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a Clinical Pharmacology Unit, University of Cambridge, Box 110, Addenbrooke's Hospital, Cambridge CB2 2QQ mjb14@medschl.cam.ac.uk
Series edited by: John Savill
The abundance of drugs now available for treating hypertension, and evidence that small
reductions in blood pressure reverse the associated risk of stroke have shifted clinical concerns
away from hypertension. However, we do not understand the cause of hypertension in
95% of patients, fail to achieve a normal blood pressure in 50% of patients, and are
unable fully to reverse the cardiac and vascular changes that predate the diagnosis and treatment
of hypertension. Consequently, hypertension remains the commonest cause of strokes in Britain
and of renal failure in the United States. Essential hypertension is a polygenic disease whose
understanding can now be advanced through molecular genetic analyses. Several different
syndromes are likely to be recognised; most will be due to interactions between genetic and
environmental factors, but there are also likely to be further monogenic syndromes in families
with multiple affected members. Recognition of these syndromes will permit accurate genetic
prediction of prognosis and optimal treatment and perhaps lead to new and more powerful classes
of antihypertensive treatment.
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