Evidence map›Paper›PMID 36109436›Full record

ArticleGeroScience2023

Episodic memory dysfunction and hypersynchrony in brain functional networks in cognitively intact subjects and MCI: a study of 379 individuals.

Brenda Chino, Pablo Cuesta, Javier Pacios, Jaisalmer de Frutos-Lucas, Lucía Torres-Simón, Sandra Doval, Alberto Marcos, Ricardo Bruña, Fernando Maestú

Open access · hybridAbstract read
In one paragraph

Article in GeroScience, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 2 pooled it
1.2field-weighted citation impact, top 23% 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

6 citing papers in PubMed, 2 syntheses or guidelines pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Review
  6. 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

9 authors at 3 institutions in 2 countries.

Brenda ChinoInstitute of Neuroscience, Autonomous University of Barcelona, Barcelona, Spain. brendanadia.chino@autonoma.cat.ORCID 0000-0002-8169-263X
Pablo CuestaCenter for Cognitive and Computational Neuroscience, Complutense University of Madrid, Madrid, Spain.
Javier PaciosCenter for Cognitive and Computational Neuroscience, Complutense University of Madrid, Madrid, Spain.
Jaisalmer de Frutos-LucasCenter for Cognitive and Computational Neuroscience, Complutense University of Madrid, Madrid, Spain.
Lucía Torres-SimónCenter for Cognitive and Computational Neuroscience, Complutense University of Madrid, Madrid, Spain.
Sandra DovalCenter for Cognitive and Computational Neuroscience, Complutense University of Madrid, Madrid, Spain.
Alberto MarcosInstituto de Investigación Sanitaria San Carlos (IdISSC), Madrid, Spain.
Ricardo BruñaCenter for Cognitive and Computational Neuroscience, Complutense University of Madrid, Madrid, Spain.
Fernando MaestúCenter for Cognitive and Computational Neuroscience, Complutense University of Madrid, Madrid, Spain.
Universidad Complutense de Madrid · ESEdith Cowan University · AUHospital Clínico San Carlos · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Delayed recall (DR) impairment is one of the most significant predictive factors in defining the progression to Alzheimer's disease (AD). Changes in brain functional connectivity (FC) could accompany this decline in the DR performance even in a resting state condition from the preclinical stages to the diagnosis of AD itself, so the characterization of the relationship between the two phenomena has attracted increasing interest. Another aspect to contemplate is the potential moderator role of the APOE genotype in this association, considering the evidence about their implication for the disease. 379 subjects (118 mild cognitive impairment (MCI) and 261 cognitively intact (CI) individuals) underwent an extensive evaluation, including MEG recording. Applying cluster-based permutation test, we identified a cluster of differences in FC and studied which connections drove such an effect in DR. The moderation effect of APOE genotype between FC results and delayed recall was evaluated too. Higher FC in beta band in the right occipital region is associated with lower DR scores in both groups. A significant anteroposterior link emerged in the seed-based analysis with higher values in MCI. Moreover, APOE genotype appeared as a moderator between beta FC and DR performance only in the CI group. An increased beta FC in the anteroposterior brain region appears to be associated with lower memory performance in MCI. This finding could help discriminate the pattern of the progression of healthy aging to MCI and the relation between resting state and memory performance.

Indexed as

Alzheimer DiseaseCognitive DysfunctionMemory, EpisodicApolipoproteins EBrainHumansApolipoproteins ECognitively normalDelayed recallFunctional connectivityMCIMEG

Identifiers

PMID36109436
PMCPMC9886758
OpenAlexW4295931480

What OpenQuestion holds

Textmetadata
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.