Evidence map›Paper›PMID 39529471›Full record

ArticleEuropean journal of neurology2025

Brain neurovascular coupling in amyotrophic lateral sclerosis: Correlations with disease progression and cognitive impairment.

Francesca Trojsi, Antonietta Canna, Minoo Sharbafshaaer, Federica di Nardo, Fabrizio Canale, Carla Passaniti, Maria Agnese Pirozzi, Marcello Silvestro, Ilaria Orologio, Antonio Russo and 4 more

Abstract read
In one paragraph

Article in European journal of neurology, 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.

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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

14 authors.

Francesca TrojsiDepartment of Advanced Medical and Surgical Sciences, MRI Research Center, Università degli Studi della Campania Luigi Vanvitelli, Naples, Italy.ORCID 0000-0002-3790-8018
Antonietta CannaDepartment of Advanced Medical and Surgical Sciences, MRI Research Center, Università degli Studi della Campania Luigi Vanvitelli, Naples, Italy.
Minoo SharbafshaaerDepartment of Advanced Medical and Surgical Sciences, MRI Research Center, Università degli Studi della Campania Luigi Vanvitelli, Naples, Italy.ORCID 0000-0001-9887-5304
Federica di NardoFirst Division of Neurology and Neurophysiopathology, AOU Università degli Studi della Campania 'Luigi Vanvitelli', Naples, Italy.
Fabrizio CanaleDepartment of Advanced Medical and Surgical Sciences, MRI Research Center, Università degli Studi della Campania Luigi Vanvitelli, Naples, Italy.ORCID 0009-0007-8435-0102
Carla PassanitiFirst Division of Neurology and Neurophysiopathology, AOU Università degli Studi della Campania 'Luigi Vanvitelli', Naples, Italy.
Maria Agnese PirozziDepartment of Advanced Medical and Surgical Sciences, MRI Research Center, Università degli Studi della Campania Luigi Vanvitelli, Naples, Italy.ORCID 0000-0002-4632-3513
Marcello SilvestroDepartment of Advanced Medical and Surgical Sciences, MRI Research Center, Università degli Studi della Campania Luigi Vanvitelli, Naples, Italy.
Ilaria OrologioDepartment of Advanced Medical and Surgical Sciences, MRI Research Center, Università degli Studi della Campania Luigi Vanvitelli, Naples, Italy.
Antonio RussoDepartment of Advanced Medical and Surgical Sciences, MRI Research Center, Università degli Studi della Campania Luigi Vanvitelli, Naples, Italy.
Mario CirilloDepartment of Advanced Medical and Surgical Sciences, MRI Research Center, Università degli Studi della Campania Luigi Vanvitelli, Naples, Italy.
Alessandro TessitoreDepartment of Advanced Medical and Surgical Sciences, MRI Research Center, Università degli Studi della Campania Luigi Vanvitelli, Naples, Italy.
Mattia SicilianoDepartment of Advanced Medical and Surgical Sciences, MRI Research Center, Università degli Studi della Campania Luigi Vanvitelli, Naples, Italy.
Fabrizio EspositoDepartment of Advanced Medical and Surgical Sciences, MRI Research Center, Università degli Studi della Campania Luigi Vanvitelli, Naples, Italy.ORCID 0000-0002-5099-9786

Funding

Ministero dell'Istruzione, dell'Università e della Ricerca NRRP project MNESYS (PE0000006, to NT)
6 · The paper itself

Abstract

background and purpose'Neurovascular coupling' (NVC) alterations, assessing the interplay between local cerebral perfusion and neural activity within a given brain region or network, may reflect neurovascular unit impairment in amyotrophic lateral sclerosis (ALS). The aim was to explore NVC as a correlation between the functional connectivity and cerebral blood flow within the large-scale resting-state functional magnetic resonance imaging brain networks in a sample of ALS patients compared to healthy controls (HCs).

methodsForty-eight ALS patients (30 males; mean age 60.64 ± 9.62 years) and 32 HC subjects (14 males; mean age 55.06 ± 16 years) were enrolled and underwent 3 T magnetic resonance imaging. ALS patients were screened by clinical and neuropsychological scales and were retrospectively classified as very fast progressors (VFPs), fast progressors and slow progressors (SPs).

resultsNeurovascular coupling reduction within the default mode network (DMN) (p = 0.005) was revealed in ALS patients compared to HCs, observing, for this network, significant NVC differences between VFP and SP groups. Receiver operating characteristic curve analysis showed that impaired NVC in the DMN at baseline best discriminated VFPs and SPs (area under the curve 75%). Significant correlations were found between NVC and the executive (r = 0.40, p = 0.01), memory (r = 0.32, p = 0.04), visuospatial ability (r = 0.40, p = 0.01) and non-ALS-specific (r = 0.40, p = 0.01) subscores of the Edinburgh Cognitive and Behavioural ALS Screen.

conclusionsThe reduction of brain NVC in the DMN may reflect largely distributed abnormalities of the neurovascular unit. NVC alterations in the DMN could play a role in anticipating a faster clinical progression in ALS patients, aiding patient selection and monitoring during clinical trials.

Indexed as

Amyotrophic Lateral SclerosisBrainCognitive DysfunctionDisease ProgressionMagnetic Resonance ImagingNeurovascular CouplingAdultAgedDefault Mode NetworkFemaleHumansMaleMiddle AgedNerve Netamyotrophic lateral sclerosiscognitive impairmentdefault mode networkdisease progressionneurovascular coupling

Identifiers

PMID39529471
PMCPMC11625914

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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.