Hypertension Clinical Trial
To continue a prospective study of the ability of ambulatory blood pressure to predict cardiovascular morbidity in patients with mild hypertension.
BACKGROUND:
This was a continuation of a prospective study of the ability of ambulatory blood pressure
to predict cardiovascular morbidity in patients with mild hypertension, which was first
started in 1978.
DESIGN NARRATIVE:
Predictor variables evaluated at entry to the longitudinal study included clinic and
ambulatory blood pressures (including measures of pressure level and variability in
different settings), left ventricular mass index (LVMI, determined by echocardiography),
renin-sodium profile, and other cardiovascular risk factors (e.g., cholesterol and smoking).
During follow-up, blood pressure, treatment status, BMI, and clinical course were evaluated.
Outcome measures were definite cardiovascular morbid events, defined as sudden cardiac
death, myocardial infarction, stroke, congestive heart failure, and coronary artery
revascularization. The main hypotheses tested were that ambulatory blood pressure would give
a better prediction of outcome than clinic pressure, and that patients with white coat
hypertension (defined as a high clinic pressure and normal ambulatory pressure) would be at
low risk relative to patients with sustained hypertension. Initial results in 729 patients
initially studied between 1978 and 1985 using Cox survival analysis showed that the four
most significant predictors of morbid events were daytime blood pressure variability, age,
male sex, and serum cholesterol. Patients with white coat hypertension appeared to be at a
level of risk intermediate between normotensives and sustained hypertensives, but the
differences were not yet significant. Expansion of the cohort size to include patients
evaluated initially between 1985 and 1990 provided nearly 2,000 patients altogether, which
together with the longer follow-up of the initial cohort provided a sufficient number of
morbid events to identify the predictive significance of the different blood pressure
measures, and their interaction with other risk factors.
The study completion date listed in this record was obtained from the "End Date" entered in
the Protocol Registration and Results System (PRS) record.
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