APOE and LDLR Gene Polymorphisms and Dyslipidemia Tracking. Rio de Janeiro Study

Bibliographic Details
Main Author: Freitas,Rossana Ghessa Andrade de
Publication Date: 2015
Other Authors: Campana,Erika Maria Gonçalves, Pozzan,Roberto, Brandão,Andréa Araujo, Brandão,Ayrton Pires, Magalhães,Maria Eliane Campos, Silva,Dayse Aparecida da
Format: Article
Language: eng
Source: Arquivos Brasileiros de Cardiologia (Online)
Download full: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0066-782X2015000600006
Summary: 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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spelling 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
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