Service Endocrinologie-Diabétologie, Centre Hospitalo-Universitaire(CHU) Rennes, University Rennes 1, INSERM UMR 991, Rennes, France.
Diabetes. 2011 Jun;60(6):1660-7. doi: 10.2337/db10-1806. Epub 2011 Apr 26.
The pathophysiological mechanisms to explain the association between risk of type 2 diabetes and elevated concentrations of γ-glutamyltransferase (GGT) and alanineaminotransferase (ALT) remain poorly characterized. We explored the association of liver enzymes with peripheral and hepatic insulin resistance, insulin secretion, insulin clearance, and glucagon concentration.
We studied 1,309 nondiabetic individuals from the Relationship between Insulin Sensitivity and Cardiovascular disease (RISC) study; all had a euglycemic-hyperinsulinemic clamp and an oral glucose tolerance test (OGTT) with assessment of insulin secretion and hepatic insulin extraction. The hepatic insulin resistance index was calculated in 393 individuals.
In both men and women, plasma concentrations of GGT and ALT were inversely related with insulin sensitivity (M/I) (all P < 0.01). Likewise, the hepatic insulin resistance index was positively correlated with both GGT (r = 0.37, P < 0.0001, men; r = 0.36, P < 0.0001, women) and ALT (r = 0.25, P = 0.0005, men; r = 0.18, P = 0.01, women). These associations persisted in multivariable models. Increased GGT and ALT were significantly associated with higher insulin secretion rates and with both reduced endogenous clearance of insulin and hepatic insulin extraction during the OGTT (P = 0.0005 in men; P = 0.003 in women). Plasma fasting glucagon levels increased over ALT quartiles (men, quartile 4 vs. quartile 1 11.2 ± 5.1 vs. 9.3 ± 3.8 pmol/L, respectively, P = 0.0002; women, 9.0 ± 4.3 vs. 7.6 ± 3.1, P = 0.001).
In healthy individuals, increased GGT and ALT were biomarkers of both systemic and hepatic insulin resistance with concomitant increased insulin secretion and decreased hepatic insulin clearance. The novel finding of a positive correlation between ALT and fasting glucagon level concentrations warrants confirmation in type 2 diabetes.
解释 2 型糖尿病风险与 γ-谷氨酰转移酶(GGT)和丙氨酸氨基转移酶(ALT)浓度升高之间关联的病理生理机制仍未得到充分描述。我们探讨了肝酶与外周和肝胰岛素抵抗、胰岛素分泌、胰岛素清除和胰高血糖素浓度之间的关系。
我们研究了来自胰岛素敏感性与心血管疾病关系(RISC)研究的 1309 名非糖尿病个体;所有个体均进行了正常血糖高胰岛素钳夹试验和口服葡萄糖耐量试验(OGTT),并评估了胰岛素分泌和肝胰岛素提取。在 393 名个体中计算了肝胰岛素抵抗指数。
在男性和女性中,血浆 GGT 和 ALT 浓度与胰岛素敏感性(M/I)呈负相关(均 P < 0.01)。同样,肝胰岛素抵抗指数与 GGT(r = 0.37,P < 0.0001,男性;r = 0.36,P < 0.0001,女性)和 ALT(r = 0.25,P = 0.0005,男性;r = 0.18,P = 0.01,女性)呈正相关。这些关联在多变量模型中仍然存在。GGT 和 ALT 升高与胰岛素分泌率升高显著相关,并且与 OGTT 期间胰岛素的内源性清除率和肝胰岛素提取率降低相关(男性,P = 0.0005;女性,P = 0.003)。血浆空腹胰高血糖素水平随 ALT 四分位升高(男性,四分位数 4 与四分位数 1 相比,分别为 11.2 ± 5.1 与 9.3 ± 3.8 pmol/L,P = 0.0002;女性,9.0 ± 4.3 与 7.6 ± 3.1,P = 0.001)。
在健康个体中,GGT 和 ALT 升高是全身和肝胰岛素抵抗的标志物,同时伴有胰岛素分泌增加和肝胰岛素清除率降低。ALT 与空腹胰高血糖素浓度之间存在正相关的新发现值得在 2 型糖尿病中进一步证实。