Evidence map›Paper›PMID 32802832›Full record

ArticleBioMed research international2020

Associations between NLRC4 Gene Polymorphisms and Autoimmune Thyroid Disease.

Xuerong Liu, Xiaogang Bai, Jing Zhao, Chaoqun Gao, Peng Du, Jin-An Zhang, Sheli Li

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 37% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
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  6. Computational and mathematical methods in medicine · 2021
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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

7 authors at 2 institutions in 1 country.

Xuerong LiuDepartment of Endocrinology, Yanan University Affiliated Hospital, Shaanxi 716000, China.ORCID https://orcid.org/0000-0002-2897-7871
Xiaogang BaiDepartment of Endocrinology, Yanan University Affiliated Hospital, Shaanxi 716000, China.
Jing ZhaoDepartment of Endocrinology, Shanghai University of Medicine & Health Sciences Affiliated Zhoupu Hospital, Shanghai 201508, China.
Chaoqun GaoDepartment of Endocrinology, Shanghai University of Medicine & Health Sciences Affiliated Zhoupu Hospital, Shanghai 201508, China.
Peng DuDepartment of Endocrinology, Shanghai University of Medicine & Health Sciences Affiliated Zhoupu Hospital, Shanghai 201508, China.
Jin-An ZhangDepartment of Endocrinology, Shanghai University of Medicine & Health Sciences Affiliated Zhoupu Hospital, Shanghai 201508, China.ORCID https://orcid.org/0000-0002-1700-4695
Sheli LiDepartment of Endocrinology, Yanan University Affiliated Hospital, Shaanxi 716000, China.ORCID https://orcid.org/0000-0002-1546-8891
Shanghai University of Medicine and Health Sciences · CNYanan University Affiliated Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMany studies have shown that NLRC4 inflammasome polymorphisms are associated with a variety of autoimmune diseases, but the associations between NLRC4 polymorphisms and autoimmune thyroid diseases (AITDs) are unclear. Our research was aimed at identifying the correlations between NLRC4 polymorphisms and AITDs.

methodsHi-SNP high-throughput genotyping technology was used for detecting four single-nucleotide polymorphisms (SNPs) of NLRC4 in 1005 AITDs patients (including 629 Graves' disease and 376 Hashimoto's thyroiditis) and 781 healthy controls.

resultsCompared with healthy controls, the allele frequencies and genotype distribution of rs385076 were statistically related to AITDs (

conclusionNLRC4 rs385076 was found to have a significant association with Hashimoto's thyroiditis for the first time. It laid a foundation for the disclosure of the pathogenesis of AITDs, and provided a possible treatment prospect for HT.

Indexed as

AdultAutoimmune DiseasesCalcium-Binding ProteinsCARD Signaling Adaptor ProteinsCase-Control StudiesFemaleGenetic Predisposition to DiseaseGenotypeGraves DiseaseHaplotypesHashimoto DiseaseHumansMalePolymorphism, Single NucleotideThyroid DiseasesCalcium-Binding ProteinsCARD Signaling Adaptor ProteinsNLRC4 protein, human

Identifiers

PMID32802832
PMCPMC7424365
OpenAlexW3047273758

What OpenQuestion holds

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LicenceCC BY
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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.