Evidence map›Paper›PMID 38795020›Full record

ArticleJournal of inherited metabolic disease2024

International validation of meaningfulness of postural sway and gait to assess myeloneuropathy in adults with adrenoleukodystrophy.

Hemmo A F Yska, Bela R Turk, Ali Fatemi, Jordan Goodman, Marije Voermans, Dan Amos, Man Amanat, Stephanie van de Stadt, Marc Engelen, Amena Smith-Fine and 1 more

Abstract readValidation StudyMulticenter Study
In one paragraph

Article in Journal of inherited metabolic disease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Clinically Relevant Outcome Measures in Women With Adrenoleukodystrophy.Annals of clinical and translational neurology · 2026
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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.

Hemmo A F YskaEmma Children's Hospital, Department of Neurology and Pediatric Neurology, Amsterdam Leukodystrophy Center, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.ORCID 0009-0002-7973-2724
Bela R TurkKennedy Krieger Institute, Baltimore, Maryland, USA.
Ali FatemiKennedy Krieger Institute, Baltimore, Maryland, USA.
Jordan GoodmanKennedy Krieger Institute, Baltimore, Maryland, USA.
Marije VoermansEmma Children's Hospital, Department of Neurology and Pediatric Neurology, Amsterdam Leukodystrophy Center, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.
Dan AmosKennedy Krieger Institute, Baltimore, Maryland, USA.
Man AmanatKennedy Krieger Institute, Baltimore, Maryland, USA.
Stephanie van de StadtEmma Children's Hospital, Department of Neurology and Pediatric Neurology, Amsterdam Leukodystrophy Center, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.
Marc EngelenEmma Children's Hospital, Department of Neurology and Pediatric Neurology, Amsterdam Leukodystrophy Center, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.ORCID 0000-0002-5346-8497
Amena Smith-FineKennedy Krieger Institute, Baltimore, Maryland, USA.
Jennifer KellerKennedy Krieger Institute, Baltimore, Maryland, USA.

Funding

Validation of the GMFC-MLDU54NS115052 · NINDS · CHILDREN'S HOSP OF PHILADELPHIA · PI Laura Ann Adang, FLORIAN S EICHLER · 2019 to 2026
$14.3M
Sleep and Circadian Dysfunction, Brain and Neurobehavioral Development in AutismP50HD103538 · NICHD · HUGO W. MOSER RES INST KENNEDY KRIEGER · PI S. Ali Fatemi, Bradley L Schlaggar · 2020 to 2026
$9.9M
National Institute of Neurological Disorders and Stroke (NINDS)/National Center for Advancing Translational Sciences (NCATS) U54NS115052Netherlands Organization for Scientific Research VIDI 016.196.310NICHD NIH HHS P50 HD103538NICHD NIH HHS P50HD103538NINDS NIH HHS U54 NS115052
6 · The paper itself

Abstract

backgroundThe most common manifestation of X-linked adrenoleukodystrophy (ALD) is a slowly progressive myeloneuropathy, which leads to imbalance and gait disturbances. The variable progression of the disease complicates evaluation of its progression rate. Wearable sensors allow for easy and frequent balance and gait collection. This study reports baseline data from a longitudinal study on the quantitative assessment of balance and gait with wearable sensors and their clinical relevance.

methodsData were collected from adult patients in two institutions. Postural body sway and gait parameters were measured using accelerometers. Disease severity was measured by the Expanded Disability Severity Scale (EDSS). Falling frequency and quality of life (QOL) were collected in men. The relationship between sway and gait variables and EDSS score, participants' use of a walking aid, and falling frequency was evaluated.

resultsOne hundred twenty individuals with ALD were included. Sway variables significantly differentiate participants' assistive device use. Sway and gait variables were correlated to the EDSS in both sexes. Both gait speed and sway were correlated with falling frequency in men from one institution. Select QOL subscores were correlated with the EDSS in males from one institution. Accelerometry generated comparable results across sites. DISCUSSION: This study confirms the clinical correlation between spinal cord disease and imbalance and gait in ALD. For the first time, this study shows clinically meaningful relationships for sway and gait with use of an assistive device, falling frequency and QOL. Wearable accelerometers are a valid means to measure sway and gait in ALD. These measures are promising outcomes for clinical trial designs to assess myeloneuropathy in ALD and to monitor disease progression in individuals.

Indexed as

AdrenoleukodystrophyGaitPostural BalanceQuality of LifeAdultDisease ProgressionFemaleHumansLongitudinal StudiesMaleMiddle AgedSeverity of Illness IndexSpinal Cord DiseasesWearable Electronic DevicesYoung Adultadrenoleukodystrophyadrenomyeloneuropathyclinical trialgaitswayvalidationwearable devices

Identifiers

PMID38795020
PMCPMC11586604

What OpenQuestion holds

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LicenceCC BY
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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.