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一项大型人群组织学研究表明,慢性乙型肝炎中丙氨酸氨基转移酶(ALT)升高与显著纤维化之间缺乏关联。

A large population histology study showing the lack of association between ALT elevation and significant fibrosis in chronic hepatitis B.

机构信息

Department of Medicine, The University of Hong Kong, Queen Mary Hospital, Hong Kong.

出版信息

PLoS One. 2012;7(2):e32622. doi: 10.1371/journal.pone.0032622. Epub 2012 Feb 28.

DOI:10.1371/journal.pone.0032622
PMID:22389715
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3289659/
Abstract

OBJECTIVE

We determined the association between various clinical parameters and significant liver injury in both hepatitis B e antigen (HBeAg)-positive and HBeAg-negative patients.

METHODS

From 1994 to 2008, liver biopsy was performed on 319 treatment-naïve CHB patients. Histologic assessment was based on the Knodell histologic activity index for necroinflammation and the Ishak fibrosis staging for fibrosis.

RESULTS

211 HBeAg-positive and 108 HBeAg-negative patients were recruited, with a median age of 31 and 46 years respectively. 9 out of 40 (22.5%) HBeAg-positive patients with normal ALT had significant histologic abnormalities (necroinflammation grading ≥ 7 or fibrosis score ≥ 3). There was a significant difference in fibrosis scores among HBeAg-positive patients with an ALT level within the Prati criteria (30 U/L for men, 19 U/L for women) and patients with a normal ALT but exceeding the Prati criteria (p = 0.024). Age, aspartate aminotransferase and platelet count were independent predictors of significant fibrosis in HBeAg-positive patients with an elevated ALT by multivariate analysis (p = 0.007, 0.047 and 0.045 respectively). HBV DNA and platelet count were predictors of significant fibrosis in HBeAg-negative disease (p = 0.020 and 0.015 respectively). An elevated ALT was not predictive of significant fibrosis for HBeAg-positive (p = 0.345) and -negative (p = 0.544) disease. There was no significant difference in fibrosis staging among ALT 1-2 × upper limit of normal (ULN) and > × 2 ULN for both HBeAg-positive (p = 0.098) and -negative (p = 0.838) disease.

CONCLUSION

An elevated ALT does not accurately predict significant liver injury. Decisions on commencing antiviral therapy should not be heavily based on a particular ALT threshold.

摘要

目的

我们确定了乙型肝炎 e 抗原(HBeAg)阳性和 HBeAg 阴性患者中各种临床参数与显著肝损伤之间的关系。

方法

1994 年至 2008 年,对 319 例未经治疗的慢性乙型肝炎患者进行了肝活检。组织学评估基于坏死性炎症的 Knodell 组织学活动指数和纤维化的 Ishak 分期。

结果

纳入 211 例 HBeAg 阳性和 108 例 HBeAg 阴性患者,中位年龄分别为 31 岁和 46 岁。40 例 HBeAg 阳性 ALT 正常患者中有 9 例(22.5%)存在显著组织学异常(坏死性炎症分级≥7 或纤维化评分≥3)。在符合 Prati 标准的 ALT 水平(男性 30 U/L,女性 19 U/L)的 HBeAg 阳性患者和 ALT 正常但超过 Prati 标准的患者之间,纤维化评分存在显著差异(p=0.024)。年龄、天冬氨酸氨基转移酶和血小板计数是 HBeAg 阳性患者 ALT 升高时发生显著纤维化的独立预测因素(p=0.007、0.047 和 0.045)。HBV DNA 和血小板计数是 HBeAg 阴性疾病显著纤维化的预测因素(p=0.020 和 0.015)。升高的 ALT 对 HBeAg 阳性(p=0.345)和阴性(p=0.544)疾病的显著纤维化没有预测作用。在 HBeAg 阳性(p=0.098)和阴性(p=0.838)疾病中,ALT 为 1-2×正常值上限(ULN)和>×2ULN 之间的纤维化分期没有显著差异。

结论

升高的 ALT 并不能准确预测显著的肝损伤。启动抗病毒治疗的决定不应过分依赖于特定的 ALT 阈值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d19/3289659/79e31c94ebea/pone.0032622.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d19/3289659/e4649d0c40d1/pone.0032622.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d19/3289659/465d27fe5223/pone.0032622.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d19/3289659/186c6f6cb239/pone.0032622.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d19/3289659/b16c6f836c19/pone.0032622.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d19/3289659/79e31c94ebea/pone.0032622.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d19/3289659/e4649d0c40d1/pone.0032622.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d19/3289659/465d27fe5223/pone.0032622.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d19/3289659/186c6f6cb239/pone.0032622.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d19/3289659/b16c6f836c19/pone.0032622.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d19/3289659/79e31c94ebea/pone.0032622.g005.jpg

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