Evidence map›Paper›PMID 34278511›Full record

ArticleNeuroradiology2022

Differences in structural and functional default mode network connectivity in amyloid positive mild cognitive impairment: a longitudinal study.

Thamires Naela Cardoso Magalhães, Christian Luiz Baptista Gerbelli, Luciana Ramalho Pimentel-Silva, Brunno Machado de Campos, Thiago Junqueira Ribeiro de Rezende, Liara Rizzi, Helena Passarelli Giroud Joaquim, Leda Leme Talib, Orestes Vicente Forlenza, Fernando Cendes and 1 more

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Article in Neuroradiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

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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

11 authors.

Thamires Naela Cardoso MagalhãesLaboratory of Neuroimaging, Department of Neurology - Medical Sciences School, University of Campinas (UNICAMP), Rua Tessália Vieira de Camargo 126, Campinas, SP, 13083-887, Brazil. thamiresncm@hotmail.com.ORCID http://orcid.org/0000-0002-0825-1387
Christian Luiz Baptista GerbelliLaboratory of Neuroimaging, Department of Neurology - Medical Sciences School, University of Campinas (UNICAMP), Rua Tessália Vieira de Camargo 126, Campinas, SP, 13083-887, Brazil.
Luciana Ramalho Pimentel-SilvaLaboratory of Neuroimaging, Department of Neurology - Medical Sciences School, University of Campinas (UNICAMP), Rua Tessália Vieira de Camargo 126, Campinas, SP, 13083-887, Brazil.
Brunno Machado de CamposLaboratory of Neuroimaging, Department of Neurology - Medical Sciences School, University of Campinas (UNICAMP), Rua Tessália Vieira de Camargo 126, Campinas, SP, 13083-887, Brazil.
Thiago Junqueira Ribeiro de RezendeLaboratory of Neuroimaging, Department of Neurology - Medical Sciences School, University of Campinas (UNICAMP), Rua Tessália Vieira de Camargo 126, Campinas, SP, 13083-887, Brazil.
Liara RizziLaboratory of Neuroimaging, Department of Neurology - Medical Sciences School, University of Campinas (UNICAMP), Rua Tessália Vieira de Camargo 126, Campinas, SP, 13083-887, Brazil.
Helena Passarelli Giroud JoaquimLaboratory of Neurosciences, (LIM 27), Department and Institute of Psychiatry, University of São Paulo (USP), São Paulo, Brazil.
Leda Leme TalibLaboratory of Neurosciences, (LIM 27), Department and Institute of Psychiatry, University of São Paulo (USP), São Paulo, Brazil.
Orestes Vicente ForlenzaLaboratory of Neurosciences, (LIM 27), Department and Institute of Psychiatry, University of São Paulo (USP), São Paulo, Brazil.
Fernando CendesLaboratory of Neuroimaging, Department of Neurology - Medical Sciences School, University of Campinas (UNICAMP), Rua Tessália Vieira de Camargo 126, Campinas, SP, 13083-887, Brazil.
Marcio Luiz Figueredo BalthazarLaboratory of Neuroimaging, Department of Neurology - Medical Sciences School, University of Campinas (UNICAMP), Rua Tessália Vieira de Camargo 126, Campinas, SP, 13083-887, Brazil.

Funding

Fundação de Amparo à Pesquisa do Estado de São Paulo 2011/17092-0Fundação de Amparo à Pesquisa do Estado de São Paulo 2013/07559-3Fundação de Amparo à Pesquisa do Estado de São Paulo 2017/13906-9Fundação de Amparo à Pesquisa do Estado de São Paulo 2018/15571-7
6 · The paper itself

Abstract

purposeDefault mode network (DMN) has emerged as a potential biomarker of Alzheimer's disease (AD); however, it is not clear whether it can differentiate amnestic mild cognitive impairment with altered amyloid (aMCI-Aβ +) who will evolve to AD. We evaluated if structural and functional connectivity (FC), hippocampal volumes (HV), and cerebrospinal fluid biomarkers (CSF-Aβ

methodsForty-eight individuals (18 normal controls and 30 aMCI subjects in the AD continuum - with altered Aβ

resultsDuring follow-up, 8/30 aMCI-Aβ + converted (26.6%) to AD dementia. There were no differences in multivariate analysis between groups in CSF biomarkers (p = 0.092) or at DMN functional connectivity (p = 0.814). aMCI-Aβ + converters had smaller right HV than controls (p = 0.013), and greater right cingulum parahippocampal bundle radial diffusivity than controls (p < 0.001) and non-converters (p = 0.036).

conclusionIn this exploratory study, structural, but not functional, DMN connectivity alterations may differentiate aMCI-Aβ + subjects who converted to AD dementia.

Indexed as

Alzheimer DiseaseCognitive DysfunctionBrainDefault Mode NetworkDiffusion Tensor ImagingHumansLongitudinal StudiesMagnetic Resonance ImagingNeuropsychological TestsDefault mode network (DMN)DementiaDiffusion tensor imagingFunctional MRIMild cognitive impairment

Identifiers

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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.