Evidence map›Paper›PMID 41022923›Full record

ArticleScientific reports2025

Revealing gait as a murine biomarker of injury, disease, and age with multivariate statistics and machine learning.

Bilal A Naved, Shuling Han, Kyle M Koss, Mary J Kando, Jiao-Jing Wang, Jill Chang, Craig Weiss, Maya G Passman, Jason A Wertheim, Yuan Luo and 1 more

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

11 authors.

Bilal A NavedDepartment of Biomedical Engineering, McCormick School of Engineering, Northwestern University, Evanston, IL, USA.
Shuling HanComprehensive Transplant Center, Department of Surgery, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Kyle M KossComprehensive Transplant Center, Department of Surgery, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Mary J KandoBehavioral Phenotyping Core, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Jiao-Jing WangComprehensive Transplant Center, Department of Surgery, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Jill ChangDepartment of Pediatrics, University of Colorado School of Medicine, Aurora, CO, USA.
Craig WeissBehavioral Phenotyping Core, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Maya G PassmanBarnard College, Columbia University, New York, NY, USA.
Jason A WertheimUniversity of Arizona College of Medicine, Tucson, Arizona, 85724, USA.
Yuan LuoDivision of Health and Biomedical Informatics, Department of Preventive Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA. yuan.luo@northwestern.edu.
Zheng J ZhangComprehensive Transplant Center, Department of Surgery, Northwestern University Feinberg School of Medicine, Chicago, IL, USA. zjzhang@northwestern.edu.

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM008152 · NIGMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ARDEHALI, HOSSEIN · 1987 to 2021
$24.0M
Strategies in Renal Nanomedicine to Impact Treatment Paradigms in Kidney DiseaseF30DK123985 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI NAVED, BILAL ABDULLAH · 2019 to 2023
$238k
NIDDK NIH HHS F30DK123985NIGMS NIH HHS T32GM008152U.S. Department of Defense W81XWH2110862U.S. National Library of Medicine R01LM013337
6 · The paper itself

Abstract

Hundreds of rodent gait studies have been published over the past two decades, according to a PubMed search. Treadmill gait data, for example from the DigiGait system, generates over 30 + spatial and temporal measures. Despite this multi-dimensional data, all but a handful of the published literature on rodent gait has conducted univariate analysis that reveals limited information on the relationships that are characteristic of different gait states. This study conducted rigorous multivariate analysis in the form of sequential feature selection and factor analysis on gait data from a variety of gait deviations (due to injury i.e. peripheral nerve transection and transplantation, disease i.e. IUGR and hyperoxia, and age-related changes) and used machine learning to train a classifier to distinguish among and score different gait states. Treadmill gait data (DigiGait) of three different types of gait deviations were collected. Data were collected from B6 mice using the DigiGait system, with gait measurements taken at standardized treadmill speeds of 10, 17, and 24 cm/s over a period of 3-4 s per observation. Each mouse underwent at least two trials at each speed. Data were collected on B6 mice that were healthy and had various types of gait deficit due to: (a) a peripheral nerve injury model with increasing degrees of damage to the neuromusculoskeletal sequence of gait i.e. nerve transection, total hind limb transplantation, (b) a central nerve injury model of increasing degrees of damage to the motor regions responsible for gait i.e. IUGR, IUGR + hyperoxia, and (c) gait changes due to increasing age. Multivariate factor analysis (using MATLAB's factoran) and forward feature selection (with ten-fold cross-validation) were conducted to identify those features and factors most descriptive of each gait state for comparison. Various machine learning classifier models were trained with ten-fold cross-validation and evaluated (e.g. random forest, regression, discriminant analysis, support vector machine, and ensemble) in a 70 - 30 training-testing split for their accuracy, precision, recall, and F-score. The highest performing model was used to score each type of gait for direct comparison on a scale of -0.5 to 0.5. The score distributions were plotted on a histogram for direct comparisons of score populations among various gait states. Multivariate feature selection revealed that not all 30 + features were relevant to describing the gait states. Plotting misclassification error (MCE) as a function of number of features included revealed that there was a critical number of features (~ 16) that minimized MCE (0.17 via univariate feature selection vs. 0.12 via multivariate feature selection). Incorporating more than 16 features led MCE to increase linearly indicating overfitting. Relationships among the identified features were understood via factor analysis. The factor analysis results were consistent with the biological differences between the groups (e.g. total hind limb transplantation was distinguishable via features descriptive of the positioning of the paw in relation to the body while nerve transection injury alone was distinguishable via features descriptive of changes to fine motor movements). Across all gait states, there was significant conservation of features and factors. This suggests certain relationships may be fundamental to rodent gait analysis regardless of the gait pathology in question. The highest performing machine learning classifier model (ensemble) was able to distinguish between gait deficits with high performance (F-score, recall, precision, and accuracy all > 0.90). This included the ability to distinguish between peripheral vs. central gait deficit, between individual types of peripheral deficit, between individual types of central deficit, and between younger vs. older animals. Using the classifier to score individual animals and plot the scores by group revealed score distributions that were consistent with biological phenomena. For example, the multivariate gait score trends as a result of increasing central nerve injury were consistent with the trends of white matter volume loss in relevant motor regions of the brain as measured via MRI. Finally, the degrees of separation between multivariate gait scores were consistent with the degree of biological difference between gaits (e.g. central injury had greater separation from healthy vs. peripheral injury; older and younger animals had more moderate, yet still statistically significant, separation in scores vs. any of the injury / disease states did with each other). In conclusion, this study establishes a new methodology to quantify and evaluate gait deviations across a variety of different models. Its novelty is in using multivariate statistics to describe the features and factors that characterize gait states due to injury, disease, and age for use in machine learning model training. This includes statistically describing the differences in gait between diseases with vastly different etiologies of gait deficits (peripheral vs. central). In doing so the methodology's novelty includes accounting for relationships between groupings of features in model training; something that traditional univariate analysis is unable to do. It used multivariate statistics and machine learning to reveal gait as a quantifiable, preclinical biomarker of injury, disease, and age. It collapsed a multi-dimensional biological phenomena (gait) into a single score by encoding revealed biological relationships allowing for direct, quantifiable comparisons of function as it pertains to ambulation. It revealed how these multivariate gait scores can visualize biologically consistent separation and combined effects. Finally, we demonstrate the application of this methodology to already published univariate study that is representative of the hundreds of univariate treadmill gait analysis published over the last two decades. Thereby, opening the door to a new class of multivariate gait analyses that provides greater insight and value than the current state-of-the art.

Indexed as

GaitMachine LearningAnimalsBiomarkersGait AnalysisMaleMiceMice, Inbred C57BLMultivariate AnalysisBiomarkersBiomarkerCentral nerve injuryDigigaitFactor analysisGait analysisHind-limb transplantHyperoxiaIntrauterine growth restrictionMachine learningMultivariate statisticsNeuromotor recoveryPeripheral nerve injuryVascularized composite allotransplantation

Identifiers

PMID41022923
PMCPMC12480750

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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.