André P, Balkau B, Born C, Charles M A, Eschwège E
INSERM U780-IFR69, 16 avenue Paul Vaillant-Couturier, 94807 Villejuif Cedex, France,
Diabetologia. 2006 Nov;49(11):2599-603. doi: 10.1007/s00125-006-0418-x. Epub 2006 Sep 13.
AIMS/HYPOTHESIS: Among hepatic markers, gamma-glutamyltransferase (GGT) is the main predictor for development of type 2 diabetes, but there are no data to date on changes in GGT and type 2 diabetes incidence.
Data at baseline and at 3 years from the D.E.S.I.R. cohort were used, comprising 2,071 men and 2,130 women without baseline diabetes.
Changes in GGT level were correlated with changes in markers of insulin resistance (fasting insulin, homeostasis model assessment of insulin resistance), as well as with the following elements of the metabolic syndrome: central obesity, and increased fasting glucose, triglycerides and blood pressure (systolic and diastolic). The 3-year increase in GGT was associated with incident type 2 diabetes in both sexes, after adjusting for age and baseline GGT. After further adjustment for baseline confounding factors, including alanine-aminotransferase, alcohol intake, obesity and fasting insulin, the odds ratios (95% CI) for an association between incident type 2 diabetes and unchanged or increased (as opposed to decreased) GGT levels were 2.54 (1.38-4.68) in men (p=0.003) and 2.78 (1.20-6.42) in women (p=0.02). These associations were slightly attenuated after adjusting for the 3-year change in BMI, alcohol consumption and fasting insulin, the odds ratios being 2.49 (1.28-4.86) in men and 2.53 (1.01-6.40) in women. This relationship was not dependent on intra-individual variability.
CONCLUSIONS/INTERPRETATION: An unchanged or increased GGT level over time, even when GGT is in the normal range, is correlated with increasing insulin resistance and is associated with a risk of incident type 2 diabetes in both sexes, independently of baseline GGT, which is itself a diabetes risk factor.
目的/假设:在肝脏标志物中,γ-谷氨酰转移酶(GGT)是2型糖尿病发生的主要预测指标,但迄今为止尚无关于GGT变化与2型糖尿病发病率的数据。
使用了来自D.E.S.I.R.队列的基线数据和3年随访数据,该队列包括2071名男性和2130名无基线糖尿病的女性。
GGT水平的变化与胰岛素抵抗标志物(空腹胰岛素、胰岛素抵抗稳态模型评估)的变化相关,也与代谢综合征的以下因素相关:中心性肥胖、空腹血糖升高、甘油三酯升高和血压升高(收缩压和舒张压)。在调整年龄和基线GGT后,GGT的3年升高与男女2型糖尿病的发生均相关。在进一步调整包括丙氨酸氨基转移酶、酒精摄入量、肥胖和空腹胰岛素在内的基线混杂因素后,2型糖尿病发生与GGT水平不变或升高(与降低相反)之间关联的比值比(95%CI)在男性中为2.54(1.38-4.68)(p=0.003),在女性中为2.78(1.20-6.42)(p=0.02)。在调整BMI、酒精摄入量和空腹胰岛素的3年变化后,这些关联略有减弱,男性的比值比为2.49(1.28-4.86),女性为2.53(1.01-6.40)。这种关系不依赖于个体内变异性。
结论/解读:随着时间推移GGT水平不变或升高,即使GGT在正常范围内,也与胰岛素抵抗增加相关,且与男女2型糖尿病发生风险相关,独立于基线GGT,而基线GGT本身就是糖尿病风险因素。