Evidence map›Paper›PMID 26885047›Full record

ArticleInternational journal of clinical and experimental medicine2015

Genetic association between hOGG1 C8069G polymorphism and colorectal cancer risk.

Xiaoge Sun, Hao Yang, Yu Lin, Jianguo Zhao, Yinna Bao, Xiulan Liu, Zhen Qi, Shaojun Wang, Congxiu Huang, Zhilong Yu

Abstract 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 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
–field-weighted citation impact
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. 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

10 authors.

Xiaoge SunDepartment of Radiation Oncology, The Affiliated Hospital of Inner Mongolia Medical University Tongdao Road, Hohhot 10050, Inner Mongolia, P.R. China.
Hao YangDepartment of Radiation Oncology, Inner Mongolia Cancer Hospital & The Affiliated People's Hospital of Inner Mongolia Medical University Hohhot, Inner Mongolia, China.
Yu LinDepartment of Radiation Oncology, The Affiliated Hospital of Inner Mongolia Medical University Tongdao Road, Hohhot 10050, Inner Mongolia, P.R. China.
Jianguo ZhaoDepartment of Radiation Oncology, The Affiliated Hospital of Inner Mongolia Medical University Tongdao Road, Hohhot 10050, Inner Mongolia, P.R. China.
Yinna BaoDepartment of Radiation Oncology, The Affiliated Hospital of Inner Mongolia Medical University Tongdao Road, Hohhot 10050, Inner Mongolia, P.R. China.
Xiulan LiuDepartment of Radiation Oncology, The Affiliated Hospital of Inner Mongolia Medical University Tongdao Road, Hohhot 10050, Inner Mongolia, P.R. China.
Zhen QiDepartment of Radiation Oncology, The Affiliated Hospital of Inner Mongolia Medical University Tongdao Road, Hohhot 10050, Inner Mongolia, P.R. China.
Shaojun WangDepartment of Radiation Oncology, The Affiliated Hospital of Inner Mongolia Medical University Tongdao Road, Hohhot 10050, Inner Mongolia, P.R. China.
Congxiu HuangDepartment of Radiation Oncology, The Affiliated Hospital of Inner Mongolia Medical University Tongdao Road, Hohhot 10050, Inner Mongolia, P.R. China.
Zhilong YuDepartment of Radiation Oncology, The Affiliated Hospital of Inner Mongolia Medical University Tongdao Road, Hohhot 10050, Inner Mongolia, P.R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundhOGG1 C8069G polymorphism has been extensively investigated in single studies as well as meta-analyses in terms of the association with colorectal cancer (CRC). But the results remain contradictory. This study was undertaken to comprehensively evaluate the association of the commonly studied hOGG1 C8069G polymorphism and the susceptibility to CRC.

methodsBy searching the electronic databases of PubMed, Embase, and Web of science, 16 available publications consisting of 4,866 cases and 7,363 controls were finally included in our meta-analysis. Stratified analyses by ethnicity and source of control were also carried out to further assess the association between hOGG1 C8069G polymorphism and CRC risk.

resultshOGG1 C8069G polymorphism was not observed to have statistical significance with the susceptibility to CRC (ORCC vs. GG = 0.97, 95% CI = 0.91-1.05; P = 0.995; ORCC + CG vs. GG = 0.98, 95% CI = 0.93-1.04; P = 0.993; ORCC vs. CG + GG = 0.96, 95% CI = 0.90-1.02; P = 0.339; ORallele C vs. allele G = 0.98, 95% CI = 0.94-1.02; P = 0.912; ORCG vs. GG = 0.95, 95% CI = 0.88-1.03; P = 0.526). Similarly, no association was found in the subgroup analysis by ethnicity or the source of control.

conclusionsThe results of our meta-analysis did not demonstrate any evidence for significant association between hOGG1 C8069G polymorphism and CRC risk. Future large-scale studies are expected to be conducted to further confirm our findings.

Indexed as

C8069GCRChOGG1polymorphismsusceptibility

Identifiers

PMID26885047
PMCPMC4723892

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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.