Rilmenidine is an antihypertensive agent with selectivity for I-1 imidazoli
ne receptors that acts both centrally by reducing sympathetic overactivity
and in the kidney by inhibiting the Na+/H+ antiport.
Rilmenidine provides antihypertensive efficacy comparable with that of diur
etics, beta-blockers, calcium channel blockers, and angiotensin-converting
enzyme (ACE) inhibitors.
Experience from trials and clinical practice highlights rilmenidine's clini
cal and metabolic acceptability in hypertensive populations, including thos
e at special risk because of old age, renal impairment, diabetes mellitus,
or dyslipidemia.
In the at-risk hypertensive, rilmenidine reduces left ventricular hypertrop
hy to a similar degree to other reference agents. New studies show a signif
icant improvement in glucose metabolism in metabolic syndrome patients trea
ted with rilmenidine, and a significant reduction in microalbuminuria durin
g rilmenidine treatment of hypertensive type 2 diabetics.
Thus the efficacy/tolerance ratio of rilmenidine supports its role as a fir
st-line antihypertensive option for all groups of hypertensive patient, wit
h specific advantages in some at-risk populations. (C) 2000 American Journa
l of Hypertension, Ltd.