Hypertension Clinical Trial
Official title:
A Randomised Double-blind Cross-over Single-centre Study on Molecular Genetics of Drug Responsiveness in Essential Hypertension
Blood pressure variation and the risk of essential hypertension have an important genetic
component. In most cases susceptibility to essential hypertension is likely determined by the
action of more than one gene.
The identification of genes causing susceptibility to hypertension is important, since it
would give new tools for the diagnosis and enable better etiological classification and
specific treatment of the disease.
The innovation of this study is to use the response to antihypertensive therapy as an
intermediate phenotype.
In the study, each subject uses one of four antihypertensive drugs, each as a monotherapy in
a rotational fashion, for 28 days in a randomized order. The antihypertensive drugs to be
tested include a thiazide diuretic, a beta-adrenergic antagonist, an angiotensin-II receptor
antagonist and a calcium channel blocker. The drugs that are selected for the study are
"typical" representatives of their groups and long-acting, and the dosages are sufficient but
well tolerable.
Blood pressure variation and the risk of essential hypertension have an important genetic
component. In most cases susceptibility to essential hypertension is likely determined by the
action of more than one gene.
The identification of genes causing susceptibility to hypertension is important, since it
would give new tools for the diagnosis and enable better etiological classification and
specific treatment of the disease. Finland is an ideal place for a study like this because of
the genetic homogeneity of the population, the relatively high prevalence of the disease and
the established protocols for the treatment and follow-up of hypertension in public health
care.
The molecular genetic studies on hypertension performed so far (by 1999) have primarily been
association studies, which are based on case-control classification and may produce erroneous
results. Particularly, a reliable phenotyping of cases and controls has been difficult.
Consequently, more attention should be paid to the phenotyping of patients, and novel
intermediate phenotypes characteristic of certain subtypes of hypertension should be used to
facilitate the search for hypertension genes. The innovation of this study is to use the
response to antihypertensive therapy as an intermediate phenotype.
In the study, each subject uses one of four antihypertensive drugs, each as a monotherapy in
a rotational fashion, for 28 days in a randomized order. The antihypertensive drugs to be
tested include a thiazide diuretic, a beta-adrenergic antagonist, an angiotensin-II receptor
antagonist and a calcium channel blocker. The drugs that are selected for the study are
"typical" representatives of their groups and long-acting, and the dosages are sufficient but
well tolerable. The study design does not necessitate the use of equipotent doses of the
various agents, since the study is not designed to compare the antihypertensive effectiveness
of the study drugs or, due to the short treatment periods, their effects on clinical
endpoints.
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