Evidence map›Paper›PMID 42327136›Full record

ArticlebioRxiv : the preprint server for biology2026

A novel machine-learning classification model detects oxidative fiber type transitions in a rabbit model of cerebral palsy.

Cassandra Kramer, Emily J Reedich, Hope McCann, Sadie Drouin, Destiny Sanders, Elian Gonzalez, Tiffany Ung, Alexandra Mukisa, Elvia Mena Avila, Brendan Moline and 7 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

17 authors.

Cassandra KramerGeorge and Anne Ryan Institute for Neuroscience, University of Rhode Island, Kingston, RI, USA.
Emily J ReedichGeorge and Anne Ryan Institute for Neuroscience, University of Rhode Island, Kingston, RI, USA.ORCID 0000-0002-7861-7778
Hope McCannGeorge and Anne Ryan Institute for Neuroscience, University of Rhode Island, Kingston, RI, USA.
Sadie DrouinGeorge and Anne Ryan Institute for Neuroscience, University of Rhode Island, Kingston, RI, USA.
Destiny SandersGeorge and Anne Ryan Institute for Neuroscience, University of Rhode Island, Kingston, RI, USA.
Elian GonzalezGeorge and Anne Ryan Institute for Neuroscience, University of Rhode Island, Kingston, RI, USA.
Tiffany UngGeorge and Anne Ryan Institute for Neuroscience, University of Rhode Island, Kingston, RI, USA.
Alexandra MukisaGeorge and Anne Ryan Institute for Neuroscience, University of Rhode Island, Kingston, RI, USA.
Elvia Mena AvilaGeorge and Anne Ryan Institute for Neuroscience, University of Rhode Island, Kingston, RI, USA.
Brendan MolineGeorge and Anne Ryan Institute for Neuroscience, University of Rhode Island, Kingston, RI, USA.
Landon GenryGeorge and Anne Ryan Institute for Neuroscience, University of Rhode Island, Kingston, RI, USA.
Jess GlennonGeorge and Anne Ryan Institute for Neuroscience, University of Rhode Island, Kingston, RI, USA.
Camila QuirogaGeorge and Anne Ryan Institute for Neuroscience, University of Rhode Island, Kingston, RI, USA.
Lisa DowalibyGeorge and Anne Ryan Institute for Neuroscience, University of Rhode Island, Kingston, RI, USA.
Christine J DiDonatoDepartment of Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Katharina A QuinlanGeorge and Anne Ryan Institute for Neuroscience, University of Rhode Island, Kingston, RI, USA.ORCID 0000-0002-6177-4849
Marin ManuelGeorge and Anne Ryan Institute for Neuroscience, University of Rhode Island, Kingston, RI, USA.ORCID 0000-0002-5344-3572

Funding

Training CoreP20GM103430 · NIGMS · UNIVERSITY OF RHODE ISLAND · PI Bongsup P Cho · 2012 to 2026
$63.6M
Tracking and Evaluation CoreU54GM115677 · NIGMS · BROWN UNIVERSITY · PI SCHMID, CHRISTOPHER H. · 2016 to 2025
$45.0M
Validation of Prenatal Rabbit Hypoxia Ischemia as a Model of Cerebral Palsy-induced PainRF1NS135580 · NINDS · UNIVERSITY OF RHODE ISLAND · PI MEGAN R DETLOFF, Katharina Ann Quinlan · 2023 to 2026
$4.6M
Impairment of Spinal Development in Cerebral PalsyR01NS104436 · NINDS · UNIVERSITY OF RHODE ISLAND · PI Katharina Ann Quinlan · 2017 to 2026
$4.3M
Serotonin Based Therapeutics in Cerebral PalsyR01NS132728 · NINDS · UNIVERSITY OF RHODE ISLAND · PI Katharina Ann Quinlan · 2023 to 2026
$2.5M
Leica Cryostat for shared use at URIS10OD032209 · OD · UNIVERSITY OF RHODE ISLAND · PI CHEN, XINYUAN · 2022 to 2022
$61k
NIGMS NIH HHS P20 GM103430NIGMS NIH HHS U54 GM115677NIH HHS S10 OD032209NINDS NIH HHS R01 NS104436NINDS NIH HHS R01 NS132728NINDS NIH HHS RF1 NS135580
6 · The paper itself

Abstract

The distribution of slow- and fast-twitch fiber types in a skeletal muscle heavily influences its physiology. Muscle biopsy studies indicate atypical fiber type composition and fiber size variation in children with cerebral palsy (CP), but subjects have variable treatment history and a variety of muscles affected, so uncertainties remain. In this study, we developed a novel machine-learning classification model to perform high-throughput fiber typing of complete transverse muscle sections. Our XGBoost algorithm-based prediction model yielded a balanced accuracy score of 0.89 and a macro F1-score of 0.89, reflecting its ability to robustly predict muscle fiber type from myosin heavy chain (MyHC) isoform immunofluorescence intensities and morphological descriptors. This is the first reported fiber type classifier to consider hybrid fibers, which is a major advance, considering at least 20% of myofibers are hybrid yet they are routinely overlooked due to difficulty in their detection. We used this classification model to define fiber types of more than 7 million myofibers from flexor-extensor muscle pairs in rabbits that experienced hypoxia-ischemia (HI) injury in utero (modeling CP), and typically developing sham rabbits. We observed an oxidative fiber type shift in flexor muscles (biceps brachii and tibialis anterior) of HI rabbits at postnatal day (P)14-20 and P30-32 (weaning age). This altered fiber type composition imparts reduced contractile force and is amenable to sustained muscle activity; it may reflect chronic low-frequency motor unit activation. This work supports prior clinical reports that developmental trajectories of muscle fibers are disrupted in CP.

Indexed as

classifierdevelopmental injuryfiber type compositionHypoxia-ischemiamyosin heavy chain isoform

Identifiers

PMID42327136
PMCPMC13277925

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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.