Tumor necrosis factor α and insulin resistance in obese type 2 diabetic patients

被引:95
作者
Miyazaki, Y
Pipek, R
Mandarino, LJ
DeFronzo, RA
机构
[1] Univ Texas, Hlth Sci Ctr, Diabet Div, San Antonio, TX 78229 USA
[2] Texas Diabet Inst, San Antonio, TX USA
关键词
type; 2; diabetes; tumor necrosis factor alpha; insulin sensitivity;
D O I
10.1038/sj.ijo.0802187
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The relationship between basal serum tumor necrosis factor alpha (TNFalpha) levels and peripheral tissue (muscle) sensitivity to insulin was examined in 63 subjects with normal glucose tolerance (NGT), 18 subjects with impaired glucose tolerance (IGT), and 123 patients with type 2 diabetes mellitus (T2DM). The BMI was similar in NGT (28.8 +/- 0.7 kg/m(2)), IGT (31.1 +/- 1.0), and T2DM (30.0 +/- 0.4) groups. The fasting serum TNFalpha concentration in T2DM (4.4 +/- 0.2 pg/ml) was significantly higher than in NGT (3.1 +/- 0.2) and IGT (3.4 +/- 0.2; both P < 0.05). In T2DM the fasting plasma glucose (PPG 183 +/- 5 mg/dl) and insulin (FPI = 17 +/- 1 μU/ml) concentrations were significantly higher than in NGT (FPG = 95 +/- 1; FPI = 10 +/- 1) and IGT (FPG = 100 +/- 2; FPI = 13 +/- 1; all P < 0.01). The rate of total body insulin-mediated glucose disposal (Rd; 40 mU/m(2) min euglycemic insulin clamp in combination with H-3-glucose) was reduced in T2DM (102 +/- 3 mg/m(2) min) compared with NGT (177 10) and IGT (151 +/- 14; both P<0.01). The serum TNFα concentration was inversely correlated with Rd (r=-0.47, P<0.0001) and positively correlated with both FPG (r=0.32, P=0.004) and FPI (r=0.32, P=0.004) in NGT plus IGT. No correlation was observed between serum TNFalpha and Rd (r= -0.02), FPG (r= 0.15), or FPI (r= 0.15) in T2DM. In stepwise multiple regression analysis using age, sex, BMI, FPG, FPI and serum TNFalpha concentration as independent variables, only BMI and serum TNFalpha concentration were significant and independent predictors of Rd (r(2) = 0.29, P < 0.0001) in the NGT plus IGT group, while FPG and FPI were significant and independent predictors of Rd (r(2) = 0.13, P < 0.0001) in T2DM. These results suggest that: (i) an increase in circulating TNFalpha concentration is associated with peripheral insulin resistance and increased plasma glucose and insulin levels prior to the onset of type 2 diabetes; and (ii) the further deterioration in peripheral insulin resistance in T2DM (compared with NGT and IGT) is unrelated to the increase in serum TNFalpha concentration.
引用
收藏
页码:88 / 94
页数:7
相关论文
共 42 条
[1]  
Arner P, 2001, BIOCHEM SOC T, V29, P72, DOI 10.1042/bst0290072
[2]   Leptin selectively decreases visceral adiposity and enhances insulin action [J].
Barzilai, N ;
Wang, JL ;
Massilon, D ;
Vuguin, P ;
Hawkins, M ;
Rossetti, L .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (12) :3105-3110
[3]  
BEMELMANS MHA, 1997, CRIT REV IMMUNOL, V16, P1
[4]   Role of fatty acids in the pathogenesis of insulin resistance and NIDDM [J].
Boden, G .
DIABETES, 1997, 46 (01) :3-10
[5]   An in vivo model for elucidation of the mechanism of tumor necrosis factor-α (TNF-α)-induced insulin resistance:: Evidence for differential regulation of insulin signaling by TNF-α [J].
Cheung, AT ;
Ree, D ;
Kolls, JK ;
Fuselier, J ;
Coy, DH ;
Bryer-Ash, M .
ENDOCRINOLOGY, 1998, 139 (12) :4928-4935
[6]  
Chung HY, 2001, ANN NY ACAD SCI, V928, P327
[7]   Serum immunoreactive leptin concentrations in normal-weight and obese humans [J].
Considine, RV ;
Sinha, MK ;
Heiman, ML ;
Kriauciunas, A ;
Stephens, TW ;
Nyce, MR ;
Ohannesian, JP ;
Marco, CC ;
McKee, LJ ;
Bauer, TL ;
Caro, JF .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (05) :292-295
[8]   MONOKINE REGULATION OF GLUCOSE TRANSPORTER MESSENGER-RNA IN L6 MYOTUBES [J].
CORNELIUS, P ;
LEE, MD ;
MARLOWE, M ;
PEKALA, PH .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 165 (01) :429-436
[9]   Tumor necrosis factor-α in sera of obese patients:: Fall with weight loss [J].
Dandona, P ;
Weinstock, R ;
Thusu, K ;
Abdel-Rahman, E ;
Aljada, A ;
Wadden, T .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1998, 83 (08) :2907-2910
[10]   INSULIN RESISTANCE - A MULTIFACETED SYNDROME RESPONSIBLE FOR NIDDM, OBESITY, HYPERTENSION, DYSLIPIDEMIA, AND ATHEROSCLEROTIC CARDIOVASCULAR-DISEASE [J].
DEFRONZO, RA ;
FERRANNINI, E .
DIABETES CARE, 1991, 14 (03) :173-194