Leptina sérica, calprotectina fecal e composição corporal em pacientes com doença de Crohn.
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Tipo de documento: | Dissertação |
Idioma: | por |
Título da fonte: | Repositório Institucional da UFMG |
Texto Completo: | http://hdl.handle.net/1843/49475 |
Resumo: | Inflammatory bowel diseases (IBDs), such as Crohn's disease (CD) and ulcerative colitis (UC), are serious diseases of the digestive tract. The diagnosis and follow-up of IBDs remains a major challenge in clinical practice. The aim of this study was to investigate the serum levels of the adipokine leptin and fecal calprotectin in patients with Crohn's disease (CD). Serum leptin and fecal calprotectin values, considered the “gold standard”, were analyzed to identify a correlation between these proteins and disease activity (inflammation). For comparison purposes, a control group containing participants (n = 8) without Crohn's disease was also evaluated following the same criteria for collecting and evaluating the samples. Fifteen patients with Crohn's disease were selected. Serum levels of leptin and calprotectin were not influenced by the gender factor in patients, nor were they influenced by controls. Leptin was not able to differentiate the disease activity (8.1 (1.30 - 13.40) ng/mL – active disease ng/mL; 8 (3.125 - 15.35) ng/mL – active disease; p = 0.614), unlike calprotectin, which was higher in patients with active disease, 514 (224 - 1231) mcg/g (remission 145.50 (59.50 - 387.50) mcg/g), p = 0.039. Leptin was positively influenced by anthropometric values (body fat and waist circumference). This work showed that leptin has low specificity and selectivity for differentiating forms of Crohn's disease. Regarding the stage of the disease, only calprotectin proved to be efficient in differentiating active disease from disease in remission. |
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Leptina sérica, calprotectina fecal e composição corporal em pacientes com doença de Crohn.Serum leptin, fecal calprotectin and body composition in patients with Crohn's disease.Doença de crohnBiomarcadoresLeptinaCalprotectinaDiagnósticoDoenças inflamatórias intestinaisInflamaçãoInflammatory bowel diseases (IBDs), such as Crohn's disease (CD) and ulcerative colitis (UC), are serious diseases of the digestive tract. The diagnosis and follow-up of IBDs remains a major challenge in clinical practice. The aim of this study was to investigate the serum levels of the adipokine leptin and fecal calprotectin in patients with Crohn's disease (CD). Serum leptin and fecal calprotectin values, considered the “gold standard”, were analyzed to identify a correlation between these proteins and disease activity (inflammation). For comparison purposes, a control group containing participants (n = 8) without Crohn's disease was also evaluated following the same criteria for collecting and evaluating the samples. Fifteen patients with Crohn's disease were selected. Serum levels of leptin and calprotectin were not influenced by the gender factor in patients, nor were they influenced by controls. Leptin was not able to differentiate the disease activity (8.1 (1.30 - 13.40) ng/mL – active disease ng/mL; 8 (3.125 - 15.35) ng/mL – active disease; p = 0.614), unlike calprotectin, which was higher in patients with active disease, 514 (224 - 1231) mcg/g (remission 145.50 (59.50 - 387.50) mcg/g), p = 0.039. Leptin was positively influenced by anthropometric values (body fat and waist circumference). This work showed that leptin has low specificity and selectivity for differentiating forms of Crohn's disease. Regarding the stage of the disease, only calprotectin proved to be efficient in differentiating active disease from disease in remission.As doenças inflamatórias intestinais (DIIs), como a doença de Crohn (DC) e a colite ulcerativa (CU), são doenças graves do trato digestivo. O diagnóstico e acompanhamento das DIIs permanece sendo um grande desafio na prática clínica. O objetivo deste estudo foi investigar os níveis séricos da adipocina leptina e calprotectina fecal nos pacientes portadores da doença de crohn (DC). Os valores de leptina sérica e calprotectina fecal, considerado o “padrão-ouro”, foram analisados para identificar uma correlação entre essas proteínas com a atividade da doença (inflamação). Para título de comparação, um grupo controle contendo participantes (n = 8) sem a doença de Crohn, também foi avaliado seguindo os mesmos critérios de coleta e avaliação das amostras. Foram selecionados 15 pacientes com a doença de Crohn. Os níveis séricos de leptina e calprotectina não se mostraram influenciáveis pelo fator gênero em pacientes tão pouco para controles. A leptina não foi capaz de diferenciar a atividade da doença (8,1 (1,30 - 13,40) ng/mL – doença ativa ng/mL; 8 (3,125 - 15,35) ng/mL– doença ativa; p = 0,614), ao contrário da calprotectina que se mostrou mais alta nos pacientes com a doença ativa, 514 (224 - 1231) mcg/g (remissão 145,50 (59,50 - 387,50) mcg/g), p = 0,039. A leptina se mostrou positivamente influenciada pelos valores antropométricos (gordura corporal e circunferência abdominal). Este trabalho mostrou que a leptina tem baixa especificidade e seletividade para diferenciar as formas da doença de Crohn. Com relação ao estágio da doença, apenas a calprotectina mostrou ser eficiente na diferenciação de doença ativa de doença em remissão.CAPES - Coordenação de Aperfeiçoamento de Pessoal de Nível SuperiorUniversidade Federal de Minas GeraisBrasilFARMACIA - FACULDADE DE FARMACIAPrograma de Pós-Graduação em Ciências FarmacêuticasUFMGSimone Odília Antunes Fernandeshttp://lattes.cnpq.br/3333466607118191Valbert Nascimento CardosoValbert Nascimento CardosoLuiz Gonzaga Vaz CoelhoFrancisco Guilherme Cancela e PennaLarissa Gabriela Ferreira de Carvalho2023-02-02T17:09:20Z2023-02-02T17:09:20Z2022-09-28info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisapplication/pdfhttp://hdl.handle.net/1843/494750000-0002-9134-9536porinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFMGinstname:Universidade Federal de Minas Gerais (UFMG)instacron:UFMG2023-02-02T17:09:21Zoai:repositorio.ufmg.br:1843/49475Repositório InstitucionalPUBhttps://repositorio.ufmg.br/oairepositorio@ufmg.bropendoar:2023-02-02T17:09:21Repositório Institucional da UFMG - Universidade Federal de Minas Gerais (UFMG)false |
dc.title.none.fl_str_mv |
Leptina sérica, calprotectina fecal e composição corporal em pacientes com doença de Crohn. Serum leptin, fecal calprotectin and body composition in patients with Crohn's disease. |
title |
Leptina sérica, calprotectina fecal e composição corporal em pacientes com doença de Crohn. |
spellingShingle |
Leptina sérica, calprotectina fecal e composição corporal em pacientes com doença de Crohn. Larissa Gabriela Ferreira de Carvalho Doença de crohn Biomarcadores Leptina Calprotectina Diagnóstico Doenças inflamatórias intestinais Inflamação |
title_short |
Leptina sérica, calprotectina fecal e composição corporal em pacientes com doença de Crohn. |
title_full |
Leptina sérica, calprotectina fecal e composição corporal em pacientes com doença de Crohn. |
title_fullStr |
Leptina sérica, calprotectina fecal e composição corporal em pacientes com doença de Crohn. |
title_full_unstemmed |
Leptina sérica, calprotectina fecal e composição corporal em pacientes com doença de Crohn. |
title_sort |
Leptina sérica, calprotectina fecal e composição corporal em pacientes com doença de Crohn. |
author |
Larissa Gabriela Ferreira de Carvalho |
author_facet |
Larissa Gabriela Ferreira de Carvalho |
author_role |
author |
dc.contributor.none.fl_str_mv |
Simone Odília Antunes Fernandes http://lattes.cnpq.br/3333466607118191 Valbert Nascimento Cardoso Valbert Nascimento Cardoso Luiz Gonzaga Vaz Coelho Francisco Guilherme Cancela e Penna |
dc.contributor.author.fl_str_mv |
Larissa Gabriela Ferreira de Carvalho |
dc.subject.por.fl_str_mv |
Doença de crohn Biomarcadores Leptina Calprotectina Diagnóstico Doenças inflamatórias intestinais Inflamação |
topic |
Doença de crohn Biomarcadores Leptina Calprotectina Diagnóstico Doenças inflamatórias intestinais Inflamação |
description |
Inflammatory bowel diseases (IBDs), such as Crohn's disease (CD) and ulcerative colitis (UC), are serious diseases of the digestive tract. The diagnosis and follow-up of IBDs remains a major challenge in clinical practice. The aim of this study was to investigate the serum levels of the adipokine leptin and fecal calprotectin in patients with Crohn's disease (CD). Serum leptin and fecal calprotectin values, considered the “gold standard”, were analyzed to identify a correlation between these proteins and disease activity (inflammation). For comparison purposes, a control group containing participants (n = 8) without Crohn's disease was also evaluated following the same criteria for collecting and evaluating the samples. Fifteen patients with Crohn's disease were selected. Serum levels of leptin and calprotectin were not influenced by the gender factor in patients, nor were they influenced by controls. Leptin was not able to differentiate the disease activity (8.1 (1.30 - 13.40) ng/mL – active disease ng/mL; 8 (3.125 - 15.35) ng/mL – active disease; p = 0.614), unlike calprotectin, which was higher in patients with active disease, 514 (224 - 1231) mcg/g (remission 145.50 (59.50 - 387.50) mcg/g), p = 0.039. Leptin was positively influenced by anthropometric values (body fat and waist circumference). This work showed that leptin has low specificity and selectivity for differentiating forms of Crohn's disease. Regarding the stage of the disease, only calprotectin proved to be efficient in differentiating active disease from disease in remission. |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022-09-28 2023-02-02T17:09:20Z 2023-02-02T17:09:20Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/masterThesis |
format |
masterThesis |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/1843/49475 0000-0002-9134-9536 |
url |
http://hdl.handle.net/1843/49475 |
identifier_str_mv |
0000-0002-9134-9536 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Universidade Federal de Minas Gerais Brasil FARMACIA - FACULDADE DE FARMACIA Programa de Pós-Graduação em Ciências Farmacêuticas UFMG |
publisher.none.fl_str_mv |
Universidade Federal de Minas Gerais Brasil FARMACIA - FACULDADE DE FARMACIA Programa de Pós-Graduação em Ciências Farmacêuticas UFMG |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UFMG instname:Universidade Federal de Minas Gerais (UFMG) instacron:UFMG |
instname_str |
Universidade Federal de Minas Gerais (UFMG) |
instacron_str |
UFMG |
institution |
UFMG |
reponame_str |
Repositório Institucional da UFMG |
collection |
Repositório Institucional da UFMG |
repository.name.fl_str_mv |
Repositório Institucional da UFMG - Universidade Federal de Minas Gerais (UFMG) |
repository.mail.fl_str_mv |
repositorio@ufmg.br |
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1823248319705513984 |