Evidence map›Paper›PMID 26099307›Full record

ArticleMolecular neurobiology2016

Common Aging Signature in the Peripheral Blood of Vascular Dementia and Alzheimer's Disease.

Hongbo Luo, Guangchun Han, Jiajia Wang, Fan Zeng, Yuanming Li, Shaoju Shao, Fuhai Song, Zhouxian Bai, Xing Peng, Yan-Jiang Wang and 2 more

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular neurobiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–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

8 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Addition of AβNeuropsychiatric disease and treatment · 2021
    Article
  5. Article
  6. Article
  7. Article
  8. Towards Personalized Intervention for Alzheimer's Disease.Genomics, proteomics & bioinformatics · 2016
    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

12 authors.

Hongbo LuoDepartment of Neurology, Lanzhou General Hospital, Lanzhou military Area Command, Lanzhou, Gansu, 730050, China.
Guangchun HanCAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing, 100101, China.
Jiajia WangCAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing, 100101, China.
Fan ZengDepartment of Neurology and Center for Clinical Neuroscience, Daping Hospital, Third Military Medical University, Chongqing, 100053, China.
Yuanming LiDepartment of Neurology, Lanzhou General Hospital, Lanzhou military Area Command, Lanzhou, Gansu, 730050, China.
Shaoju ShaoDepartment of Neurology, Lanzhou General Hospital, Lanzhou military Area Command, Lanzhou, Gansu, 730050, China.
Fuhai SongCAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing, 100101, China.
Zhouxian BaiCAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing, 100101, China.
Xing PengCAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing, 100101, China.
Yan-Jiang WangDepartment of Neurology and Center for Clinical Neuroscience, Daping Hospital, Third Military Medical University, Chongqing, 100053, China.
Xiangqun ShiDepartment of Neurology, Lanzhou General Hospital, Lanzhou military Area Command, Lanzhou, Gansu, 730050, China. shixq_2003@163.com.
Hongxing LeiCAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing, 100101, China. leihx@big.ac.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alzheimer's disease (AD) and vascular dementia (VaD) are the two most dominant forms of dementia in elderly people. Due to the large overlap between AD and VaD in clinical observations, great controversies exist regarding the distinction and connection between these two types of senile dementia. Here for the first time, we resort to the gene expression pattern of the peripheral blood to compare AD and VaD objectively. In our previous work, we have demonstrated that the dysregulation of gene expression in AD is unique among the examined diseases including neurological diseases, cancer, and metabolic diseases. In this study, we found that the dysregulation of gene expression in AD and VaD is quite similar to each other at both functional and gene levels. Interestingly, the dysregulation started at the early stages of the diseases, namely mild cognitive impairment (MCI) and vascular cognitive impairment (VCI). We have also shown that this signature is distinctive from that of peripheral vascular diseases. Comparison with aging studies revealed that the most profound change in AD and VaD, namely ribosome, is consistent with the accelerated aging scenario. This study may have implications to the common mechanism between AD and VaD.

Indexed as

Gene Expression ProfilingAgedAgingAlzheimer DiseaseDatabases, GeneticDementia, VascularDisease ProgressionHumansS100A12 ProteinS100A12 ProteinS100A12 protein, humanAlzheimer’s diseaseGene expressionPeripheral bloodRibosomeVascular dementia

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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.