Evidence map›Paper›PMID 33715398›Full record

ArticleStem cells and development2021

High Frequency Spectral Ultrasound Imaging Detects Early Heterotopic Ossification in Rodents.

Nicole J Edwards, Eric Hobson, Devaveena Dey, Alisha Rhodes, Archie Overmann, Benjamin Hoyt, Sarah A Walsh, Chase A Pagani, Amy L Strong, Geoffrey E Hespe and 5 more

Open access · greenAbstract read
In one paragraph

Article in Stem cells and development, 2021. 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
1.4field-weighted citation impact, top 20% 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

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Revisiting Heinz-Lippman disease as a complication of chronic venous insufficiency.Journal of vascular surgery cases and innovative techniques · 2024
    Article
  2. Review
  3. 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

15 authors at 4 institutions in 1 country.

Nicole J EdwardsDepartment of Surgery, University of Michigan, Ann Arbor, Michigan, USA.
Eric HobsonDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, Michigan, USA.
Devaveena DeyDepartment of Surgery, Uniformed Services University of the Health Sciences, Bethesda, Maryland, USA.
Alisha RhodesDepartment of Surgery, Uniformed Services University of the Health Sciences, Bethesda, Maryland, USA.
Archie OvermannDepartment of Surgery, Uniformed Services University of the Health Sciences, Bethesda, Maryland, USA.
Benjamin HoytDepartment of Surgery, Uniformed Services University of the Health Sciences, Bethesda, Maryland, USA.
Sarah A WalshDepartment of Surgery, Uniformed Services University of the Health Sciences, Bethesda, Maryland, USA.
Chase A PaganiDepartment of Surgery, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Amy L StrongDepartment of Surgery, University of Michigan, Ann Arbor, Michigan, USA.
Geoffrey E HespeDepartment of Surgery, University of Michigan, Ann Arbor, Michigan, USA.
Karthik R PadmanabhanEpigenomic Core, University of Michigan, Ann Arbor, Michigan, USA.
Amanda HuberDepartment of Surgery, University of Michigan, Ann Arbor, Michigan, USA.
Cheri DengDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, Michigan, USA.
Thomas A DavisDepartment of Surgery, Uniformed Services University of the Health Sciences, Bethesda, Maryland, USA.
Benjamin LeviDepartment of Surgery, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
University of Michigan–Ann Arbor · USUniformed Services University of the Health Sciences · USThe University of Texas Southwestern Medical Center · USHenry M. Jackson Foundation · US

Funding

TRAINING PROGRAM IN ORGANOGENESIST32HD007505 · NICHD · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PASCA DI MAGLIANO, MARINA, SPENCE, JASON · 1997 to 2021
$6.9M
University of Michigan Surgical Oncology Research Training ProgramT32CA009672 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI JACQUELINE SARA JERUSS, WEIPING ZOU · 1991 to 2026
$6.0M
Targeting Molecular and Cellular Mediators of Inflammation to Prevent Pathologic Cell Differentiation and Heterotopic OssificationR01AR071379 · NIAMS · UT SOUTHWESTERN MEDICAL CENTER · PI LEVI, BENJAMIN · 2017 to 2021
$1.5M
Developing New Diagnostic and Timed, TAK1 Specific Treatment Strategies for Trauma Induced Heterotopic OssificationR01GM123069 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI LEVI, BENJAMIN · 2017 to 2020
$1.2M
NCI NIH HHS T32 CA009672NIAMS NIH HHS R01 AR071379NICHD NIH HHS T32 HD007505NIGMS NIH HHS R01 GM123069
6 · The paper itself

Abstract

Heterotopic ossification (HO) is a devastating condition in which ectopic bone forms inappropriately in soft tissues following traumatic injuries and orthopedic surgeries as a result of aberrant mesenchymal progenitor cell (MPC) differentiation. HO leads to chronic pain, decreased range of motion, and an overall decrease in quality of life. While several treatments have shown promise in animal models, all must be given during early stages of formation. Methods for early determination of whether and where endochondral ossification/soft tissue mineralization (HO anlagen) develop are lacking. At-risk patients are not identified sufficiently early in the process of MPC differentiation and soft tissue endochondral ossification for potential treatments to be effective. Hence, a critical need exists to develop technologies capable of detecting HO anlagen soon after trauma, when treatments are most effective. In this study, we investigate high frequency spectral ultrasound imaging (SUSI) as a noninvasive strategy to identify HO anlagen at early time points after injury. We show that by determining quantitative parameters based on tissue organization and structure, SUSI identifies HO anlagen as early as 1-week postinjury in a mouse model of burn/tenotomy and 3 days postinjury in a rat model of blast/amputation. We analyze single cell RNA sequencing profiles of the MPCs responsible for HO formation and show that the early tissue changes detected by SUSI match chondrogenic and osteogenic gene expression in this population. SUSI identifies sites of soft tissue endochondral ossification at early stages of HO formation so that effective intervention can be targeted when and where it is needed following trauma-induced injury. Furthermore, we characterize the chondrogenic to osteogenic transition that occurs in the MPCs during HO formation and correlate gene expression to SUSI detection of the HO anlagen.

Indexed as

Disease Models, AnimalAnimalsBurnsCell DifferentiationChondrogenesisGene Expression ProfilingGene OntologyHumansMaleMesenchymal Stem CellsMiceMice, Inbred C57BLOssification, HeterotopicOsteogenesisRatsRats, Sprague-Dawleyheterotopic ossificationhigh frequency spectral ultrasound imagingmesenchymal progenitor cellstraumatic injury

Identifiers

PMID33715398
PMCPMC8106252
OpenAlexW3136180459

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.