Evidence map›Paper›PMID 31878257›Full record

ReviewInternational journal of molecular sciences2019

Modeling Resilience to Damage in Multiple Sclerosis: Plasticity Meets Connectivity.

Mario Stampanoni Bassi, Ennio Iezzi, Luigi Pavone, Georgia Mandolesi, Alessandra Musella, Antonietta Gentile, Luana Gilio, Diego Centonze, Fabio Buttari

Registry-linked trialOpen access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05811013 (Effects of Transcranial Static Magnetic Field Stimulation), which is not on this map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.1field-weighted citation impact, top 22% 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.

NCT05811013 narecruitingnot on this mapstarted 2023, after this paper: background citation

Effects of Transcranial Static Magnetic Field Stimulation (tSMS) in Progressive Multiple Sclerosis

TypeinterventionalSponsorNeuromed IRCCSRan2023 to 2026Enrolled40ConditionsProgressive Multiple SclerosisArmsTranscranial static magnetic field stimulation (tSMS), Sham Transcranial static magnetic field stimulation (tSMS)
3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Review
  3. RegenerativeAesthetic plastic surgery · 2025
    Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
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

9 authors at 3 institutions in 1 country.

Mario Stampanoni BassiUnit of Neurology & Neurorehabilitation, IRCCS Neuromed, 86077 Pozzilli (IS), Italy.
Ennio IezziUnit of Neurology & Neurorehabilitation, IRCCS Neuromed, 86077 Pozzilli (IS), Italy.
Luigi PavoneUnit of Neurology & Neurorehabilitation, IRCCS Neuromed, 86077 Pozzilli (IS), Italy.
Georgia MandolesiLaboratory of Synaptic Immunopathology, IRCCS San Raffaele Pisana, 00163 Rome, Italy.
Alessandra MusellaLaboratory of Synaptic Immunopathology, IRCCS San Raffaele Pisana, 00163 Rome, Italy.
Antonietta GentileLaboratory of Synaptic Immunopathology, IRCCS San Raffaele Pisana, 00163 Rome, Italy.
Luana GilioUnit of Neurology & Neurorehabilitation, IRCCS Neuromed, 86077 Pozzilli (IS), Italy.
Diego CentonzeUnit of Neurology & Neurorehabilitation, IRCCS Neuromed, 86077 Pozzilli (IS), Italy.
Fabio ButtariUnit of Neurology & Neurorehabilitation, IRCCS Neuromed, 86077 Pozzilli (IS), Italy.
Istituto Neurologico Mediterraneo · ITIstituto di Ricovero e Cura a Carattere Scientifico San RaffaeleSan Raffaele University of Rome · IT

Funding

Fondazione Italiana Sclerosi Multipla 2019/S/1Ministero della Salute Ricerca Correnteundefined <span style="color:gray;font-size:10px;">undefined</span> 5 × 1000 grant to IRCCS Neuromed
6 · The paper itself

Abstract

Multiple sclerosis (MS) is a chronic inflammatory disease of the central nervous system (CNS) characterized by demyelinating white matter lesions and neurodegeneration, with a variable clinical course. Brain network architecture provides efficient information processing and resilience to damage. The peculiar organization characterized by a low number of highly connected nodes (hubs) confers high resistance to random damage. Anti-homeostatic synaptic plasticity, in particular long-term potentiation (LTP), represents one of the main physiological mechanisms underlying clinical recovery after brain damage. Different types of synaptic plasticity, including both anti-homeostatic and homeostatic mechanisms (synaptic scaling), contribute to shape brain networks. In MS, altered synaptic functioning induced by inflammatory mediators may represent a further cause of brain network collapse in addition to demyelination and grey matter atrophy. We propose that impaired LTP expression and pathologically enhanced upscaling may contribute to disrupting brain network topology in MS, weakening resilience to damage and negatively influencing the disease course.

Indexed as

AnimalsBrainHumansInflammationLong-Term PotentiationMultiple SclerosisNeuronal Plasticitybrain networksconnectivityinflammationlong-term potentiation (LTP)multiple sclerosisresting state functional MRI (rs-fMRI)synaptic plasticitysynaptic scaling

Identifiers

PMID31878257
PMCPMC6981966
OpenAlexW2998665239

What OpenQuestion holds

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Registered trials

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.