Evidence map›Paper›PMID 28824302›Full record

ArticleInternational journal of medical sciences2017

Association of Genes Variants in RANKL/RANK/OPG Signaling Pathway with the Development of Osteonecrosis of the Femoral Head in Chinese Population.

Yang Song, Zhen-Wu Du, Qi-Wei Yang, Ming Ren, Qing-Yu Wang, Ao Wang, Gao-Yang Chen, Hai-Yue Zhao, Tao Yu, Gui-Zhen Zhang

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in International journal of medical sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 14% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Pooled it
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  12. [Microarchitecture features and pathology of necrotic region in patients with steroid-induced and alcohol-induced osteonecrosis of femoral head].Zhongguo xiu fu chong jian wai ke za zhi = Zhongguo xiufu chongjian waike zazhi = Chinese journal of reparative and reconstructive surgery · 2018
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Yang SongDepartment of Orthopedics of Second Clinical College, Jilin University, Changchun, 130041, China.
Zhen-Wu DuDepartment of Orthopedics of Second Clinical College, Jilin University, Changchun, 130041, China.
Qi-Wei YangResearch Center of Second Clinical College, Jilin University, Changchun, 130041, China.
Ming RenDepartment of Orthopedics of Second Clinical College, Jilin University, Changchun, 130041, China.
Qing-Yu WangResearch Center of Second Clinical College, Jilin University, Changchun, 130041, China.
Ao WangDepartment of Orthopedics of Second Clinical College, Jilin University, Changchun, 130041, China.
Gao-Yang ChenResearch Center of Second Clinical College, Jilin University, Changchun, 130041, China.
Hai-Yue ZhaoResearch Center of Second Clinical College, Jilin University, Changchun, 130041, China.
Tao YuDepartment of Orthopedics of Second Clinical College, Jilin University, Changchun, 130041, China.
Gui-Zhen ZhangDepartment of Orthopedics of Second Clinical College, Jilin University, Changchun, 130041, China.
Jilin University · CNSecond Affiliated Hospital of Jilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The RANKL/RANK/OPG pathway plays an important role in regulating bone remodeling and bone turnover. However, the association of the genes variants with the risk of ONFH has rarely been reported. Here, we analyzed the correlation of the 10 SNPs polymorphisms of RANKL, RANK, OPG, TRAF6, and NFATC1 genes with the risk and development of ONFH in 200 ONFH patients and 177 health controls of Chinese population with using Mass ARRAY® platform. The results showed that the recessive model of NFATC1rs9518 was significantly associated with increased ONFH risk (OR:8.223,

Indexed as

AgedChinaFemaleFemur Head NecrosisGenetic Association StudiesGenetic Predisposition to DiseaseGenotypeHaplotypesHumansMaleMiddle AgedNFATC Transcription FactorsOsteonecrosisOsteoprotegerinPolymorphism, Single NucleotideRANK LigandNFATC1 protein, humanNFATC Transcription FactorsOsteoprotegerinRANK LigandReceptor Activator of Nuclear Factor-kappa BTNFRSF11A protein, humanTNFRSF11B protein, humanTNFSF11 protein, humanTRAF7 protein, humanTumor Necrosis Factor Receptor-Associated Peptides and Proteinsgene polymorphismNFATC1.ONFHRANKL/RANK/OPG pathwayTRAF6

Identifiers

PMID28824302
PMCPMC5562121
OpenAlexW2734491599

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.