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Diabetes Care, Vol 21, Issue 5 796-799, Copyright © 1998 by American Diabetes Association
Troglitazone decreases the proportion of small, dense LDL and increases the resistance of LDL to oxidation in obese subjects
CJ Tack, P Smits, PN Demacker and AF Stalenhoef
Department of Internal Medicine, University Hospital Nijmegen, The Netherlands.
OBJECTIVE: Insulin resistance is associated with a predominance of small,
atherogenic LDL particles that are more prone to oxidative modification.
Treatment with the insulin-sensitizer troglitazone may improve LDL
composition and resistance to oxidation. RESEARCH DESIGN AND METHODS: In a
randomized double-blind crossover design, 15 obese subjects were treated
with either 400 mg troglitazone daily or placebo for 8 weeks. Insulin
sensitivity (clamp), (apo)lipoproteins, LDL subclass pattern, plasma TBARS,
and ex vivo LDL oxidation were determined. RESULTS: Troglitazone treatment
improved insulin sensitivity. LDL cholesterol increased from 2.58 +/- 0.18
to 2.77 +/- 0.20 mmol/l (P = 0.03) because of an increase in large
(buoyant) LDL1 (from 0.45 +/- 0.04 to 0.62 +/- 0.09 mmol/l, P = 0.008).
Because small (dense) LDL3 decreased, LDL1:LDL3 ratio increased (P = 0.02).
Plasma TBARS concentration declined significantly, and the lag time of ex
vivo LDL oxidation showed a small but significant increase. CONCLUSIONS: In
obese subjects, treatment with troglitazone improves insulin sensitivity,
increases the ratio of large buoyant to small dense LDL, and appears to
enhance the resistance of the LDL particle to oxidation. These qualitative
changes in lipoproteins may have a beneficial effect on cardiovascular risk
profile and compensate for a small increase in LDL cholesterol.

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Copyright © 1998 by the American Diabetes Association.
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