type 2 diabetes;
tumor necrosis factor α;
insulin sensitivity;
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摘要:
The relationship between basal serum tumor necrosis factor alpha (TNFα) 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/m2), IGT (31.1±1.0), and T2DM (30.0±0.4) groups. The fasting serum TNFα 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 (FPG=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/m2 min euglycemic insulin clamp in combination with 3H-glucose) was reduced in T2DM (102±3 mg/m2 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 TNFα 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 TNFα concentration as independent variables, only BMI and serum TNFα concentration were significant and independent predictors of Rd (r2=0.29, P<0.0001) in the NGT plus IGT group, while FPG and FPI were significant and independent predictors of Rd (r2=0.13, P<0.0001) in T2DM. These results suggest that: (i) an increase in circulating TNFα 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 TNFα concentration.
机构:
Massachusetts Gen Hosp, Div Gen Med, Dept Med, Boston, MA 02114 USA
Harvard Univ, Sch Med, Boston, MA 02115 USAMassachusetts Gen Hosp, Div Gen Med, Dept Med, Boston, MA 02114 USA
Hivert, Marie-France
Sullivan, Lisa M.
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机构:
Boston Univ, Sch Publ Hlth, Dept Biostat, Boston, MA 02118 USAMassachusetts Gen Hosp, Div Gen Med, Dept Med, Boston, MA 02114 USA
Sullivan, Lisa M.
Shrader, Peter
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机构:
Massachusetts Gen Hosp, Div Gen Med, Dept Med, Boston, MA 02114 USAMassachusetts Gen Hosp, Div Gen Med, Dept Med, Boston, MA 02114 USA
Shrader, Peter
Fox, Caroline S.
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机构:
NHLBI, Framingham Heart Study, Framingham, MA 01702 USA
Brigham & Womens Hosp, Dept Endocrinol & Metab, Boston, MA 02115 USAMassachusetts Gen Hosp, Div Gen Med, Dept Med, Boston, MA 02114 USA
Fox, Caroline S.
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Nathan, David M.
D'Agostino, Ralph B., Sr.
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机构:
Boston Univ, Dept Math & Stat, Consulting Unit, Boston, MA 02115 USAMassachusetts Gen Hosp, Div Gen Med, Dept Med, Boston, MA 02114 USA
D'Agostino, Ralph B., Sr.
Wilson, Peter W. F.
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机构:
Emory Univ, Sch Med, Atlanta, GA 30322 USAMassachusetts Gen Hosp, Div Gen Med, Dept Med, Boston, MA 02114 USA
Wilson, Peter W. F.
Benjamin, Emelia J.
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机构:
NHLBI, Framingham Heart Study, Framingham, MA 01702 USA
Boston Univ, Sch Med, Prevent Med Sect, Boston, MA 02118 USA
Boston Univ, Sch Med, Prevent Cardiol Sect, Boston, MA 02118 USA
Boston Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02118 USAMassachusetts Gen Hosp, Div Gen Med, Dept Med, Boston, MA 02114 USA
Benjamin, Emelia J.
Meigs, James B.
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机构:
Massachusetts Gen Hosp, Div Gen Med, Dept Med, Boston, MA 02114 USA
Harvard Univ, Sch Med, Boston, MA 02115 USAMassachusetts Gen Hosp, Div Gen Med, Dept Med, Boston, MA 02114 USA
Meigs, James B.
METABOLISM-CLINICAL AND EXPERIMENTAL,
2010,
59
(04):
: 540
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546