Evidence map›Paper›PMID 31938263›Full record

ArticleInternational journal of clinical and experimental pathology2018

Sequence variation in microRNA-34a is associated with diabetes mellitus susceptibility in a southwest Chinese Han population.

Yan Sun, Rui Peng, Ailing Li, Luyu Zhang, Handeng Liu, Huiming Peng, Zheng Zhang

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.6field-weighted citation impact, top 38% 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

10 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Decreased Urinary Levels ofInternational journal of molecular sciences · 2020
    Article
  9. Association of microRNA gene polymorphisms with Type 2 diabetes mellitus: A systematic review and meta-analysis.Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences · 2020
    Review
  10. 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

7 authors at 1 institution in 1 country.

Yan SunMolecular Medicine and Cancer Research Center, Chongqing Medical University Chongqing 400016, China.
Rui PengDepartment of Bioinformatics, Chongqing Medical University Chongqing, China.
Ailing LiMolecular Medicine and Cancer Research Center, Chongqing Medical University Chongqing 400016, China.
Luyu ZhangMolecular Medicine and Cancer Research Center, Chongqing Medical University Chongqing 400016, China.
Handeng LiuMolecular Medicine and Cancer Research Center, Chongqing Medical University Chongqing 400016, China.
Huiming PengMolecular Medicine and Cancer Research Center, Chongqing Medical University Chongqing 400016, China.
Zheng ZhangMolecular Medicine and Cancer Research Center, Chongqing Medical University Chongqing 400016, China.
Chongqing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Type 2 diabetes mellitus (T2DM) and diabetic nephropathy (DN) seriously impact the prognosis and survival of patients. Abundant studies suggest that single nucleotide polymorphisms (SNPs) within regulatory regions of miRNAs modulate progression of various diseases including DM and DN. However, evidence for exploring the mechanism in DM and DN are still insufficient. This study was performed to discuss the association of SNPs in the regulatory region of hsa-miR-34a with DM or DN susceptibility in the southwest Chinese Han population. Three SNPs (rs12128240, rs2666433, rs6577555) in miR-34a were analyzed in the T2DM patients with or without DN and normal controls. RT-qPCR was performed to measure expression of miR-34a. Real-time PCR was used for amplification of SNPs. MiR-34a was over-expressed in T2DM and DM patients. Both the distribution of GG genotypes and the G allele frequency of rs2666433 were significantly different between the T2DM and control groups (

Indexed as

Diabetic nephropathypolymorphismtype 2 diabetes

Identifiers

PMID31938263
PMCPMC6958157
OpenAlexW3015130918

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.