Evidence map›Paper›PMID 30020560›Full record

ReviewBrain pathology (Zurich, Switzerland)2018

Exploring the heterogeneity of MS lesions using positron emission tomography: a reappraisal of their contribution to disability.

Bruno Stankoff, Emilie Poirion, Matteo Tonietto, Benedetta Bodini

2 registry-linked trialsOpen access · greenAbstract readReview
In one paragraph

Review in Brain pathology (Zurich, Switzerland), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.5field-weighted citation impact, top 11% 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.

NCT05147532 naunknown statusnot on this mapstarted 2022, after this paper: background citation

Remyelination in Multiple Sclerosis: a PET-MR Longitudinal Study Investigating Individual Profiles of Myelin Repair and the Contribution of Neuroinflammation

TypeinterventionalSponsorAssistance Publique - Hôpitaux de ParisRan2022 to 2024Enrolled80ConditionsMultiple Sclerosis, Inflammatory DiseaseArmsPET-MRI with [18F]-Florbetaben and PET-MRI with [18F]-DPA-714
NCT05783934 nacompletednot on this mapstarted 2021, after this paper: background citation

Evaluation of the Degree of Demyelination and Remyelination in Multiple Sclerosis (MS) Detected by Brain Positron Emission Tomography With Amyloid Markers (PET-CT 18F-Florbetaben) and Comparison With MRI Findings

TypeinterventionalSponsorIstituti Clinici Scientifici Maugeri SpARan2021 to 2024Enrolled6ConditionsMultiple SclerosisArms18F-florbetaben PET/CT
3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
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  3. Article
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  6. Article
  7. Neuroprotection in Cerebral Cortex Induced by the Pregnancy Hormone Estriol.Laboratory investigation; a journal of technical methods and pathology · 2023
    Article
  8. Article
  9. Innate immune cells and myelin profile in multiple sclerosis: a multi-tracer PET/MR study.European journal of nuclear medicine and molecular imaging · 2022
    Article
  10. Review
  11. Review
  12. Review
  13. Potential Biomarkers Associated with Multiple Sclerosis Pathology.International journal of molecular sciences · 2021
    Review
  14. Article
  15. Review
  16. Profiles of cortical inflammation in multiple sclerosis byMultiple sclerosis (Houndmills, Basingstoke, England) · 2020
    Article
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 at 1 institution in 1 country.

Bruno StankoffSorbonne Universités, UPMC Paris 06, Institut du Cerveau et de la Moelle épinière, ICM, Hôpital de la Pitié Salpêtrière, Inserm UMR S 1127, CNRS UMR 7225, Paris, France.ORCID 0000-0002-9631-4674
Emilie PoirionSorbonne Universités, UPMC Paris 06, Institut du Cerveau et de la Moelle épinière, ICM, Hôpital de la Pitié Salpêtrière, Inserm UMR S 1127, CNRS UMR 7225, Paris, France.
Matteo ToniettoSorbonne Universités, UPMC Paris 06, Institut du Cerveau et de la Moelle épinière, ICM, Hôpital de la Pitié Salpêtrière, Inserm UMR S 1127, CNRS UMR 7225, Paris, France.
Benedetta BodiniSorbonne Universités, UPMC Paris 06, Institut du Cerveau et de la Moelle épinière, ICM, Hôpital de la Pitié Salpêtrière, Inserm UMR S 1127, CNRS UMR 7225, Paris, France.
Centre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The biological mechanisms driving disability worsening in multiple sclerosis (MS) are only partly understood. Monitoring changes in lesion load on MRI has a limited predictive value on the progression of clinical disability, and there is an essential need for novel imaging markers specific for the main candidate mechanisms underlying neurodegeneration which include failing myelin repair, innate immune cell activation and gray matter neuronal damage. Positron Emission Tomography (PET) is an imaging technology based on the injection of radiotracers directed against specific molecular targets, which has recently allowed the selective quantification in-vivo of the key biological mechanisms relevant to MS pathophysiology. Pilot PET studies performed in patients with all forms of MS allowed to revisit the contribution of MS lesions to disability worsening and showed that the evolution of lesions toward chronic activation, together with their remyelination profile were relevant predictors of disability worsening. PET offers the opportunity to bridge a critical gap between neuropathology and in-vivo imaging. This technique provides an original approach to disentangle some of the most relevant pathological components driving MS progression, to follow-up their temporal evolution, to investigate their clinical relevance and to evaluate novel therapeutics aimed to prevent disease progression.

Indexed as

Positron-Emission TomographyAnimalsHumansMultiple Sclerosisclinical progressiondisability worseninginnate immune cellmicrogliamultiple sclerosispositron emission tomographyremyelinationwhite matter lesions

Identifiers

PMID30020560
PMCPMC8099240
OpenAlexW2883994607

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.