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Circulation. 2002;106:337-341
Published online before print June 10, 2002, doi: 10.1161/01.CIR.0000022663.26468.5B
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(Circulation. 2002;106:337.)
© 2002 American Heart Association, Inc.


Clinical Investigation and Reports

Evidence for Heritability of Abdominal Aortic Calcific Deposits in the Framingham Heart Study

Christopher J. O’Donnell, MD, MPH; Irmarie Chazaro, MA; Peter W.F. Wilson, MD; Caroline Fox, MD; Marian T. Hannan, ScD; Douglas P. Kiel, MD, MPH; L. Adrienne Cupples, PhD

From the National Heart, Lung and Blood Institute’s Framingham Heart Study (C.J.O., P.W.F.W., C.F.), Framingham, Mass; the Cardiology Division (C.J.O.), Department of Medicine, Massachusetts General Hospital, the Hebrew Rehabilitation Center for Aged Research and Training Institute and the Division on Aging (M.H., D.K.), Harvard Medical School, Boston, Mass; the Boston University School of Public Health Department of Epidemiology and Biostatistics (I.C., L.A.C.), Boston, Mass; and the National Heart, Lung and Blood Institute, National Institutes of Health (C.J.O.), Bethesda, Md.

Correspondence to Christopher J. O’Donnell, MD, MPH, Framingham Heart Study, 73 Mount Wayte Ave, Framingham, MA 01702. E-mail chris{at}fram.nhlbi.nih.gov

Background Atherosclerosis is a systemic disease that underlies clinical cardiovascular disease. The radiographic finding of abdominal aortic calcific deposits is an indicator of the presence of aortic atherosclerosis and an independent predictor of cardiovascular disease events. Little is known about the heritability of aortic calcification.

Methods and Results Original Framingham Heart Study cohort participants (2151) in 1109 extended pedigrees had a lateral lumbar radiograph. The presence and severity of abdominal aortic calcific (AAC) deposits at the levels of the first through fourth lumbar vertebrae was graded by a previously validated rating scale. Correlation coefficients were calculated in pairs of siblings, parent-offspring, and spouses. Age-, sex-, and multivariable-adjusted correlation coefficients for AAC were 0.52 for parent-offspring pairs and 0.20 for sibling pairs. In contrast, the multivariable-adjusted correlation for AAC in spouse pairs was -0.02. Using variance component methods implemented in SOLAR, the estimated heritability for age-, sex-, and multivariable-adjusted AAC was 0.49 (P<0.001). Thirty-one percent of the overall variance in AAC deposits was due to measured covariates, and 49% to heritable factors.

Conclusions In our large, population-based sample, heritable factors play a role in the presence and extent of abdominal aortic calcification. Thus, a substantial proportion of the variation in AAC is due to additive effects of genes, which have yet to be characterized. Measures of aortic atherosclerosis may provide heritable quantitative phenotypes for the genetic dissection of the complex condition of atherosclerosis in human populations.


Key Words: atherosclerosis • calcification • abdominal aorta • genetics • heritability




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