The 1988 recommendations from the Joint National Committee revolutionized the step-care approach to the treatment of hypertension: the calcium- channel blockers, a new class of agents, are now included as first-line agents. That they lower blood pressure is clear. But no randomized trial has yet evaluated their safety and efficacy in terms of the clinical endpoints of stroke and coronary heart disease (CHD). Because the results of previous randomized trials suggest that the treatment of hypertension does not reduce the incidence of CHD, we have designed a population-based, case-control study to determine whether the calcium- channel blockers reduce the incidence of myocardial infarction (MI) in patients with hypertension. Our secondary aims include the evaluation of the relative efficacy and safety of other major classes, including ACE inhibitors, beta-blockers, and alpha blockers. This revised proposal includes the results of three pilot studies that address questions raised in previous reviews. The setting is Group Health Cooperative (GHC). We will use the GHC computerized files to identify potential cases: all treated hypertensive patients, aged 30 to 79 yrs., will be eligible as cases if, according to WHO criteria, they present with an incident, fatal or non-fatal MI. A random sample of members listed in the GHC enrollment files will serve as our source of potential controls. Review of the outpatient medical records will ensure that all study subjects meet the same entrance criteria. This effort will also secure information about blood pressures, duration of hypertension, and past medical history. A telephone interview will provide information about other potential confounders, including smoking, diet, and physical activity. The GHC computerized pharmacy records, a database of all prescriptions filled by enrollees, will serve as the primary source of information about the use of calcium-channel blockers. Frequency matching will control for the potential confounding effects of age and year of presentation, and data analysis will involve logistic regression. Collecting data for 7 years will identify a number of study subjects sufficient to provide 80% power for detecting a relative risk of 0.70. The use of population-based controls will enhance the validity of our findings--results which will provide evidence about the overall risk or benefit from the use of calcium-channel blockers and other anti- hypertensive agents in patients with high blood pressure.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
1R01HL043201-01A2
Application #
3361755
Study Section
Epidemiology and Disease Control Subcommittee 2 (EDC)
Project Start
1991-09-30
Project End
1995-12-31
Budget Start
1991-09-30
Budget End
1992-09-29
Support Year
1
Fiscal Year
1991
Total Cost
Indirect Cost
Name
University of Washington
Department
Type
Schools of Medicine
DUNS #
135646524
City
Seattle
State
WA
Country
United States
Zip Code
98195
Maloney, James P; Branchford, Brian R; Brodsky, Gary L et al. (2017) The ENTPD1 promoter polymorphism -860 A > G (rs3814159) is associated with increased gene transcription, protein expression, CD39/NTPDase1 enzymatic activity, and thromboembolism risk. FASEB J 31:2771-2784
Harrington, L B; Marck, B T; Wiggins, K L et al. (2017) Cross-sectional association of endogenous steroid hormone, sex hormone-binding globulin, and precursor steroid levels with hemostatic factor levels in postmenopausal women. J Thromb Haemost 15:80-90
Lindström, Sara; Germain, Marine; Crous-Bou, Marta et al. (2017) Assessing the causal relationship between obesity and venous thromboembolism through a Mendelian Randomization study. Hum Genet 136:897-902
Postmus, Iris; Warren, Helen R; Trompet, Stella et al. (2016) Meta-analysis of genome-wide association studies of HDL cholesterol response to statins. J Med Genet 53:835-845
Smith, N L; Harrington, L B; Blondon, M et al. (2016) The association of statin therapy with the risk of recurrent venous thrombosis. J Thromb Haemost 14:1384-92
Harrington, Laura B; Weiss, Noel S; Wiggins, Kerri L et al. (2016) Prior hysterectomy and oophorectomy and incident venous thrombosis risk among postmenopausal women: a population-based, case-control study. Menopause 23:143-9
Harrington, Laura B; Wiggins, Kerri L; Sitlani, Colleen M et al. (2016) The association of F11 genetic variants with the risk of incident venous thrombosis among women, by statin use. Thromb Haemost 115:682-4
Germain, Marine; Chasman, Daniel I; de Haan, Hugoline et al. (2015) Meta-analysis of 65,734 individuals identifies TSPAN15 and SLC44A2 as two susceptibility loci for venous thromboembolism. Am J Hum Genet 96:532-42
Smith, Nicholas L; Blondon, Marc; Wiggins, Kerri L et al. (2014) Lower risk of cardiovascular events in postmenopausal women taking oral estradiol compared with oral conjugated equine estrogens. JAMA Intern Med 174:25-31
Blondon, M; van Hylckama Vlieg, A; Wiggins, K L et al. (2014) Differential associations of oral estradiol and conjugated equine estrogen with hemostatic biomarkers. J Thromb Haemost 12:879-86

Showing the most recent 10 out of 111 publications