Evidence map›Paper›PMID 28058582›Full record

ArticleMolecular neurobiology2018

Genome-Wide DNA Methylation Patterns Analysis of Noncoding RNAs in Temporal Lobe Epilepsy Patients.

Wenbiao Xiao, Yuze Cao, Hongyu Long, Zhaohui Luo, Shuyu Li, Na Deng, Jianjian Wang, Xiaoyan Lu, Tianfeng Wang, Shangwei Ning and 2 more

Abstract read
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In one paragraph

Article in Molecular neurobiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

30 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. MicroRNAs in temporal lobe epilepsy: a systematic review.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2021
    Pooled it
  2. Article
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  6. Review
  7. Review
  8. Complexity in Genetic Epilepsies: A Comprehensive Review.International journal of molecular sciences · 2023
    Review
  9. The regulatory function of lncRNA and constructed network in epilepsy.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2023
    Review
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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

12 authors.

Wenbiao XiaoDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, 410008, China.
Yuze CaoDepartment of Neurology, The Second Affiliated Hospital, Harbin Medical University, Harbin, 150081, China.
Hongyu LongDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, 410008, China.
Zhaohui LuoDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, 410008, China.
Shuyu LiDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, 410008, China.
Na DengDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, 410008, China.
Jianjian WangDepartment of Neurology, The Second Affiliated Hospital, Harbin Medical University, Harbin, 150081, China.
Xiaoyan LuDepartment of Neurology, The Second Affiliated Hospital, Harbin Medical University, Harbin, 150081, China.
Tianfeng WangDepartment of Neurology, The Second Affiliated Hospital, Harbin Medical University, Harbin, 150081, China.
Shangwei NingCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, 150081, China. ningsw@ems.hrbmu.edu.cn.
Lihua WangDepartment of Neurology, The Second Affiliated Hospital, Harbin Medical University, Harbin, 150081, China. wanglh211@163.com.
Bo XiaoDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, 410008, China. mdboxiao@163.com.

Funding

National Natural Science Foundation of China 81371435National Natural Science Foundation of China 81401078
6 · The paper itself

Abstract

Temporal lobe epilepsy (TLE) is the most common form of adult epilepsy and frequently evolving drug resistance. Although there is growing consensus that noncoding ribonucleic acids (ncRNAs) are modulators of TLE, the knowledge about the deoxyribonucleic acid (DNA) methylation patterns of ncRNAs in TLE remains limited. In the current study, we constructed DNA methylation profiles from 30 TLE patients and 30 healthy controls for ncRNAs, primarily focusing on long ncRNAs (lncRNAs) and microRNAs (miRNAs), by reannotating data of DNA methylation BeadChip. Statistics analyses have revealed a global hypermethylation pattern in miRNA and lncRNA gene in TLE patients. Bioinformatic analyses have found aberrantly methylated miRNAs and lncRNAs are related to ion channel activity, drug metabolism, mitogen-activated protein kinase (MAPK) signaling pathway, and neurotrophin signaling pathway. Aberrantly methylated ncRNA and pathway target might be involved in TLE development and progression. The methylated and demethylated ncRNAs identified in this study provide novel insights for developing TLE biomarkers and potential therapeutic targets.

Indexed as

Genome, HumanAdultCluster AnalysisDNA MethylationEpilepsy, Temporal LobeFemaleHumansMaleMicroRNAsMolecular Sequence AnnotationRNA, UntranslatedMicroRNAsRNA, UntranslatedDNA methylationEpigeneticLong noncoding RNA (lncRNA)MicroRNA (miRNA)Temporal lobe epilepsy (TLE)

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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.