Evidence map›Paper›PMID 27982479›Full record

ReviewJournal of cellular biochemistry2017

Hypermethylation: Causes and Consequences in Skeletal Muscle Myopathy.

Avisek Majumder, Jyotirmaya Behera, Nevena Jeremic, Suresh C Tyagi

Open access · greenAbstract readReview
In one paragraph

Review in Journal of cellular biochemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
3.6field-weighted citation impact, top 7% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

  1. Pooled it
  2. Significance of GSH and HRedox report : communications in free radical research · 2026
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  7. NArchives of microbiology · 2024
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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

4 authors at 1 institution in 1 country.

Avisek MajumderDepartment of Biochemistry and Molecular Genetics, School of Medicine, University of Louisville, Louisville, Kentucky, 40202.
Jyotirmaya BeheraDepartment of Physiology, School of Medicine, University of Louisville, Louisville, Kentucky, 40202.
Nevena JeremicDepartment of Physiology, School of Medicine, University of Louisville, Louisville, Kentucky, 40202.
Suresh C TyagiDepartment of Biochemistry and Molecular Genetics, School of Medicine, University of Louisville, Louisville, Kentucky, 40202.
University of Louisville · US

Funding

Reversing diabetic muscle myopathy by exercise and exosomesR01HL074185 · NHLBI · UNIVERSITY OF LOUISVILLE · PI TYAGI, SURESH C. · 2003 to 2018
$5.7M
Remote Hind Limb Ischemia Mechanism of CardioprotectionR01HL139047 · NHLBI · UNIVERSITY OF LOUISVILLE · PI TYAGI, SURESH C. · 2018 to 2021
$1.8M
Reversing Skeletal Muscle Myopathy by Hydrogen SulfideR01AR071789 · NIAMS · UNIVERSITY OF LOUISVILLE · PI TYAGI, SURESH C. · 2018 to 2023
$1.7M
NHLBI NIH HHS R01 HL074185NHLBI NIH HHS R01 HL139047NIAMS NIH HHS R01 AR071789
6 · The paper itself

Abstract

A detrimental consequence of hypermethylation is hyperhomocysteinemia (HHcy), that causes oxidative stress, inflammation, and matrix degradation, which leads to multi-pathology in different organs. Although, it is well known that hypermethylation leads to overall gene silencing and hypomethylation leads to overall gene activation, the role of such process in skeletal muscle dysfunction during HHcy condition is unclear. In this study, we emphasized the multiple mechanisms including epigenetic alteration by which HHcy causes skeletal muscle myopathy. This review also highlights possible role of methylation, histone modification, and RNA interference in skeletal muscle dysfunction during HHcy condition and potential therapeutic molecules, putative challenges, and methodologies to deal with HHcy mediated skeletal muscle dysfunction. We also highlighted that B vitamins (mainly B12 and B6), with folic acid supplementation, could be useful as an adjuvant therapy to reverse these consequences associated with this HHcy conditions in skeletal muscle. However, we would recommend to further study involving long-term trials could help to assess efficacy of the use of these therapeutic agents. J. Cell. Biochem. 118: 2108-2117, 2017. © 2017 Wiley Periodicals, Inc.

Indexed as

Epigenesis, GeneticAnimalsDNA MethylationFolic AcidHistonesHomocysteineHumansHyperhomocysteinemiaMetforminMuscle, SkeletalMuscular DiseasesOxidative StressRNA InterferenceThiazolidinedionesVitamin B 12Vitamin B 6Folic AcidHistonesHomocysteineMetforminThiazolidinedionesVitamin B 12Vitamin B 6ECM REMODELINGHOMOCYSTEINEHYPERMETHYLATIONMUSCLE DYSFUNCTIONOXIDATIVE STRESS

Identifiers

PMID27982479
PMCPMC6563903
OpenAlexW2567545900

What OpenQuestion holds

Textmetadata
LicenceTDM
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.