Evolução do estado nutricional de pacientes com Distrofia Muscular de Duchenne

Detalhes bibliográficos
Autor(a) principal: Cunha, Thais
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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spelling 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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dc.identifier.pr_BR.fl_str_mv 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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dc.publisher.department.fl_str_mv Nutrição
publisher.none.fl_str_mv Universidade Federal do Rio Grande do Norte
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