Evidence map›Paper›PMID 37453552›Full record

ArticleActa biomaterialia2023

In vivo shear wave elasticity imaging for assessment of diaphragm function in muscular dystrophy.

Jeehyun Lee, Nia O Myrie, Gun-Jae Jeong, Woojin M Han, Young C Jang, Andrés J García, Stanislav Emelianov

Open access · greenAbstract read
In one paragraph

Article in Acta biomaterialia, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. 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

7 authors at 3 institutions in 2 countries.

Jeehyun LeeSchool of Electrical and Computer Engineering, Georgia Institute of Technology, Atlanta, GA 30332, USA.
Nia O MyrieWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University School of Medicine, Atlanta, GA 30332, USA.
Gun-Jae JeongInstitute of Cell and Tissue Engineering, The Catholic University of Korea, Seoul 06591, Republic of Korea.
Woojin M HanDepartment of Orthopedics, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Young C JangWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University School of Medicine, Atlanta, GA 30332, USA; Department of Orthopedics, Emory Musculoskeletal Institute, Emory School of Medicine, Atlanta, GA 30329, USA. Electronic address: young.jang@emory.edu.
Andrés J GarcíaGeorge W. Woodruff School of Mechanical Engineering, Georgia Institute of Technology, Atlanta, GA 30332, USA. Electronic address: andres.garcia@me.gatech.edu.
Stanislav EmelianovSchool of Electrical and Computer Engineering, Georgia Institute of Technology, Atlanta, GA 30332, USA; Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University School of Medicine, Atlanta, GA 30332, USA. Electronic address: stas@gatech.edu.
Georgia Institute of Technology · USCatholic University of Korea · KRIcahn School of Medicine at Mount Sinai · US

Funding

Hydrogels for hMSC delivery & engraftmentR01AR062368 · NIAMS · GEORGIA INSTITUTE OF TECHNOLOGY · PI GARCIA, ANDRES J · 2012 to 2022
$3.5M
Trimodal Vitality Imaging of Neural Progenitor Cells in the Spinal CordR01NS117613 · NINDS · GEORGIA INSTITUTE OF TECHNOLOGY · PI EMELIANOV, STANISLAV Y · 2020 to 2025
$3.0M
Engineered Heterochronic Parabiosis on 3D Microphysiological SystemsR01AG072309 · NIA · GEORGIA INSTITUTE OF TECHNOLOGY · PI JANG, YOUNG CHARLES · 2021 to 2025
$1.9M
Replicating heterochronic parabiosis on a 3D microfluidic chip to study systematic regulation of muscle stem cellR56AG063928 · NIA · GEORGIA INSTITUTE OF TECHNOLOGY · PI JANG, YOUNG CHARLES · 2019 to 2019
$384k
Implantable biofunctional hydrogel for muscle stem cell transplantationR21AR072287 · NIAMS · GEORGIA INSTITUTE OF TECHNOLOGY · PI JANG, YOUNG CHARLES · 2017 to 2018
$377k
Synthetic hydrogel for satellite cell delivery to the dystrophic diaphragmF32HL140821 · NHLBI · GEORGIA INSTITUTE OF TECHNOLOGY · PI HAN, WOOJIN · 2018 to 2020
$183k
NHLBI NIH HHS F32 HL140821NIAMS NIH HHS R01 AR062368NIAMS NIH HHS R21 AR072287NIA NIH HHS R01 AG072309NIA NIH HHS R56 AG063928NINDS NIH HHS R01 NS117613
6 · The paper itself

Abstract

Duchenne muscular dystrophy (DMD) causes patients to suffer from ambulatory disability and cardiorespiratory failure, the latter of which leads to premature death. Due to its role in respiration, the diaphragm is an important muscle for study. A common method for evaluating diaphragm function is ex vivo force testing, which only allows for an end point measurement. In contrast, ultrasound shear wave elastography imaging (US-SWEI) can assess diaphragm function over time; however, US-SWEI studies in dystrophic patients to date have focused on the limbs without preclinical studies. In this work, we used US-SWEI to estimate the shear wave speed (SWS) in diaphragm muscles of healthy (WT) mice, mdx mice, and mdx mice haploinsufficient for utrophin (mdx-utr) at 6 and 12 months of age. Diaphragms were then subjected to ex vivo force testing and histological analysis at 12 months of age. Between 6 and 12 months, a 23.8% increase in SWS was observed in WT mice and a 27.8% increase in mdx mice, although no significant difference was found in mdx-utr mice. Specific force generated by mdx-utr diaphragms was lower than that of WT diaphragms following twitch stimulus. A strong correlation between SWS and collagen deposition was observed, as well as between SWS and muscle fiber size. Together, these data demonstrate the ability of US-SWEI to evaluate dystrophic diaphragm functionality over time and predict the biochemical and morphological make-up of the diaphragm. Additionally, our results highlight the advantage of US-SWEI over ex vivo testing by obtaining longitudinal measurements in the same subject. STATEMENT OF SIGNIFICANCE: In DMD patients, muscles experience cycles of regeneration and degeneration that contribute to chronic inflammation and muscle weakness. This pathology only worsens with time and leads to muscle wasting, including in respiratory and cardiac muscles. Because respiratory failure is a major contributor to premature death in DMD patients, the diaphragm muscle is an important muscle to evaluate and treat over time. Currently, diaphragm function is assessed using ex vivo force testing, a technique that only allows measurement at sacrifice. In contrast, ultrasonography, particularly shear wave elasticity imaging (USSWEI), is a promising tool for longitudinal assessment; however, most US-SWEI in DMD patients aimed for limb muscles only with the absence of preclinical studies. This work broadens the applications of US-SWE imaging by demonstrating its ability to track properties and function of dystrophic diaphragm muscles longitudinally in multiple dystrophic mouse models.

Indexed as

DiaphragmMuscular Dystrophy, DuchenneAnimalsDisease Models, AnimalElasticityMiceMice, Inbred C57BLMice, Inbred mdxMuscle, SkeletalDiaphragmDuchenne muscular dystrophyMuscle functionShear wave elasticity imagingUltrasonography

Identifiers

PMID37453552
PMCPMC10540053
OpenAlexW4384156750

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.