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(Circulation. 1999;99:1407-1410.)
© 1999 American Heart Association, Inc.


Brief Rapid Communication

Genome-Wide Linkage Analyses of Systolic Blood Pressure Using Highly Discordant Siblings

Julia Krushkal, PhD; Robert Ferrell, PhD; Stephen C. Mockrin, PhD; Stephen T. Turner, MD; Charles F. Sing, PhD; Eric Boerwinkle, PhD

From the Institute of Molecular Medicine (J.K., E.B.) and the Human Genetics Center (E.B.), University of Texas–Houston Health Science Center, Houston, Tex; Department of Human Genetics (R.F.), University of Pittsburgh, Pittsburgh, Pa; National Heart, Lung, and Blood Institute (S.C.M.), Bethesda, Md; Division of Hypertension (S.T.T.), Department of Internal Medicine, Mayo Clinic, Rochester, Minn; and Department of Human Genetics (C.F.S.), University of Michigan, Ann Arbor, Mich.

Correspondence to Eric Boerwinkle, PhD, Human Genetics Center, University of Texas–Houston Health Science Center, PO Box 20334, Houston, TX 77225. E-mail eboerwin{at}gsbs.gs.uth.tmc.edu

Background—Elevated blood pressure is a risk factor for cardiovascular, cerebrovascular, and renal diseases. Complex mechanisms of blood pressure regulation pose a challenge to identifying genetic factors that influence interindividual blood pressure variation in the population at large.

Methods and Results—We performed a genome-wide linkage analysis of systolic blood pressure in humans using an efficient, highly discordant, full-sibling design. We identified 4 regions of the human genome that show statistical significant linkage to genes that influence interindividual systolic blood pressure variation (2p22.1 to 2p21, 5q33.3 to 5q34, 6q23.1 to 6q24.1, and 15q25.1 to 15q26.1). These regions contain a number of candidate genes that are involved in physiological mechanisms of blood pressure regulation.

Conclusions—These results provide both novel information about genome regions in humans that influence interindividual blood pressure variation and a basis for identifying the contributing genes. Identification of the functional mutations in these genes may uncover novel mechanisms for blood pressure regulation and suggest new therapies and prevention strategies.


Key Words: hypertension • blood pressure • genetics • genes




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Circulation, November 30, 1999; 100(22): 2231 - 2236.
[Abstract] [Full Text] [PDF]


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S. B. HARRAP, Z. Y. H. WONG, M. STEBBING, A. LAMANTIA, and M. BAHLO
Blood pressure QTLs identified by genome-wide linkage analysis and dependence on associated phenotypes
Physiol Genomics, February 28, 2002; 8(2): 99 - 105.
[Abstract] [Full Text] [PDF]