Evidence map›Paper›PMID 31759186›Full record

ArticleMultiple sclerosis and related disorders2020

Technology-enabled comprehensive characterization of multiple sclerosis in clinical practice.

Laura E Baldassari, Kunio Nakamura, Brandon P Moss, Gabrielle Macaron, Hong Li, Malory Weber, Stephen E Jones, Stephen M Rao, Deborah Miller, Devon S Conway and 4 more

Abstract 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 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Observational
  5. Review
  6. Depression in multiple sclerosis across the adult lifespan.Multiple sclerosis (Houndmills, Basingstoke, England) · 2021
    Article
  7. Review
  8. Review
  9. Article
  10. Multiple sclerosis management during the COVID-19 pandemic.Multiple sclerosis (Houndmills, Basingstoke, England) · 2020
    Article
  11. Article
  12. Association of Spinal Cord Radiomic Features and Disability in Multiple Sclerosis.Journal of neuroimaging : official journal of the American Society of Neuroimaging
    Article
  13. 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

14 authors.

Laura E BaldassariMellen Center for Multiple Sclerosis, Cleveland Clinic, Cleveland, OH, United States.
Kunio NakamuraDepartment of Biomedical Engineering, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, United States.
Brandon P MossMellen Center for Multiple Sclerosis, Cleveland Clinic, Cleveland, OH, United States.
Gabrielle MacaronMellen Center for Multiple Sclerosis, Cleveland Clinic, Cleveland, OH, United States.
Hong LiDepartment of Quantitative Health Sciences, Cleveland Clinic, Cleveland, OH, United States.
Malory WeberMellen Center for Multiple Sclerosis, Cleveland Clinic, Cleveland, OH, United States.
Stephen E JonesImaging Institute, Cleveland Clinic, Cleveland, OH, United States.
Stephen M RaoLou Ruvo Center for Brain Health, Cleveland Clinic, Cleveland, OH, United States.
Deborah MillerMellen Center for Multiple Sclerosis, Cleveland Clinic, Cleveland, OH, United States.
Devon S ConwayMellen Center for Multiple Sclerosis, Cleveland Clinic, Cleveland, OH, United States.
Robert A BermelMellen Center for Multiple Sclerosis, Cleveland Clinic, Cleveland, OH, United States.
Jeffrey A CohenMellen Center for Multiple Sclerosis, Cleveland Clinic, Cleveland, OH, United States.
Daniel OntanedaMellen Center for Multiple Sclerosis, Cleveland Clinic, Cleveland, OH, United States.
Marisa P McGinleyMellen Center for Multiple Sclerosis, Cleveland Clinic, Cleveland, OH, United States. Electronic address: mcginlm@ccf.org.

Funding

Institutional Career Development CoreKL2TR002547 · NCATS · CASE WESTERN RESERVE UNIVERSITY · PI DWEIK, RAED A. · 2018 to 2022
$7.7M
NCATS NIH HHS KL2 TR002547
6 · The paper itself

Abstract

backgroundObjective and longitudinal measurements of disability in patients with multiple sclerosis (MS) are desired in order to monitor disease status and response to disease-modifying and symptomatic therapies. Technology-enabled comprehensive assessment of MS patients, including neuroperformance tests (NPTs), patient-reported outcome measures (PROMs), and MRI, is incorporated into clinical care at our center. The relationships of each NPT with PROMs and MRI measures in a real-world setting are incompletely studied, particularly in larger datasets.

objectivesTo demonstrate the utility of comprehensive neurological assessment and determine the association between NPTs, PROMs, and quantitative MRI measures in a large MS clinical cohort.

methodsNPTs (processing speed [PST], contrast sensitivity [CST], manual dexterity [MDT], and walking speed [WST]) and physical disability-related PROMs (Quality of Life in Neurological Disorders [Neuro-QoL], Patient Determined Disease Steps [PDDS], and Patient-Reported Outcomes Measurement Information System Global-10 [PROMIS-10] physical) were collected as part of routine clinical care. Fully-automated MRI analysis calculated T2-lesion volume (T2LV), whole brain fraction (WBF), thalamic volume (TV), and cervical spinal cord cross-sectional area (CA) for brain MRIs completed within 3 months of a clinic visit during which NPTs and PROMs were assessed. Spearman's rank correlation coefficients evaluated the cross-sectional associations of NPTs with PROMs and MRI measures. Linear regression was utilized to determine which combination of clinical characteristics, patient demographics, MRI measures, and PROMs best cross-sectionally explained each NPT result.

results997 unique patients (age 47.7 ± 11.4 years, 71.8% female) who underwent assessments over a 2-year period were included. Correlations among NPTs and PROMs were moderate. PST correlations were strongest for Neuro-QoL upper extremity (NQ-UE) (Spearman's rho = 0.43) and lower extremity (NQ-LE) (0.47). CST correlations were strongest for NQ-UE (0.33), NQ-LE (0.36), and PDDS (-0.31). MDT correlations were strongest for NQ-UE (-0.53), NQ-LE (-0.54), and PDDS (0.53). WST correlations were strongest for PDDS (0.64) and NQ-LE (-0.65). NPTs also had moderate correlations with MRI metrics, the strongest of which were observed with PST (with T2LV (-0.44) and WBF (0.49)). Spearman's rho for other NPT-MRI correlations ranged from 0.23 to 0.36. Linear regression identified age, disease duration, PROMIS-10 physical, NQ-UE, NQ-LE, T2LV and WBF as significant cross-sectional explanatory variables for PST (adjusted R

conclusionsImpaired performance on NPTs correlated with worse physical disability-related PROMs and MRI disease severity, but the strongest cross-sectional explanatory variables for each NPT component varied. This study supports the use of comprehensive, objective quantification of MS status in clinical and research settings. Future longitudinal analyses can determine predictors of treatment response and disability worsening.

Indexed as

Diagnosis, Computer-AssistedMagnetic Resonance ImagingNeuropsychological TestsPatient Reported Outcome MeasuresPsychomotor PerformanceSeverity of Illness IndexAdultCross-Sectional StudiesFemaleHumansMaleMiddle AgedMultiple SclerosisPersons with DisabilitiesQuality of LifeMultiple sclerosisOutcome measurementPatient-reported outcome measuresQuality of lifeQuantitative MRI

Identifiers

PMID31759186
PMCPMC6943942

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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.