Serum proinflammatory cytokines and nutritional status in pediatric chronic liver disease

Detalhes bibliográficos
Autor(a) principal: Santetti, Daniele
Data de Publicação: 2015
Outros Autores: Wilasco, Maria Inês de Albuquerque, Dornelles, Cristina Toscani Leal, Werlang, Isabel Cristina Ribas, Fontella, Fernanda Urruth, Kieling, Carlos Oscar, Santos, Jorge Luiz dos, Vieira, Sandra Maria Gonçalves, Goldani, Helena Ayako Sueno
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/131984
Resumo: AIM: To evaluate the nutritional status and its association with proinflammatory cytokines in children with chronic liver disease. METHODS: We performed a cross-sectional study with 43 children and adolescents, aged 0 to 17 years, diagnosed with chronic liver disease. All patients regularly attended the Pediatric Hepatology Unit and were under nutritional follow up. The exclusion criteria were fever from any etiology at the time of enrollment, inborn errors of the metabolism and any chronic illness. The severity of liver disease was assessed by Child-Pugh, Model for End-stage Liver Disease (MELD) and Pediatric End Stage Liver Disease (PELD) scores. Anthropometric parameters were height/age, body mass index/age and triceps skinfold/age according to World Health Organization standards. The cutoff points for nutritional status were risk of malnutrition (Z-score < -1.00) and malnutrition (Z-score < -2.00). Interleukin-1β (IL-1β), IL-6 and tumor necrosis factor-α levels were assessed by commercial ELISA kits. For multivariate analysis, linear regression was applied to assess the association between cytokine levels, disease severity and nutritional status RESULTS: The median (25th-75th centile) age of the study population was 60 (17-116)-mo-old, and 53.5% were female. Biliary atresia was the main cause of chronic liver disease (72%). With respect to Child-Pugh score, cirrhotic patients were distributed as follows: 57.1% Child-Pugh A, a mild presentation of the disease, 34.3% Child-Pugh B, a moderate stage of cirrhosis and 8.6% Child-Pugh C, were considered severe cases. PELD and MELD scores were only above the cutoff point in 5 cases. IL-6 values were increased in patients at nutritional risk (34.9%) compared with those who were well-nourished [7.12 (0.58-34.23) pg/mL vs 1.63 (0.53-3.43) pg/mL; P = 0.02], correlating inversely with triceps skinfold-for-age z-score (rs = -0.61; P < 0.001). IL-6 levels were associated with liver disease severity assessed by Child-Pugh score (P = 0.001). This association remained significant after adjusting for nutritional status in a linear regression model. CONCLUSION: High IL-6 levels were found in children with chronic liver disease at nutritional risk. Inflammatory activity may be related to nutritional status deterioration in these patients.
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spelling Santetti, DanieleWilasco, Maria Inês de AlbuquerqueDornelles, Cristina Toscani LealWerlang, Isabel Cristina RibasFontella, Fernanda UrruthKieling, Carlos OscarSantos, Jorge Luiz dosVieira, Sandra Maria GonçalvesGoldani, Helena Ayako Sueno2016-01-20T02:39:33Z20152219-2840http://hdl.handle.net/10183/131984000978823AIM: To evaluate the nutritional status and its association with proinflammatory cytokines in children with chronic liver disease. METHODS: We performed a cross-sectional study with 43 children and adolescents, aged 0 to 17 years, diagnosed with chronic liver disease. All patients regularly attended the Pediatric Hepatology Unit and were under nutritional follow up. The exclusion criteria were fever from any etiology at the time of enrollment, inborn errors of the metabolism and any chronic illness. The severity of liver disease was assessed by Child-Pugh, Model for End-stage Liver Disease (MELD) and Pediatric End Stage Liver Disease (PELD) scores. Anthropometric parameters were height/age, body mass index/age and triceps skinfold/age according to World Health Organization standards. The cutoff points for nutritional status were risk of malnutrition (Z-score < -1.00) and malnutrition (Z-score < -2.00). Interleukin-1β (IL-1β), IL-6 and tumor necrosis factor-α levels were assessed by commercial ELISA kits. For multivariate analysis, linear regression was applied to assess the association between cytokine levels, disease severity and nutritional status RESULTS: The median (25th-75th centile) age of the study population was 60 (17-116)-mo-old, and 53.5% were female. Biliary atresia was the main cause of chronic liver disease (72%). With respect to Child-Pugh score, cirrhotic patients were distributed as follows: 57.1% Child-Pugh A, a mild presentation of the disease, 34.3% Child-Pugh B, a moderate stage of cirrhosis and 8.6% Child-Pugh C, were considered severe cases. PELD and MELD scores were only above the cutoff point in 5 cases. IL-6 values were increased in patients at nutritional risk (34.9%) compared with those who were well-nourished [7.12 (0.58-34.23) pg/mL vs 1.63 (0.53-3.43) pg/mL; P = 0.02], correlating inversely with triceps skinfold-for-age z-score (rs = -0.61; P < 0.001). IL-6 levels were associated with liver disease severity assessed by Child-Pugh score (P = 0.001). This association remained significant after adjusting for nutritional status in a linear regression model. CONCLUSION: High IL-6 levels were found in children with chronic liver disease at nutritional risk. Inflammatory activity may be related to nutritional status deterioration in these patients.application/pdfengWorld journal of gastroenterology. Beijing. Vol. 21, no. 29 (Aug. 7, 2015), p. 8927-8934CitocinasInterleucina-6DesnutriçãoFibroseCriançaCytokinesInterleukin-6MalnutritionCirrhosisChildSerum proinflammatory cytokines and nutritional status in pediatric chronic liver diseaseEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSORIGINAL000978823.pdf000978823.pdfTexto completo (inglês)application/pdf875527http://www.lume.ufrgs.br/bitstream/10183/131984/1/000978823.pdf89565396e8ee130ec1d1b90b9b6f4447MD51TEXT000978823.pdf.txt000978823.pdf.txtExtracted Texttext/plain41922http://www.lume.ufrgs.br/bitstream/10183/131984/2/000978823.pdf.txtca0b2b3d1de4cebe841fcb8bfae33c6aMD52THUMBNAIL000978823.pdf.jpg000978823.pdf.jpgGenerated Thumbnailimage/jpeg2397http://www.lume.ufrgs.br/bitstream/10183/131984/3/000978823.pdf.jpg43122451f3b7aaaebb087808bb14a312MD5310183/1319842021-09-18 04:41:23.036229oai:www.lume.ufrgs.br:10183/131984Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2021-09-18T07:41:23Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Serum proinflammatory cytokines and nutritional status in pediatric chronic liver disease
title Serum proinflammatory cytokines and nutritional status in pediatric chronic liver disease
spellingShingle Serum proinflammatory cytokines and nutritional status in pediatric chronic liver disease
Santetti, Daniele
Citocinas
Interleucina-6
Desnutrição
Fibrose
Criança
Cytokines
Interleukin-6
Malnutrition
Cirrhosis
Child
title_short Serum proinflammatory cytokines and nutritional status in pediatric chronic liver disease
title_full Serum proinflammatory cytokines and nutritional status in pediatric chronic liver disease
title_fullStr Serum proinflammatory cytokines and nutritional status in pediatric chronic liver disease
title_full_unstemmed Serum proinflammatory cytokines and nutritional status in pediatric chronic liver disease
title_sort Serum proinflammatory cytokines and nutritional status in pediatric chronic liver disease
author Santetti, Daniele
author_facet Santetti, Daniele
Wilasco, Maria Inês de Albuquerque
Dornelles, Cristina Toscani Leal
Werlang, Isabel Cristina Ribas
Fontella, Fernanda Urruth
Kieling, Carlos Oscar
Santos, Jorge Luiz dos
Vieira, Sandra Maria Gonçalves
Goldani, Helena Ayako Sueno
author_role author
author2 Wilasco, Maria Inês de Albuquerque
Dornelles, Cristina Toscani Leal
Werlang, Isabel Cristina Ribas
Fontella, Fernanda Urruth
Kieling, Carlos Oscar
Santos, Jorge Luiz dos
Vieira, Sandra Maria Gonçalves
Goldani, Helena Ayako Sueno
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Santetti, Daniele
Wilasco, Maria Inês de Albuquerque
Dornelles, Cristina Toscani Leal
Werlang, Isabel Cristina Ribas
Fontella, Fernanda Urruth
Kieling, Carlos Oscar
Santos, Jorge Luiz dos
Vieira, Sandra Maria Gonçalves
Goldani, Helena Ayako Sueno
dc.subject.por.fl_str_mv Citocinas
Interleucina-6
Desnutrição
Fibrose
Criança
topic Citocinas
Interleucina-6
Desnutrição
Fibrose
Criança
Cytokines
Interleukin-6
Malnutrition
Cirrhosis
Child
dc.subject.eng.fl_str_mv Cytokines
Interleukin-6
Malnutrition
Cirrhosis
Child
description AIM: To evaluate the nutritional status and its association with proinflammatory cytokines in children with chronic liver disease. METHODS: We performed a cross-sectional study with 43 children and adolescents, aged 0 to 17 years, diagnosed with chronic liver disease. All patients regularly attended the Pediatric Hepatology Unit and were under nutritional follow up. The exclusion criteria were fever from any etiology at the time of enrollment, inborn errors of the metabolism and any chronic illness. The severity of liver disease was assessed by Child-Pugh, Model for End-stage Liver Disease (MELD) and Pediatric End Stage Liver Disease (PELD) scores. Anthropometric parameters were height/age, body mass index/age and triceps skinfold/age according to World Health Organization standards. The cutoff points for nutritional status were risk of malnutrition (Z-score < -1.00) and malnutrition (Z-score < -2.00). Interleukin-1β (IL-1β), IL-6 and tumor necrosis factor-α levels were assessed by commercial ELISA kits. For multivariate analysis, linear regression was applied to assess the association between cytokine levels, disease severity and nutritional status RESULTS: The median (25th-75th centile) age of the study population was 60 (17-116)-mo-old, and 53.5% were female. Biliary atresia was the main cause of chronic liver disease (72%). With respect to Child-Pugh score, cirrhotic patients were distributed as follows: 57.1% Child-Pugh A, a mild presentation of the disease, 34.3% Child-Pugh B, a moderate stage of cirrhosis and 8.6% Child-Pugh C, were considered severe cases. PELD and MELD scores were only above the cutoff point in 5 cases. IL-6 values were increased in patients at nutritional risk (34.9%) compared with those who were well-nourished [7.12 (0.58-34.23) pg/mL vs 1.63 (0.53-3.43) pg/mL; P = 0.02], correlating inversely with triceps skinfold-for-age z-score (rs = -0.61; P < 0.001). IL-6 levels were associated with liver disease severity assessed by Child-Pugh score (P = 0.001). This association remained significant after adjusting for nutritional status in a linear regression model. CONCLUSION: High IL-6 levels were found in children with chronic liver disease at nutritional risk. Inflammatory activity may be related to nutritional status deterioration in these patients.
publishDate 2015
dc.date.issued.fl_str_mv 2015
dc.date.accessioned.fl_str_mv 2016-01-20T02:39:33Z
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dc.relation.ispartof.pt_BR.fl_str_mv World journal of gastroenterology. Beijing. Vol. 21, no. 29 (Aug. 7, 2015), p. 8927-8934
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