Body composition in patients with classical homocystinuria: body mass relates to homocysteine and choline metabolism
Autor(a) principal: | |
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Data de Publicação: | 2014 |
Outros Autores: | , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.1016/j.gene.2014.05.015 http://repositorio.unifesp.br/handle/11600/38085 |
Resumo: | Introduction: Classical homocystinuria is a rare genetic disease caused by cystathionine beta-synthase deficiency, resulting in homocysteine accumulation. Growing evidence suggests that reduced fat mass in patients with classical homocystinuria may be associated with alterations in choline and homocysteine pathways. This study aimed to evaluate the body composition of patients with classical homocystinuria, identifying changes in body fat percentage and correlating findings with biochemical markers of homocysteine and choline pathways, lipoprotein levels and bone mineral density (BMD) T-scores.Methods: Nine patients with classical homocystinuria were included in the study. Levels of homocysteine, methionine, cysteine, choline, betaine, dimethylglycine and ethanolamine were determined. Body composition was assessed by bioelectrical impedance analysis (BIA) in patients and in 18 controls. Data on the last BMD measurement and lipoprotein profile were obtained from medical records.Results: of 9 patients, 4 (44%) had a low body fat percentage, but no statistically significant differences were found between patients and controls. Homocysteine and methionine levels were negatively correlated with body mass index (BMI), while cysteine showed a positive correlation with BMI (p < 0.05). There was a trend between total choline levels and body fat percentage (r = 0.439, p = 0.07). HDL cholesterol correlated with choline and ethanolamine levels (r = 0.757, p = 0.049; r = 0.847, p = 0.016, respectively), and total cholesterol also correlated with choline levels (r = 0.775, p = 0.041). There was no association between BMD T-scores and body composition.Conclusions: These results suggest that reduced fat mass is common in patients with classical homocystinuria, and that alterations in homocysteine and choline pathways affect body mass and lipid metabolism. (C) 2014 Elsevier B.V. All rights reserved. |
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Body composition in patients with classical homocystinuria: body mass relates to homocysteine and choline metabolismClassical homocystinuriaBody compositionHomocysteineCholineIntroduction: Classical homocystinuria is a rare genetic disease caused by cystathionine beta-synthase deficiency, resulting in homocysteine accumulation. Growing evidence suggests that reduced fat mass in patients with classical homocystinuria may be associated with alterations in choline and homocysteine pathways. This study aimed to evaluate the body composition of patients with classical homocystinuria, identifying changes in body fat percentage and correlating findings with biochemical markers of homocysteine and choline pathways, lipoprotein levels and bone mineral density (BMD) T-scores.Methods: Nine patients with classical homocystinuria were included in the study. Levels of homocysteine, methionine, cysteine, choline, betaine, dimethylglycine and ethanolamine were determined. Body composition was assessed by bioelectrical impedance analysis (BIA) in patients and in 18 controls. Data on the last BMD measurement and lipoprotein profile were obtained from medical records.Results: of 9 patients, 4 (44%) had a low body fat percentage, but no statistically significant differences were found between patients and controls. Homocysteine and methionine levels were negatively correlated with body mass index (BMI), while cysteine showed a positive correlation with BMI (p < 0.05). There was a trend between total choline levels and body fat percentage (r = 0.439, p = 0.07). HDL cholesterol correlated with choline and ethanolamine levels (r = 0.757, p = 0.049; r = 0.847, p = 0.016, respectively), and total cholesterol also correlated with choline levels (r = 0.775, p = 0.041). There was no association between BMD T-scores and body composition.Conclusions: These results suggest that reduced fat mass is common in patients with classical homocystinuria, and that alterations in homocysteine and choline pathways affect body mass and lipid metabolism. (C) 2014 Elsevier B.V. All rights reserved.Univ Fed Rio Grande do Sul, Postgrad Program Genet & Mol Biol, Porto Alegre, RS, BrazilHosp Clin Porto Alegre, BRAIN Lab Basic Res & Adv Invest Neurosci, BR-90035003 Porto Alegre, RS, BrazilHosp Clin Porto Alegre, Med Genet Serv, BR-90035003 Porto Alegre, RS, BrazilUniversidade Federal de São Paulo, Reference Ctr Inborn Errors Metab, São Paulo, BrazilUniv Fed Rio Grande do Sul, Dept Physiol, Hosp Clin Porto Alegre, Gynecol Endocrinol Unit,Div Endocrinol, Porto Alegre, RS, BrazilUniv Fed Rio Grande do Sul, Food & Nutr Res Ctr, Hosp Clin Porto Alegre, Porto Alegre, RS, BrazilRobert Debre Hosp, AP HP, Biochem Hormonol Lab, Paris, FranceUniv Med Ctr Freiburg, Dept Gen Pediat, Lab Clin Biochem & Metab, Freiburg, GermanyUniversidade Federal de São Paulo, Reference Ctr Inborn Errors Metab, São Paulo, BrazilWeb of ScienceResearch Incentive Fund (Fundo de Incentivo a Pesquisa, FIPE) of HCPAPRONEM/FAPERGSConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Research Incentive Fund (Fundo de Incentivo a Pesquisa, FIPE) of HCPA: 11-0386PRONEM/FAPERGS: 11/2043-0CNPq: 308816/2013-7CNPq: 301742/2010-3CAPES: 12785-11Elsevier B.V.Univ Fed Rio Grande do SulHosp Clin Porto AlegreUniversidade Federal de São Paulo (UNIFESP)Robert Debre HospUniv Med Ctr FreiburgPoloni, SoraiaLeistner-Segal, SandraBandeira, Isabel CristinaD'Almeida, Vânia [UNIFESP]Souza, Carolina Fischinger Moura deSpritzer, Poli MaraCastro, KamilaTonon, TássiaNalin, TatieleImbard, ApollineBlom, Henk J.Schwartz, Ida Vanessa Doederlein2016-01-24T14:37:43Z2016-01-24T14:37:43Z2014-08-10info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion443-447application/pdfhttp://dx.doi.org/10.1016/j.gene.2014.05.015Gene. Amsterdam: Elsevier B.V., v. 546, n. 2, p. 443-447, 2014.10.1016/j.gene.2014.05.015WOS000339150800044.pdf0378-1119http://repositorio.unifesp.br/handle/11600/38085WOS:000339150800044engGeneinfo:eu-repo/semantics/openAccesshttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policyreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-01T03:37:12Zoai:repositorio.unifesp.br/:11600/38085Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-01T03:37:12Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Body composition in patients with classical homocystinuria: body mass relates to homocysteine and choline metabolism |
title |
Body composition in patients with classical homocystinuria: body mass relates to homocysteine and choline metabolism |
spellingShingle |
Body composition in patients with classical homocystinuria: body mass relates to homocysteine and choline metabolism Poloni, Soraia Classical homocystinuria Body composition Homocysteine Choline |
title_short |
Body composition in patients with classical homocystinuria: body mass relates to homocysteine and choline metabolism |
title_full |
Body composition in patients with classical homocystinuria: body mass relates to homocysteine and choline metabolism |
title_fullStr |
Body composition in patients with classical homocystinuria: body mass relates to homocysteine and choline metabolism |
title_full_unstemmed |
Body composition in patients with classical homocystinuria: body mass relates to homocysteine and choline metabolism |
title_sort |
Body composition in patients with classical homocystinuria: body mass relates to homocysteine and choline metabolism |
author |
Poloni, Soraia |
author_facet |
Poloni, Soraia Leistner-Segal, Sandra Bandeira, Isabel Cristina D'Almeida, Vânia [UNIFESP] Souza, Carolina Fischinger Moura de Spritzer, Poli Mara Castro, Kamila Tonon, Tássia Nalin, Tatiele Imbard, Apolline Blom, Henk J. Schwartz, Ida Vanessa Doederlein |
author_role |
author |
author2 |
Leistner-Segal, Sandra Bandeira, Isabel Cristina D'Almeida, Vânia [UNIFESP] Souza, Carolina Fischinger Moura de Spritzer, Poli Mara Castro, Kamila Tonon, Tássia Nalin, Tatiele Imbard, Apolline Blom, Henk J. Schwartz, Ida Vanessa Doederlein |
author2_role |
author author author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Univ Fed Rio Grande do Sul Hosp Clin Porto Alegre Universidade Federal de São Paulo (UNIFESP) Robert Debre Hosp Univ Med Ctr Freiburg |
dc.contributor.author.fl_str_mv |
Poloni, Soraia Leistner-Segal, Sandra Bandeira, Isabel Cristina D'Almeida, Vânia [UNIFESP] Souza, Carolina Fischinger Moura de Spritzer, Poli Mara Castro, Kamila Tonon, Tássia Nalin, Tatiele Imbard, Apolline Blom, Henk J. Schwartz, Ida Vanessa Doederlein |
dc.subject.por.fl_str_mv |
Classical homocystinuria Body composition Homocysteine Choline |
topic |
Classical homocystinuria Body composition Homocysteine Choline |
description |
Introduction: Classical homocystinuria is a rare genetic disease caused by cystathionine beta-synthase deficiency, resulting in homocysteine accumulation. Growing evidence suggests that reduced fat mass in patients with classical homocystinuria may be associated with alterations in choline and homocysteine pathways. This study aimed to evaluate the body composition of patients with classical homocystinuria, identifying changes in body fat percentage and correlating findings with biochemical markers of homocysteine and choline pathways, lipoprotein levels and bone mineral density (BMD) T-scores.Methods: Nine patients with classical homocystinuria were included in the study. Levels of homocysteine, methionine, cysteine, choline, betaine, dimethylglycine and ethanolamine were determined. Body composition was assessed by bioelectrical impedance analysis (BIA) in patients and in 18 controls. Data on the last BMD measurement and lipoprotein profile were obtained from medical records.Results: of 9 patients, 4 (44%) had a low body fat percentage, but no statistically significant differences were found between patients and controls. Homocysteine and methionine levels were negatively correlated with body mass index (BMI), while cysteine showed a positive correlation with BMI (p < 0.05). There was a trend between total choline levels and body fat percentage (r = 0.439, p = 0.07). HDL cholesterol correlated with choline and ethanolamine levels (r = 0.757, p = 0.049; r = 0.847, p = 0.016, respectively), and total cholesterol also correlated with choline levels (r = 0.775, p = 0.041). There was no association between BMD T-scores and body composition.Conclusions: These results suggest that reduced fat mass is common in patients with classical homocystinuria, and that alterations in homocysteine and choline pathways affect body mass and lipid metabolism. (C) 2014 Elsevier B.V. All rights reserved. |
publishDate |
2014 |
dc.date.none.fl_str_mv |
2014-08-10 2016-01-24T14:37:43Z 2016-01-24T14:37:43Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1016/j.gene.2014.05.015 Gene. Amsterdam: Elsevier B.V., v. 546, n. 2, p. 443-447, 2014. 10.1016/j.gene.2014.05.015 WOS000339150800044.pdf 0378-1119 http://repositorio.unifesp.br/handle/11600/38085 WOS:000339150800044 |
url |
http://dx.doi.org/10.1016/j.gene.2014.05.015 http://repositorio.unifesp.br/handle/11600/38085 |
identifier_str_mv |
Gene. Amsterdam: Elsevier B.V., v. 546, n. 2, p. 443-447, 2014. 10.1016/j.gene.2014.05.015 WOS000339150800044.pdf 0378-1119 WOS:000339150800044 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Gene |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy |
dc.format.none.fl_str_mv |
443-447 application/pdf |
dc.publisher.none.fl_str_mv |
Elsevier B.V. |
publisher.none.fl_str_mv |
Elsevier B.V. |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
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1814268348516532224 |