Antihypertensive treatments obscure familial contributions to blood pressure variation

Cui, J. S., Hopper, J. L. and Harrap, S. B. 2003, Antihypertensive treatments obscure familial contributions to blood pressure variation, Hypertension, vol. 41, no. 2, pp. 207-210, doi: 10.1161/01.HYP.0000044938.94050.E3.

Attached Files
Name Description MIMEType Size Downloads

Title Antihypertensive treatments obscure familial contributions to blood pressure variation
Author(s) Cui, J. S.
Hopper, J. L.
Harrap, S. B.
Journal name Hypertension
Volume number 41
Issue number 2
Start page 207
End page 210
Total pages 4
Publisher Lippincott Williams & Wilkins
Place of publication Philadelphia, Pa.
Publication date 2003
ISSN 0194-911X
Keyword(s) Analysis of Variance
Antihypertensive Agents/therapeutic use
Blood Pressure/drug effects/genetics/physiology
Family Health
Middle Aged
Nuclear Family
Summary The linkage and association between inherent blood pressure and underlying genotype is potentially confounded by antihypertensive treatment. We estimated blood pressure variance components (genetic, shared environmental, individual-specific) in 767 adult volunteer families by using a variety of approaches to adjusting blood pressure of the 244 subjects (8.2%) receiving antihypertensive medications. The additive genetic component of variance for systolic pressure was 73.9 mm Hg(2) (SE, 8.8) when measured pressures (adjusted for age by gender within each generation) were used but fell to 61.4 mm Hg(2) (SE, 8.0) when treated subjects were excluded. When the relevant 95th percentile values were substituted for treated systolic pressures, the additive genetic component was 81.9 mm Hg(2) (SE, 9.5), but individual adjustments in systolic pressure ranged from -53.5 mm Hg to +64.5 mm Hg (mean, +17.2 mm Hg). Instead, when 10 mm Hg was added to treated systolic pressure, the additive genetic component rose to 86.6 mm Hg(2) (SE, 10.1). Similar changes were seen in the shared environment component of variance for systolic pressure and for the combined genetic and shared environmental (ie, familial) components of diastolic pressure. There was little change in the individual-specific variance component across any of the methods. Therefore, treated subjects contribute important information to the familial components of blood pressure variance. This information is lost if treated subjects are excluded and obscured by treatment effects if unadjusted measured pressures are used. Adding back an appropriate increment of pressure restores familial components, more closely reflects the pretreatment values, and should increase the power of genomic linkage and linkage disequilibrium analyses.
Language eng
DOI 10.1161/01.HYP.0000044938.94050.E3
Field of Research 111706 Epidemiology
110201 Cardiology (incl Cardiovascular Diseases)
HERDC Research category C1.1 Refereed article in a scholarly journal
Copyright notice ©2003, American Heart Association.
Persistent URL

Document type: Journal Article
Collection: Public Health Research, Evaluation, and Policy Cluster
Connect to link resolver
Unless expressly stated otherwise, the copyright for items in DRO is owned by the author, with all rights reserved.

Version Filter Type
Citation counts: TR Web of Science Citation Count  Cited 174 times in TR Web of Science
Scopus Citation Count Cited 177 times in Scopus
Google Scholar Search Google Scholar
Access Statistics: 413 Abstract Views, 0 File Downloads  -  Detailed Statistics
Created: Mon, 15 Mar 2010, 10:04:28 EST

Every reasonable effort has been made to ensure that permission has been obtained for items included in DRO. If you believe that your rights have been infringed by this repository, please contact