z-logo
Premium
An increase in insulin sensitivity and basal beta‐cell function in diabetic subjects treated with pioglitazone in a placebo‐controlled randomized study
Author(s) -
Wallace T. M.,
Levy J. C.,
Matthews D. R.
Publication year - 2004
Publication title -
diabetic medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.474
H-Index - 145
eISSN - 1464-5491
pISSN - 0742-3071
DOI - 10.1111/j.1464-5491.2004.01218.x
Subject(s) - pioglitazone , medicine , placebo , endocrinology , proinsulin , diabetes mellitus , insulin , basal (medicine) , type 2 diabetes , insulin resistance , adiponectin , pathology , alternative medicine
Aims  To investigate the effect of treatment with pioglitazone on beta‐cell function and insulin sensitivity in Type 2 diabetes. Methods  Thirty subjects with diet‐controlled Type 2 diabetes were randomized to 3 months treatment with pioglitazone ( n  = 19) or placebo ( n  = 11). All subjects underwent basal sampling for homeostatic model assessment (HOMA), followed by an intravenous glucose tolerance test and hyperglycaemic clamp, followed by an euglycaemic hyperinsulinaemic clamp; at baseline and after treatment. Results  All results are expressed as mean ( sem ). Pioglitazone increased basal insulin sensitivity by 24.7% (7.8) HOMA‐%S vs. 2.1% (5.9) in the placebo group ( P =  0.02). Stimulated insulin sensitivity, M/I, increased in the pioglitazone group compared with placebo: +15.1 (2.8) l kg −1  min −1 vs. +3.2 (2.9) l kg −1  min −1 , respectively ( P =  0.009). Pioglitazone increased adiponectin by 39.3 (6.3), ng/ml compared with a decrease of 0.8 (1.3) ng/ml with placebo ( P =  0.00004). HOMA‐%B increased with pioglitazone, +11.5% (4.8) vs. −2.0% (4.8) with placebo ( P =  0.049), but there was no change in stimulated beta‐cell function as determined by hyperglycaemic clamps. There was a significant reduction in the proinsulin/insulin ratio in the pioglitazone group, −0.057 (0.02) compared with placebo, +0.004 (0.02) ( P =  0.03). There was a significant reduction in HbA 1c of 0.6% (0.1) in the pioglitazone group compared with placebo ( P =  0.003). There was no significant weight gain associated with pioglitazone therapy: +0.7 ( sem 0.6) kg vs. +1.1 ( sem 0.5) kg in placebo group ( P =  NS). Conclusions  Basal beta‐cell function and insulin sensitivity improved following pioglitazone therapy. The improvement in proinsulin to insulin ratio suggests that beta‐cells are under less stress.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here