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Magnetic resonance imaging abnormalities as a marker of multiple system atrophy in isolated rapid eye movement sleep
Amaia Muñoz-Lopetegi1, Joan Berenguer2, Alex Iranzo1
1Center for Sleep Disorders, Neurology Service, Universitat de Barcelona, IDIBAPS, CIBERNED:CB06/05/0018-ISCIII, Hospital Clínic de Barcelona, Barcelona, Spain.
Study Objectives:
Patients with isolated rapid eye movement (REM) sleep behavior disorder (IRBD) develop Parkinson disease (PD), dementia with Lewy bodies (DLB), or multiple system atrophy (MSA). Magnetic resonance imaging (MRI) is abnormal in MSA showing abnormalities in the putamen, cerebellum, and brainstem. Our objective was to evaluate the usefulness of MRI to detect MRI abnormalities in IRBD and predict development of MSA and not PD and DLB.
Methods:
In IRBD patients that eventually developed PD, DLB, and MSA, we looked for the specific structural MRI abnormalities described in manifest MSA (e.g. hot cross-bun sign, putaminal rim, and cerebellar atrophy). We compared the frequency of these MRI changes among groups of converters (PD, DLB, and MSA) and analyzed their ability to predict development of MSA. The clinical and radiological features of the IRBD patients that eventually converted to MSA are described in detail.
Results:
A total of 61 IRBD patients who underwent MRI phenoconverted to PD (n = 30), DLB (n = 26), and MSA (n = 5) after a median follow-up of 2.4 years from neuroimaging. MRI changes typical of MSA were found in four of the five (80%) patients who converted to MSA and in three of the 56 (5.4%) patients who developed PD or DLB. MRI changes of MSA had sensitivity of 80.0%, specificity of 94.6%, positive likelihood ratio of 14.9 (95% CI 4.6-48.8), and negative likelihood ratio of 0.2 (95% CI 0.04-1.2) to predict MSA.
Conclusions:
In IRBD, conventional brain MRI is helpful to predict conversion to MSA. The specific MRI abnormalities of manifest MSA may be detected in its premotor stage.
Insights
Magnetic resonance imaging (MRI) can predict multiple system atrophy (MSA) development in patients with isolated rapid eye movement sleep behavior disorder (IRBD). Specific MRI findings indicative of MSA were detected in the premotor stage of the disease.
Area of Science:
- Neurology
- Radiology
- Sleep Medicine
Background:
- Patients with isolated rapid eye movement sleep behavior disorder (IRBD) have a high risk of developing neurodegenerative diseases such as Parkinson disease (PD), dementia with Lewy bodies (DLB), and multiple system atrophy (MSA).
- Specific neuroimaging findings on magnetic resonance imaging (MRI) are characteristic of manifest MSA, involving abnormalities in the putamen, cerebellum, and brainstem.
Purpose of the Study:
- To evaluate the utility of conventional brain MRI in detecting specific abnormalities in IRBD patients.
- To determine if these MRI findings can predict the future development of MSA, distinguishing it from PD and DLB.
Main Methods:
- Retrospective analysis of MRI scans from 61 IRBD patients who later developed PD, DLB, or MSA.
- Comparison of the frequency of MSA-specific MRI changes (e.g., hot cross-bun sign, putaminal rim, cerebellar atrophy) among patient groups.
- Assessment of the predictive value of these MRI changes for MSA conversion.
Main Results:
- MRI changes typical of MSA were identified in 80% of patients who converted to MSA (4 out of 5).
- These specific MRI changes were found in only 5.4% of patients who developed PD or DLB (3 out of 56).
- The MRI findings demonstrated high sensitivity (80.0%) and specificity (94.6%) for predicting MSA development.
Conclusions:
- Conventional brain MRI is a valuable tool for predicting the conversion to MSA in patients with IRBD.
- Characteristic MRI abnormalities associated with manifest MSA can be detected during its premotor stage, aiding in early diagnosis and prediction.
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