Evidence map›Paper›PMID 31978134›Full record

ArticlePloS one2020

Gait asymmetry in glucocerebrosidase mutation carriers with Parkinson's disease.

Anjali Gera, Joan A O'Keefe, Bichun Ouyang, Yuanqing Liu, Samantha Ruehl, Mark Buder, Jessica Joyce, Nicolette Purcell, Gian Pal

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 2 pooled it
1.0field-weighted citation impact, top 26% 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

7 citing papers in PubMed, 2 syntheses or guidelines pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Association of gender and age at onset with glucocerebrosidase associated Parkinson's disease: a systematic review and meta-analysis.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2021
    Pooled it
  3. Review
  4. Article
  5. Article
  6. Review
  7. 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

9 authors at 1 institution in 1 country.

Anjali GeraDepartment of Neurological Sciences, Rush University, Chicago, Illinois, United States of America.
Joan A O'KeefeCell & Molecular Medicine, Rush University, Chicago, Illinois, United States of America.
Bichun OuyangDepartment of Neurological Sciences, Rush University, Chicago, Illinois, United States of America.
Yuanqing LiuDepartment of Neurological Sciences, Rush University, Chicago, Illinois, United States of America.
Samantha RuehlDepartment of Neurological Sciences, Rush University, Chicago, Illinois, United States of America.
Mark BuderDepartment of Neurological Sciences, Rush University, Chicago, Illinois, United States of America.
Jessica JoyceCell & Molecular Medicine, Rush University, Chicago, Illinois, United States of America.
Nicolette PurcellCell & Molecular Medicine, Rush University, Chicago, Illinois, United States of America.
Gian PalDepartment of Neurological Sciences, Rush University, Chicago, Illinois, United States of America.ORCID 0000-0003-1048-6182
Rush University · US

Funding

Parkinson disease and DBS: cognitive effects in GBA mutation carriersK23NS097625 · NINDS · RUSH UNIVERSITY MEDICAL CENTER · PI PAL, GIAN D · 2017 to 2021
$936k
Impact of Cognitive function on Balance and Gait Markers for FXTASK01HD088762 · NICHD · RUSH UNIVERSITY MEDICAL CENTER · PI O'KEEFE, JOAN A · 2016 to 2021
$711k
NICHD NIH HHS K01 HD088762NINDS NIH HHS K23 NS097625
6 · The paper itself

Abstract

backgroundGBA mutation carriers with PD (PD-GBA) are at higher risk of cognitive decline, but there is limited data regarding whether there are differences in gait dysfunction between GBA mutation and non-mutation carriers with PD. OBJECTIVES/

methodsThe primary aim of this study was to use quantitative inertial sensor-based gait analysis to compare gait asymmetry in 17 PD-GBA subjects, 17 non-mutation carriers with PD, and 15 healthy control subjects using parameters that had gait laterality and were markers of bradykinesia, in particular arm swing velocity and arm swing range of motion and stride length.

resultsArm swing velocity was more symmetric in PD-GBA subjects vs. non-mutation carriers in the OFF state (12.5 +/- 8.3 vs. 22.9 +/- 11.8%, respectively, p = 0.018). In the ON-medication state, non-mutation carriers with PD, but not PD-GBA subjects, exhibited arm swing velocity (16.8 +/- 8.6 vs. 22.9 +/- 11.8%, p = 0.006) and arm range of motion (26.7 +/- 16.3 vs. 33.4 +/- 18.6%, p = 0.02) that was more asymmetric compared with the OFF-medication state.

conclusionsIn the OFF medication state, arm swing velocity asymmetry may be a useful parameter in helping to distinguish GBA mutation carriers with PD from non-mutation carriers.

Indexed as

MutationArmCase-Control StudiesCognitive DysfunctionFemaleGaitGlucosylceramidaseHeterozygoteHumansMaleMiddle AgedMovement DisordersParkinson DiseaseRange of Motion, ArticularGBA protein, humanGlucosylceramidase

Identifiers

PMID31978134
PMCPMC6980620
OpenAlexW3002063332

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.