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Different degrees of malnutrition and immunological alterations according to the aetiology of cirrhosis: a prospective and sequential study

OBJECTIVES: In this work we investigated how immunological dysfunction and malnutrition interact in alcoholic and viral aetiologies of cirrhosis. METHODS: To investigate the matter, 77 cirrhotic patients divided in three aetiologies [Alcohol, HCV and Alcohol + HCV) and 32 controls were prospectivell...

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Autores principales: Caly, Wanda Regina, Strauss, Edna, Carrilho, Flair José, Laudanna, Antonio Atílio
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC270012/
https://www.ncbi.nlm.nih.gov/pubmed/14613508
http://dx.doi.org/10.1186/1475-2891-2-10
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author Caly, Wanda Regina
Strauss, Edna
Carrilho, Flair José
Laudanna, Antonio Atílio
author_facet Caly, Wanda Regina
Strauss, Edna
Carrilho, Flair José
Laudanna, Antonio Atílio
author_sort Caly, Wanda Regina
collection PubMed
description OBJECTIVES: In this work we investigated how immunological dysfunction and malnutrition interact in alcoholic and viral aetiologies of cirrhosis. METHODS: To investigate the matter, 77 cirrhotic patients divided in three aetiologies [Alcohol, HCV and Alcohol + HCV) and 32 controls were prospectivelly and sequentially studied. Parameters of humoral immunity (Components 3 and 4 of seric complement and immunoglobulins A M, G and E) and of cellular immunity (total leukocytes and lymphocytes in peripheral blood, T lymphocytes subpopulations, CD4+ and CD8+, CD4+/CD8+ ratio and intradermic tests of delayed hypersensitivity), as well as nutrititional parameters: anthropometric measures, serum albumin and transferrin were evaluated. RESULTS: Multiple statistical comparisons showed that IgM was higher in HCV group; IgG was significantly elevated in both HCV and Alcohol + HCV, whereas for the Alcohol group, IgE was found at higher titles. The analysis of T- lymphocytes subpopulations showed no aetiologic differences, but intradermic tests of delayed hypersensitivity did show greater frequency of anergy in the Alcohol group. For anthropometric parameters, the Alcohol +HCV group displayed the lowest triceps skinfold whereas creatinine – height index evaluation was more preserved in the HCV group. Body mass index, arm muscle area and arm fat area showed that differently from alcohol group, the HCV group was similar to control. CONCLUSION: Significant differences were found among the main aetiologies of cirrhosis concerning immunological alterations and nutritional status: better nutrition and worse immunology for HCV and vice-versa for alcohol.
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spelling pubmed-2700122003-11-21 Different degrees of malnutrition and immunological alterations according to the aetiology of cirrhosis: a prospective and sequential study Caly, Wanda Regina Strauss, Edna Carrilho, Flair José Laudanna, Antonio Atílio Nutr J Research OBJECTIVES: In this work we investigated how immunological dysfunction and malnutrition interact in alcoholic and viral aetiologies of cirrhosis. METHODS: To investigate the matter, 77 cirrhotic patients divided in three aetiologies [Alcohol, HCV and Alcohol + HCV) and 32 controls were prospectivelly and sequentially studied. Parameters of humoral immunity (Components 3 and 4 of seric complement and immunoglobulins A M, G and E) and of cellular immunity (total leukocytes and lymphocytes in peripheral blood, T lymphocytes subpopulations, CD4+ and CD8+, CD4+/CD8+ ratio and intradermic tests of delayed hypersensitivity), as well as nutrititional parameters: anthropometric measures, serum albumin and transferrin were evaluated. RESULTS: Multiple statistical comparisons showed that IgM was higher in HCV group; IgG was significantly elevated in both HCV and Alcohol + HCV, whereas for the Alcohol group, IgE was found at higher titles. The analysis of T- lymphocytes subpopulations showed no aetiologic differences, but intradermic tests of delayed hypersensitivity did show greater frequency of anergy in the Alcohol group. For anthropometric parameters, the Alcohol +HCV group displayed the lowest triceps skinfold whereas creatinine – height index evaluation was more preserved in the HCV group. Body mass index, arm muscle area and arm fat area showed that differently from alcohol group, the HCV group was similar to control. CONCLUSION: Significant differences were found among the main aetiologies of cirrhosis concerning immunological alterations and nutritional status: better nutrition and worse immunology for HCV and vice-versa for alcohol. BioMed Central 2003-10-07 /pmc/articles/PMC270012/ /pubmed/14613508 http://dx.doi.org/10.1186/1475-2891-2-10 Text en Copyright © 2003 Caly et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
spellingShingle Research
Caly, Wanda Regina
Strauss, Edna
Carrilho, Flair José
Laudanna, Antonio Atílio
Different degrees of malnutrition and immunological alterations according to the aetiology of cirrhosis: a prospective and sequential study
title Different degrees of malnutrition and immunological alterations according to the aetiology of cirrhosis: a prospective and sequential study
title_full Different degrees of malnutrition and immunological alterations according to the aetiology of cirrhosis: a prospective and sequential study
title_fullStr Different degrees of malnutrition and immunological alterations according to the aetiology of cirrhosis: a prospective and sequential study
title_full_unstemmed Different degrees of malnutrition and immunological alterations according to the aetiology of cirrhosis: a prospective and sequential study
title_short Different degrees of malnutrition and immunological alterations according to the aetiology of cirrhosis: a prospective and sequential study
title_sort different degrees of malnutrition and immunological alterations according to the aetiology of cirrhosis: a prospective and sequential study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC270012/
https://www.ncbi.nlm.nih.gov/pubmed/14613508
http://dx.doi.org/10.1186/1475-2891-2-10
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