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Genetics of smoking and risk of clonal hematopoiesis

Levin, Michael G. (author)
University of Pennsylvania,Veterans Health Administration
Nakao, Tetsushi (author)
Brigham and Women's Hospital / Harvard Medical School,Dana-Farber Cancer Institute,Broad Institute,Massachusetts General Hospital
Zekavat, Seyedeh M. (author)
Yale University,Broad Institute
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Koyama, Satoshi (author)
Broad Institute
Bick, Alexander G. (author)
Vanderbilt University
Niroula, Abhishek (author)
Lund University,Lunds universitet,Hematogenomics,Forskargrupper vid Lunds universitet,LUCC: Lunds universitets cancercentrum,Övriga starka forskningsmiljöer,Lund University Research Groups,LUCC: Lund University Cancer Centre,Other Strong Research Environments,Broad Institute,Dana-Farber Cancer Institute
Ebert, Benjamin (author)
Dana-Farber Cancer Institute,Harvard Medical School,Howard Hughes Medical Institute
Damrauer, Scott M. (author)
University of Pennsylvania,Veterans Health Administration
Natarajan, Pradeep (author)
Massachusetts General Hospital,Broad Institute,Harvard Medical School
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 (creator_code:org_t)
2022-05-04
2022
English.
In: Scientific Reports. - : Springer Science and Business Media LLC. - 2045-2322. ; 12:1
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • 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.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Medicinsk genetik (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Medical Genetics (hsv//eng)

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