APOE and LDLR Gene Polymorphisms and Dyslipidemia Tracking. Rio de Janeiro Study
Autor(a) principal: | |
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Data de Publicação: | 2015 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Arquivos Brasileiros de Cardiologia (Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0066-782X2015000600006 |
Resumo: | Background:Studies show an association between changes in apolipoprotein E (ApoE) and LDLR receptor with the occurrence of dyslipidemia.Objectives:To investigate the association between polymorphisms of the APOE (ε2, ε3, ε4) and LDLR (A370T) genes with the persistence of abnormal serum lipid levels in young individuals followed up for 17 years in the Rio de Janeiro Study.Methods:The study included 56 individuals (35 males) who underwent three assessments at different ages: A1 (mean age 13.30 ± 1.53 years), A2 (22.09 ± 1.91 years) and A3 (31.23 ± 1.99 years). Clinical evaluation with measurement of blood pressure (BP) and body mass index (BMI) was conducted at all three assessments. Measurement of waist circumference (WC) and serum lipids, and analysis of genetic polymorphisms by PCR-RFLP were performed at A2 and A3. Based on dyslipidemia tracking, three groups were established: 0 (no abnormal lipid value at A2 and A3), 1 (up to one abnormal lipid value at A2 or A3) and 2 (one or more abnormal lipid values at A2 and A3).Results:Compared with groups 0 and 1, group 2 presented higher mean values of BP, BMI, WC, LDL-c and TG (p < 0.01) and lower mean values of HDL-c (p = 0.001). Across the assessments, all individuals with APOE genotypes ε2/ε4 and ε4/ε4 maintained at least one abnormal lipid variable, whereas those with genotype ε2/ε3 did not show abnormal values (χ2 = 16.848, p = 0.032). For the LDLR genotypes, there was no significant difference among the groups.Conclusions:APOE gene polymorphisms were associated with dyslipidemia in young individuals followed up longitudinally from childhood. |
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Arquivos Brasileiros de Cardiologia (Online) |
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APOE and LDLR Gene Polymorphisms and Dyslipidemia Tracking. Rio de Janeiro StudyPolymorphism, GeneticDyslipidemiasYoung AdultEpidemiologyApolipoproteins EBackground:Studies show an association between changes in apolipoprotein E (ApoE) and LDLR receptor with the occurrence of dyslipidemia.Objectives:To investigate the association between polymorphisms of the APOE (ε2, ε3, ε4) and LDLR (A370T) genes with the persistence of abnormal serum lipid levels in young individuals followed up for 17 years in the Rio de Janeiro Study.Methods:The study included 56 individuals (35 males) who underwent three assessments at different ages: A1 (mean age 13.30 ± 1.53 years), A2 (22.09 ± 1.91 years) and A3 (31.23 ± 1.99 years). Clinical evaluation with measurement of blood pressure (BP) and body mass index (BMI) was conducted at all three assessments. Measurement of waist circumference (WC) and serum lipids, and analysis of genetic polymorphisms by PCR-RFLP were performed at A2 and A3. Based on dyslipidemia tracking, three groups were established: 0 (no abnormal lipid value at A2 and A3), 1 (up to one abnormal lipid value at A2 or A3) and 2 (one or more abnormal lipid values at A2 and A3).Results:Compared with groups 0 and 1, group 2 presented higher mean values of BP, BMI, WC, LDL-c and TG (p < 0.01) and lower mean values of HDL-c (p = 0.001). Across the assessments, all individuals with APOE genotypes ε2/ε4 and ε4/ε4 maintained at least one abnormal lipid variable, whereas those with genotype ε2/ε3 did not show abnormal values (χ2 = 16.848, p = 0.032). For the LDLR genotypes, there was no significant difference among the groups.Conclusions:APOE gene polymorphisms were associated with dyslipidemia in young individuals followed up longitudinally from childhood.Sociedade Brasileira de Cardiologia - SBC2015-06-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0066-782X2015000600006Arquivos Brasileiros de Cardiologia v.104 n.6 2015reponame:Arquivos Brasileiros de Cardiologia (Online)instname:Sociedade Brasileira de Cardiologia (SBC)instacron:SBC10.5935/abc.20150036info:eu-repo/semantics/openAccessFreitas,Rossana Ghessa Andrade deCampana,Erika Maria GonçalvesPozzan,RobertoBrandão,Andréa AraujoBrandão,Ayrton PiresMagalhães,Maria Eliane CamposSilva,Dayse Aparecida daeng2015-09-01T00:00:00Zoai:scielo:S0066-782X2015000600006Revistahttp://www.arquivosonline.com.br/https://old.scielo.br/oai/scielo-oai.php||arquivos@cardiol.br1678-41700066-782Xopendoar:2015-09-01T00:00Arquivos Brasileiros de Cardiologia (Online) - Sociedade Brasileira de Cardiologia (SBC)false |
dc.title.none.fl_str_mv |
APOE and LDLR Gene Polymorphisms and Dyslipidemia Tracking. Rio de Janeiro Study |
title |
APOE and LDLR Gene Polymorphisms and Dyslipidemia Tracking. Rio de Janeiro Study |
spellingShingle |
APOE and LDLR Gene Polymorphisms and Dyslipidemia Tracking. Rio de Janeiro Study Freitas,Rossana Ghessa Andrade de Polymorphism, Genetic Dyslipidemias Young Adult Epidemiology Apolipoproteins E |
title_short |
APOE and LDLR Gene Polymorphisms and Dyslipidemia Tracking. Rio de Janeiro Study |
title_full |
APOE and LDLR Gene Polymorphisms and Dyslipidemia Tracking. Rio de Janeiro Study |
title_fullStr |
APOE and LDLR Gene Polymorphisms and Dyslipidemia Tracking. Rio de Janeiro Study |
title_full_unstemmed |
APOE and LDLR Gene Polymorphisms and Dyslipidemia Tracking. Rio de Janeiro Study |
title_sort |
APOE and LDLR Gene Polymorphisms and Dyslipidemia Tracking. Rio de Janeiro Study |
author |
Freitas,Rossana Ghessa Andrade de |
author_facet |
Freitas,Rossana Ghessa Andrade de Campana,Erika Maria Gonçalves Pozzan,Roberto Brandão,Andréa Araujo Brandão,Ayrton Pires Magalhães,Maria Eliane Campos Silva,Dayse Aparecida da |
author_role |
author |
author2 |
Campana,Erika Maria Gonçalves Pozzan,Roberto Brandão,Andréa Araujo Brandão,Ayrton Pires Magalhães,Maria Eliane Campos Silva,Dayse Aparecida da |
author2_role |
author author author author author author |
dc.contributor.author.fl_str_mv |
Freitas,Rossana Ghessa Andrade de Campana,Erika Maria Gonçalves Pozzan,Roberto Brandão,Andréa Araujo Brandão,Ayrton Pires Magalhães,Maria Eliane Campos Silva,Dayse Aparecida da |
dc.subject.por.fl_str_mv |
Polymorphism, Genetic Dyslipidemias Young Adult Epidemiology Apolipoproteins E |
topic |
Polymorphism, Genetic Dyslipidemias Young Adult Epidemiology Apolipoproteins E |
description |
Background:Studies show an association between changes in apolipoprotein E (ApoE) and LDLR receptor with the occurrence of dyslipidemia.Objectives:To investigate the association between polymorphisms of the APOE (ε2, ε3, ε4) and LDLR (A370T) genes with the persistence of abnormal serum lipid levels in young individuals followed up for 17 years in the Rio de Janeiro Study.Methods:The study included 56 individuals (35 males) who underwent three assessments at different ages: A1 (mean age 13.30 ± 1.53 years), A2 (22.09 ± 1.91 years) and A3 (31.23 ± 1.99 years). Clinical evaluation with measurement of blood pressure (BP) and body mass index (BMI) was conducted at all three assessments. Measurement of waist circumference (WC) and serum lipids, and analysis of genetic polymorphisms by PCR-RFLP were performed at A2 and A3. Based on dyslipidemia tracking, three groups were established: 0 (no abnormal lipid value at A2 and A3), 1 (up to one abnormal lipid value at A2 or A3) and 2 (one or more abnormal lipid values at A2 and A3).Results:Compared with groups 0 and 1, group 2 presented higher mean values of BP, BMI, WC, LDL-c and TG (p < 0.01) and lower mean values of HDL-c (p = 0.001). Across the assessments, all individuals with APOE genotypes ε2/ε4 and ε4/ε4 maintained at least one abnormal lipid variable, whereas those with genotype ε2/ε3 did not show abnormal values (χ2 = 16.848, p = 0.032). For the LDLR genotypes, there was no significant difference among the groups.Conclusions:APOE gene polymorphisms were associated with dyslipidemia in young individuals followed up longitudinally from childhood. |
publishDate |
2015 |
dc.date.none.fl_str_mv |
2015-06-01 |
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://old.scielo.br/scielo.php?script=sci_arttext&pid=S0066-782X2015000600006 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0066-782X2015000600006 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.5935/abc.20150036 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Sociedade Brasileira de Cardiologia - SBC |
publisher.none.fl_str_mv |
Sociedade Brasileira de Cardiologia - SBC |
dc.source.none.fl_str_mv |
Arquivos Brasileiros de Cardiologia v.104 n.6 2015 reponame:Arquivos Brasileiros de Cardiologia (Online) instname:Sociedade Brasileira de Cardiologia (SBC) instacron:SBC |
instname_str |
Sociedade Brasileira de Cardiologia (SBC) |
instacron_str |
SBC |
institution |
SBC |
reponame_str |
Arquivos Brasileiros de Cardiologia (Online) |
collection |
Arquivos Brasileiros de Cardiologia (Online) |
repository.name.fl_str_mv |
Arquivos Brasileiros de Cardiologia (Online) - Sociedade Brasileira de Cardiologia (SBC) |
repository.mail.fl_str_mv |
||arquivos@cardiol.br |
_version_ |
1752126565170282496 |