Progressive Brain Atrophy in Multiple System Atrophy: A Longitudinal, Multicenter, Magnetic Resonance Imaging Study
Movement Disorders. 2023-11-07; :
DOI: 10.1002/mds.29633
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ObjectiveTo determine the rates of brain atrophy progression in vivo in patients with multiple system atrophy (MSA).BackgroundSurrogate biomarkers of disease progression are a major unmet need in MSA. Small‐scale longitudinal studies in patients with MSA using magnetic resonance imaging (MRI) to assess progression of brain atrophy have produced inconsistent results. In recent years, novel MRI post‐processing methods have been developed enabling reliable quantification of brain atrophy in an automated fashion.MethodsSerial 3D‐T1‐weighted MRI assessments (baseline and after 1 year of follow‐up) of 43 patients with MSA were analyzed and compared to a cohort of early‐stage Parkinson’s disease (PD) patients and healthy controls (HC). FreeSurfer’s longitudinal analysis stream was used to determine the brain atrophy rates in an observer‐independent fashion.ResultsMean ages at baseline were 64.4 ± 8.3, 60.0 ± 7.5, and 59.8 ± 9.2 years in MSA, PD patients and HC, respectively. A mean disease duration at baseline of 4.1 ± 2.5 years in MSA patients and 2.3 ± 1.4 years in PD patients was observed. Brain regions chiefly affected by MSA pathology showed progressive atrophy with annual rates of atrophy for the cerebellar cortex, cerebellar white matter, pons, and putamen of −4.24 ± 6.8%, −8.22 ± 8.8%, −4.67 ± 4.9%, and − 4.25 ± 4.9%, respectively. Similar to HC, atrophy rates in PD patients were minimal with values of −0.41% ± 1.8%, −1.47% ± 4.1%, −0.04% ± 1.8%, and −1.54% ± 2.2% for cerebellar cortex, cerebellar white matter, pons, and putamen, respectively.ConclusionsPatients with MSA show significant brain volume loss over 12 months, and cerebellar, pontine, and putaminal volumes were the most sensitive to change in mid‐stage disease. © 2023 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.