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Acute sporadic non-A, non-B hepatitis in northeastern Brazil:: Etiology and natural history
被引:30
|作者:
Paraná, R
Vitvitski, L
Andrade, Z
Trepo, C
Cotrim, H
Bertillon, P
Silva, F
Silva, L
de Oliveira, IR
Lyra, L
机构:
[1] Hepatol Unit, Bahia, Brazil
[2] INSERM, U271, F-69008 Lyon, France
[3] CPGM Fiocruz, Bahia, Brazil
来源:
关键词:
D O I:
10.1002/hep.510300143
中图分类号:
R57 [消化系及腹部疾病];
学科分类号:
摘要:
In a 4-year follow-up study, patients with acute sporadic non-A, non-B (NANB) hepatitis were evaluated to determine the etiology and natural history of the disease. Acute hepatitis C virus (HCV) was detected in 13 of 43 (30%) of patients, anti-hepatitis E virus (HEV) IgG in 5 (12%), and 25 (58%) were considered non-A-E. The HCV RNA was detected in all HCV patients but none of the non-A-E cases. The initial clinical and biochemical presentation of the HCV and non-A-E cases was quite similar, although 2 of the non-A-E patients had severe disease. The 5 patients who were found to be anti-HEV IgG-reactive recovered within 6 months of follow-up. Of the 13 HCV cases, alanine transaminase (ALT) levels returned to normal in 7 (53.8%), while 6 (46.2%) continued to show abnormal ALT after 6 months of follow-up. However, 9 (69.2%) of them remained HCV-RNA-positive, denoting virological/biochemical dissociation. Longterm follow-up showed a reappearance of HCV RNA in 2 of the 4 patients who were in virological remission performing 84% of chronicity rate. Acute non-A-E hepatitis patients were less likely to evolve toward chronicity, as compared with acute HCV cases (16% vs. 84%; P = .0001). Only 4 (16%) of the non-A-E patients were hepatitis G virus (HGV)-RNA-positive. Concerning risk factors for acquiring parenterally transmitted viruses, tattooing was the only one that could be associated with HCV transmission (P = .002). No risk factors could be identified for putative non-A-E virus transmission. Liver biopsies performed for chronic HCV patients showed a variable degree of inflammation, while the non-A-E patients presented less severe histological disease.
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页码:289 / 293
页数:5
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