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Submitted on February 3, 2005
From the Tulane Center for Cardiovascular Health and Department of Epidemiology (W.C., S.L., S.R.S., G.S.B.), Tulane School of Public Health & Tropical Medicine, New Orleans, La; and the Human Genetics Center and Institute of Molecular Medicine (E.B.), University of Texas-Houston Health Science Center, Houston, Tex. * To whom correspondence should be addressed. E-mail: berenson{at}mailhost.tcs.tulane.edu.
Abstract--Genetic loci influencing the long-term levels and trends of blood pressure over time were investigated using 775 white siblings, ages 13 to 43 years, enrolled in the Bogalusa Heart Study, and 357 microsatellite markers on the 22 autosomal chromosomes. Subjects had been examined serially 2 to 12 times with 4365 serial observations over an average of 22 years from childhood to adulthood. Total and incremental area under the curve was calculated based on a cubic growth curve and used as long-term levels and trends, respectively. After adjusting for age, sex, and body mass index, heritability estimates of total area were 0.66 for systolic and 0.68 for diastolic blood pressure. Heritability of incremental area was 0.38 for systolic and 0.46 for diastolic blood pressure. Significant linkage to the total area of diastolic blood pressure (peak logarithm of odds [LOD]=3.9 at 73 cM) was observed on chromosome 2, with a region spanning from 44 cM to 103 cM showing supporting linkage evidence of LOD >3.0. In addition, suggestive linkage for total area of systolic (LOD=1.6 at 182 cM) and diastolic blood pressure (LOD=2.0 at 36 cM) on chromosome 4 and diastolic blood pressure incremental area (LOD=2.2 at 28 cM) on chromosome 18 was noted. Several hypertension candidate genes such as
Revised on February 3, 2005
Autosomal Genome Scan for Loci Linked to Blood Pressure Levels and Trends Since Childhood. The Bogalusa Heart Study
Wei Chen;
-adducin,
-adducin, sodium bicarbonate co-transporter, and G protein-coupled receptor kinase 4 are located in these regions. Linkage evidence found in this community-based study indicates that regions on these chromosomes harbor genetic loci that affect the propensity for development of hypertension from childhood.
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