Evidence map›Paper›PMID 27904696›Full record

ArticleAmerican journal of translational research2016

A study on the correlation between MTHFR promoter methylation and diabetic nephropathy.

Xiao-Hui Yang, Ren-Fang Cao, Yang Yu, Miao Sui, Tao Zhang, Jing-Yi Xu, Xiao-Mei Wang

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 16% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Accelerated epigenetic age in hypertension: a systematic review and meta-analysis.Hypertension research : official journal of the Japanese Society of Hypertension · 2026
    Pooled it
  2. Article
  3. Review
  4. Association Between DNA Methylation ofJournal of diabetes research · 2025
    Article
  5. Article
  6. Pathomechanisms of Diabetic Kidney Disease.Journal of clinical medicine · 2023
    Review
  7. Review
  8. Physical Activity Level InfluencesFrontiers in physiology · 2020
    Article
  9. Article
  10. Review
  11. TheDiabetology & metabolic syndrome · 2019
    Article
  12. Review
  13. Hypermethylation in the promoter of theDiabetology & metabolic syndrome · 2017
    Article
  14. 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 2 institutions in 2 countries.

Xiao-Hui YangDepartment of Endocrinology, Affiliated Zhongshan Hospital of Dalian University Dalian 116001, China.
Ren-Fang CaoDepartment of Outpatient, The Royal Hong Kong Slow Disease Hospital Dalian, China.
Yang YuDepartment of Endocrinology, Affiliated Zhongshan Hospital of Dalian University Dalian 116001, China.
Miao SuiDepartment of Endocrinology, Affiliated Zhongshan Hospital of Dalian University Dalian 116001, China.
Tao ZhangDepartment of Endocrinology, Affiliated Zhongshan Hospital of Dalian University Dalian 116001, China.
Jing-Yi XuDepartment of Endocrinology, Affiliated Zhongshan Hospital of Dalian University Dalian 116001, China.
Xiao-Mei WangDepartment of Endocrinology, Affiliated Zhongshan Hospital of Dalian University Dalian 116001, China.
Affiliated Zhongshan Hospital of Dalian University · CNRoyal Hospital · OM

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveIn order to observe the relationship between MTHFR promoter and DN, the determinations on MTHFR promoter methylation level and expression of HCY from DN patients have been carried out.

methodsAccording to the Diabetes diagnosis and classification standard from WHO in 1999, 85 patients with DM diagnosed by Endocrinology and 30 healthy participants from our medical examination center were chosen as control specimen to study in this paper. All this specimen were divided into A, B, C and D four groups , which are corresponding simple diabetes mellitus group (SDM), early diabetic nephropathy group (EDN), clinical diabetic nephropathy group (CDN) and normal control group. And then, all common materials and clinical experiments data have been collected respectively. (1) Extracted the peripheral blood DNA of each group and determinate the methylation status of MTHFR gene promoter by PCR (MSP). (2) Determinated the serum HCY protein expression of each group.

results(1) The MTHFR promoter methylation of SDM and diabetic nephropathy group are wear off comparied with normal control group. And MTHFR promoter was in demethylation state in normal control group, a slightly weak in SDN, a obviously weak in early diabetic nephropathy group; the MTHFR promoter was in methylation state in clinical diabetic nephropathy group. (2) The HCY protein of simple diabetes mellitus group, early diabetic nephropathy group and clinical diabetic nephropathy group are Pitch with normal control group. HCY protein level of each group are as 7.41±1.61 umol/L, 10.34±2.89 umol/L, 10.95±5.89 umol/L and 13.03±6.14 umol/L corresponding normal control group, simple diabetes mellitus group, early diabetic nephropathy group and clinical diabetic nephropathy group. And there is no statistical significance about the differences among four groups.

conclusionThe demethylation state of MTHFR promoter was obviously weaker in clinical diabetic nephropathy group than in SDM. The level of serum HCY was obviously higher in clinical diabetic nephropathy group than in SDM. It suggested that MTHFR promoter demethylation may be involoed in the pathogenesis of DN.

Indexed as

Diabetes meilltusdiabetic nephropathyDNA methylationhomocysteinemethylenetetrahydrofolate reductase

Identifiers

PMID27904696
PMCPMC5126338
OpenAlexW2593360419

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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.