Evidence map›Paper›PMID 31781662›Full record

ArticleJournal of diabetes research2019

The Association between Genomic DNA Methylation and Diabetic Peripheral Neuropathy in Patients with Type 2 Diabetes Mellitus.

Hong-Hong Zhang, Xingfa Han, Mengmeng Wang, Qingfang Hu, Sicheng Li, Meng Wang, Ji Hu

Open access · goldAbstract readComparative Study
In one paragraph

Article in Journal of diabetes research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

19 citing papers in PubMed, 42 citations in OpenAlex.

  1. Review
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  7. Metabolic memory: mechanisms and diseases.Signal transduction and targeted therapy · 2024
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  15. Article
  16. Review
  17. Epigenetic modifications in diabetes.Metabolism: clinical and experimental · 2022
    Review
  18. Article
  19. Genetic and Epigenomic Modifiers of Diabetic Neuropathy.International journal of molecular sciences · 2021
    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.

Hong-Hong ZhangDepartment of Endocrinology, The Second Affiliated Hospital, Soochow University, Suzhou 215004, China.ORCID https://orcid.org/0000-0002-6979-9020
Xingfa HanDepartment of Endocrinology, Suzhou Science and Technology Town Hospital, Nanjing Medical University, Suzhou 215004, China.
Mengmeng WangClinical Pharmacology Laboratory, The Second Affiliated Hospital, Soochow University, Suzhou 215004, China.
Qingfang HuDepartment of Endocrinology, The Second Affiliated Hospital, Soochow University, Suzhou 215004, China.
Sicheng LiDepartment of Endocrinology, The Second Affiliated Hospital, Soochow University, Suzhou 215004, China.
Meng WangClinical Pharmacology Laboratory, The Second Affiliated Hospital, Soochow University, Suzhou 215004, China.ORCID https://orcid.org/0000-0001-6679-5166
Ji HuDepartment of Endocrinology, The Second Affiliated Hospital, Soochow University, Suzhou 215004, China.ORCID https://orcid.org/0000-0002-3443-999X
Soochow University · CNNanjing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimDNA methylation is thought to be involved in regulating the expression of key genes and inducing diabetic peripheral neuropathy (DPN). However, clinically, the level of whole-genome DNA methylation and its relationship with DPN remains unclear.

methods186 patients with type 2 diabetes mellitus (T2DM) admitted to the Second Affiliated Hospital of Soochow University since Jul. 2016 to Oct. 2017 were enrolled in the study, including 100 patients in the DPN group and 86 patients in the non-DPN group, diagnosed with Toronto Clinical Scoring System (TCSS). Clinical and biochemical characteristics between the two groups were compared, and the correlations with TCSS scores were analyzed. Furthermore, the levels of genomic DNA methylation of leukocytes, measured with high-performance liquid chromatography-tandem mass spectrometry (LC-MS/MS), were also analyzed between the two groups.

resultsAge, duration, triglyceride (TG), total cholesterol (TC), low-density lipoprotein (LDL-C), creatinine, uric acid (UA), blood urea nitrogen (BUN), and C-reactive protein (CRP) were significantly higher in the DPN group. Estimated glomerular filtration rate (eGFR) and the level of genomic DNA methylation were much lower in the DPN group. Spearman correlation analysis showed that TCSS was positively correlated with age, duration, UA, and CRP and was negatively correlated with body mass index (BMI), eGFR, and the level of genomic DNA methylation. Interestingly, multiple stepwise regression analysis showed that only duration, genomic DNA methylation, and eGFR had impacts on TCSS. The results also showed that the levels of genomic DNA methylation did not change significantly whether or not there was renal injury. Another multiple stepwise regression analysis showed that TCSS and BMI were the influencing factors of genomic DNA methylation. Finally, we found that genomic DNA methylation levels were decreased significantly in the DPN group compared with the non-DPN group when the duration is ≥5 years or BMI ≥ 25 kg/m

conclusionLow level of genomic DNA methylation is a relative specific risk factor of diabetic peripheral neuropathy in patients with type 2 diabetes.

Indexed as

DNA MethylationBiomarkersBody Mass IndexCase-Control StudiesCross-Sectional StudiesDiabetes Mellitus, Type 2Diabetic NephropathiesDiabetic NeuropathiesFemaleGenetic Predisposition to DiseaseHumansMaleMiddle AgedPhenotypeRisk AssessmentRisk FactorsBiomarkers

Identifiers

PMID31781662
PMCPMC6875377
OpenAlexW2988888954

What OpenQuestion holds

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LicenceCC BY
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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.