Genetic information improves the prediction of major adverse cardiovascular events in the GENEMACOR population

Detalhes bibliográficos
Autor(a) principal: Mendonça,Maria Isabel
Data de Publicação: 2021
Outros Autores: Henriques,Eva, Borges,Sofia, Sousa,Ana Célia, Pereira,Andreia, Santos,Marina, Temtem,Margarida, Freitas,Sónia, Monteiro,Joel, Sousa,João Adriano, Rodrigues,Ricardo, Guerra,Graça, Reis,Roberto Palma dos
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Genetics and Molecular Biology
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572021000300113
Resumo: Abstract The inclusion of a genetic risk score (GRS) can modify the risk prediction of coronary artery disease (CAD), providing an advantage over the use of traditional models. The predictive value of the genetic information on the recurrence of major adverse cardiovascular events (MACE) remains controversial. A total of 33 genetic variants previously associated with CAD were genotyped in 1587 CAD patients from the GENEMACOR study. Of these, 18 variants presented an hazard ratio >1, so they were selected to construct a weighted GRS (wGRS). MACE discrimination and reclassification were evaluated by C-Statistic, Net Reclassification Index and Integrated Discrimination Improvement methodologies. After the addition of wGRS to traditional predictors, the C-index increased from 0.566 to 0.572 (p=0.0003). Subsequently, adding wGRS to traditional plus clinical risk factors, this model slightly improved from 0.620 to 0.622 but with statistical significance (p=0.004). NRI showed that 17.9% of the cohort was better reclassified when the primary model was associated with wGRS. The Kaplan-Meier estimator showed that, at 15-year follow-up, the group with a higher number of risk alleles had a significantly higher MACE occurrence (p=0.011). In CAD patients, wGRS improved MACE risk prediction, discrimination and reclassification over the conventional factors, providing better cost-effective therapeutic strategies.
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spelling Genetic information improves the prediction of major adverse cardiovascular events in the GENEMACOR populationTraditional risk factorsgenetic risk scoreevents risk discrimination and reclassificationNet Reclassification Indexsecondary prevention of coronary artery diseaseAbstract The inclusion of a genetic risk score (GRS) can modify the risk prediction of coronary artery disease (CAD), providing an advantage over the use of traditional models. The predictive value of the genetic information on the recurrence of major adverse cardiovascular events (MACE) remains controversial. A total of 33 genetic variants previously associated with CAD were genotyped in 1587 CAD patients from the GENEMACOR study. Of these, 18 variants presented an hazard ratio >1, so they were selected to construct a weighted GRS (wGRS). MACE discrimination and reclassification were evaluated by C-Statistic, Net Reclassification Index and Integrated Discrimination Improvement methodologies. After the addition of wGRS to traditional predictors, the C-index increased from 0.566 to 0.572 (p=0.0003). Subsequently, adding wGRS to traditional plus clinical risk factors, this model slightly improved from 0.620 to 0.622 but with statistical significance (p=0.004). NRI showed that 17.9% of the cohort was better reclassified when the primary model was associated with wGRS. The Kaplan-Meier estimator showed that, at 15-year follow-up, the group with a higher number of risk alleles had a significantly higher MACE occurrence (p=0.011). In CAD patients, wGRS improved MACE risk prediction, discrimination and reclassification over the conventional factors, providing better cost-effective therapeutic strategies.Sociedade Brasileira de Genética2021-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572021000300113Genetics and Molecular Biology v.44 n.2 2021reponame:Genetics and Molecular Biologyinstname:Sociedade Brasileira de Genética (SBG)instacron:SBG10.1590/1678-4685-gmb-2020-0448info:eu-repo/semantics/openAccessMendonça,Maria IsabelHenriques,EvaBorges,SofiaSousa,Ana CéliaPereira,AndreiaSantos,MarinaTemtem,MargaridaFreitas,SóniaMonteiro,JoelSousa,João AdrianoRodrigues,RicardoGuerra,GraçaReis,Roberto Palma doseng2021-06-09T00:00:00Zoai:scielo:S1415-47572021000300113Revistahttp://www.gmb.org.br/ONGhttps://old.scielo.br/oai/scielo-oai.php||editor@gmb.org.br1678-46851415-4757opendoar:2021-06-09T00:00Genetics and Molecular Biology - Sociedade Brasileira de Genética (SBG)false
dc.title.none.fl_str_mv Genetic information improves the prediction of major adverse cardiovascular events in the GENEMACOR population
title Genetic information improves the prediction of major adverse cardiovascular events in the GENEMACOR population
spellingShingle Genetic information improves the prediction of major adverse cardiovascular events in the GENEMACOR population
Mendonça,Maria Isabel
Traditional risk factors
genetic risk score
events risk discrimination and reclassification
Net Reclassification Index
secondary prevention of coronary artery disease
title_short Genetic information improves the prediction of major adverse cardiovascular events in the GENEMACOR population
title_full Genetic information improves the prediction of major adverse cardiovascular events in the GENEMACOR population
title_fullStr Genetic information improves the prediction of major adverse cardiovascular events in the GENEMACOR population
title_full_unstemmed Genetic information improves the prediction of major adverse cardiovascular events in the GENEMACOR population
title_sort Genetic information improves the prediction of major adverse cardiovascular events in the GENEMACOR population
author Mendonça,Maria Isabel
author_facet Mendonça,Maria Isabel
Henriques,Eva
Borges,Sofia
Sousa,Ana Célia
Pereira,Andreia
Santos,Marina
Temtem,Margarida
Freitas,Sónia
Monteiro,Joel
Sousa,João Adriano
Rodrigues,Ricardo
Guerra,Graça
Reis,Roberto Palma dos
author_role author
author2 Henriques,Eva
Borges,Sofia
Sousa,Ana Célia
Pereira,Andreia
Santos,Marina
Temtem,Margarida
Freitas,Sónia
Monteiro,Joel
Sousa,João Adriano
Rodrigues,Ricardo
Guerra,Graça
Reis,Roberto Palma dos
author2_role author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Mendonça,Maria Isabel
Henriques,Eva
Borges,Sofia
Sousa,Ana Célia
Pereira,Andreia
Santos,Marina
Temtem,Margarida
Freitas,Sónia
Monteiro,Joel
Sousa,João Adriano
Rodrigues,Ricardo
Guerra,Graça
Reis,Roberto Palma dos
dc.subject.por.fl_str_mv Traditional risk factors
genetic risk score
events risk discrimination and reclassification
Net Reclassification Index
secondary prevention of coronary artery disease
topic Traditional risk factors
genetic risk score
events risk discrimination and reclassification
Net Reclassification Index
secondary prevention of coronary artery disease
description Abstract The inclusion of a genetic risk score (GRS) can modify the risk prediction of coronary artery disease (CAD), providing an advantage over the use of traditional models. The predictive value of the genetic information on the recurrence of major adverse cardiovascular events (MACE) remains controversial. A total of 33 genetic variants previously associated with CAD were genotyped in 1587 CAD patients from the GENEMACOR study. Of these, 18 variants presented an hazard ratio >1, so they were selected to construct a weighted GRS (wGRS). MACE discrimination and reclassification were evaluated by C-Statistic, Net Reclassification Index and Integrated Discrimination Improvement methodologies. After the addition of wGRS to traditional predictors, the C-index increased from 0.566 to 0.572 (p=0.0003). Subsequently, adding wGRS to traditional plus clinical risk factors, this model slightly improved from 0.620 to 0.622 but with statistical significance (p=0.004). NRI showed that 17.9% of the cohort was better reclassified when the primary model was associated with wGRS. The Kaplan-Meier estimator showed that, at 15-year follow-up, the group with a higher number of risk alleles had a significantly higher MACE occurrence (p=0.011). In CAD patients, wGRS improved MACE risk prediction, discrimination and reclassification over the conventional factors, providing better cost-effective therapeutic strategies.
publishDate 2021
dc.date.none.fl_str_mv 2021-01-01
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=S1415-47572021000300113
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572021000300113
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/1678-4685-gmb-2020-0448
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 Genética
publisher.none.fl_str_mv Sociedade Brasileira de Genética
dc.source.none.fl_str_mv Genetics and Molecular Biology v.44 n.2 2021
reponame:Genetics and Molecular Biology
instname:Sociedade Brasileira de Genética (SBG)
instacron:SBG
instname_str Sociedade Brasileira de Genética (SBG)
instacron_str SBG
institution SBG
reponame_str Genetics and Molecular Biology
collection Genetics and Molecular Biology
repository.name.fl_str_mv Genetics and Molecular Biology - Sociedade Brasileira de Genética (SBG)
repository.mail.fl_str_mv ||editor@gmb.org.br
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