Evidence map›Paper›PMID 38478535›Full record

ArticlePloS one2024

Impact of genetic background as a risk factor for atherosclerotic cardiovascular disease: A protocol for a nationwide genetic case-control (CV-GENES) study in Brazil.

Haliton Alves de Oliveira, Precil Diego Miranda de Menezes Neves, Gustavo Bernardes de Figueiredo Oliveira, Frederico Rafael Moreira, Maria Carolina Tostes Pintão, Viviane Zorzanelli Rocha, Cristiane de Souza Rocha, Viviane Nakano Katz, Elisa Napolitano Ferreira, Diana Rojas-Málaga and 9 more

Erratum issued Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to trial NCT05515653 (Impact of the Genetic Background as a Risk Factor for Atherosclerotic Cardiovascular Disease in the Brazilian Population), which is not on this map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.7field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT05515653 unknown statusnot on this map

Impact of the Genetic Background as a Risk Factor for Atherosclerotic Cardiovascular Disease in the Brazilian Population

TypeobservationalSponsorHospital Alemão Oswaldo CruzRan2022 to 2024Enrolled3,974ConditionsCardiovascular Diseases, Acute MI, Stroke, Peripheral Arterial DiseaseArmsExposure to genetics (polygenic)
3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 3 citations in OpenAlex.

  1. Trial
  2. Article
  3. Observational
  4. Article
  5. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 2 institutions in 1 country.

Haliton Alves de OliveiraSustainability and Social Responsibility, Hospital Alemão Oswaldo Cruz, São Paulo, São Paulo, Brazil.ORCID 0000-0002-0289-4947
Precil Diego Miranda de Menezes NevesInternational Research Center, Hospital Alemão Oswaldo Cruz, São Paulo, São Paulo, Brazil.
Gustavo Bernardes de Figueiredo OliveiraInternational Research Center, Hospital Alemão Oswaldo Cruz, São Paulo, São Paulo, Brazil.ORCID 0000-0002-1815-6498
Frederico Rafael MoreiraSustainability and Social Responsibility, Hospital Alemão Oswaldo Cruz, São Paulo, São Paulo, Brazil.
Maria Carolina Tostes PintãoDepartment of Research and Development, Fleury Group, São Paulo, São Paulo, Brazil.
Viviane Zorzanelli RochaDepartment of Research and Development, Fleury Group, São Paulo, São Paulo, Brazil.
Cristiane de Souza RochaDepartment of Research and Development, Fleury Group, São Paulo, São Paulo, Brazil.
Viviane Nakano KatzDepartment of Research and Development, Fleury Group, São Paulo, São Paulo, Brazil.
Elisa Napolitano FerreiraDepartment of Research and Development, Fleury Group, São Paulo, São Paulo, Brazil.
Diana Rojas-MálagaDepartment of Research and Development, Fleury Group, São Paulo, São Paulo, Brazil.
Celso Ferraz VianaDepartment of Research and Development, Fleury Group, São Paulo, São Paulo, Brazil.
Fabiula Fagundes da SilvaInternational Research Center, Hospital Alemão Oswaldo Cruz, São Paulo, São Paulo, Brazil.ORCID 0000-0002-5228-8187
Juliete Jorge VidottiInternational Research Center, Hospital Alemão Oswaldo Cruz, São Paulo, São Paulo, Brazil.ORCID 0000-0003-0658-9429
Natalia Mariana FelicioInternational Research Center, Hospital Alemão Oswaldo Cruz, São Paulo, São Paulo, Brazil.
Leticia de Araújo VitorSustainability and Social Responsibility, Hospital Alemão Oswaldo Cruz, São Paulo, São Paulo, Brazil.
Karina Gimenez CesarSustainability and Social Responsibility, Hospital Alemão Oswaldo Cruz, São Paulo, São Paulo, Brazil.
Camila Araújo da SilvaSustainability and Social Responsibility, Hospital Alemão Oswaldo Cruz, São Paulo, São Paulo, Brazil.
Lucas Bassolli de Oliveira AlvesSustainability and Social Responsibility, Hospital Alemão Oswaldo Cruz, São Paulo, São Paulo, Brazil.
Álvaro AvezumInternational Research Center, Hospital Alemão Oswaldo Cruz, São Paulo, São Paulo, Brazil.
Hospital Alemão Oswaldo Cruz · BRFleury S.A. (Brazil) · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Atherosclerotic Cardiovascular Disease (ASCVD) represents the leading cause of death worldwide, and individual screening should be based on behavioral, metabolic, and genetic profile derived from data collected in large population-based studies. Due to the polygenic nature of ASCVD, we aimed to assess the association of genomics with ASCVD risk and its impact on the occurrence of acute myocardial infarction, stroke, or peripheral artery thrombotic-ischemic events at population level. CardioVascular Genes (CV-GENES) is a nationwide, multicenter, 1:1 case-control study of 3,734 patients in Brazil. Inclusion criterion for cases is the first occurrence of one of the ASCVD events. Individuals without known ASCVD will be eligible as controls. A core lab will perform the genetic analyses through low-pass whole genome sequencing and whole exome sequencing. In order to estimate the independent association between genetic polymorphisms and ASCVD, a polygenic risk score (PRS) will be built through a hybrid approach including effect size of each Single Nucleotide Polymorphism (SNP), number of effect alleles observed, sample ploidy, total number of SNPs included in the PRS, and number of non-missing SNPs in the sample. In addition, the presence of pathogenic or likely pathogenic variants will be screened in 8 genes (ABCG5, ABCG8, APOB, APOE, LDLR, LDLRAP1, LIPA, PCSK9) associated with atherosclerosis. Multiple logistic regression will be applied to estimate adjusted odds ratios (OR) and 95% confidence intervals (CI), and population attributable risks will be calculated. Clinical trial registration: This study is registered in clinicaltrials.gov (NCT05515653).

Indexed as

AtherosclerosisCardiovascular DiseasesBrazilCase-Control StudiesGenetic BackgroundHumansMulticenter Studies as TopicProprotein Convertase 9Risk FactorsPCSK9 protein, humanProprotein Convertase 9

Identifiers

PMID38478535
PMCPMC10936812
OpenAlexW4392775712

What OpenQuestion holds

Texttitle and abstract
LicenceCC BY
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.