Evidence map›Paper›PMID 29310478›Full record

ArticleThe Journal of international medical research2018

Genetic variation of SMAD3 is associated with hip osteoarthritis in a Chinese Han population.

Fuhua Zhong, Jianwei Lu, Yangxin Wang, Hongpu Song

Open access · goldAbstract read
In one paragraph

Article in The Journal of international medical research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 2 pooled it
1.4field-weighted citation impact, top 20% 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

7 citing papers in PubMed, 2 syntheses or guidelines pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Bioscience reports · 2018
    Pooled it
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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

4 authors at 2 institutions in 1 country.

Fuhua Zhong1 Department of Orthopedics, 414282 Tongde Hospital of Zhejiang Province , Zhejiang, CN, P.R. China.
Jianwei Lu1 Department of Orthopedics, 414282 Tongde Hospital of Zhejiang Province , Zhejiang, CN, P.R. China.
Yangxin Wang2 Department of Orthopedic Surgery, Second Affiliated Hospital's Campus in Binjiang District, School of Medicine, Zhejiang University, Hangzhou, Zhejiang, CN, P.R. China.
Hongpu Song1 Department of Orthopedics, 414282 Tongde Hospital of Zhejiang Province , Zhejiang, CN, P.R. China.
Tongde Hospital of Zhejiang Province · CNSecond Affiliated Hospital of Zhejiang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective This study was performed to investigate the association between genetic variation in SMAD3 and hip osteoarthritis (OA) in a Chinese Han population. Methods The frequency of two single nucleotide polymorphisms of SMAD3, rs1470002 and rs12901499, was examined in 500 patients with hip OA and 1080 healthy controls in a Chinese Han population. Further analysis was performed according to sex and age. Results We detected statistically significant differences in the allele frequency and genotype between the hip OA and healthy control groups. The frequency of the GA+GG and GA genotypes of rs12901499 and the G variant were much higher in patients with hip OA than in healthy controls. This association was also present when the participants were stratified by sex and age. However, there was no significant association between the risk of hip OA and the presence of rs1470002 GA, AA, or GA+AA genotypes, even after sex- and age-stratified analysis. Conclusions The SMAD3 SNP rs12901499 GA genotype and G variant may increase the risk of hip OA in Chinese Han patients.

Indexed as

Genetic Predisposition to DiseasePolymorphism, Single NucleotideAgedAllelesAsian PeopleCase-Control StudiesFemaleGene ExpressionGene FrequencyHumansMaleMiddle AgedOsteoarthritis, HipRiskSmad3 ProteinSmad3 ProteinSMAD3 protein, humancase–control studyChinese HanHip osteoarthritisPCRsingle nucleotide polymorphismSMAD3

Identifiers

PMID29310478
PMCPMC5972263
OpenAlexW2784292354

What OpenQuestion holds

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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.