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Diagnosis and Treatment of Autoimmune Liver Diseases in a Tertiary Referral Center in Cuba
BACKGROUND: Autoimmune liver diseases (AILD) comprise a set of entities characterized by tissue damage as a result of the loss of self-tolerance. There are few reports of AILD from Caribbean countries. OBJECTIVES: The aim of our study was to investigate the clinical patterns, laboratory findings, an...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5681282/ https://www.ncbi.nlm.nih.gov/pubmed/29158853 http://dx.doi.org/10.1016/j.curtheres.2017.04.002 |
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author | Fernández, Marlen Ivón Castellanos Hernández, Deyanira la Rosa Cabrera Eugenio, Diego Enrique Palanca, Wilson Guridi, Zaily Dorta González Fabián, Licet |
author_facet | Fernández, Marlen Ivón Castellanos Hernández, Deyanira la Rosa Cabrera Eugenio, Diego Enrique Palanca, Wilson Guridi, Zaily Dorta González Fabián, Licet |
author_sort | Fernández, Marlen Ivón Castellanos |
collection | PubMed |
description | BACKGROUND: Autoimmune liver diseases (AILD) comprise a set of entities characterized by tissue damage as a result of the loss of self-tolerance. There are few reports of AILD from Caribbean countries. OBJECTIVES: The aim of our study was to investigate the clinical patterns, laboratory findings, and immunologic features, treatment responses, and prognoses of AILD in adult patients at a Cuban tertiary referral center. METHODS: A prospective study was conducted at the National Institute of Gastroenterology in Havana, Cuba, from May 2012 to April 2016. Clinical, immunologic, and histologic features of autoimmune hepatitis (AIH), primary biliary cirrhosis, AIH/primary biliary cirrhosis overlap syndrome, autoimmune cholangiopathy, and primary sclerosing cholangitis were recorded. Response to therapy was assessed by serum alanine aminotransferase and bilirubin levels at 3, 6, 12, and 24 months after treatment initiation. RESULTS: Of the 106 patients included in the study, 85.5% were women. The median age at presentation was 47 years. AIH was the most common AILD and was diagnosed in 60 patients (56.6%), 55 of whom had type 1 AIH. Primary biliary cirrhosis was diagnosed in 22 patients (20.7%), overlap syndrome in 16 patients (15%), autoimmune cholangiopathy in 5 patients (4.71%), and PSC in 3 patients (2.8%). Most patients were symptomatic; 48 patients (45.2%) presented with liver cirrhosis, 14.5% of whom had decompensated cirrhosis. Follow-up of treatment was between 6 and 24 months. Prednisone monotherapy was used in 22 AIH patients (36.6%) and a combination of prednisone and azathioprine was used in 28 (46.6%) AIH patients. Response to treatment was seen in 41 AIH patients (68.3%), 33 of whom (55%) had a complete response and 8 of whom (24.2%) relapsed after 12 months of maintenance therapy. No or incomplete response to treatment was seen in 18 patients (30%). In 46 patients with autoimmune cholestasis, ursodeoxycholic acid was used as monotherapy in 25 patients (54.3%). CONCLUSIONS: The clinical profile of AILD in a sample of the Cuban population is similar to that reported in South areas (Developing countries). AIH was more frequent than PBC, and usually presented with advanced liver disease that responded poorly to treatment. |
format | Online Article Text |
id | pubmed-5681282 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-56812822017-11-20 Diagnosis and Treatment of Autoimmune Liver Diseases in a Tertiary Referral Center in Cuba Fernández, Marlen Ivón Castellanos Hernández, Deyanira la Rosa Cabrera Eugenio, Diego Enrique Palanca, Wilson Guridi, Zaily Dorta González Fabián, Licet Curr Ther Res Clin Exp Article BACKGROUND: Autoimmune liver diseases (AILD) comprise a set of entities characterized by tissue damage as a result of the loss of self-tolerance. There are few reports of AILD from Caribbean countries. OBJECTIVES: The aim of our study was to investigate the clinical patterns, laboratory findings, and immunologic features, treatment responses, and prognoses of AILD in adult patients at a Cuban tertiary referral center. METHODS: A prospective study was conducted at the National Institute of Gastroenterology in Havana, Cuba, from May 2012 to April 2016. Clinical, immunologic, and histologic features of autoimmune hepatitis (AIH), primary biliary cirrhosis, AIH/primary biliary cirrhosis overlap syndrome, autoimmune cholangiopathy, and primary sclerosing cholangitis were recorded. Response to therapy was assessed by serum alanine aminotransferase and bilirubin levels at 3, 6, 12, and 24 months after treatment initiation. RESULTS: Of the 106 patients included in the study, 85.5% were women. The median age at presentation was 47 years. AIH was the most common AILD and was diagnosed in 60 patients (56.6%), 55 of whom had type 1 AIH. Primary biliary cirrhosis was diagnosed in 22 patients (20.7%), overlap syndrome in 16 patients (15%), autoimmune cholangiopathy in 5 patients (4.71%), and PSC in 3 patients (2.8%). Most patients were symptomatic; 48 patients (45.2%) presented with liver cirrhosis, 14.5% of whom had decompensated cirrhosis. Follow-up of treatment was between 6 and 24 months. Prednisone monotherapy was used in 22 AIH patients (36.6%) and a combination of prednisone and azathioprine was used in 28 (46.6%) AIH patients. Response to treatment was seen in 41 AIH patients (68.3%), 33 of whom (55%) had a complete response and 8 of whom (24.2%) relapsed after 12 months of maintenance therapy. No or incomplete response to treatment was seen in 18 patients (30%). In 46 patients with autoimmune cholestasis, ursodeoxycholic acid was used as monotherapy in 25 patients (54.3%). CONCLUSIONS: The clinical profile of AILD in a sample of the Cuban population is similar to that reported in South areas (Developing countries). AIH was more frequent than PBC, and usually presented with advanced liver disease that responded poorly to treatment. Elsevier 2017-04-07 /pmc/articles/PMC5681282/ /pubmed/29158853 http://dx.doi.org/10.1016/j.curtheres.2017.04.002 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Fernández, Marlen Ivón Castellanos Hernández, Deyanira la Rosa Cabrera Eugenio, Diego Enrique Palanca, Wilson Guridi, Zaily Dorta González Fabián, Licet Diagnosis and Treatment of Autoimmune Liver Diseases in a Tertiary Referral Center in Cuba |
title | Diagnosis and Treatment of Autoimmune Liver Diseases in a Tertiary Referral Center in Cuba |
title_full | Diagnosis and Treatment of Autoimmune Liver Diseases in a Tertiary Referral Center in Cuba |
title_fullStr | Diagnosis and Treatment of Autoimmune Liver Diseases in a Tertiary Referral Center in Cuba |
title_full_unstemmed | Diagnosis and Treatment of Autoimmune Liver Diseases in a Tertiary Referral Center in Cuba |
title_short | Diagnosis and Treatment of Autoimmune Liver Diseases in a Tertiary Referral Center in Cuba |
title_sort | diagnosis and treatment of autoimmune liver diseases in a tertiary referral center in cuba |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5681282/ https://www.ncbi.nlm.nih.gov/pubmed/29158853 http://dx.doi.org/10.1016/j.curtheres.2017.04.002 |
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