Evidence map›Paper›PMID 27047576›Full record

ArticleThe open rheumatology journal2016

Association Study of Single Nucleotide Polymorphisms Rs4552569/Rs17095830 with Ankylosing Spondylitis in A Chinese Population.

Qingwen Wang, Yuanyuan Yang, Jiyang Lv, Qi Lin, Luo Wang, Zhengyu Fanga

Open access · diamondAbstract read
In one paragraph

Article in The open rheumatology journal, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
0.3field-weighted citation impact, top 36% 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

1 citing paper in PubMed, 1 synthesis or guideline pooled it, 1 citations in OpenAlex.

  1. Pooled it
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

6 authors at 2 institutions in 2 countries.

Qingwen WangDepartment of Rheumatism and Immunology, Peking University Shenzhen Hospital, Shenzhen, Guangdong, PR China.
Yuanyuan YangDepartment of Rheumatism and Immunology, Peking University Shenzhen Hospital, Shenzhen, Guangdong, PR China.
Jiyang LvDepartment of Rheumatism and Immunology, Peking University Shenzhen Hospital, Shenzhen, Guangdong, PR China.
Qi LinDepartment of Rheumatism and Immunology, Peking University Shenzhen Hospital, Shenzhen, Guangdong, PR China.
Luo WangBiomedical Research Institute, Shenzhen Peking University- The Hong Kong University of Science and Technology Medical Center, Guangdong Province, China.
Zhengyu FangaDepartment of Rheumatism and Immunology, Peking University Shenzhen Hospital, Shenzhen, Guangdong, PR China; Biomedical Research Institute, Shenzhen Peking University- The Hong Kong University of Science and Technology Medical Center, Guangdong Province, China.
Peking University Shenzhen Hospital · CNUniversity of Hong Kong · HK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetics play a key role in ankylosing spondylitis (AS). A previous genome-wide association study (GWAS) showed that rs4552569 (on 5q14.3) and rs17095830 (on 12q12) were associated with the risk of AS in Han Chinese, which was not replicated in other two studies. In the current study, rs4552569 and rs17095830 were genotyped in 735 Han Chinese AS patients and 1204 healthy controls using high resolution melting analysis (HRMA). We compared the distributions of genotypes and alleles between AS cases and healthy controls. Rs30187 and rs10865331, which were reported to be associated with AS susceptibility in various populations, were also genotyped and analyzed as positive controls. The results showed that no association between rs4552569/rs17095830 polymorphisms and AS susceptibility was found. On the other hand, an association between rs17095830 and one of AS complication (inflammatory bowel disease) was observed (allelic P value=0.0180; odds ratio[OR]=1.739; 95% confidence interval [CI]=1.146-2.639).

Indexed as

Ankylosing spondylitishigh resolution melting single nucleotide polymorphismrs17095830rs4552569

Identifiers

PMID27047576
PMCPMC4792219
OpenAlexW2255803379

What OpenQuestion holds

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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.