Evidence map›Paper›PMID 28855613›Full record

ArticleScientific reports2017

A comprehensive analysis of the association of common variants of ABCG2 with gout.

Kuang-Hui Yu, Pi-Yueh Chang, Shih-Cheng Chang, Yah-Huei Wu-Chou, Li-An Wu, Ding-Pin Chen, Fu-Sung Lo, Jang-Jih Lu

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 3 pooled it
2.9field-weighted citation impact, top 9% 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

18 citing papers in PubMed, 3 syntheses or guidelines pooled it, 35 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Observational
  5. Article
  6. Article
  7. The Evolving Landscape of Gout in the Female: A Narrative Review.Gout, urate, and crystal deposition disease · 2023
    Article
  8. The frequency of majorPharmacogenomics · 2023
    Article
  9. Article
  10. Article
  11. Multidrug efflux transporter ABCG2: expression and regulation.Cellular and molecular life sciences : CMLS · 2021
    Review
  12. Impact ofGenes · 2021
    Article
  13. Article
  14. Article
  15. Review
  16. Polymorphisms ofMedicina (Kaunas, Lithuania) · 2019
    Article
  17. Review
  18. Article
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 3 institutions in 1 country.

Kuang-Hui YuDivision of Rheumatology, Allergy and Immunology, Chang Gung Memorial Hospital and Chang Gung University, Taoyuan, Taiwan.
Pi-Yueh ChangDepartment of Laboratory Medicine, Chang-Gung Memorial Hospital at LinKou, Taoyuan, Taiwan.
Shih-Cheng ChangDepartment of Laboratory Medicine, Chang-Gung Memorial Hospital at LinKou, Taoyuan, Taiwan.
Yah-Huei Wu-ChouDepartment of Medical Research, Chang Gung Memorial Hospital and Chang Gung University, Taoyuan, Taiwan.
Li-An WuDepartment of Laboratory Medicine, Chang-Gung Memorial Hospital at LinKou, Taoyuan, Taiwan.
Ding-Pin ChenDepartment of Laboratory Medicine, Chang-Gung Memorial Hospital at LinKou, Taoyuan, Taiwan.
Fu-Sung LoDivision of Pediatric Endocrinology and Genetics, Chang Gung Memorial Hospital and Chang Gung University, Taoyuan, Taiwan.
Jang-Jih LuDepartment of Laboratory Medicine, Chang-Gung Memorial Hospital at LinKou, Taoyuan, Taiwan. jjlpcp@cgmh.org.tw.
Chang Gung University · TWLinkou Chang Gung Memorial Hospital · TWChang Gung Memorial Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The objective of the present study was to determine whether there was an association between single nucleotide polymorphisms (SNPs) in ABCG2 and gout. We recruited 333 participants including 210 patients with gout and 123 controls and genotyped 45 SNPs in both cohorts. We found that 24 SNPs in ABCG2 are susceptibility loci associated with gout. Haplotype analysis revealed five blocks across the ABCG2 locus were associated with an increased risk of gout with odds ratios (ORs) from 2.59-3.17 (all P < 0.0001). A novel finding in the present study was the identification of rs3114018 in block 3 and its association with increased gout risk. We found that the rs2231142T allele in block 2 and the rs3114018C-rs3109823T (C-T) risk haplotype in block 3 conferred the greatest evidence of association to gout risk (P = 1.19 × 10

Indexed as

Genetic Predisposition to DiseaseGenotypeATP Binding Cassette Transporter, Subfamily G, Member 2Gene FrequencyGoutHumansNeoplasm ProteinsPolymorphism, Single NucleotideABCG2 protein, humanATP Binding Cassette Transporter, Subfamily G, Member 2Neoplasm Proteins

Identifiers

PMID28855613
PMCPMC5577061
OpenAlexW2747289605

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.