Evidence map›Paper›PMID 30397880›Full record

ArticleJournal of molecular neuroscience : MN2018

NLRP1 and NTN1, Deregulated Blood Differentially Methylated Regions in Mild Cognitive Impairment Patients.

Min-Koo Park, Ji-Won Lee, Jeong-Chan Lee, Sung-Joo Hwang, Hyun Woong Roh, Chang Hyung Hong, Sang Joon Son

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of molecular neuroscience : MN, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 36% 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

2 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. 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.

Min-Koo ParkBio-Innovation Park, Erom, Inc., Chuncheon, Gangwon, 24427, Republic of Korea.
Ji-Won LeeBio-Innovation Park, Erom, Inc., Chuncheon, Gangwon, 24427, Republic of Korea.
Jeong-Chan LeeBio-Innovation Park, Erom, Inc., Chuncheon, Gangwon, 24427, Republic of Korea.
Sung-Joo HwangBio-Innovation Park, Erom, Inc., Chuncheon, Gangwon, 24427, Republic of Korea.
Hyun Woong RohDepartment of Brain Science, Ajou University School of Medicine, Suwon, Gyeonggi, 16499, Republic of Korea.
Chang Hyung HongDepartment of Psychiatry, Ajou University School of Medicine, Suwon, Gyeonggi, 16499, Republic of Korea.
Sang Joon SonDepartment of Psychiatry, Ajou University School of Medicine, Suwon, Gyeonggi, 16499, Republic of Korea. sjsonpsy@ajou.ac.kr.
Ajou University · KR

Funding

Small and Medium Business Administration (KR) S2261274
6 · The paper itself

Abstract

Epigenetic dysregulation has been known to be involved in neurodegenerative diseases, including amnestic mild cognitive impairment (MCI). The aim of this study was to investigate the genome-wide DNA methylation analysis, in order to identify epigenetic dysregulation in blood from patients with MCI. Here, we investigated whether epigenetic dysregulation in MCI and whether such an aberration could be detected in blood circulation. Genome-wide bisulfite sequencing targeted 84 million bases covering 3.7 million CpG sites was comparatively analyzed in MCI and control groups. And correlation between DNA methylation and transcriptomic changes was sought. Significant differentially methylated regions (DMRs) distinguishing the MCI and control groups were identified and functionally annotated. Most DMRs specific to MCI were enriched between - 2 kb and + 2 kb of the CpG island start sites located within or near gene promoters. Representative hypo- and hypermethylated DMRs in MCI were confirmed to be correlated to mRNA expression changes with the comparative delta Ct method. DNA methylation aberrations involving metal ion homeostasis, axon growth, inflammasome, and others in this study may be less-invasive, easily measurable blood biomarker candidates for MCI.

Indexed as

DNA MethylationAdaptor Proteins, Signal TransducingAgedAged, 80 and overApoptosis Regulatory ProteinsBiomarkersCognitive DysfunctionCpG IslandsEpigenesis, GeneticFemaleHumansMaleNetrin-1NLR ProteinsTranscriptomeAdaptor Proteins, Signal TransducingApoptosis Regulatory ProteinsBiomarkersNetrin-1NLRP1 protein, humanNLR ProteinsNTN1 protein, humanDifferentially methylated region (DMR)Mild cognitive impairment (MCI)NLRP1NTN1Reverse transcription-quantitative PCR (RT-QPCR)

Identifiers

PMID30397880
OpenAlexW2899661390

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.