Evidence map›Paper›PMID 40747637›Full record

ArticleAlzheimer's & dementia : the journal of the Alzheimer's Association2025

Neurovascular coupling and functional connectivity changes through the Alzheimer's disease spectrum: Effects of simvastatin treatment.

Aline R Zimmer, Miled Bourourou, Frédéric Lesage, Edith Hamel

Abstract read
In one paragraph

Article in Alzheimer's & dementia : the journal of the Alzheimer's Association, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Simvastatin rescues cognitive impairment in an AβNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Article
  2. A cerebrospinal fluid blood-brain barrier dysfunction score is associated with progression from mild cognitive impairment to Alzheimer's disease.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
    Article
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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

4 authors.

Aline R ZimmerGraduate Program in Pharmaceutical Science, Federal University of Rio Grande do Sul (UFRGS), Porto Alegre, Brazil.ORCID 0000-0002-8309-7068
Miled BourourouLaboratory of Cerebrovascular Research, Montreal Neurological Institute-Hospital, McGill University, Montréal, Quebec, Canadá.
Frédéric LesageDepartment of Electrical Engineering, Ecole Polytechnique de Montréal, Montréal, Quebec, Canadá.
Edith HamelLaboratory of Cerebrovascular Research, Montreal Neurological Institute-Hospital, McGill University, Montréal, Quebec, Canadá.

Funding

Canada First Research Excellence FundCanadian Consortium on Neurodegeneration in AgingCanadian Institutes of Health Research (CIHR) 436352Canadian Institutes of Health Research (CIHR) MOP-126001Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES/PRINT) 88887.363553/2019-00Fonds de recherche du Québec-SantéMcGill Healthy Brains Healthy LivesNatural Sciences and Engineering Research Council of Canada RGPIN-2017-06140Quebec's Ministère de l'Économie et de l'Innovation
6 · The paper itself

Abstract

introductionAlzheimer's disease (AD) is a leading cause of dementia, with vascular dysfunction being an early pathogenic event. Cardiovascular interventions show therapeutic promise, hence may improve neurovascular coupling (NVC) and resting-state functional connectivity (RSFC) hemodynamic responses.

methodsNVC and RSFC were recorded longitudinally in control and AD transgenic mice treated or not with simvastatin (SV) using optical imaging of intrinsic signals (OIS), together with memory testing.

resultsAD mice showed early decreases in NVC and bilateral connectivity (BC) in motor and cingulate cortex, and hypoconnectivity within the sensory-motor network. Early default-mode network (DMN) hyperconnectivity was followed by hypoconnectivity, together with a decreased BC in somatosensory (S) cortex. SV restored NVC, prevented aberrant DMN hyperconnectivity, improved BC of S, and preserved memory. DISCUSSION: Our results indicate that OIS can detect early AD-related changes in NVC and RSFC, and that a preventive cardiovascular strategy may bear therapeutic promise in at-risk individuals. HIGHLIGHTS: Optical imaging of intrinsic signals captures Alzheimer's disease (AD) progression and response to therapy. Neurovascular coupling (NVC) and resting-state functional connectivity (RSFC) disruptions precede memory decline in AD transgenic mice. Simvastatin prevented NVC and AD-specific RSFC disruptions and protected memory. This study supports translational value of hemodynamic signal in early AD detection.

Indexed as

Alzheimer DiseaseBrainHydroxymethylglutaryl-CoA Reductase InhibitorsNerve NetNeurovascular CouplingSimvastatinAnimalsDisease Models, AnimalHumansMaleMiceMice, TransgenicHydroxymethylglutaryl-CoA Reductase InhibitorsSimvastatinAlzheimer's diseaseneurovascular couplingresting‐state functional connectivitysimvastatin

Identifiers

PMID40747637
PMCPMC12314550

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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.