Evidence map›Paper›PMID 27638852›Full record

ArticleJournal of the renin-angiotensin-aldosterone system : JRAAS2016

The association of ACE gene polymorphism with diabetic kidney disease and renoprotective efficacy of valsartan.

Yuying Wang, Wen Peng, Xiaoxue Zhang, Huibo Qiao, Li Wang, Zhigang Xu, Chenguang Wu

Open access · hybridAbstract read
In one paragraph

Article in Journal of the renin-angiotensin-aldosterone system : JRAAS, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 19% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Observational
  3. Article
  4. Review
  5. Article
  6. The Susceptibility Genes in Diabetic Nephropathy.Kidney diseases (Basel, Switzerland) · 2018
    Review
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

7 authors at 2 institutions in 1 country.

Yuying WangDepartment of Endocrinology, Affiliated People's Hospital, Jiangsu University, Zhenjiang, China.
Wen PengDepartment of Endocrinology, Affiliated People's Hospital, Jiangsu University, Zhenjiang, China.
Xiaoxue ZhangDepartment of Endocrinology, Affiliated People's Hospital, Jiangsu University, Zhenjiang, China.
Huibo QiaoDepartment of Endocrinology, Affiliated People's Hospital, Jiangsu University, Zhenjiang, China.
Li WangDepartment of Endocrinology, Affiliated People's Hospital, Jiangsu University, Zhenjiang, China.
Zhigang XuDepartment of Endocrinology, Affiliated People's Hospital, Jiangsu University, Zhenjiang, China.
Chenguang WuDepartment of Endocrinology, Affiliated People's Hospital, Jiangsu University, Zhenjiang, China Wcgzj1128@aliyun.com.
Affiliated Hospital of Jiangsu University · CNJiangsu University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionTo investigate the associations between the insertion/deletion (I/D) polymorphisms in the angiotensin converting enzyme (ACE) gene and susceptibility to diabetic kidney disease (DKD); and the efficacy of valsartan in reducing the urine protein in Type 2 diabetes mellitus (T2DM) patients. MATERIALS AND

methodsWe enrolled 128 T2DM patients in this study, including 54 cases with DKD (DKD+) and 74 controls (DKD-). The ACE polymorphism was assayed by polymerase chain reaction (PCR), and the genotype distribution and allele frequency were analyzed. The DKD+ group was subdivided into the DD, ID and II subgroups, based on their genotypes. In addition, patients with DKD received valsartan treatment for 12 weeks. We determined changes in the urinary albumin to creatinine ratio (ACR) and serum creatinine (SCr).

resultsThe frequencies of the genotypes DD and ID were higher in the DKD+ than in the DKD- group. The frequency of allele D was higher, and of allele I was lower, in the DKD+ than in DKD- group (p < 0.05). Following valsartan treatment, albuminuria was significantly decreased in subgroups DD and ID (p < 0.05).

conclusionsIn T2DM patients, the ACE I/D polymorphism was associated with onset of DKD. Furthermore, the ACE I/D polymorphism influenced the renoprotective response to valsartan: Patients with the DD genotype benefitted the most from this treatment.

Indexed as

Genetic Association StudiesGenetic Predisposition to DiseaseDiabetic NephropathiesFemaleGene FrequencyHumansMaleMiddle AgedPeptidyl-Dipeptidase AProtective AgentsValsartanACE protein, humanPeptidyl-Dipeptidase AProtective AgentsValsartanAngiotensin converting enzymediabetesdiabetes mellitus Type 2diabetic kidney diseaseend stage renal diseasegene polymorphismskidney diseasemicroangiopathymicrovascular complicationsvalsartan

Identifiers

PMID27638852
PMCPMC5843882
OpenAlexW2519778034

What OpenQuestion holds

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Registered trials

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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.