Evolução do estado nutricional de pacientes com Distrofia Muscular de Duchenne
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Tipo de documento: | Trabalho de conclusão de curso |
Idioma: | por |
Título da fonte: | Repositório Institucional da UFRN |
Texto Completo: | https://repositorio.ufrn.br/handle/123456789/40026 |
Resumo: | Introduction Duchenne Muscular Dystrophy is a hereditary recessive disease linked to the X chromosome, in the dystrophin gene, which is an essential protein for muscle contraction, and when deficient or absent leads to exhaustive cycles of degeneration and regeneration of muscle fiber, causing the replacement of muscle fibers by connective and adipose tissue. Objective To analyze the evolution of the nutritional status of patients with Duchenne Muscular Dystrophy. Methodology The study is observational of the prospective type. For analysis, the parameters of the Corrected Arm Muscle Area, Tricipital Cutaneous Fold, and Body Mass Index, assessed in the first and second evaluation with the nutritionist. Results During the 11.1 (4.4) month period, the 26 children and adolescents (ages 9.3 - 18.4 years) evaluated presented p = 0.553 with a variation of +0.67 (5.09) cm² for the corrected Arm Muscle Area; p <0.001 with +5.10 (5.35) mm for Tricipital Cutaneous Fold; and p = 0.007 with +2.17 (2.88) kg/m² for the Body Mass Index. Significance level was considered p <0.05. Conclusion From the results, it was possible to observe a positive variation of the Body Mass Index presented by the individuals with Duchenne Muscular Dystrophy, and could be caused by the increase of the body fat in detriment of the muscular mass, based on the information of the Tricipital Cutaneous Fold and Area Muscle of the corrected arm, respectively. |
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Cunha, ThaisVale, SanchaGrilo, EvellynLeal, LeilaneVale, Sancha2018-06-26T14:42:39Z2021-09-29T11:40:49Z2018-062014088874CUNHA, Thais Alves. Evolução do estado nutricional de pacientes com a Distrofia Muscular de Duchenne. Trabalho de Conclusão de Curso (Graduação em Nutrição) - Curso de Nutrição, Departamento de Nutrição, Universidade Federal do Rio Grande do Norte, Natal, 2018.https://repositorio.ufrn.br/handle/123456789/40026Introduction Duchenne Muscular Dystrophy is a hereditary recessive disease linked to the X chromosome, in the dystrophin gene, which is an essential protein for muscle contraction, and when deficient or absent leads to exhaustive cycles of degeneration and regeneration of muscle fiber, causing the replacement of muscle fibers by connective and adipose tissue. Objective To analyze the evolution of the nutritional status of patients with Duchenne Muscular Dystrophy. Methodology The study is observational of the prospective type. For analysis, the parameters of the Corrected Arm Muscle Area, Tricipital Cutaneous Fold, and Body Mass Index, assessed in the first and second evaluation with the nutritionist. Results During the 11.1 (4.4) month period, the 26 children and adolescents (ages 9.3 - 18.4 years) evaluated presented p = 0.553 with a variation of +0.67 (5.09) cm² for the corrected Arm Muscle Area; p <0.001 with +5.10 (5.35) mm for Tricipital Cutaneous Fold; and p = 0.007 with +2.17 (2.88) kg/m² for the Body Mass Index. Significance level was considered p <0.05. Conclusion From the results, it was possible to observe a positive variation of the Body Mass Index presented by the individuals with Duchenne Muscular Dystrophy, and could be caused by the increase of the body fat in detriment of the muscular mass, based on the information of the Tricipital Cutaneous Fold and Area Muscle of the corrected arm, respectively.Introdução A Distrofia Muscular de Duchenne é uma doença hereditária recessiva ligada ao cromossomo X, no gene da distrofina, que é uma proteína essencial para a contração muscular, e quando está deficiente ou ausente leva a exaustivos ciclos de degeneração e regeneração da fibra muscular, provocando a substituição de fibras musculares por tecido conectivo e adiposo. Objetivo Analisar a evolução do estado nutricional de pacientes com a Distrofia Muscular de Duchenne. Metodologia O estudo é observacional do tipo prospectivo. Para análise foram utilizados os parâmetros da Área Muscular do Braço corrigida, Dobra Cutânea Tricipital, e o Índice de Massa Corporal, aferidos na primeira e segunda avaliação com o nutricionista. Resultados Durante o período de 11,1 (4,4) meses, as 26 crianças e adolescentes (idade entre 9,3 – 18,4 anos) avaliados apresentaram p= 0,553 com variação de +0,67 (5,09) cm² para a Área Muscular do Braço corrigida; p<0,001 com +5,10 (5,35) mm para a Dobra Cutânea Tricipital; e p=0,007 com +2,17 (2,88) kg/m² para o Índice de Massa Corporal. Foi considerado nível de significância p < 0,05. Conclusão A partir dos resultados, foi possível observar uma variação positiva do Índice de Massa Corporal apresentada pelos indíviduos com a Distrofia Muscular de Duchenne, podendo ser ocasionada pelo aumento da gordura corporal em detrimento da massa muscular, com base nas informações da Dobra Cutânea Tricipital e Área Muscular do Braço corrigida, respectivamente.2021-07-21O trabalho é em formato de artigo científico, e a revista exige exclusividade.Universidade Federal do Rio Grande do NorteUFRNBrasilNutriçãoDistrofia Muscular de DuchenneComposição corporalAntropometriaCNPQ::CIENCIAS DA SAUDEEvolução do estado nutricional de pacientes com Distrofia Muscular de DuchenneEvolution of nutritional status of patients with Duchenne Muscular Dystrophyinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/bachelorThesisinfo:eu-repo/semantics/embargoedAccessporreponame:Repositório Institucional da UFRNinstname:Universidade Federal do Rio Grande do Norte (UFRN)instacron:UFRNCC-LICENSElicense_urlapplication/octet-stream49https://repositorio.ufrn.br/bitstream/123456789/40026/1/license_url4afdbb8c545fd630ea7db775da747b2fMD51license_textapplication/octet-stream0https://repositorio.ufrn.br/bitstream/123456789/40026/2/license_textd41d8cd98f00b204e9800998ecf8427eMD52license_rdfapplication/octet-stream0https://repositorio.ufrn.br/bitstream/123456789/40026/3/license_rdfd41d8cd98f00b204e9800998ecf8427eMD53ORIGINALEvoluçãoestadonutricional_2018_Trabalho de Conclusão de CursoTexto Completoapplication/octet-stream77659https://repositorio.ufrn.br/bitstream/123456789/40026/4/Evolu%c3%a7%c3%a3oestadonutricional_2018_Trabalho%20de%20Conclus%c3%a3o%20de%20Cursoe893699570fd9fc242e91541cac932f0MD54LICENSElicense.txttext/plain756https://repositorio.ufrn.br/bitstream/123456789/40026/5/license.txta80a9cda2756d355b388cc443c3d8a43MD55123456789/400262024-03-19 01:06:07.403oai:https://repositorio.ufrn.br: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ório de PublicaçõesPUBhttp://repositorio.ufrn.br/oai/opendoar:2024-03-19T04:06:07Repositório Institucional da UFRN - Universidade Federal do Rio Grande do Norte (UFRN)false |
dc.title.pr_BR.fl_str_mv |
Evolução do estado nutricional de pacientes com Distrofia Muscular de Duchenne |
dc.title.alternative.pr_BR.fl_str_mv |
Evolution of nutritional status of patients with Duchenne Muscular Dystrophy |
title |
Evolução do estado nutricional de pacientes com Distrofia Muscular de Duchenne |
spellingShingle |
Evolução do estado nutricional de pacientes com Distrofia Muscular de Duchenne Cunha, Thais Distrofia Muscular de Duchenne Composição corporal Antropometria CNPQ::CIENCIAS DA SAUDE |
title_short |
Evolução do estado nutricional de pacientes com Distrofia Muscular de Duchenne |
title_full |
Evolução do estado nutricional de pacientes com Distrofia Muscular de Duchenne |
title_fullStr |
Evolução do estado nutricional de pacientes com Distrofia Muscular de Duchenne |
title_full_unstemmed |
Evolução do estado nutricional de pacientes com Distrofia Muscular de Duchenne |
title_sort |
Evolução do estado nutricional de pacientes com Distrofia Muscular de Duchenne |
author |
Cunha, Thais |
author_facet |
Cunha, Thais |
author_role |
author |
dc.contributor.referees1.none.fl_str_mv |
Vale, Sancha |
dc.contributor.referees2.none.fl_str_mv |
Grilo, Evellyn |
dc.contributor.referees3.none.fl_str_mv |
Leal, Leilane |
dc.contributor.author.fl_str_mv |
Cunha, Thais |
dc.contributor.advisor1.fl_str_mv |
Vale, Sancha |
contributor_str_mv |
Vale, Sancha |
dc.subject.pr_BR.fl_str_mv |
Distrofia Muscular de Duchenne Composição corporal Antropometria |
topic |
Distrofia Muscular de Duchenne Composição corporal Antropometria CNPQ::CIENCIAS DA SAUDE |
dc.subject.cnpq.fl_str_mv |
CNPQ::CIENCIAS DA SAUDE |
description |
Introduction Duchenne Muscular Dystrophy is a hereditary recessive disease linked to the X chromosome, in the dystrophin gene, which is an essential protein for muscle contraction, and when deficient or absent leads to exhaustive cycles of degeneration and regeneration of muscle fiber, causing the replacement of muscle fibers by connective and adipose tissue. Objective To analyze the evolution of the nutritional status of patients with Duchenne Muscular Dystrophy. Methodology The study is observational of the prospective type. For analysis, the parameters of the Corrected Arm Muscle Area, Tricipital Cutaneous Fold, and Body Mass Index, assessed in the first and second evaluation with the nutritionist. Results During the 11.1 (4.4) month period, the 26 children and adolescents (ages 9.3 - 18.4 years) evaluated presented p = 0.553 with a variation of +0.67 (5.09) cm² for the corrected Arm Muscle Area; p <0.001 with +5.10 (5.35) mm for Tricipital Cutaneous Fold; and p = 0.007 with +2.17 (2.88) kg/m² for the Body Mass Index. Significance level was considered p <0.05. Conclusion From the results, it was possible to observe a positive variation of the Body Mass Index presented by the individuals with Duchenne Muscular Dystrophy, and could be caused by the increase of the body fat in detriment of the muscular mass, based on the information of the Tricipital Cutaneous Fold and Area Muscle of the corrected arm, respectively. |
publishDate |
2018 |
dc.date.accessioned.fl_str_mv |
2018-06-26T14:42:39Z 2021-09-29T11:40:49Z |
dc.date.issued.fl_str_mv |
2018-06 |
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info:eu-repo/semantics/publishedVersion |
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publishedVersion |
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2014088874 |
dc.identifier.citation.fl_str_mv |
CUNHA, Thais Alves. Evolução do estado nutricional de pacientes com a Distrofia Muscular de Duchenne. Trabalho de Conclusão de Curso (Graduação em Nutrição) - Curso de Nutrição, Departamento de Nutrição, Universidade Federal do Rio Grande do Norte, Natal, 2018. |
dc.identifier.uri.fl_str_mv |
https://repositorio.ufrn.br/handle/123456789/40026 |
identifier_str_mv |
2014088874 CUNHA, Thais Alves. Evolução do estado nutricional de pacientes com a Distrofia Muscular de Duchenne. Trabalho de Conclusão de Curso (Graduação em Nutrição) - Curso de Nutrição, Departamento de Nutrição, Universidade Federal do Rio Grande do Norte, Natal, 2018. |
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Universidade Federal do Rio Grande do Norte |
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Brasil |
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Nutrição |
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Universidade Federal do Rio Grande do Norte |
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