Evidence map›Paper›PMID 32272444›Full record

ArticleMultiple sclerosis and related disorders2020

Longitudinal ultra-high field MRI of brain lesions in neuromyelitis optica spectrum disorders.

Sanjeev Chawla, Yulin Ge, Jens Wuerfel, Shadi Asadollahi, Suyash Mohan, Friedemann Paul, Tim Sinnecker, Ilya Kister

Open access · greenAbstract read
In one paragraph

Article in Multiple sclerosis and related disorders, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. 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

8 authors at 5 institutions in 3 countries.

Sanjeev ChawlaCenter for Advanced Imaging Innovation and Research (CAI2R), Bernard and Irene Schwartz Center for Biomedical Imaging, United States; Department of Radiology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, United States. Electronic address: Sanjeev.Chawla@pennmedicine.upenn.edu.
Yulin GeCenter for Advanced Imaging Innovation and Research (CAI2R), Bernard and Irene Schwartz Center for Biomedical Imaging, United States.
Jens WuerfelMIAC AG and Department of Biomedical Engineering, University of Basel, Switzerland; NeuroCure Clinical Research Center and Experimental and Clinical Research Center, Max Delbrueck Center for Molecular Medicine, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Shadi AsadollahiDepartment of Radiology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, United States.
Suyash MohanDepartment of Radiology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, United States.
Friedemann PaulNeuroCure Clinical Research Center and Experimental and Clinical Research Center, Max Delbrueck Center for Molecular Medicine, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Tim SinneckerNeuroCure Clinical Research Center and Experimental and Clinical Research Center, Max Delbrueck Center for Molecular Medicine, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Ilya KisterDepartment of Neurology, New York University School of Medicine, Prague, New York, NY 10016, United States.
Advanced Imaging Research (United States) · USMax Delbrück Center · DEUniversity of Pennsylvania · USNew York University · USUniversity of Basel · CH

Funding

TR&D 4: Revealing Microstructure: Biophysical modeling and validation for discovery and clinical careP41EB017183 · NIBIB · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Hersh Chandarana · 2014 to 2026
$19.3M
In vivo insights of small vessel changes with age using USPIO-enhanced MRIR01NS108491 · NINDS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI GE, YULIN, HAACKE, EWART MARK · 2018 to 2022
$3.7M
The next generation of vascular imaging using contrast-enhanced MICRO MRIR56AG060822 · NIA · WAYNE STATE UNIVERSITY · PI GE, YULIN, HAACKE, EWART MARK · 2018 to 2018
$728k
Assessment of tDCS-Induced Neuronal Responses with Advanced MRIR21HD094424 · NICHD · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI CHARVET, LEIGH, GE, YULIN · 2018 to 2019
$466k
NIA NIH HHS R56 AG060822NIBIB NIH HHS P41 EB017183NICHD NIH HHS R21 HD094424NINDS NIH HHS R01 NS108491
6 · The paper itself

Abstract

backgroundIn neuromyelitis optica spectrum disorder (NMOSD), clinical disability in NMOSD patients is relapse-related and progressive phase is rare. This observation raises the question whether there is any radiographic disease activity. The aim of present study was to determine the longitudinal changes in cerebral lesion number, lesion size, lesion-to-venule relationship, and morphological patterns of lesions in NMOSD using multiparametric 7T MR imaging. We also aimed to assess brain volume changes in NMOSD.

methodsA cohort of 22 patients with NMOSD underwent high-resolution 3D-susceptibility weighted imaging (SWI) and 2D-gradient-echo (GRE-T2*) weighted imaging on 7T MRI of brain at baseline and after ~2.8 years of follow-up. Morphologic imaging characteristics, and signal intensity patterns of lesions were recorded at both time points. Lesions were classified as "iron-laden" if they demonstrated hypointense signal on GRE-T2* images and/or SWI as well as hyperintense signal on quantitative susceptibility mapping (QSM). Lesions were considered "non-iron-laden" if they were hyperintense on GRE-T2*/SWI and isointense or hyperintense on QSM. Additionally, fractional brain parenchymal volume (fBPV) was computed at both time points.

resultsA total of 169 lesions were observed at baseline. At follow-up, 6 new lesions were found in 5 patients. In one patient, a single lesion could not be detected on the follow-up scan. No appreciable change in lesion size and vessel-lesion relationship was observed at follow up. All lesions demonstrated hyperintense signal intensity on GRE-T2* weighted images and isointense signal on QSM at both time points. Therefore, these lesions were considered as non-associated with iron pathology. Additionally, no significant change in brain volume was observed: fBPV 0.78 ± 0.06 at baseline vs. 0.77 ± 0.05 at follow up, p>0.05.

conclusionCerebral lesions in NMOSD patients remain 'inert' and do not show any substantial variations in morphological characteristics during a 2-3-year follow-up period.

Indexed as

Disease ProgressionMagnetic Resonance ImagingAdultBrainFemaleHumansLongitudinal StudiesMaleMiddle AgedNeuromyelitis OpticaRetrospective Studies7T Magnetic resonance imagingFollow-upNeuromyelitis optica spectrum disorderQuantitative susceptibility mappingSusceptibility weighted imaging

Identifiers

PMID32272444
PMCPMC7410392
OpenAlexW3013500075

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.