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MRI volumetry and diffusion tensor imaging for diagnosis and follow-up of late post-traumatic injuries - 27/03/24

Doi : 10.1016/j.rehab.2023.101783 
Alice Jacquens a, , Pierre-Romain Delmotte a, Claire Gourbeix a, Nicolas Farny a, Bérenger Perret-Liaudet a, Dany Hijazi a, Valentine Batisti a, Grégory Torkomian a, Didier Cassereau b, c, Clara Debarle d, Eimad Shotar e, Celia Gellman f, Bertrand Mathon g, Eleonor Bayen h, Damien Galanaud i, Vincent Perlbarg j, Louis Puybasset a, j, Vincent Degos a
a Sorbonne University, GRC 29, AP-HP, DMU DREAM, Department of Anaesthesiology and Critical Care Medicine, AP–HP, Pitié-Salpêtrière Hospital, 47-83, boulevard de l'Hôpital, 75013, Paris, France 
b Laboratoire d'Imagerie Biomédicale, Sorbonne Université, 15 rue de l'Ecole de Médecine, 75006, Paris, France 
c ESPCI, 10 rue Vauquelin, 75005, Paris, France 
d Physical Medicine and Rehabilitation Department, Centre Hospitalier Saint-Anne, 1 rue Cabanis, GHU Paris psychiatrie et neurosciences, 75014, Paris, France 
e Department of Interventional Neuroradiology, Pitié-Salpêtrière Hospital, Paris, France 
f Icahn School of Medicine at Mount Sinai, NYC Health + Hospitals/Elmhurst, Internal Medicine Residency Program, United States 
g Department of Neurosurgery, APHP - Sorbonne University, La Pitié-Salpêtrière Hospital, 47-83, Boulevard de L'Hôpital, 75651 Cedex 13, Paris, France 
h UGECAM-IdF, groupe hospitalier Pitié-Salpêtrière, service de médecine physique et de réadaptation, Paris France 
i Sorbonne Université, Assistance Publique-Hôpitaux de Paris, Hôpital de la Pitié-Salpêtrière, Service de Neuroradiologie, 75013, Paris, France 
j BRAINTALE SAS, Paris, France 

Corresponding author at: Anesthesiology department, 47-83, Boulevard de l'Hôpital, 75013, Paris, France.Anesthesiology department47-83, Boulevard de l'HôpitalParis75013France

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Highlights

DTI is a key element in the diagnosis and follow-up care for people following a TBI.
DTI markers (particularly FA) are more correlated to post-TBI neurological outcomes than FLAIR.
DTI markers allow a regional analysis of post-TBI white matter injuries.
DTI markers show that in the 10 years post-TBI lesions evolve in a biphasic pattern: their incidence increases for the first 5 years, before stabilizing.

El texto completo de este artículo está disponible en PDF.

Abstract

Background

Traumatic Brain Injury (TBI) is a major cause of acquired disability and can cause devastating and progressive post-traumatic encephalopathy. TBI is a dynamic condition that continues to evolve over time. A better understanding of the pathophysiology of these late lesions is important for the development of new therapeutic strategies.

Objectives

The primary objective was to compare the ability of fluid-attenuated reversion recovery (FLAIR) and diffusion tensor imaging (DTI) magnetic resonance imaging (MRI) markers to identify participants with a Glasgow outcome scale extended (GOS-E) score of 7–8, up to 10 years after their original TBI. The secondary objective was to study the brain regionalization of DTI markers. Finally, we analyzed the evolution of late-developing brain lesions using repeated MRI images, also taken up to 10 years after the TBI.

Methods

In this retrospective study, participants were included from a cohort of people hospitalized following a severe TBI. Following their discharge, they were followed-up and clinically assessed, including a DTI-MRI scan, between 2012 and 2016. We performed a cross-sectional analysis on 97 participants at a median (IQR) of 5 years (3–6) post-TBI, and a further post-TBI longitudinal analysis over 10 years on a subpopulation (n = 17) of the cohort.

Results

Although the area under the curve (AUC) of FLAIR, fractional anisotropy (FA), and mean diffusivity (MD) were not significantly different, only the AUC of FA was statistically greater than 0.5. In addition, only the FA was correlated with clinical outcomes as assessed by GOS-E score (P<10−4). On the cross-sectional analysis, DTI markers allowed study post-TBI white matter lesions by region. In the longitudinal subpopulation analysis, the observed number of brain lesions increased for the first 5 years post-TBI, before stabilizing over the next 5 years.

Conclusions

This study has shown for the first time that post-TBI lesions can present in a two-phase evolution. These results must be confirmed in larger studies. French Data Protection Agency (Commission nationale de l'informatique et des libertés; CNIL) study registration no: 1934708v0.

El texto completo de este artículo está disponible en PDF.

Keywords : Traumatic brain injury, Diffusion tensor imaging

Abbreviations : AUC, CENTER-TBI, CSF, CT, DTI, DTIFIT, FA, FLAIR, FMRIB, GM, GOS-E, IMPACT-TBI, JHU, MD, MRI, NICU, ROC, SAPS II, STROBE, TBI, TE, TIV, TR, WM, 3DT1


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