Evidence map›Paper›PMID 18368489›Full record

ArticleDigestive diseases and sciences2008

Mannan-binding lectin (MBL) polymorphism and gastric cancer risk in Japanese population.

Fang-Yu Wang, Tomomitsu Tahara, Tomiyasu Arisawa, Tomoyuki Shibata, Hiromi Yamashita, Masakatsu Nakamura, Daisuke Yoshioka, Masaaki Okubo, Naoko Maruyama, Toshiaki Kamano and 9 more

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Article in Digestive diseases and sciences, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.8field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

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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

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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

13 citing papers in PubMed, 20 citations in OpenAlex.

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  10. Role of bacteria in oncogenesis.Clinical microbiology reviews · 2010
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 2 institutions in 1 country.

Fang-Yu WangDepartment of Gastroenterology, Fujita Health University School of Medicine, Aichi Prefecture, 470-1192, Japan.
Tomomitsu Tahara
Tomiyasu Arisawa
Tomoyuki Shibata
Hiromi Yamashita
Masakatsu Nakamura
Daisuke Yoshioka
Masaaki Okubo
Naoko Maruyama
Toshiaki Kamano
Yoshio Kamiya
Masahiko Nakamura
Hiroshi Fujita
Mitsuo Nagasaka
Masami Iwata
Kazuya Takahama
Makoto Watanabe
Hiroshi Nakano
Ichiro Hirata
Fujita Health University Hospital · JPFujita Health University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMannan-binding lectin (MBL) is believed to be an important constituent of the innate immune system. It has been reported that the codon 54 G/A polymorphism of exon-1 affects the MBL2 gene and alters its activity.

aimsWe investigated the association between polymorphism of the MBL2 gene and gastric cancer risk as well as Helicobacter pylori infection in a Japanese population.

methodsThe study cohort comprised 388 gastric cancer patients and 144 healthy volunteers. Polymorphism at codon 54 of exon 1 of the MBL2 gene was investigated by PCR-based restriction fragment length polymorphism analysis.

resultsThere was no significant difference in the distribution of the MBL2 genotype among the gastric cancer patients and healthy controls. However, the carrier of the A allele was more prevalent among patients with a more advanced stage gastric cancer [odds ratio (OR) 1.68, 95% confidence interval (CI) 1.05-2.67; P = 0.03] and also had an increased risk of gastric cancer among patients 65 years of age or younger (OR = 1.6, 95%CI = 1.01-2.52, <0.05).

conclusionThe codon 54 polymorphism of the MBL2 gene is associated with more advanced phenotypes of gastric cancer and the risk of gastric cancer in Japanese patients 65 years of age or younger.

Indexed as

AdultAgedCase-Control StudiesExonsFemaleGenetic Predisposition to DiseaseGenotypeHelicobacter InfectionsHelicobacter pyloriHumansJapanMaleMannose-Binding LectinMiddle AgedPolymorphism, Restriction Fragment LengthPrevalenceMannose-Binding LectinMBL2 protein, human

Identifiers

PMID18368489
OpenAlexW2063392974

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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.