Liver enzymes, the metabolic syndrome, and incident diabetes: The Mexico City Diabetes Study

被引:249
作者
Nannipieri, M
Gonzales, C
Baldi, S
Posadas, R
Williams, K
Haffner, SM
Stern, MP
Ferrannini, E [1 ]
机构
[1] Univ Pisa, Sch Med, Dept Internal Med, Metab Unit, I-56126 Pisa, Italy
[2] Univ Pisa, Sch Med, CNR, Inst Clin Physiol, I-56126 Pisa, Italy
[3] Mexican Social Secur Inst, Specialty Hosp Natl Med Ctr, Endocrinol & Metab Serv, Mexico City, DF, Mexico
[4] Mexican Social Secur Inst, Amer British Cowdray Hosp, Mexico City, DF, Mexico
[5] Univ Texas, Hlth Sci Ctr, Div Clin Epidemiol, San Antonio, TX 78285 USA
关键词
D O I
10.2337/diacare.28.7.1757
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE - To test the hypothesis that enzymes conventionally associated with liver dysfunction (aspartate aminotransferase, alanine aminotranlsferase, gamma-glutamyltransferase [GGTI, and alkaline phosphatase) may predict diabetes. RESEARCH DESIGN AND METHODS - From a population-based diabetes survey, we selected 1,441 men and women in whom serum enzyme levels were <= 3 SDs of the mean population value, alcohol intake was < 250 g/week, and hepatitis B and C virus testing was negative. At follow-up (7 years), 94 subjects developed diabetes and 93 impaired glucose tolerance (IGT). RESULTS - At baseline, all four enzymes were related to most of the features of the metabolic syndrome. After controlling for sex, age, adiposity/fat distribution, alcohol intake, serum lipids, and blood pressure, higher alanine aminotransferase and GGT values were significantly (P < 0.01) associated with both IGT and diabetes, whereas alkaline phosphatase was associated with diabetes only (P = 0.0004) and aspartate aminotransferase with IGT only (P = 0.0001). Raised GIST alone was associated with all the features of the metabolic syndrome. Raised GGT was a significant predictor of either IGT or diabetes (odds ratio 1.62 [95% CI 1.08-2.421 top quartile vs. lower quartiles, P < 0.02) after controlling for sex, age, adiposity/fat distribution, alcohol consumption, fasting plasma insulin and proinsulin levels, and 2-h postglucose plasma glucose concentrations. CONCLUSIONS - Although mild elevations in liver enzymes are associated with features of the metabolic syndrome, only raised GIST is an independent predictor of deterioration of glucose tolerance to IGT or diabetes. As GGT signals oxidative stress, the association With diabetes may reflect both hepatic steatosis and enhanced oxidative stress.
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页码:1757 / 1762
页数:6
相关论文
共 36 条
[1]   THE TROMSO HEART-STUDY - DISTRIBUTION OF, AND DETERMINANTS FOR, GAMMA-GLUTAMYL-TRANSFERASE IN A FREE-LIVING POPULATION [J].
ARNESEN, E ;
HUSEBY, NE ;
BRENN, T ;
TRY, K .
SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION, 1986, 46 (01) :63-70
[2]  
BANERJI MA, 1995, INT J OBESITY, V19, P846
[3]   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
[4]   Nonalcoholic fatty liver disease: Predictors of nonalcoholic steatohepatitis and liver fibrosis in the severely obese [J].
Dixon, JB ;
Bhathal, PS ;
O'Brien, PE .
GASTROENTEROLOGY, 2001, 121 (01) :91-100
[5]   γ-glutamyltransferase dependent generation of reactive oxygen species from a glutathione/transferrin system [J].
Drozdz, R ;
Parmentier, C ;
Hachad, H ;
Leroy, P ;
Siest, G ;
Wellman, M .
FREE RADICAL BIOLOGY AND MEDICINE, 1998, 25 (07) :786-792
[6]   Prevalence of abnormal serum alanine aminotransferase levels in obese patients and patients with type 2 diabetes [J].
Erbey, JR ;
Silberman, C ;
Lydick, E .
AMERICAN JOURNAL OF MEDICINE, 2000, 109 (07) :588-590
[7]  
ERIKSSON S, 1986, ACTA MED SCAND, V220, P83
[8]  
Gavin JR, 1999, DIABETES CARE, V22, pS5
[9]  
GOTO T, 1995, INT J OBESITY, V19, P841
[10]   Total immunoreactive proinsulin, immunoreactive insulin and specific insulin in relation to conversion to NIDDM: The Mexico City Diabetes Study [J].
Haffner, SM ;
Gonzalez, C ;
Mykkanen, L ;
Stern, M .
DIABETOLOGIA, 1997, 40 (07) :830-837