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American Journal of Epidemiology Vol. 143, No. 12: 1219-1228
Copyright © 1996 by The Johns Hopkins University School of Hygiene and Public Health


other

NHLBI Family Heart Study: Objectives and Design

Millicent Higgins1, Michael Province2, Gerardo Heiss3, John Eckfeldt4, R. Curtis Ellison5, Aaron R. Folsom4, D. C. Rao2,, J. Michael Sprafka4 and Roger Williams6

1National Heart, Lung, and Blood Institute Bethesda, MD.
2Washington University St. Louis, MO
3University of North Carolina Chapel Hill, NC
4University of Minnesota Minneapolis, MN
5Boston University Framingham, MA
6University of Utah Salt Lake City, UT

Reprint requests to Dr. D. C. Rao, Washington University School of Medicine, Division of Bbstatistics, Box 8067, 660 South Euclid, St. Louis, MO 63110.

The NHLBI Family Heart Study is a multicenter, population-based study of genetic and nongenetic determinants of coronary heart disease (CHD), atherosclerosis, and cardiovascular risk factors. In phase I, 2, 000 randomly selected participants and 2, 000 with family histories of CHD were identified among 14, 592 middle-aged participants in epidemiologic studies. Medical histories from these individuals, their parents, and their siblings were used to calculate family risk scores that compared the number of reported and validated CHD events with the number expected based on the size, sex, and age of family members. A total of 657 families with the highest risk scores and early-onset CHD and 588 randomly sampled families had clinic examinations that included electrocardiograms, carotid artery ultrasound scans, spirometry, measurements of body size, blood pressure, lipids, lipoproteins, hemostatic factors, insulin, glucose, and routine chemistries. Additional biochemical and genetic studies are being performed on selected participants. Serum, plasma, lymphocytes, red cells, and DNA are stored for future studies, including genotyping of candidate genes and anonymous markers. Contributions of genes, shared and individual environments, and behaviors to variations in risk factors, preclinical atherosclerosis, and CHD will be estimated. Linkage studies, including the quantitative trait loci approach, are planned. Am J Epidemiol 1996; 143: 1219–28.

coronary heart disease; genetics; hypertension; risk factors


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