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Birth Weight Is Associated With Clonal Hematopoiesis of Indeterminate Potential and Cardiovascular Outcomes in Adulthood

Schuermans, Art (author)
Broad Institute,Massachusetts General Hospital
Nakao, Tetsushi (author)
Massachusetts General Hospital,Broad Institute,Brigham and Women's Hospital / Harvard Medical School
Ruan, Yunfeng (author)
Broad Institute,Massachusetts General Hospital
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Koyama, Satoshi (author)
Broad Institute,Massachusetts General Hospital
Yu, Zhi (author)
Massachusetts General Hospital,Broad Institute
Uddin, Md Mesbah (author)
Broad Institute,Massachusetts General Hospital
Haidermota, Sara (author)
Massachusetts General Hospital,Broad Institute
Hornsby, Whitney (author)
Broad Institute,Massachusetts General Hospital
Lewandowski, Adam J. (author)
University of Oxford
Bick, Alexander G. (author)
Vanderbilt University Medical Center
Niroula, Abhishek (author)
Lund University,Lunds universitet,Institutionen för laboratoriemedicin,Medicinska fakulteten,Department of Laboratory Medicine,Faculty of Medicine,Dana-Farber Cancer Institute,Broad Institute
Jaiswal, Siddhartha (author)
Stanford University School of Medicine
Ebert, Benjamin L. (author)
Dana-Farber Cancer Institute,Howard Hughes Medical Institute
Natarajan, Pradeep (author)
Harvard Medical School,Broad Institute,Massachusetts General Hospital
Honigberg, Michael C. (author)
Massachusetts General Hospital,Broad Institute,Harvard Medical School
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 (creator_code:org_t)
2023
2023
English.
In: Journal of the American Heart Association. - 2047-9980. ; 12:13
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • BACKGROUND: High and low birth weight are independently associated with increased cardiovascular disease risk in adulthood. Clonal hematopoiesis of indeterminate potential (CHIP), the age-related clonal expansion of hematopoietic cells with preleu-kemic somatic mutations, predicts incident cardiovascular disease independent of traditional cardiovascular risk factors. Whether birth weight predicts development of CHIP later in life is unknown. METHODS AND RESULTS: A total of 221 047 adults enrolled in the UK Biobank with whole exome sequences and self-reported birth weight were analyzed. Of those, 22 030 (11.5%) had low (<2.5 kg) and 29 292 (14.7%) high birth weight (>4.0 kg). CHIP prevalence was higher among participants with low (6.0%, P=0.049) and high (6.3%, P<0.001) versus normal birth weight (5.7%, ref.). Multivariable-adjusted logistic regression analyses demonstrated that each 1-kg increase in birth weight was associated with a 3% increased risk of CHIP (odds ratio, 1.03 [95% CI, 1.00–1.06]; P=0.04), driven by a stronger association ob-served between birth weight and DNMT3A CHIP (odds ratio, 1.04 per 1-kg increase [95% CI, 1.01–1.08]; P=0.02). Mendelian randomization analyses supported a causal relationship of longer gestational age at delivery with DNMT3A CHIP. Multivariable Cox regression demonstrated that CHIP was independently and additively associated with incident cardiovascular disease or death across birth weight groups, with highest absolute risks in those with CHIP plus high or low birth weight. CONCLUSIONS: Higher birth weight is associated with increased risk of developing CHIP in midlife, especially DNMT3A CHIP. These findings identify a novel risk factor for CHIP and provide insights into the relationships among early-life environment, CHIP, cancer, and cardiovascular disease.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Kardiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cardiac and Cardiovascular Systems (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Hälsovetenskap -- Folkhälsovetenskap, global hälsa, socialmedicin och epidemiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Health Sciences -- Public Health, Global Health, Social Medicine and Epidemiology (hsv//eng)

Keyword

birth weight
cardiovascular disease
clonal hematopoiesis
early life
genetics

Publication and Content Type

art (subject category)
ref (subject category)

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