Home LiteratureArticle Details
PMID: 8386693 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Cirrhosis of undefined pathogenesis: absence of evidence for unknown viruses or autoimmune processes.

Hepatology (Baltimore, Md.) ·Vol. 17 ·No. 4 ·1993-04-00 ·Pages 593-8

Greeve M, Ferrell L, Kim M, Combs C, Roberts J, Ascher N, Wright TL

Abstract

To examine whether unknown viruses or autoimmune processes contribute to the development of cryptogenic liver disease, we studied 48 patients undergoing liver transplantation who had non-A, non-B cirrhosis; non-blood-borne cirrhosis of unknown etiology; or autoimmune cirrhosis. After the diagnosis of hepatitis C virus infection was established by the presence of viral antibodies or viral RNA, patients were reclassified into three groups: hepatitis C virus infection, autoimmune cirrhosis and cryptogenic cirrhosis. Explant histological appearance, incidence of posttransplant hepatitis and immunological features were compared in the three groups. Thirty-one percent of patients had neither hepatitis C virus infection nor classical autoimmune cirrhosis and were classified as having cryptogenic cirrhosis. Unlike histological appearance in hepatitis C virus infection but similar to that in autoimmune cirrhosis, explant histological appearance of cryptogenic cirrhosis showed inactive cirrhosis with little inflammation. After transplantation, histological hepatitis of the allograft was demonstrated in 44% of patients with hepatitis C infection but in no patient with autoimmune or cryptogenic cirrhosis. The autoimmune score, developed from clinical criteria associated with autoimmune liver disease, was significantly lower in cryptogenic cirrhosis and hepatitis C virus infection than in autoimmune cirrhosis. Autoantibodies--including antinuclear antibodies, smooth muscle antibodies and liver-kidney microsomal antibodies--were not commonly present in serum of patients with cryptogenic cirrhosis, whereas antibodies to soluble liver antigens were found with increased frequency in this entity. We conclude that in many patients with liver disease, no pathogenesis can be identified.(ABSTRACT TRUNCATED AT 250 WORDS)

MeSH Terms
Autoimmune Diseases/diagnosis,pathology Base Sequence Enzyme-Linked Immunosorbent Assay Hepacivirus/genetics,isolation & purification Hepatitis C/diagnosis,pathology Humans Liver Cirrhosis/etiology,immunology,pathology Molecular Sequence Data Oligodeoxyribonucleotides Polymerase Chain Reaction/methods RNA, Viral/analysis,blood,genetics Retrospective Studies Serum Globulins/analysis
Chemicals
Oligodeoxyribonucleotides RNA, Viral Serum Globulins
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Greeve M
Department of Medicine, University of California, San Francisco 94121.
Ferrell L
Kim M
Combs C
Roberts J
Ascher N
Wright T L
Article Info
Journal
Hepatology (Baltimore, Md.)
Abbr.
Hepatology
ISSN
0270-9139
Published
1993-04-00
Pages
593-8
Language
English
Region
United States
NLM ID
8302946
Subset
IM
Grants
PHS HHS · R29A132242-01 · United States
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