Evidence map›Paper›PMID 24489705›Full record

ArticlePloS one2014

Association study to evaluate FoxO1 and FoxO3 gene in CHD in Han Chinese.

Ying Zhao, Yanbo Yu, Xiaoli Tian, Xi Yang, Xueqi Li, Feng Jiang, Yundai Chen, Maowei Shi

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

11 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. FoxO proteins in the nervous system.Analytical cellular pathology (Amsterdam) · 2015
    Review
  9. New Insights for Oxidative Stress and Diabetes Mellitus.Oxidative medicine and cellular longevity · 2015
    Review
  10. Review
  11. Review
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

8 authors at 5 institutions in 1 country.

Ying ZhaoDepartment of Geriatrics, Jinan Military General Hospital, Jinan, China.
Yanbo YuDepartment of Gastroenterology, Qilu Hospital of Shandong University, Jinan, China.
Xiaoli TianDepartment of Human Population Genetics, Institute of Molecular Medicine, Peking University, Beijing, China.
Xi YangDepartment of Human Population Genetics, Institute of Molecular Medicine, Peking University, Beijing, China.
Xueqi LiDepartment of Cardiology, the Fourth Affiliated Hospital of Harbin Medical University, Harbin, China.
Feng JiangDepartment of Cardiology, the Fourth Affiliated Hospital of Harbin Medical University, Harbin, China.
Yundai ChenDepartment of Cardiology, Chinese PLA General Hospital, Beijing, China.
Maowei ShiDepartment of Geriatrics, Jinan Military General Hospital, Jinan, China.
Harbin Medical University · CNJinan Military General Hospital · CNPeking University · CNChinese PLA General Hospital · CNShandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCoronary heart disease (CHD) is one of the leading causes of mortality and morbidity in China. Genetic factors that predispose individuals to CHD are unclear. In the present study, we aimed to determine whether the variation of FoxOs, a novel genetic factor associated with longevity, was associated with CHD in Han Chinese populations.

methods1271 CHD patients and 1287 age-and sex-matched controls from Beijing and Harbin were included. We selected four tagging single nucleotide polymorphisms (SNPs) of FoxO1 (rs2755209, rs2721072, rs4325427 and rs17592371) and two tagging SNPs of FoxO3 (rs768023 and rs1268165). And the genotypes of these SNPs were determined in both CHD patients and non-CHD controls.

resultsFor population from Beijing, four SNPs of FoxO1 and two SNPs of FoxO3 were found not to be associated with CHD (p>0.05). And this was validated in the other population from Harbin (p>0.05). After combining the two geographically isolated case-control populations, the results showed that the six SNPs did not necessarily predispose to CHD in Han Chinese(p>0.05). In stratified analysis according to gender, the history of smoking, hypertension, diabetes mellitus, hyperlipidemia and the metabolic syndrome, we further explored that neither the variants of FoxO1 nor the variants of FoxO3 might be associated with CHD (p>0.05).

conclusionThe variants of FoxO1 and FoxO3 may not increase the prevalence of CHD in Han Chinese population.

Indexed as

AgedAged, 80 and overChinaCoronary DiseaseFemaleForkhead Box Protein O1Forkhead Box Protein O3Forkhead Transcription FactorsGenetic Predisposition to DiseaseHumansMaleMiddle AgedPolymorphism, Single NucleotideForkhead Box Protein O1Forkhead Box Protein O3Forkhead Transcription FactorsFOXO1 protein, humanFOXO3 protein, human

Identifiers

PMID24489705
PMCPMC3904908
OpenAlexW2081414649

What OpenQuestion holds

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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.