Body composition in patients with classical homocystinuria: body mass relates to homocysteine and choline metabolism

Detalhes bibliográficos
Autor(a) principal: Poloni, Soraia
Data de Publicação: 2014
Outros Autores: 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
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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spelling 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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