肝纤维化评估在慢性乙型肝炎感染患者管理中的作用:来自单一中心经验的教训。

Hepatitis research and treatment Pub Date : 2011-01-01 Epub Date: 2011-10-30 DOI:10.1155/2011/524027
Raza Malik, Patrick Kennedy, Deepak Suri, Ashley Brown, Rob Goldin, Janice Main, Howard Thomas, Mark Thursz
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引用次数: 2

摘要

背景与目的评估Prati标准和ALT正常(6 log拷贝/ml)和ALT正常(肝活检显示有中度/重度纤维化)的临床应用。HBeAg(-)组:ALT正常,肝活检中重度纤维化10例;其中4例患者HBV DNA水平>3 log拷贝/ml, 6例患者HBV DNA水平阴性,ALT正常,中/重度纤维化,被错误归类为“非活性携带者”(6/84-7% HBeAg(-)组)。两名男性HBeAg(+)和三名男性HBeAg(-)患者,ALT在20至30 IU/L之间,肝活检显示中度/重度纤维化,使用Prati标准诊断正常ALT会进一步被错误诊断。在多变量分析中,年龄和种族是中度/重度纤维化更重要的预测因素。结论。在正常范围(ALT 20-40 IU/L)上端的“正常”患者中,应研究HBeAg状态、年龄、民族血统与LFTs和病毒载量的纵向评估,以便对患者进行适当分类,并确定患者进行肝纤维化评估,为治疗决策提供信息。
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The role of liver fibrosis assessment in the management of patients with chronic hepatitis B infection: lessons learned from a single centre experience.

Background & Aims. Assess the clinical utility of the Prati criteria and normal ALT (<40 IU/L) in a cohort of patients with chronic hepatitis B infection (CHB). Methods. Serology, radiology, and histology were obtained in 140 patients with CHB. Results. HBeAg(+) group: 7 patients (7/56-12% HBeAg(+) group) misclassified as "immunotolerant", with HBV DNA > 6 log copies/ml and normal ALT, who in fact had moderate/severe fibrosis on liver biopsy. HBeAg(-) group: 10 patients with normal ALT and moderate/severe fibrosis on liver biopsy; 4 of these patients had >3 log copies/ml HBV DNA levels and 6 patients misclassified as "inactive carriers" with negative HBV DNA levels normal ALT and moderate/severe fibrosis (6/84-7% HBeAg(-) group). Two male HBeAg(+) and three male HBeAg(-) patients with ALT between 20 and 30 IU/L and moderate/severe fibrosis on liver biopsy would have been further mischaracterised using the Prati criteria for normal ALT. Age and ethnic group were more important predictors of moderate/severe fibrosis in multivariate analysis. Conclusion. HBeAg status, age, ethnic origin with longitudinal assessment of LFTs and viral load should be studied in patients with "normal ALT" at the upper end of normal range (ALT 20-40 IU/L) to appropriately classify patients and identify patients for liver fibrosis assessment to inform treatment decisions.

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