Evidence map›Paper›PMID 31818276›Full record

ArticleBMC neurology2019

Autoregressive modeling to assess stride time pattern stability in individuals with Huntington's disease.

Helia Mahzoun Alzakerin, Yannis Halkiadakis, Kristin D Morgan

Abstract read
In one paragraph

Article in BMC neurology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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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

3 citing papers in PubMed.

  1. Observational
  2. Dynamic modeling of hospitalized COVID-19 patients reveals disease state-dependent risk factors.Journal of the American Medical Informatics Association : JAMIA · 2022
    Article
  3. 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

3 authors.

Helia Mahzoun AlzakerinBiomedical Engineering, School of Engineering, University of Connecticut, 260 Glenbrook Road, Storrs, CT, 06269-3247, USA.
Yannis HalkiadakisBiomedical Engineering, School of Engineering, University of Connecticut, 260 Glenbrook Road, Storrs, CT, 06269-3247, USA.
Kristin D MorganBiomedical Engineering, School of Engineering, University of Connecticut, 260 Glenbrook Road, Storrs, CT, 06269-3247, USA. Kristin.2.Morgan@uconn.edu.ORCID http://orcid.org/0000-0003-3731-1374

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHuntington's disease (HD) is a progressive, neurological disorder that results in both cognitive and physical impairments. These impairments affect an individual's gait and, as the disease progresses, it significantly alters one's stability. Previous research found that changes in stride time patterns can help delineate between healthy and pathological gait. Autoregressive (AR) modeling is a statistical technique that models the underlying temporal patterns in data. Here the AR models assessed differences in gait stride time pattern stability between the controls and individuals with HD. Differences in stride time pattern stability were determined based on the AR model coefficients and their placement on a stationarity triangle that provides a visual representation of how the patterns mean, variance and autocorrelation change with time. Thus, individuals who exhibit similar stride time pattern stability will reside in the same region of the stationarity triangle. It was hypothesized that individuals with HD would exhibit a more altered stride time pattern stability than the controls based on the AR model coefficients and their location in the stationarity triangle.

methodsSixteen control and twenty individuals with HD performed a five-minute walking protocol. Time series' were constructed from consecutive stride times extracted during the protocol and a second order AR model was fit to the stride time series data. A two-sample t-test was performed on the stride time pattern data to identify differences between the control and HD groups.

resultsThe individuals with HD exhibited significantly altered stride time pattern stability than the controls based on their AR model coefficients (AR1 p < 0.001; AR2 p < 0.001).

conclusionsThe AR coefficients successfully delineated between the controls and individuals with HD. Individuals with HD resided closer to and within the oscillatory region of the stationarity triangle, which could be reflective of the oscillatory neuronal activity commonly observed in this population. The ability to quantitatively and visually detect differences in stride time behavior highlights the potential of this approach for identifying gait impairment in individuals with HD.

Indexed as

Models, StatisticalAdultCase-Control StudiesFemaleGaitGait Disorders, NeurologicHumansHuntington DiseaseMaleMiddle AgedWalkingYoung AdultGait biomarkersGait stabilityHuntington’s diseasePattern analysis

Identifiers

PMID31818276
PMCPMC6902547

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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.