Evidence map›Paper›PMID 36337705›Full record

ArticleFrontiers in aging neuroscience2022

Brain signal complexity in adults with Down syndrome: Potential application in the detection of mild cognitive impairment.

Alberto Fernández, Federico Ramírez-Toraño, Ricardo Bruña, Pilar Zuluaga, Susanna Esteba-Castillo, Daniel Abásolo, Fernando Moldenhauer, Elizabeth Shumbayawonda, Fernando Maestú, Javier García-Alba

Open access · goldAbstract read
In one paragraph

Article in Frontiers in aging neuroscience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. The entropic brain today.Brain : a journal of neurology · 2026
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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 6 institutions in 2 countries.

Alberto FernándezDepartment of Legal Medicine, Psychiatry and Pathology, Universidad Complutense de Madrid, Madrid, Spain.
Federico Ramírez-TorañoCenter for Cognitive and Computational Neuroscience, Universidad Complutense de Madrid, Madrid, Spain.
Ricardo BruñaCenter for Cognitive and Computational Neuroscience, Universidad Complutense de Madrid, Madrid, Spain.
Pilar ZuluagaStatistics & Operations Research Department, Faculty of Medicine, Universidad Complutense de Madrid, Madrid, Spain.
Susanna Esteba-CastilloNeurodevelopmental Group, Girona Biomedical Research Institute-IDIBGI, Institute of Health Assistance (IAS), Parc Hospitalari Martí i Julià, Girona, Spain.
Daniel AbásoloCentre for Biomedical Engineering, School of Mechanical Engineering Sciences, University of Surrey, Guildford, United Kingdom.
Fernando MoldenhauerAdult Down Syndrome Unit, Internal Medicine Department, Health Research Institute, Hospital Universitario de La Princesa, Madrid, Spain.
Elizabeth ShumbayawondaCentre for Biomedical Engineering, School of Mechanical Engineering Sciences, University of Surrey, Guildford, United Kingdom.
Fernando MaestúCenter for Cognitive and Computational Neuroscience, Universidad Complutense de Madrid, Madrid, Spain.
Javier García-AlbaDepartment of Research and Psychology in Education, Universidad Complutense de Madrid, Madrid, Spain.
Universidad Complutense de Madrid · ESUniversity of Surrey · GBHospital Universitario de La Princesa · ESInstitut d'Investigació Biomèdica de Girona · ESInstituto de Investigación Sanitaria del Hospital Clínico San Carlos · ESUniversidad de La Laguna · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Down syndrome (DS) is considered the most frequent cause of early-onset Alzheimer's disease (AD), and the typical pathophysiological signs are present in almost all individuals with DS by the age of 40. Despite of this evidence, the investigation on the pre-dementia stages in DS is scarce. In the present study we analyzed the complexity of brain oscillatory patterns and neuropsychological performance for the characterization of mild cognitive impairment (MCI) in DS. Materials and methods: Lempel-Ziv complexity (LZC) values from resting-state magnetoencephalography recordings and the neuropsychological performance in 28 patients with DS [control DS group (CN-DS) ( Results: Lempel-Ziv complexity was lowest in the frontal region within the MCI-DS group, while the CN-DS group showed reduced values in parietal areas when compared with the CN-no-DS group. Also, the CN-no-DS group exhibited the expected pattern of significant increase of LZC as a function of age, while MCI-DS cases showed a decrease. The combination of reduced LZC values and a divergent trajectory of complexity evolution with age, allowed the discrimination of CN-DS vs. MCI-DS patients with a 92.9% of sensitivity and 85.7% of specificity. Finally, a pattern of mnestic and praxic impairment was significantly associated in MCI-DS cases with the significant reduction of LZC values in frontal and parietal regions ( Conclusion: Brain signal complexity measured with LZC is reduced in DS and its development with age is also disrupted. The combination of both features might assist in the detection of MCI within this population.

Indexed as

adultbrain signal complexityDown syndromemagnetoencephalographymild cognitive impairmentneuropsychological performance

Identifiers

PMID36337705
PMCPMC9631477
OpenAlexW4306868880

What Socratic holds

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LicenceCC BY
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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 Socratic graph.