Division of Gastroenterology, Department of Internal Medicine, Buddhist Tzu Chi General Hospital, Taipei Branch, Taiwan.
J Gastroenterol Hepatol. 2010 May;25(5):970-7. doi: 10.1111/j.1440-1746.2009.06186.x.
Metabolic profiles are associated with severity of liver histology in chronic hepatitis C (CHC) infection. However, the influence of hepatitis C virus (HCV) genotypes, especially genotype 1 and 2, on the association between metabolic profiles and hepatic fibrosis remains unknown.
We consecutively enrolled 528 CHC patients infected by HCV genotype 1 or 2, and used univariate and multivariate approaches to determine the influence of HCV genotype on the association of metabolic characteristics with severity of liver histology.
In univariate analysis, diabetes mellitus, obesity, higher grades of hepatic steatosis, homeostasis model assessment-insulin resistance index and alanine aminotransferase level, but lower serum total cholesterol and low-density lipoprotein level, were associated with advanced hepatic fibrosis. Advanced hepatic fibrosis was associated with an adjusted odds ratio of 13.72 (95% confidence interval, 2.15-87.7) for serum fasting blood glucose, 1.07 (1.01 to 1.13) for body mass index (BMI), and 0.03 (0.00-0.32) for total cholesterol level. Older age, lower serum total cholesterol level and more necro-inflammatory activity were associated with advanced hepatic fibrosis in both genotype 1 and 2 patients (P < 0.05). Advanced hepatic fibrosis was associated with an adjusted odds ratio of 31.18 (2.31-421.4) for fasting blood glucose level in genotype 1 infection, whereas 1.16 (1.05-1.28) for BMI in genotype 2 infection.
Age, serum total cholesterol, and hepatic necro-inflammation have important associations with severity of hepatic fibrosis in CHC patients. Moreover, these associations are different between HCV genotype: the effects of fasting blood glucose level and BMI are increased on genotype 1 and genotype 2 patients, respectively.
代谢特征与慢性丙型肝炎(CHC)感染的肝组织学严重程度相关。然而,丙型肝炎病毒(HCV)基因型,尤其是基因型 1 和 2,对代谢特征与肝纤维化严重程度之间关联的影响尚不清楚。
我们连续纳入了 528 名感染 HCV 基因型 1 或 2 的 CHC 患者,采用单因素和多因素方法确定 HCV 基因型对代谢特征与肝组织学严重程度之间关联的影响。
在单因素分析中,糖尿病、肥胖、更严重的肝脂肪变性、稳态模型评估-胰岛素抵抗指数和丙氨酸氨基转移酶水平,但血清总胆固醇和低密度脂蛋白水平较低,与晚期肝纤维化相关。晚期肝纤维化与空腹血糖的校正比值比为 13.72(95%可信区间,2.15-87.7),体质指数(BMI)为 1.07(1.01-1.13),总胆固醇水平为 0.03(0.00-0.32)。年龄较大、血清总胆固醇水平较低和更多的坏死性炎症活动与基因型 1 和 2 患者的晚期肝纤维化相关(P<0.05)。在基因型 1 感染中,空腹血糖水平与晚期肝纤维化的校正比值比为 31.18(2.31-421.4),而在基因型 2 感染中,BMI 为 1.16(1.05-1.28)。
年龄、血清总胆固醇和肝坏死性炎症与 CHC 患者肝纤维化的严重程度有重要关联。此外,这些关联在 HCV 基因型之间存在差异:空腹血糖水平和 BMI 的影响在基因型 1 和基因型 2 患者中分别增加。