Evidence map›Paper›PMID 28225862›Full record

ArticleArchives of endocrinology and metabolism

Association between C1q gene polymorphisms and autoimmune thyroid diseases.

Qiuming Yao, Jie Li, Xiaofei An, Wenjuan Jiang, Qiu Qin, Ronghua Song, Ni Yan, Danfeng Li, Yanfei Jiang, Wen Wang and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Archives of endocrinology and metabolism. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
0.2field-weighted citation impact, top 48% 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

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 5 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
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

12 authors at 3 institutions in 1 country.

Qiuming YaoDepartment of Endocrinology, Jinshan Hospital of Fudan University, Shanghai, China.
Jie LiDepartment of Nephrology, Xi'an Central Hospital, Xi'an, China.
Xiaofei AnDepartment of Endocrinology, Jinshan Hospital of Fudan University, Shanghai, China.
Wenjuan JiangDepartment of Endocrinology, Jinshan Hospital of Fudan University, Shanghai, China.
Qiu QinDepartment of Endocrinology, Jinshan Hospital of Fudan University, Shanghai, China.
Ronghua SongDepartment of Endocrinology, Jinshan Hospital of Fudan University, Shanghai, China.
Ni YanDepartment of Endocrinology, Jinshan Hospital of Fudan University, Shanghai, China.
Danfeng LiDepartment of Endocrinology, Jinshan Hospital of Fudan University, Shanghai, China.
Yanfei JiangDepartment of Endocrinology, Jinshan Hospital of Fudan University, Shanghai, China.
Wen WangDepartment of Endocrinology, Jinshan Hospital of Fudan University, Shanghai, China.
Liangfeng ShiDepartment of Endocrinology, Jinshan Hospital of Fudan University, Shanghai, China.
Jin-An ZhangDepartment of Endocrinology, Jinshan Hospital of Fudan University, Shanghai, China.
Jinshan Hospital of Fudan University · CNFudan University · CNFirst Hospital of Xi'an · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveIn the present study, we aimed to assess the associations of C1q gene polymorphisms with autoimmune thyroid diseases (AITD) susceptibility. SUBJECTS AND

methodsA set of 1,003 AITD patients (661 with Graves' disease and 342 with Hashimoto's thyroiditis) and 880 ethnically- and geographically-matched controls from Chinese Han population were included. Five common single nucleotide polymorphisms (SNPs) (rs294185, rs292001, rs682658, rs665691 and rs294179) in C1q gene locus were genotyped. Frequencies of genotypes and alleles were compared between patients and controls, and haplotype analysis was also performed.

resultsThere was no statistically significant difference between AITD patients and controls in the frequencies of alleles of rs294185 (P = 0.41), rs292001 (P = 0.71), rs682658 (P = 0.68), rs665691 (P = 0.68) and rs294179 (P = 0.69). There was also no statistically significant difference between AITD patients and controls in the frequencies of genotypes of rs294185 (P = 0.72), rs292001 (P = 0.89), rs682658 (P = 0.83), rs665691 (P = 0.90) and rs294179 (P = 0.43). Stratified analyses showed that none of those five SNPs in C1q gene were associated with Graves' disease or Hashimoto's thyroiditis (all P values > 0.05). Haplotype analysis revealed that there were no obvious genetic associations of C1q gene polymorphisms with AITD susceptibility.

conclusionsWe, for the first time, identified the associations between C1q gene SNPs and AITD, and our findings suggested that five common SNPs in C1q gene were not associated with AITD susceptibility in Chinese Han population.

Indexed as

AdultAsian PeopleCase-Control StudiesChinaComplement C1qFemaleGenetic Association StudiesGenetic Predisposition to DiseaseGraves DiseaseHashimoto DiseaseHumansLinkage DisequilibriumMaleMiddle AgedPolymorphism, Single NucleotideYoung AdultComplement C1q

Identifiers

PMID28225862
PMCPMC10118932
OpenAlexW2588556039

What OpenQuestion holds

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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.