Evidence map›Paper›PMID 25885804›Full record

SynthesisEuropean journal of medical research2015

Is rs759853 polymorphism in promoter of aldose reductase gene a risk factor for diabetic nephropathy? A meta-analysis.

Wenpeng Cui, Bing Du, Yingchun Cui, Lili Kong, Hao Wu, Yangwei Wang, Lining Miao, Wenhua Zhou

Abstract readMeta-Analysis
In one paragraph

Synthesis in European journal of medical research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. The A allele of the rs759853 single nucleotide polymorphism in theArchives of endocrinology and metabolism · 2022
    Article
  4. Article
  5. Article
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

8 authors.

Wenpeng CuiDepartment of Nephrology, Second Hospital of Jilin University, 218 Ziqiang Street, Changchun, Jilin, 130041, China. wenpengcui@163.com.
Bing DuDepartment of Cardiology, the Second Part of First Hospital, Jilin University, 3302 Jilin Road, Changchun, Jilin, 130032, China. dbdavina@126.com.
Yingchun CuiDepartment of Nephrology, Second Hospital of Jilin University, 218 Ziqiang Street, Changchun, Jilin, 130041, China. yingcc16@163.com.
Lili KongDepartment of Nephrology, Second Hospital of Jilin University, 218 Ziqiang Street, Changchun, Jilin, 130041, China. konglili2004@126.com.
Hao WuDepartment of Nephrology, Second Hospital of Jilin University, 218 Ziqiang Street, Changchun, Jilin, 130041, China. 65480256@qq.com.
Yangwei WangDepartment of Nephrology, Second Hospital of Jilin University, 218 Ziqiang Street, Changchun, Jilin, 130041, China. wywhanfeng@163.com.
Lining MiaoDepartment of Nephrology, Second Hospital of Jilin University, 218 Ziqiang Street, Changchun, Jilin, 130041, China. miaolining55@163.com.
Wenhua ZhouDepartment of Nephrology, Second Hospital of Jilin University, 218 Ziqiang Street, Changchun, Jilin, 130041, China. 153762368@qq.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSo far, a number of case-control or cohort studies have been carried out to investigate the relationship between rs759853 polymorphism in the promoter of aldose reductase (AR) gene and the risk of diabetic nephropathy (DN). However, the results have generated considerable controversy. We performed this study to clarify the linkage between this gene mutation and the risk of DN.

methodsA comprehensive literature search of electronic databases and a well-organized meta-analysis were conducted.

resultsTwelve comparisons and 4,735 individuals from nine published case-control or cohort studies were included finally. From none to large heterogeneity was observed, therefore, both fixed and random models were used. Significant differences were found between AR rs759853 polymorphism and susceptibility of DN from both type 1 and type 2 diabetes in all genetic models (allele contrast, OR = 1.37, CI (1.18, 1.59), P < 0.0001; additive model, OR = 1.78, CI (1.25, 2.53), P = 0.01; recessive model OR = 1.33 CI (1.08, 1.63), P = 0.008; dominant model, OR = 1.52, CI (1.26, 1.84), P < 0.0001; codominance model OR = 1.30 (1.15, 1.47), P < 0.0001). In stratified meta-analyses for type 2 diabetes by ethnicity, the significant relationship was found in allele contrast and dominant model in Caucasians, and in allele contrast and codominance model in Asians. However, data do not support the linkage between this gene mutation and the progression of DN. There was no significant publication bias.

conclusionsThe evidence currently available shows that the AR rs759853 polymorphism may correlate with the susceptibility of DN. However, data do not support the association between this DNA variation and the progression of DN.

Indexed as

Polymorphism, Single NucleotidePromoter Regions, GeneticAldehyde ReductaseCase-Control StudiesDiabetic NephropathiesHumansMiddle AgedAldehyde Reductase

Identifiers

PMID25885804
PMCPMC4335367

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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.