Evidence map›Paper›PMID 26064388›Full record

ArticleInternational journal of clinical and experimental medicine2015

Association of genetic polymorphisms in HTR3A and HTR3E with diarrhea predominant irritable bowel syndrome.

Qiao-Yan Gu, Jun Zhang, Yi-Chao Feng, Guang-Rong Dai, Wei-Ping Du

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
1.9field-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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. The serotonin receptor 3E variant is a risk factor for female IBS-D.Journal of molecular medicine (Berlin, Germany) · 2022
    Pooled it
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  7. 5-HTAmerican journal of physiology. Gastrointestinal and liver physiology · 2019
    Article
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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

5 authors at 1 institution in 1 country.

Qiao-Yan GuDepartment of Gastroenterology, Second Affiliated Hospital of Xi'an Jiaotong University Xi'an 710004, Shaanxi Province, P. R. China ; Department of Gastroenterology, Affiliated Hospital of Yan'an University Yan'an 716000, Shaanxi Province, P. R. China.
Jun ZhangDepartment of Gastroenterology, Second Affiliated Hospital of Xi'an Jiaotong University Xi'an 710004, Shaanxi Province, P. R. China.
Yi-Chao FengDepartment of Gastroenterology, Affiliated Hospital of Yan'an University Yan'an 716000, Shaanxi Province, P. R. China.
Guang-Rong DaiDepartment of Gastroenterology, Affiliated Hospital of Yan'an University Yan'an 716000, Shaanxi Province, P. R. China.
Wei-Ping DuDepartment of Gastroenterology, Affiliated Hospital of Yan'an University Yan'an 716000, Shaanxi Province, P. R. China.
Xi'an Jiaotong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe present study aims to investigate the relationship between genetic polymorphisms in HTR3A and HTR3E and diarrhea predominant irritable bowel syndrome (D-IBS) in a Chinese population.

methodsWe enrolled 500 D-IBS patients and 500 age- and sex-matched healthy control subjects to detect the genotypes in HTR3A and HTR3B gene by using of PCR-RFLP method.

resultsThere were significant difference between the D-IBS patients and the health control subjects in the distribution of genotype and allele of rs1062613 in HTR3A gene. As regarding rs62625044 in HTR3E gene, we found there was a significant different between the case and the control group in the distribution of GA genotype and A allele in female but not in male.

conclusionThe present study suggested that there are associations of D-IBS risk with genetic polymorphisms in HTR3A and HTR3E.

Indexed as

Diarrhea predominant irritable bowel syndromegeneHTR3AHTR3Epolymorphism

Identifiers

PMID26064388
PMCPMC4443222
OpenAlexW2414179833

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.