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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...

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Autores principales: Fernández, Marlen Ivón Castellanos, Hernández, Deyanira la Rosa, Cabrera Eugenio, Diego Enrique, Palanca, Wilson, Guridi, Zaily Dorta, González Fabián, Licet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
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.
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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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