Evidence map›Paper›PMID 28437430›Full record

ArticlePloS one2017

Cerebellar volume as imaging outcome in progressive multiple sclerosis.

Matilde Inglese, Maria Petracca, Enricomaria Mormina, Anat Achiron, Rebecca Straus-Farber, Shmuel Miron, Michelle Fabian, Stephen Krieger, Aaron Miller, Fred Lublin and 1 more

Abstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Article
  6. Cerebellar volume loss in radiologically isolated syndrome.Multiple sclerosis (Houndmills, Basingstoke, England) · 2021
    Article
  7. Laminar analysis of the cortical T1/T2-weighted ratio at 7T.Neurology(R) neuroimmunology & neuroinflammation · 2020
    Observational
  8. Article
  9. Review
  10. Article
  11. An MRI evaluation of grey matter damage in African Americans with MS.Multiple sclerosis and related disorders · 2018
    Article
  12. Observational
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

11 authors.

Matilde IngleseDepartment of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY, United States of America.ORCID http://orcid.org/0000-0002-9610-0297
Maria PetraccaDepartment of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY, United States of America.ORCID http://orcid.org/0000-0001-9429-2769
Enricomaria MorminaDepartment of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY, United States of America.
Anat AchironMultiple Sclerosis Center, Sheba Medical Center, Tel Hashomer, Israel.
Rebecca Straus-FarberDepartment of Neurology, Columbia University, New York, NY, United States of America.
Shmuel MironMultiple Sclerosis Center, Sheba Medical Center, Tel Hashomer, Israel.
Michelle FabianDepartment of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY, United States of America.
Stephen KriegerDepartment of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY, United States of America.
Aaron MillerDepartment of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY, United States of America.
Fred LublinDepartment of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY, United States of America.
Maria Pia SormaniBiostatistics Unit, University of Genoa, Genoa, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeTo assess whether cerebellar volumes changes could represent a sensitive outcome measure in primary-progressive MS. MATERIAL AND

methodsChanges in cerebellar volumes over one-year follow-up, estimated in 26 primary-progressive MS patients and 20 controls with Freesurfer longitudinal pipeline, were assessed using Wilcoxon test and tested for their correlation with disability worsening by a logistic regression. Clinical worsening was defined as EDSS score increase or change of >20% for 25-foot walk test or 9-hole peg test scores at follow-up. Sample sizes for given treatment effects and power were calculated. The findings were validated in an independent cohort of 20 primary-progressive MS patients.

resultsSignificant changes were detected in brain T1 lesion volume (p<0.01), cerebellar T2 and T1 lesion volume (p<0.01 and p<0.05), cerebellar volume, cerebellar cortex volume, and cerebellar WM volume (p<0.001). Only cerebellar volume and cerebellar cortex volume percentage change were significantly reduced in clinically progressed patients when compared to patients who did not progress (p<0.01; respectively AUC of 0.91 and 0.96). Cerebellar volume percentage changes were consistent in the exploration and validation cohorts (cerebellar volume -1.90±1.11% vs -1.47±2.30%; cerebellar cortex volume -1.68±1.41% vs -1.56±2.23%). Based on our results the numbers of patients required to detect a 30% effect are 81 per arm for cerebellar volume and 162 per arm for cerebellar cortex volume (90% power, type 1 error alpha = 0.05).

conclusionsOur results suggest a role for cerebellar cortex volume and cerebellar volume as potential short-term imaging metrics to monitor treatment effect in primary-progressive MS clinical trials.

Indexed as

Magnetic Resonance ImagingAdultBrainCerebellumDisability EvaluationDisease ProgressionFemaleHumansMiddle AgedMultiple Sclerosis, Chronic ProgressiveOrgan SizeSeverity of Illness Index

Identifiers

PMID28437430
PMCPMC5402974

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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.