Hypertension Clinical Trial
Official title:
Contribution of Angiotensin II to Supine Hypertension in Autonomic Failure
The purpose of this study is to test the hypothesis that angiotensin II plays a role in the supine hypertension of primary autonomic failure. To determine the contribution of angiotensin II to renin and blood pressure regulation in autonomic failure, patients with multiple system atrophy [MSA] or pure autonomic failure [PAF] and supine hypertension will undergo medication testing with the angiotensin II receptor blocker losartan. The investigators will compare the biochemical and hemodynamic effects between MSA and PAF patients. In a subset of patients, the investigators will also give the ACE inhibitor captopril. Our primary endpoint will be changes in plasma renin activity, and subsequent components of the circulating renin-angiotensin system, in response to angiotensin II blockade. Our secondary outcome will be changes in hemodynamic measures during administration of these drugs.
Primary autonomic failure is a disabling condition characterized by orthostatic hypotension.
It is less well appreciated that at least 50% of these patients have high blood pressure when
lying down [supine hypertension]. The mechanisms underlying supine hypertension in autonomic
failure remain poorly understood. The hypertension in MSA patients may be explained by
residual sympathetic tone, possibly acting on hypersensitive adrenoreceptors and unrestrained
by the lack of baroreflex modulation. In contrast, the hypertension in PAF is associated with
increased vascular resistance in the absence of residual sympathetic tone. However, the
factors driving an elevation in either sympathetic or vascular tone in these patients remain
unclear.
The investigators hypothesize that angiotensin II, a hormone widely implicated in blood
pressure regulation, plays a role in the supine hypertension of autonomic failure. To
determine the contribution of angiotensin II to renin and blood pressure regulation in
autonomic failure, the investigators will administer the angiotensin II receptor blocker
losartan to MSA and PAF patients with supine hypertension. The primary endpoint will be
changes in plasma renin activity, and subsequent components of the circulating
renin-angiotensin system, in response to angiotensin II blockade. The secondary outcomes will
be the decrease in blood pressure and changes in heart rate, cardiac output, stroke volume
and systemic vascular resistance during administration of these drugs.
Subjects will be studied on 2 separate days, one with oral administration of placebo and the
other with losartan [50 mg]. The order of administration will be randomized in a single-blind
manner. The investigators will collect blood samples before and every 2 hours after
administration for up to 6 hours to determine if angiotensin II regulates plasma renin
activity, and other components of the circulating renin-angiotensin system, in autonomic
failure. The investigators will also obtain hemodynamic measurements before and every 1 hour
(blood pressure and heart rate) or 2 hours (cardiac output, stroke volume and systemic
vascular resistance) after drug administration.
In a subset of patients the investigators will also administer the ACE inhibitor captopril
[50 mg] on a separate study day using the same methods. Captopril is less specific for
assessing the role of angiotensin II to hypertension. However, it may provide important
information on the mechanism for angiotensin II formation in these patients.
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