Prevention of diabetes with pioglitazone in ACT NOW: physiologic correlates.
Prevention of diabetes with pioglitazone in ACT NOW: physiologic correlates.
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DOI:
10.2337/db13-0265
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发表时间:
2013-11
期刊:
影响因子:
7.7
通讯作者:
ACT NOW Study
中科院分区:
文献类型:
--
作者:
Defronzo RA;Tripathy D;Schwenke DC;Banerji M;Bray GA;Buchanan TA;Clement SC;Gastaldelli A;Henry RR;Kitabchi AE;Mudaliar S;Ratner RE;Stentz FB;Musi N;Reaven PD;ACT NOW Study
We examined the metabolic characteristics that attend the development of type 2 diabetes (T2DM) in 441 impaired glucose tolerance (IGT) subjects who participated in the ACT NOW Study and had complete end-of-study metabolic measurements. Subjects were randomized to receive pioglitazone (PGZ; 45 mg/day) or placebo and were observed for a median of 2.4 years. Indices of insulin sensitivity (Matsuda index [MI]), insulin secretion (IS)/insulin resistance (IR; ΔI0–120/ΔG0–120, ΔIS rate [ISR]0–120/ΔG0–120), and β-cell function (ΔI/ΔG × MI and ΔISR/ΔG × MI) were calculated from plasma glucose, insulin, and C-peptide concentrations during oral glucose tolerance tests at baseline and study end. Diabetes developed in 45 placebo-treated vs. 15 PGZ-treated subjects (odds ratio [OR] 0.28 [95% CI 0.15–0.49]; P < 0.0001); 48% of PGZ-treated subjects reverted to normal glucose tolerance (NGT) versus 28% of placebo-treated subjects (P < 0.005). Higher final glucose tolerance status (NGT > IGT > T2DM) was associated with improvements in insulin sensitivity (OR 0.61 [95% CI 0.54–0.80]), IS (OR 0.61 [95% CI 0.50–0.75]), and β-cell function (ln IS/IR index and ln ISR/IR index) (OR 0.26 [95% CI 0.19–0.37]; all P < 0.0001). Of the factors measured, improved β-cell function was most closely associated with final glucose tolerance status.
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影响因子:
3.8
作者:
Abdul-Ghani, Muhammad A.;Molina-Carrion, Marjorie;DeFronzo, Ralph A.
通讯作者:
DeFronzo, Ralph A.
影响因子:
2.7
作者:
DeFronzo, Ralph A.;Banerji, MaryAnn;Tripathy, Devjit
通讯作者:
Tripathy, Devjit
影响因子:
7.7
作者:
Kim, SH;Abbasi, F;Reaven, GM
通讯作者:
Reaven, GM
影响因子:
168.9
作者:
Dormandy, JA;Charbonnel, B;Taton, J
通讯作者:
Taton, J
影响因子:
16.2
作者:
Cowie, Catherine C.;Engelgau, Michael M.;Gregg, Edward W.
通讯作者:
Gregg, Edward W.