Evidence map›Paper›PMID 28464463›Full record

ArticleCNS neuroscience & therapeutics2017

Resting-state connectivity and modulated somatomotor and default-mode networks in Huntington disease.

Cristina Sánchez-Castañeda, Francesco de Pasquale, Chiara Falletta Caravasso, Massimo Marano, Sabrina Maffi, Simone Migliore, Umberto Sabatini, Ferdinando Squitieri

Abstract read
In one paragraph

Article in CNS neuroscience & therapeutics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 2 pooled it
1.0field-weighted citation impact, top 30% 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

12 citing papers in PubMed, 2 syntheses or guidelines pooled it, 20 citations in OpenAlex.

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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

8 authors at 5 institutions in 2 countries.

Cristina Sánchez-CastañedaDepartment of Medicine, School of Medicine and Health Sciences, IDIBAPS, Neuroscience Institute, University of Barcelona, Barcelona, Spain.
Francesco de PasqualeRadiology Department, IRCCS Santa Lucia Foundation, Rome, Italy.
Chiara Falletta CaravassoRadiology Department, IRCCS Santa Lucia Foundation, Rome, Italy.
Massimo MaranoHuntington and Rare Diseases Unit, IRCSS Casa Sollievo della Sofferenza Hospital, San Giovanni Rotondo, Italy.
Sabrina MaffiHuntington and Rare Diseases Unit, IRCSS Casa Sollievo della Sofferenza Hospital, San Giovanni Rotondo, Italy.
Simone MiglioreHuntington and Rare Diseases Unit, IRCSS Casa Sollievo della Sofferenza Hospital, San Giovanni Rotondo, Italy.
Umberto SabatiniRadiology Department, IRCCS Santa Lucia Foundation, Rome, Italy.
Ferdinando SquitieriHuntington and Rare Diseases Unit, IRCSS Casa Sollievo della Sofferenza Hospital, San Giovanni Rotondo, Italy.ORCID http://orcid.org/0000-0002-7397-1727
Casa Sollievo della Sofferenza · ITFondazione Santa Lucia · ITInstitut d'Investigacions Biomèdiques de Barcelona · ESMagna Graecia University · ITUniversity of Teramo · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsTo analyze brain functional connectivity in the somatomotor and default-mode networks (DMNs) of patients with Huntington disease (HD), its relationship with gray matter (GM) volume loss, and functional changes after pridopidine treatment.

methodsTen patients and ten untreated controls underwent T1-weighted imaging and resting-state functional magnetic resonance imaging (fMRI); four patients were also assessed after 3 months of pridopidine treatment (90 mg/d). The seed-based functional connectivity patterns from the posterior cingulate cortex and the supplementary motor area (SMA), considered cortical hubs of the DMN and somatomotor networks, respectively, were computed. FMRIB Software Library voxel-based morphometry measured GM volume.

resultsPatients had GM volume decrease in all cortical and subcortical areas of the somatomotor network with preservation of the SMA, and increased somatomotor and DMN connectivity. In DMN structures, functional connectivity impairment preceded volume loss. Pridopidine reduced the intensity of these aberrant connections.

conclusionThe abnormal connectivity of the somatomotor and DMN observed in HD patients may represent an early dysfunction marker, as it preceded volume loss in DMN. Pridopidine reduced connectivity of these networks in all four treated patients, suggesting that connectivity is sensitive to treatment response.

Indexed as

Models, NeurologicalRestAdultAgedBrain MappingFemaleGray MatterGyrus CinguliHumansHuntingtin ProteinHuntington DiseaseImage Processing, Computer-AssistedMagnetic Resonance ImagingMaleMiddle AgedMotor CortexHTT protein, humanHuntingtin ProteinOxygenPiperidinespridopidinebiomarkerHuntington diseasemagnetic resonance imagingpridopidine

Identifiers

PMID28464463
PMCPMC6492661
OpenAlexW2610225842

What OpenQuestion holds

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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.