An advanced magnetic resonance imaging perspective on the etiology of deep tissue injury

Author:

Nelissen Jules L.12ORCID,Traa Willeke A.3,de Boer Hans H.4,de Graaf Larry1,Mazzoli Valentina156,Savci-Heijink C. Dilara4,Nicolay Klaas1,Froeling Martijn7,Bader Dan L.38,Nederveen Aart J.5,Oomens Cees W. J.3,Strijkers Gustav J.2

Affiliation:

1. Biomedical NMR, Biomedical Engineering, Eindhoven University of Technology, Eindhoven, The Netherlands

2. Biomedical Engineering and Physics, Academic Medical Center, Amsterdam, The Netherlands

3. Soft Tissue Engineering and Mechanobiology, Biomedical Engineering, Eindhoven University of Technology, Eindhoven, The Netherlands

4. Department of Pathology, Academic Medical Center, Amsterdam, The Netherlands

5. Department of Radiology and Nuclear Medicine, Academic Medical Center, Amsterdam, The Netherlands

6. Orthopedic Research Laboratory, Radboud UMC, Nijmegen, The Netherlands

7. Department of Radiology, University Medical Center Utrecht, Utrecht, The Netherlands

8. Department of Health Sciences, University of Southampton, Southampton, United Kingdom

Abstract

Early diagnosis of deep tissue injury remains problematic due to the complicated and multifactorial nature of damage induction and the many processes involved in damage development and recovery. In this paper, we present a comprehensive assessment of deep tissue injury development and remodeling in a rat model by multiparametric magnetic resonance imaging (MRI) and histopathology. The tibialis anterior muscle of rats was subjected to mechanical deformation for 2 h. Multiparametric in vivo MRI, consisting of T2, T2*, mean diffusivity (MD), and angiography measurements, was applied before, during, and directly after indentation as well as at several time points during a 14-day follow-up. MRI readouts were linked to histological analyses of the damaged tissue. The results showed dynamic change in various MRI parameters, reflecting the histopathological status of the tissue during damage induction and repair. Increased T2 corresponded with edema, muscle cell damage, and inflammation. T2* was related to tissue perfusion, hemorrhage, and inflammation. MD increase and decrease was reported on the tissue’s microstructural integrity and reflected muscle degeneration and edema as well as fibrosis. Angiography provided information on blockage of blood flow during deformation. Our results indicate that the effects of a single damage-causing event of only 2 h of deformation were present up to 14 days. The initial tissue response to deformation, as observed by MRI, starts at the edge of the indentation. The quantitative MRI readouts provided distinct and complementary information on the extent, temporal evolution, and microstructural basis of deep tissue injury-related muscle damage. NEW & NOTEWORTHY We have applied a multiparametric MRI approach linked to histopathology to characterize damage development and remodeling in a rat model of deep tissue injury. Our approach provided several relevant insights in deep tissue injury. Response to damage, as observed by MRI, started at some distance from the deformation. Damage after a single indentation period persisted up to 14 days. The MRI parameters provided distinct and complementary information on the microstructural basis of the damage.

Funder

Netherlands Organisation for Scientific Research | Technologiestichting STW (Technology Foundation STW)

European Cooperation in Science and Technology (COST)

Publisher

American Physiological Society

Subject

Physiology (medical),Physiology

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