Evidence map›Paper›PMID 27796522›Full record

ArticleRheumatology international2017

The association between MEFV gene polymorphisms and Henoch-Schönlein purpura, and additional SNP-SNP interactions in Chinese Han children.

Shunjun Xiong, Ying Xiong, Qian Huang, Jierong Wang, Xiaofang Zhang

Abstract read
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In one paragraph

Article in Rheumatology international, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 34% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Associations ofHeliyon · 2024
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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

5 authors at 2 institutions in 1 country.

Shunjun XiongDepartment of Pediatrics, Zhongnan Hospital of Wuhan University, No. 169 East Lake Road, Wuchang District, Wuhan City, 430071, Hubei Province, China. xiongssjj23@163.com.
Ying XiongDepartment of Pediatrics, Zhongnan Hospital of Wuhan University, No. 169 East Lake Road, Wuchang District, Wuhan City, 430071, Hubei Province, China.
Qian HuangDepartment of Pediatrics, Zhongnan Hospital of Wuhan University, No. 169 East Lake Road, Wuchang District, Wuhan City, 430071, Hubei Province, China.
Jierong WangDepartment of Pediatrics, Zhongnan Hospital of Wuhan University, No. 169 East Lake Road, Wuchang District, Wuhan City, 430071, Hubei Province, China.
Xiaofang ZhangDepartment of Pediatrics, Zhongnan Hospital of Wuhan University, No. 169 East Lake Road, Wuchang District, Wuhan City, 430071, Hubei Province, China.
Wuhan University · CNZhongnan Hospital of Wuhan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was to investigate the association between single-nucleotide polymorphisms (SNP) within MEFV gene and Henoch-Schönlein purpura (HSP) risk, and the impact of SNP-SNP interaction on HSP risk in Chinese children. A total of 662 subjects with a mean age of 7.9 ± 2.4 years old were selected, including 320 HSP patients and 342 normal controls. Logistic regression was performed to investigate association between SNP and HSP risk, and generalized multifactor dimensionality reduction (GMDR) was used to analyze the SNP-SNP interaction. Logistic analysis showed a significant association between genotypes of variants in rs3743930 and increased HSP risk. The carriers of homozygous mutant of rs3743930 polymorphism revealed increased HSP risk than those with wild-type homozygotes; OR (95% CI) was 1.55 (1.23-1.85). GMDR analysis suggested a significant two-locus model (p = 0.0107) involving rs3743930 and rs28940580, indicating a potential SNP-SNP interaction between rs3743930 and rs28940580. Overall, the two-locus models had a cross-validation consistency of 10 of 10 and had the testing accuracy of 60.72%. Subjects with rs3743930-GC or CC and rs28940580-GA or AA genotype have the highest HSP risk, compared to subjects with rs3743930-GG and rs28940580-GG genotype; OR (95% CI) was 2.13 (1.52-2.89). The variants in rs3743930 and interaction between rs3743930 and rs28940580 were associated with increased HSP risk in Chinese children.

Indexed as

Polymorphism, Single NucleotideAsian PeopleCase-Control StudiesChildChild, PreschoolChinaFemaleGenetic Association StudiesGenetic Predisposition to DiseaseGenotypeHumansIgA VasculitisLogistic ModelsMalePyrinRisk FactorsMEFV protein, humanPyrinHenoch–Schönlein purpuraInteractionMEFVSNP

Identifiers

PMID27796522
OpenAlexW2543073749

What OpenQuestion holds

Textmetadata
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.