Evidence map›Paper›PMID 42124858›Full record

ReviewJBMR plus2026

Opportunities for deep learning techniques to advance the histological analysis of preclinical models of osteoarthritis beyond ordinal rank systems.

Jacob L Griffith, Yenisel Cruz-Almeida, Alejandro Almarza, Robert Caudle, Kyle D Allen

Abstract readReview
In one paragraph

Review in JBMR plus, 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

5 authors.

Jacob L GriffithJ. Crayton Pruitt Family Department of Biomedical Engineering, Herbert Wertheim College of Engineering, University of Florida, Gainesville, FL 32611, United States.
Yenisel Cruz-AlmeidaPain Research and Intervention Center of Excellence, College of Dentistry, University of Florida, Gainesville, FL 32603, United States.ORCID https://orcid.org/0000-0002-0065-0236
Alejandro AlmarzaDepartment of Oral and Craniofacial Sciences, College of Dentistry, University of Pittsburgh, Pittsburgh, PA 15213, United States.
Robert CaudlePain Research and Intervention Center of Excellence, College of Dentistry, University of Florida, Gainesville, FL 32603, United States.
Kyle D AllenJ. Crayton Pruitt Family Department of Biomedical Engineering, Herbert Wertheim College of Engineering, University of Florida, Gainesville, FL 32611, United States.ORCID https://orcid.org/0000-0002-4470-9148

Funding

RE-JOIN NEURONAL ANATOMY, CONNECTIVITY, AND PHENOTYPIC INNERVATION OF THE KNEE JOINTUC2AR082200 · NIAMS · BAYLOR COLLEGE OF MEDICINE · PI Benjamin R Arenkiel, Brendan Lee · 2022 to 2026
$14.4M
Innervation of the knee and TMJUC2AR082196 · NIAMS · UNIVERSITY OF FLORIDA · PI Kyle D Allen, Alejandro Jose Almarza · 2022 to 2026
$11.2M
OA Pathogenesis beyond Cartilage: A preclinical study of the sources of OA painR01AR071431 · NIAMS · UNIVERSITY OF FLORIDA · PI ALLEN, KYLE D · 2018 to 2022
$2.3M
NIAMS NIH HHS R01 AR071431NIAMS NIH HHS UC2 AR082196NIAMS NIH HHS UC2 AR082200
6 · The paper itself

Abstract

Tools for assessing disease progression are needed to identify and confirm new mechanisms driving osteoarthritis (OA) progression and guide therapeutic development. This review focuses on the advantages and feasibility of leveraging deep learning techniques for quantitative analysis of rodent knee histology in preclinical OA models. Previous studies using radiographs and micro-CT have used deep-learning driven analysis, including convolutional neural networks (CNNs), to evaluate disease progression in OA patients and preclinical models. However, the use of these tools to analyze histology in rodent OA models is limited. The discrepancy between clinical and preclinical histological quantification partly relates to the size constraints of imaging, where the larger scale of clinical samples requires complex mapping and multiple samples to obtain a complete picture of the entire joint. Rodent OA samples provide a view of the entire joint on an individual slide and thereby enable the quantification of changes across the width of the joint. Here, we discuss approaches for using CNN-based pipelines to quantify and visualize joint remodeling in rodent OA models, complementing existing grading schemes and potentially providing insight into mechanisms driving joint pain and disability.

Indexed as

Analysis/Quantitation of BoneAnimal ModelsBone HistomorphometryOsteoarthritisStatistical Methods

Identifiers

PMID42124858
PMCPMC13160421

What OpenQuestion holds

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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.