Evidence map›Paper›PMID 24558171›Full record

ArticleAmerican journal of Alzheimer's disease and other dementias2014

Gene expression profiles of entorhinal cortex in Alzheimer's disease.

Bingqian Ding, Yan Xi, Ming Gao, Zhenjiang Li, Chenyang Xu, Shaokang Fan, Weiya He

Open access · greenAbstract read
In one paragraph

Article in American journal of Alzheimer's disease and other dementias, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 2 pooled it
1.4field-weighted citation impact, top 19% 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, 2 syntheses or guidelines pooled it, 34 citations in OpenAlex.

  1. Pooled it
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  20. A transcriptional signature of Alzheimer's disease is associated with a metastable subproteome at risk for aggregation.Proceedings of the National Academy of Sciences of the United States of America · 2016
    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 1 country.

Bingqian DingDepartment of Neurosurgery, Huaihe Hospital of Henan University, Kaifeng, China.
Yan XiDepartment of Pathology, Medical College of Henan University, Kaifeng, China.
Ming GaoDepartment of Neurosurgery, Huaihe Hospital of Henan University, Kaifeng, China.
Zhenjiang LiDepartment of Neurosurgery, Huaihe Hospital of Henan University, Kaifeng, China.
Chenyang XuDepartment of Neurosurgery, Huaihe Hospital of Henan University, Kaifeng, China.
Shaokang FanDepartment of Neurosurgery, Huaihe Hospital of Henan University, Kaifeng, China.
Weiya HeDepartment of Neurosurgery, Huaihe Hospital of Henan University, Kaifeng, China weiyahe@126.com.
Henan University Huaihe Hospital and Huaihe Clinical Institute · CNHenan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The incidence of Alzheimer's disease (AD) has been increasing in the recent years but the underlying mechanisms remain uncertain. This study aimed to analyze the differentially expressed genes (DEGs) in entorhinal cortex with AD and identify featured genes related to AD. Gene expression profile GSE5281 was downloaded from Gene Expression Omnibus, including 10 AD and 13 control samples. Differentially expressed genes were identified by Student t test including 119 upregulated and 591 downregulated DEGs. Then, we obtained 14 enrichment Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways among which 11 pathways were significantly enriched (adjusted P value < .05). The KEGG pathway network which was constructed by 14 KEGG pathways showed that 6-phosphofructokinase, muscle type, phosphoglucomutase 1, aldolase A, and adolase C had high degree. Glycometabolism pathways network which was constructed by 4 glycometabolism pathways showed that adenosine triphosphate (ATP) synthase, H+transporting, mitochondrial F1 complex ATP5B, ATP5C1, ATP5D, and ATP5G1 had high degree related to ATP metabolism. These findings suggested that these genes with high degree may be the underlying potential therapeutic targets for AD.

Indexed as

Gene Expression ProfilingAlzheimer DiseaseEntorhinal CortexGene ExpressionGene Regulatory NetworksGenetic Predisposition to DiseaseGenetic TestingHumansAlzheimer’s diseasedifferentially expressed genesentorhinal cortexglycometabolism pathway

Identifiers

PMID24558171
PMCPMC10852653
OpenAlexW2045013649

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.