Evidence map›Paper›PMID 37846762›Full record

ArticleHuman brain mapping2023

Morphological connectivity differences in Alzheimer's disease correlate with gene transcription and cell-type.

Huiying Yu, Yanhui Ding, Yongbin Wei, Martin Dyrba, Dong Wang, Xiaopeng Kang, Weizhi Xu, Kun Zhao, Yong Liu, Alzheimer's Disease Neuroimaging Initiative

Open access · goldAbstract read
In one paragraph

Article in Human brain mapping, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 11% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
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  3. Review
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  11. Beyond Macrostructure: Is There a Role for Radiomics Analysis in Neuroimaging ?Magnetic resonance in medical sciences : MRMS : an official journal of Japan Society of Magnetic Resonance in Medicine · 2024
    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

10 authors at 4 institutions in 2 countries.

Huiying YuSchool of Information Science and Engineering, Shandong Normal University, Jinan, China.ORCID 0009-0008-3289-0745
Yanhui DingSchool of Information Science and Engineering, Shandong Normal University, Jinan, China.
Yongbin WeiSchool of Artificial Intelligence, Beijing University of Posts and Telecommunications, Beijing, China.
Martin DyrbaGerman Center for Neurodegenerative Diseases (DZNE), Rostock, Germany.ORCID 0000-0002-3353-3167
Dong WangSchool of Information Science and Engineering, Shandong Normal University, Jinan, China.
Xiaopeng KangSchool of Artificial Intelligence, University of Chinese Academy of Sciences, Beijing, China.
Weizhi XuSchool of Information Science and Engineering, Shandong Normal University, Jinan, China.
Kun ZhaoSchool of Artificial Intelligence, Beijing University of Posts and Telecommunications, Beijing, China.ORCID 0000-0002-5196-100X
Yong LiuSchool of Artificial Intelligence, Beijing University of Posts and Telecommunications, Beijing, China.ORCID 0000-0002-1862-3121
Alzheimer's Disease Neuroimaging Initiative
Shandong Normal University · CNBeijing University of Posts and Telecommunications · CNBeijing Academy of Artificial Intelligence · CNGerman Center for Neurodegenerative Diseases · DE

Funding

Alzheimer's Disease Neuroimaging Initiative - SupplementU01AG024904 · NIA · NORTHERN CALIFORNIA INSTITUTE RES &EDUC · PI WEINER, MICHAEL W · 2004 to 2015
$121.0M
NIA NIH HHS U01 AG024904
6 · The paper itself

Abstract

Alzheimer's disease (AD) is one of the most prevalent forms of dementia in older individuals. Convergent evidence suggests structural connectome abnormalities in specific brain regions are linked to AD progression. The biological basis underpinnings of these connectome changes, however, have remained elusive. We utilized an individual regional mean connectivity strength (RMCS) derived from a regional radiomics similarity network to capture altered morphological connectivity in 1654 participants (605 normal controls, 766 mild cognitive impairment [MCI], and 283 AD). Then, we also explored the biological basis behind these morphological changes through gene enrichment analysis and cell-specific analysis. We found that RMCS probes of the hippocampus and medial temporal lobe were significantly altered in AD and MCI, with these differences being spatially related to the expression of AD-risk genes. In addition, gene enrichment analysis revealed that the modulation of chemical synaptic transmission is the most relevant biological process associated with the altered RMCS in AD. Notably, neuronal cells were found to be the most pertinent cells in the altered RMCS. Our findings shed light on understanding the biological basis of structural connectome changes in AD, which may ultimately lead to more effective diagnostic and therapeutic strategies for this devastating disease.

Indexed as

Alzheimer DiseaseCognitive DysfunctionConnectomeAgedBrainHumansMagnetic Resonance ImagingTemporal LobeTranscription, GeneticAlzheimer's diseasecell-typegene expressionregional radiomics similarity networkstructural connectomes

Identifiers

PMID37846762
PMCPMC10681645
OpenAlexW4387692359

What OpenQuestion holds

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LicenceCC BY
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.