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Diabetes, Vol 46, Issue 3 433-439, Copyright © 1997 by American Diabetes Association
Cardiac and glycemic benefits of troglitazone treatment in NIDDM. The Troglitazone Study Group
MN Ghazzi, JE Perez, TK Antonucci, JH Driscoll, SM Huang, BW Faja and RW Whitcomb
Parke-Davis Pharmaceutical Research, Diabetes and Metabolic Diseases, Ann Arbor, Michigan 48105, USA.
Troglitazone is a thiazolidinedione under development for the treatment of
NIDDM and potentially other insulin-resistant disease states. Treatment
with troglitazone is associated with an improvement in hyperglycemia,
hyperinsulinemia, and insulin-mediated glucose disposal. No significant
side effects have been observed in humans. Because of reported cardiac
changes in animals treated with drugs of this class, this multicenter
48-week study was conducted to evaluate whether NIDDM patients treated with
troglitazone develop any cardiac mass increase or functional impairment. A
total of 154 NIDDM patients were randomized to receive troglitazone 800 mg
q.d. or glyburide titrated to achieve glycemic control (< or =20 mg
b.i.d. or q.d.). Two-dimensional echocardiography and pulsed Doppler were
used to measure left ventricular mass index (LVMI), cardiac index (CI), and
stroke volume index (SVI). All echocardiograms were performed at each
center (baseline, 12, 24, 36, and 48 weeks), recorded on videotape, and
forwarded to a blinded central echocardiographic interpreter for analysis.
The results showed that LVMI of patients treated with troglitazone was not
statistically or clinically different from baseline after 24 or 48 weeks.
Statistically significant increases in SVI and CI and a statistically
significant decrease in diastolic pressure and estimated peripheral
resistance were observed in troglitazone-treated patients. These results
were not sex-specific. Glycemic benefits of troglitazone treatment were
observed as evidenced by long-term improvement of HbA1c and C-peptide
levels. Furthermore, triglycerides were significantly lower, and HDL was
significantly higher at weeks 24 and 48. In conclusion, NIDDM patients
treated with troglitazone do not show any cardiac mass increase or cardiac
function impairment. Conversely, patients on troglitazone benefited from
enhanced cardiac output and stroke volume, possibly as a result of
decreased peripheral resistance. Treatment with troglitazone appears to
have a favorable impact on known cardiovascular risk factors and could
potentially lower cardiovascular morbidity in NIDDM patients.

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Copyright © 1997 by the American Diabetes Association.
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