afiliação
  • Levin MG; Division of Cardiovascular Medicine, Department of Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
  • Nakao T; Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA, USA.
  • Zekavat SM; Program in Medical and Population Genetics and Cardiovascular Disease Initiative, Broad Institute of Harvard and MIT, Cambridge, MA, USA.
  • Koyama S; Cardiovascular Research Center, Massachusetts General Hospital, 185 Cambridge Street, CPZN 3.184, Boston, MA, 02114, USA.
  • Bick AG; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
  • Niroula A; Division of Cardiovascular Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, MA, USA.
  • Ebert B; Program in Medical and Population Genetics and Cardiovascular Disease Initiative, Broad Institute of Harvard and MIT, Cambridge, MA, USA.
  • Damrauer SM; Yale University School of Medicine, New Haven, CT, USA.
  • Natarajan P; Program in Medical and Population Genetics and Cardiovascular Disease Initiative, Broad Institute of Harvard and MIT, Cambridge, MA, USA.
Sci Rep ; 12(1): 7248, 2022 05 04.
Article em En | MEDLINE | ID: mdl-35508625
Clonal hematopoiesis of indeterminate potential (CHIP) and mosaic chromosomal alterations (mCAs) represent two forms of clonal hematopoiesis where clones bearing expanded somatic mutations have been linked to both oncologic and non-oncologic clinical outcomes including atherosclerosis and all-cause mortality. Epidemiologic studies have highlighted smoking as an important driver of somatic mutations across multiple tissues. However, establishing the causal role of smoking in clonal hematopoiesis has been limited by observational study designs, which may suffer from confounding and reverse-causality. We performed two complementary analyses to investigate the role of smoking in mCAs and CHIP. First, using an observational study design among UK Biobank participants, we confirmed strong associations between smoking and mCAs. Second, using two-sample Mendelian randomization, smoking was strongly associated with mCA but not with CHIP. Overall, these results support a causal association between smoking and mCAs and suggest smoking may variably shape the fitness of clones bearing somatic mutations.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Aterosclerose / Hematopoiese Clonal Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Aterosclerose / Hematopoiese Clonal Idioma: En Ano de publicação: 2022 Tipo de documento: Article