Evidence map›Paper›PMID 28116820›Full record

ArticleJournal of clinical laboratory analysis2017

The association of NLRP3 and TNFRSF1A polymorphisms with risk of ankylosing spondylitis and treatment efficacy of etanercept.

Shengchun Zhao, Hongwei Chen, Guolin Wu, Chen Zhao

Open access · bronzeAbstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 23% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 32 citations in OpenAlex.

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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 3 institutions in 1 country.

Shengchun ZhaoSecond Department of Orthopaedics, Yiwu City Central Hospital, Yiwu, Zhejiang, China.
Hongwei ChenDepartment of Orthopaedics, Yiwu City Central Hospital, Yiwu, Zhejiang, China.
Guolin WuDepartment of Orthopaedics, Yiwu City Central Hospital, Yiwu, Zhejiang, China.
Chen ZhaoDepartment of Orthopaedics, Zhejiang Provincial People's Hospital, Hangzhou, Zhejiang, China.
Yiwu Science and Technology Research Institute · CNYichang Central People's Hospital · CNZhejiang Provincial People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTo discover how NLRP3 and TNFRSF1A polymorphisms affect the efficacy of traditional medicine and etanercept for ankylosing spondylitis (AS) patients.

methodsSingle nucleotide polymorphism (SNP) and haplotype analyses were conducted based on determined NLRP3 and TNFRSF1A among AS patients. We subsequently analyzed the relationship between relevant clinical indexes and polymorphisms of NLRP3 and TNFRSF1A.

resultsThe 4 SNP loci on NLRP3 and 3 SNP loci on TNFRSF1A showed significant linkage disequilibrium, respectively. The T allele of NLRP3 rs4612666 and the T allele of TFRSF1A rs4149570 are both associated with AS (P<.05). The T-A-C-T haplotype of NLRP3 as well as the G-C-C, T-C-C, T-C-T, and T-T-T haplotypes of TFRSF1A are associated with AS (P<.05). The morning stiffness time, BASDAI scoring, and ESR of patients receiving etanercept were significantly higher than those receiving traditional medicine. T allele of NLRP3 rs4612666 had a significantly greater negative impact on the ASAS20 improvement than C allele. Whereas the A allele of NLRP3 rs3806268 had a significantly greater positive impact on the ASAS20 improvement than G allele. There is no significant association between SNP and efficacy of traditional medicine in the treatment of AS.

conclusionNLRP3 and TFRSF1A (rs4149570) are associated with AS susceptibility. There is a significant association between NLRP3 polymorphisms and treatment of etanercept.

Indexed as

Spondylitis, AnkylosingAdolescentAdultCohort StudiesEtanerceptFemaleHumansImmunosuppressive AgentsLinkage DisequilibriumMaleMiddle AgedNLR Family, Pyrin Domain-Containing 3 ProteinPolymorphism, Single NucleotideReceptors, Tumor Necrosis Factor, Type IYoung AdultEtanerceptImmunosuppressive AgentsNLR Family, Pyrin Domain-Containing 3 ProteinNLRP3 protein, humanReceptors, Tumor Necrosis Factor, Type ITNFRSF1A protein, humanankylosing spondylitisetanerceptNLRP3single nucleotide polymorphismTNFRSF1A

Identifiers

PMID28116820
PMCPMC6817003
OpenAlexW2580114732

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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.