Effects of Pioglitazone in Nondiabetic Patients with Arterial Hypertension: A Double-Blind, Placebo-Controlled Study
S. Füllert,
F. Schneider,
E. Haak,
H. Rau,
K. Badenhoop,
G. Lübben,
K.-H. Usadel and
T. Konrad
Medical Department I, J. W. Goethe University (S.F., F.S., E.H.,
H.R., K.B., K.-H.U.), Frankfurt, Germany; Institute for Metabolic
Research (T.K.), Frankfurt, Germany; and Takeda Pharma (G.L.), Aachen,
Germany
Address correspondence to: Thomas Konrad, M.D., Institut für Stoffwechselforschung, European RISC Study Centre, Heidelbergerstrasse 13, D-60327 Frankfurt, Germany.
Abstract
Hypertension is often associated with insulin resistance,
dyslipidemiaand obesity, which indicate a prediabetic state and
increasedrisk of cardiovascular disease. Pioglitazone treatment of
patientswith type 2 diabetes reduces insulin resistance and improves
lipidprofiles. The present double-blind placebo-controlled studyis
the first study to report effects of pioglitazone in non-diabetic
patientswith arterial hypertension. Following a one week run-in, 60
patientswere randomized to receive either pioglitazone (45 mg/day) or
placebofor 16 weeks. Insulin sensitivity (M-value) increased by 1.2±
1.7 mg/min/kg with pioglitazone compared with 0.4 ±1.4 mg/min/kg
(P = 0.022) with placebo. HOMA index was decreased
(-22.5± 45.8) by pioglitazone but not by placebo (+0.8 ±26.5;
P < 0.001). Decreases in fasting insulin and glucose
weresignificantly (P = 0.002 and P =
0.004, respectively) greaterwith pioglitazone than placebo. Body
weight did not change significantlywith either treatment.
HDL-cholesterol was increased and apolipoproteinB was decreased to a
significantly greater extent with pioglitazone.There was a
significantly (P = 0.016) greater decrease frombaseline
in diastolic blood pressure with pioglitazone. Thesechanges would
suggest improved glucose metabolism and a possiblereduction in risk of
cardiovascular disease with pioglitazonetreatment of non-diabetic
patients with arterial hypertension.
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