Tahan Veysel, Canbakan Billur, Balci Huriye, Dane Faysal, Akin Hakan, Can Guray, Hatemi Ibrahim, Olgac Vakur, Sonsuz Abdullah, Ozbay Gulsen, Yurdakul Ibrahim, Senturk Hakan
Department of Gastroenterology, Pasabahce State Hospital, 34800 Istanbul, Turkey.
Hepatogastroenterology. 2008 Jul-Aug;55(85):1433-8.
BACKGROUND/AIMS: Hepatocyte apoptosis is an important and invasive predictor of liver injury and fibrosis in non-alcoholic fatty liver disease (NAFLD). Increased gamma-glutamyltranspeptidase (GGT) level is frequently observed in NAFLD. Hepatocyte growth factor (HGF) stimulates fibrogenesis and is correlated with GGT. The study aimed to determine whether GGT can distinguish NAFLD patients at high risk.
Fifty biopsy-proven NAFLD patients (M/F: 24/26) were divided as the normal GGT group (n = 25) and the high GGT group (n = 25) (each patients' GGT > two fold of upper-limit of normal). Liver histology was graded according to Brunt et al. TNF-sRp55, caspase-3 and 8, NFkappaB and Bcl-2 were measured by immunohistochemical methods. For statistical analysis, Student's t test, chi-square test, multivariate regression analysis and the area under receiver operating characteristic (ROC) curve were used.
The high GGT group had significantly higher NFkappaB, caspase-3 and 8, and Bcl-2 levels (54.52 +/- 26.02, p = 0.002; 55.95 +/- 27.18, p = 0.002; 47.85 +/- 28.04, p = 0.001; 11.19 +/- 12.33, p = 0.016, respectively). Serum TNF-sRp55 levels of both groups were similar (2922.93 +/- 307.26, and 2885 +/- 194.47; p = 0.78). Differences in reference to histological steatosis grade and inflammation were not significant. However, fibrosis stage was higher in the high GGT group (p = 0.048).
Multinominal logistic regression analysis showed that increased GGT level was a risk factor for advanced fibrosis in NAFLD (OR: 1.0, CI: 0.98-1.01; p =0.032). Using serum GGT levels the area under the ROC curve for the prediction of advanced fibrosis was 0.74 (95% CI: 0.54-0.94). The serum GGT cut-off value for the prediction of advanced fibrosis was 96.5 U/L; with 83% sensitivity and 69% specificity.
背景/目的:肝细胞凋亡是非酒精性脂肪性肝病(NAFLD)中肝损伤和纤维化的重要且具有侵袭性的预测指标。NAFLD患者中经常观察到γ-谷氨酰转肽酶(GGT)水平升高。肝细胞生长因子(HGF)刺激纤维生成并与GGT相关。本研究旨在确定GGT是否能够区分高危NAFLD患者。
50例经活检证实的NAFLD患者(男/女:24/26)被分为正常GGT组(n = 25)和高GGT组(n = 25)(每位患者的GGT>正常上限的两倍)。根据Brunt等人的方法对肝脏组织学进行分级。通过免疫组织化学方法测量TNF-sRp55、半胱天冬酶-3和8、NFκB和Bcl-2。进行统计分析时,使用了学生t检验、卡方检验、多元回归分析以及受试者操作特征(ROC)曲线下面积。
高GGT组的NFκB、半胱天冬酶-3和8以及Bcl-2水平显著更高(分别为54.52±26.02,p = 0.002;55.95±27.18,p = 0.002;47.85±28.04,p = 0.001;11.19±12.33,p = 0.016)。两组的血清TNF-sRp55水平相似(2922.93±307.26和2885±194.47;p = 0.78)。在组织学脂肪变性分级和炎症方面的差异不显著。然而,高GGT组的纤维化阶段更高(p = 0.048)。
多项逻辑回归分析表明,GGT水平升高是NAFLD中晚期纤维化的危险因素(比值比:1.0,可信区间:0.98 - 1.01;p = 0.032)。使用血清GGT水平预测晚期纤维化的ROC曲线下面积为0.74(95%可信区间:0.54 - 0.94)。预测晚期纤维化的血清GGT临界值为96.5 U/L;敏感性为83%,特异性为69%。