Spatiotemporal profile of atrophy in the first year following moderate‐severe traumatic brain injury

Author:

Brennan Daniel J.12ORCID,Duda Jeffrey34ORCID,Ware Jeffrey B.3,Whyte John5,Choi Joon Yul26ORCID,Gugger James7,Focht Kristen8,Walter Alexa E.7,Bushnik Tamara9,Gee James C.34,Diaz‐Arrastia Ramon7,Kim Junghoon J.12ORCID

Affiliation:

1. CUNY Neuroscience Collaborative, The Graduate Center City University of New York New York New York United States

2. Department of Molecular, Cellular, and Biomedical Sciences CUNY School of Medicine, The City College of New York New York New York United States

3. Department of Radiology University of Pennsylvania Perelman School of Medicine Philadelphia Pennsylvania United States

4. Penn Image Computing and Science Laboratory University of Pennsylvania Philadelphia Pennsylvania United States

5. Moss Rehabilitation Research Institute, Einstein Healthcare Network Elkins Park Pennsylvania United States

6. Department of Biomedical Engineering Yonsei University Wonju Republic of Korea

7. Department of Neurology University of Pennsylvania Perelman School of Medicine Philadelphia Pennsylvania United States

8. Widener University School for Graduate Clinical Psychology Chester Pennsylvania United States

9. NYU Grossman School of Medicine New York New York United States

Abstract

AbstractTraumatic brain injury (TBI) triggers progressive neurodegeneration resulting in brain atrophy that continues months‐to‐years following injury. However, a comprehensive characterization of the spatial and temporal evolution of TBI‐related brain atrophy remains incomplete. Utilizing a sensitive and unbiased morphometry analysis pipeline optimized for detecting longitudinal changes, we analyzed a sample consisting of 37 individuals with moderate‐severe TBI who had primarily high‐velocity and high‐impact injury mechanisms. They were scanned up to three times during the first year after injury (3 months, 6 months, and 12 months post‐injury) and compared with 33 demographically matched controls who were scanned once. Individuals with TBI already showed cortical thinning in frontal and temporal regions and reduced volume in the bilateral thalami at 3 months post‐injury. Longitudinally, only a subset of cortical regions in the parietal and occipital lobes showed continued atrophy from 3 to 12 months post‐injury. Additionally, cortical white matter volume and nearly all deep gray matter structures exhibited progressive atrophy over this period. Finally, we found that disproportionate atrophy of cortex along sulci relative to gyri, an emerging morphometric marker of chronic TBI, was present as early as 3 month post‐injury. In parallel, neurocognitive functioning largely recovered during this period despite this pervasive atrophy. Our findings demonstrate msTBI results in characteristic progressive neurodegeneration patterns that are divergent across regions and scale with the severity of injury. Future clinical research using atrophy during the first year of TBI as a biomarker of neurodegeneration should consider the spatiotemporal profile of atrophy described in this study.

Funder

National Institute of Neurological Disorders and Stroke

Publisher

Wiley

Subject

Neurology (clinical),Neurology,Radiology, Nuclear Medicine and imaging,Radiological and Ultrasound Technology,Anatomy

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