OBJECTIVE - Troglitazone, which improves peripheral insulin resistance
of experimental diabetic animals and diabetic patients, affects ob ge
ne expression in the adipose tissue of rodents. The present study was
undertaken to examine a hypothesis that clinical administration of tro
glitazone may reduce circulating leptin levels and affect eating behav
ior in NIDDM patients. RESEARCH DESIGN AND METHODS - Troglitazone was
administered at a dosage of 200 mg twice daily for 12 weeks in 20 poor
ly controlled NIDDM patients. Chronological changes in glycemic contro
l, serum lipids, immunoreactive leptin (IRL) levels, and BMI were meas
ured. Body fat weight was also assessed by bioelectric impedance. RESU
LTS - Troglitazone significantly decreased fasting plasma glucose, ser
um immunoreactive insulin, and HbA(1c) levels. Serum levels of IRL and
triglyceride were significantly reduced by troglitazone administered
for 4, 8, and 12 weeks. Troglitazone administration significantly incr
eased the BMI in NIDDM patients, and two-thirds of the patients compla
ined of increased hunger after the start of troglitazone administratio
n. CONCLUSIONS - Troglitazone significantly reduces circulating leptin
levels at clinical doses. It may affect the eating behavior of poorly
controlled NIDDM patients through the improvement of glycemic control
and/or the reduction of circulating leptin.