Evidence map›Paper›PMID 26261478›Full record

SynthesisInternational journal of clinical and experimental pathology2015

Association between HSD17B1 rs605059 polymorphisms and the risk of uterine diseases: a systemic review and meta-analysis.

Xiyan Mu, Xue Du, Kui Yao, Jitong Zhao, Ce Bian, Qiao Wang, Hongwei Ma, Tao Yi, Yang Wu, Xia Zhao

Abstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–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

4 citing papers in PubMed.

  1. Article
  2. 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

10 authors.

Xiyan MuDepartment of Gynecology and Obstetrics, West China Second Hospital, Sichuan University Chengdu 610041, Sichuan, P. R. China ; State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, and Collaborative Innovation Center for Biotherapy Chengdu 610041, Sichuan, P. R. China.
Xue DuDepartment of Gynecology and Obstetrics, West China Second Hospital, Sichuan University Chengdu 610041, Sichuan, P. R. China.
Kui YaoDepartment of Gynecology and Obstetrics, West China Second Hospital, Sichuan University Chengdu 610041, Sichuan, P. R. China.
Jitong ZhaoDepartment of Gynecology and Obstetrics, West China Second Hospital, Sichuan University Chengdu 610041, Sichuan, P. R. China.
Ce BianDepartment of Gynecology and Obstetrics, West China Second Hospital, Sichuan University Chengdu 610041, Sichuan, P. R. China.
Qiao WangDepartment of Gynecology and Obstetrics, West China Second Hospital, Sichuan University Chengdu 610041, Sichuan, P. R. China.
Hongwei MaDepartment of Gynecology and Obstetrics, West China Second Hospital, Sichuan University Chengdu 610041, Sichuan, P. R. China.
Tao YiDepartment of Gynecology and Obstetrics, West China Second Hospital, Sichuan University Chengdu 610041, Sichuan, P. R. China.
Yang WuState Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, and Collaborative Innovation Center for Biotherapy Chengdu 610041, Sichuan, P. R. China.
Xia ZhaoDepartment of Gynecology and Obstetrics, West China Second Hospital, Sichuan University Chengdu 610041, Sichuan, P. R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was to evaluate the HSD17B1 gene polymorphisms in the risks of endometrial cancer, endometriosis and uterine leiomyoma by meta-analysis. A comprehensive electronic search was conducted in PubMed, Medline (Ovid), Embase, Weipu, Wanfang and CNKI. The pooled ORs were performed using the Revman 5.2 softerware. 8 case-control studies were included: 3 were about endometrial cancer, 4 were about endometriosis and 1 was about uterine leiomyoma. The result showed no significant association between HSD17B1 rs605059 gene polymorphisms and risks of endometrial cancer (AA vs. AG+GG: OR = 1.11, 95% CI = 0.94-1.32; AA+AG vs. GG: OR = 1.79, 95% CI = 0.42-7.52; AG vs. AA+ GG: OR = 0.87, 95% CI = 0.76-1.00; AA vs. GG: OR = 1.43, 95% CI = 0.62-3.30; A vs. G: OR = 1.00, 95% CI = 0.91-1.11) or endometriosis (AA vs. AG+GG: OR = 0.99, 95% CI = 0.75-1.32; AA+AG vs. GG: OR = 1.73, 95% CI = 0.92-3.25; AG vs. AA+ GG: OR = 1.24, 95% CI = 1.00-1.53; AA vs. GG: OR = 1.54, 95% CI = 0.79-2.97; A vs. G: OR = 1.23, 95% CI = 0.90-1.68). No association was found in a subgroup analysis based on Asian ethnicity for endometriosis. This meta-analysis suggested that HSD17B1 rs605059 polymorphisms were not associated with the risks of endometrial cancer and endometriosis. Further studies are needed to validate the conclusion and clarify the relationship between HSD17B1 rs605059 polymorphisms and the risk of uterine leiomyoma.

Indexed as

Polymorphism, GeneticCase-Control StudiesEndometrial NeoplasmsEndometriosisEstradiol DehydrogenasesFemaleGene FrequencyGenetic Association StudiesGenetic Predisposition to DiseaseHeterozygoteHomozygoteHumansLeiomyomaOdds RatioRisk FactorsUterine NeoplasmsEstradiol DehydrogenasesHSD17B1 protein, humanEndometrial cancerendometriosisHSD17B1leiomyomameta-analysispolymorphism

Identifiers

PMID26261478
PMCPMC4525812

What OpenQuestion holds

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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.