Evidence map›Paper›PMID 18756601›Full record

ArticleWorld journal of gastroenterology2008

OCTN and CARD15 gene polymorphism in Chinese patients with inflammatory bowel disease.

Mei Li, Xiang Gao, Chang-Cun Guo, Kai-Chun Wu, Xin Zhang, Pin-Jin Hu

Open access · hybridAbstract readMulticenter Study
In one paragraph

Article in World journal of gastroenterology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 3 pooled it
3.2field-weighted citation impact, top 8% 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

24 citing papers in PubMed, 3 syntheses or guidelines pooled it, 50 citations in OpenAlex.

  1. Pooled it
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  4. Review
  5. Current status of IBD and surgery of Crohn's disease in Thailand.Annals of gastroenterological surgery · 2021
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  12. Association study betweenThe Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2017
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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

6 authors at 4 institutions in 2 countries.

Mei LiDepartment of Gastroenterology, the First Affiliated Hospital of Zhongshan University, Guangzhou 510089, Guangdong Province, China. pjhumd@vip.163.com
Xiang Gao
Chang-Cun Guo
Kai-Chun Wu
Xin Zhang
Pin-Jin Hu
The First Affiliated Hospital, Sun Yat-sen University · CNAir Force Medical University · CNHarvard University · USXijing Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo investigate the single nucleotide polymorphism (SNPs) distribution of NOD2/CARD15 (R702W, G908R), OCTN1 1672C/T and OCTN2-207G/C in Chinese patients with inflammatory bowel disease (IBD).

methodsA total of 61 patients with Crohn's disease (CD), 151 patients with ulcerative colitis (UC), and 200 unrelated healthy controls were genotyped. Genotyping was performed by sequence specific primer polymerase chain reaction (PCR-SSP) or by restriction fragment length polymorphism (PCR-RFLP) analysis.

resultsAmong the subjects in our study groups, including patients with CD, UC and healthy controls, none had OCTN and CARD15 variants and very rare IBD family history was found in our patients with the percentage of 0 (0/61 with CD) and 1.3% (2/151 with UC).

conclusionOur results indicate that although OCTN or CARD15 variation is associated with susceptibility to IBD in Western populations, these might be rare and may not be associated with susceptibility to IBD in Chinese patients.

Indexed as

Polymorphism, Single NucleotideAdultAsian PeopleCase-Control StudiesChinaFemaleGene FrequencyGenetic Predisposition to DiseaseHumansInflammatory Bowel DiseasesMaleMiddle AgedNod2 Signaling Adaptor ProteinOrganic Cation Transport ProteinsProspective StudiesSolute Carrier Family 22 Member 5NOD2 protein, humanNod2 Signaling Adaptor ProteinOrganic Cation Transport ProteinsSLC22A4 protein, humanSLC22A5 protein, humanSolute Carrier Family 22 Member 5Symporters

Identifiers

PMID18756601
PMCPMC2739946
OpenAlexW2116561312

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.