Evidence map›Paper›PMID 37443413›Full record

ArticleAnnals of clinical and translational neurology2023

Defining the natural history of tumefactive demyelination: A retrospective cohort of 257 patients.

Mahboubeh Fereidan-Esfahani, Paul A Decker, Stephen D Weigand, Alfonso S Lopez Chiriboga, Eoin P Flanagan, Jan-Mendelt Tillema, Claudia F Lucchinetti, Jeanette E Eckel-Passow, W Oliver Tobin

Abstract read
In one paragraph

Article in Annals of clinical and translational neurology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
–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

15 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  15. Tumefactive demyelination in older adults: A scoping review of published cases.Multiple sclerosis journal - experimental, translational and clinical
    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.

Mahboubeh Fereidan-EsfahaniDepartment of Neurology, Mayo Clinic, Rochester, Minnesota, USA.
Paul A DeckerDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, Minnesota, USA.
Stephen D WeigandDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, Minnesota, USA.
Alfonso S Lopez ChiribogaDepartment of Neurology, Mayo Clinic, Jacksonville, Florida, USA.ORCID 0000-0001-5653-5600
Eoin P FlanaganDepartment of Neurology, Mayo Clinic, Rochester, Minnesota, USA.
Jan-Mendelt TillemaDepartment of Neurology, Mayo Clinic, Rochester, Minnesota, USA.
Claudia F LucchinettiDepartment of Neurology, Mayo Clinic, Rochester, Minnesota, USA.ORCID 0000-0001-5070-1196
Jeanette E Eckel-PassowDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, Minnesota, USA.
W Oliver TobinDepartment of Neurology, Mayo Clinic, Rochester, Minnesota, USA.ORCID 0000-0002-8141-2394

Funding

Diagnosis of indeterminate brain lesions using MRI-based machine learning and polygenic risk modelsR01NS113803 · NINDS · MAYO CLINIC ROCHESTER · PI ECKEL PASSOW, JEANETTE E, TOBIN, W. OLIVER · 2020 to 2024
$3.1M
Characterizing the serum metabolome in multiple sclerosisR01NS121928 · NINDS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI BRIGGS, FARREN B. S. · 2021 to 2023
$1.4M
NINDS NIH HHS R01 NS113803NINDS NIH HHS R01 NS121928
6 · The paper itself

Abstract

objectiveTo describe demographic, clinical, and radiographic features of tumefactive demyelination (TD) and identify factors associated with severe attacks and poor outcomes.

methodsRetrospective review of TD cases seen at Mayo Clinic, 1990-2021.

resultsOf 257 patients with TD, 183/257 (71%) fulfilled the 2017 multiple sclerosis (MS) McDonald criteria at the last follow-up, 12/257 (5%) had myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD), 0 had aquaporin-4-IgG seropositive neuromyelitis optic spectrum disorders (AQP4+ NMOSD), and 62/257 (24%) were cryptogenic. Onset before age 18 was present in 18/257 (7%). Female to male ratio was 1.3:1. Cerebrospinal fluid oligoclonal (CSF) bands were present in 95/153 (62%). TD was the first demyelinating attack in 176/257 (69%). At presentation, 59/126 (47%) fulfilled Barkhof criteria for dissemination in space, 59/100 (59%) had apparent diffusion coefficient (ADC) restriction, and 57/126 (45%) had mass effect. Despite aggressive clinical presentation at onset, 181/257 (70%) of patients remained fully ambulatory (Expanded Disability Status Scale [EDSS] ≤4) after a 3.0-year median follow-up duration. Severe initial attack-related disability (EDSS ≥4) was more common in patients with motor symptoms (81/143 vs. 35/106, p < 0.0001), encephalopathy (20/143 vs. 2/106, p < 0.0001) and ADC restriction on initial MRI (42/63 vs. 15/33, p = 0.04). Poor long-term outcome (EDSS ≥4) was more common in patients with older onset age (41.9 ± 15 vs. 36.8 ± 15.6, p = 0.02) and motor symptoms at onset (49/76 vs. 66/171, p < 0.0001).

interpretationMost TD patients should be considered part of the MS spectrum after excluding MOGAD and NMOSD. Motor symptoms and older age at presentation portend a poor outcome.

Indexed as

Brain DiseasesMultiple SclerosisNeuromyelitis OpticaAquaporin 4FemaleHumansMaleRetrospective StudiesAquaporin 4

Identifiers

PMID37443413
PMCPMC10502639

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.