Plasma resistin concentration, hepatic fat content, and hepatic and peripheral insulin resistance in pioglitazone-treated type II diabetic patients

被引:121
作者
Bajaj, M [1 ]
Suraamornkul, S [1 ]
Hardies, LJ [1 ]
Pratipanawatr, T [1 ]
DeFronzo, RA [1 ]
机构
[1] Univ Texas, Hlth Sci Ctr, Dept Med, Diabet Div, San Antonio, TX 78284 USA
关键词
pioglitazone; hepatic fat content; hepatic insulin resistance; resistin; type II diabetes mellitus;
D O I
10.1038/sj.ijo.0802625
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: To study the effect of pioglitazone (PIO) on plasma resistin concentration, endogenous glucose production (EGP), and hepatic fat content (HFC) in patients with type II diabetes (T2DM). Subjects: A total of 13 T2DM patients (age=51+/-2 y, BMI=29.7+/-1.1 kg/m(2), HbA(1c)=8.0+/-0.5%). Methods: HFC (magnetic resonance spectroscopy) and basal plasma resistin concentration were quantitated before and after PIO treatment (45 mg/day) for 16 weeks. Subjects received a 3 h euglycemic insulin (100 mU/m(2)/min) clamp with 3-[H-3] glucose to determine rates of EGP and tissue glucose disappearance (Rd) before and after PIO. Results: PIO reduced fasting plasma glucose (10.3+/-0.7 to 7.6+/-0.6 mmol/l, P<0.001) and HbA(1c) (8.0 +/- 0.4 to 6.8 +/- 0.3%, P<0.001) despite increased body weight (83.2+/-3.4 to 86.3+/-3.4 kg, P<0.001). PIO improved Rd (4.9 +/- 0.4 to 6.6 +/- 0.5 mg/kg/min, P<0.005) and reduced EGP (0.22+/-0.04 to 0.06+/-0.02 mg/kg/min, P<0.01) during the insulin clamp. Following PIO, HFC decreased from 21.1 +/- 3.5 to 11.2 +/- 2.1% (P<0.005), and plasma resistin decreased from 5.3+/-0.6 to 3.5+/-0.3 ng/ml (P<0.01). Plasma resistin concentration correlated positively with HFC before (r=0.58, P<0.05) and after (r=0.55, P<0.05) PIO treatment. Taken collectively, plasma resistin concentration, before and after PIO treatment, correlated positively with hepatic fat content (r=0.66, P<0.001) and EGP during the insulin clamp (r=0.41, P<0.05). However, the plasma resistin concentration did not correlate with whole body glucose disposal (Rd) during the insulin clamp either before (r=-0.18, P=NS) or after (r=-0.13, P=NS) PIO treatment. Conclusions: PIO treatment in T2DM causes a significant decrease in plasma resistin concentration. The decrease in plasma resistin is positively correlated with the decrease in hepatic fat content and improvement in hepatic insulin sensitivity.
引用
收藏
页码:783 / 789
页数:7
相关论文
共 35 条
[1]   Pioglitazone reduces hepatic fat content and augments splanchnic glucose uptake in patients with type 2 diabetes [J].
Bajaj, M ;
Suraamornkul, S ;
Pratipanawatr, T ;
Hardies, LJ ;
Pratipanawatr, W ;
Glass, L ;
Cersosimo, E ;
Miyazaki, Y ;
DeFronzo, RA .
DIABETES, 2003, 52 (06) :1364-1370
[2]  
BANERJI MA, 1995, INT J OBESITY, V19, P846
[3]   SPATIAL LOCALIZATION IN NMR-SPECTROSCOPY INVIVO [J].
BOTTOMLEY, PA .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1987, 508 :333-348
[4]   Pharmacologic therapy for type 2 diabetes mellitus [J].
DeFronzo, RA .
ANNALS OF INTERNAL MEDICINE, 1999, 131 (04) :281-303
[5]  
DeFronzo RA, 1997, DIABETES REV, V5, P177
[6]  
DEFRONZO RA, 1979, AM J PHYSIOL, V237, pE214
[7]  
FELBER JP, 1988, INT J OBESITY, V12, P377
[8]  
GOTO T, 1995, INT J OBESITY, V19, P841
[9]   GLUCOSE AND FREE FATTY-ACID METABOLISM IN NON-INSULIN-DEPENDENT DIABETES-MELLITUS - EVIDENCE FOR MULTIPLE SITES OF INSULIN RESISTANCE [J].
GROOP, LC ;
BONADONNA, RC ;
DELPRATO, S ;
RATHEISER, K ;
ZYCK, K ;
FERRANNINI, E ;
DEFRONZO, RA .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 84 (01) :205-213
[10]   Pioglitazone induces in vivo adipocyte differentiation in the obese Zucker fa/fa rat [J].
Hallakou, S ;
Doare, L ;
Foufelle, F ;
Kergoat, M ;
GuerreMillo, M ;
Berthault, MF ;
Dugail, I ;
Morin, J ;
Auwerx, J ;
Ferre, P .
DIABETES, 1997, 46 (09) :1393-1399