Evidence map›Paper›PMID 26131702›Full record

ArticleArquivos brasileiros de cardiologia2015

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

Rossana Ghessa Andrade de Freitas, Erika Maria Gonçalves Campana, Roberto Pozzan, Andréa Araujo Brandão, Ayrton Pires Brandão, Maria Eliane Campos Magalhães, Dayse Aparecida da Silva

Open access · diamondAbstract read
In one paragraph

Article in Arquivos brasileiros de cardiologia, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 24% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. The physiological effects of APOE genotype in healthy young/middle-aged individuals.Biological reviews of the Cambridge Philosophical Society · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Rossana Ghessa Andrade de FreitasUniversidade do Estado do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Erika Maria Gonçalves CampanaUniversidade do Estado do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Roberto PozzanUniversidade do Estado do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Andréa Araujo BrandãoUniversidade do Estado do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Ayrton Pires BrandãoUniversidade do Estado do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Maria Eliane Campos MagalhãesUniversidade do Estado do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Dayse Aparecida da SilvaUniversidade do Estado do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Universidade do Estado do Rio de Janeiro · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundStudies show an association between changes in apolipoprotein E (ApoE) and LDLR receptor with the occurrence of dyslipidemia.

objectivesTo 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.

methodsThe 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).

resultsCompared 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.

conclusionsAPOE gene polymorphisms were associated with dyslipidemia in young individuals followed up longitudinally from childhood.

Indexed as

Genetic Association StudiesAdolescentAdultApolipoprotein E2Apolipoprotein E3Apolipoprotein E4Apolipoproteins EBlood PressureBody Mass IndexBrazilChildDyslipidemiasFemaleGene FrequencyGenotypeHumansApolipoprotein E2Apolipoprotein E3Apolipoprotein E4Apolipoproteins ELDLR protein, humanReceptors, LDL

Identifiers

PMID26131702
PMCPMC4484679
OpenAlexW2126387090

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Registered trials

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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.