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KMID : 1197720200130010039
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대한파킨슨병 및 이상운동질환 학회지
2020 Volume.13 No. 1 p.39 ~ p.46
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Automated Brainstem Segmentation Detects Differential Involvement in Atypical Parkinsonian Syndromes
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Bocchetta Martina
Iglesias Juan Eugenio
Chelban Viorica
Jabbari Edwin
Lamb Ruth
Russell Lucy L.
Greaves Caroline V.
Neason Mollie
Cash David M.
Thomas David L.
Warren Jason D.
Woodside John
Houlden Henry
Morris Huw R.
Rohrer Jonathan D.
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Abstract
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Objective: Brainstem segmentation has been useful in identifying potential imaging biomarkers for diagnosis and progression in atypical parkinsonian syndromes (APS). However, the majority of work has been performed using manual segmentation, which is time consuming for large cohorts.
Methods: We investigated brainstem involvement in APS using an automated method. We measured the volume of the medulla, pons, superior cerebellar peduncle (SCP) and midbrain from T1-weighted MRIs in 67 patients and 42 controls. Diagnoses were corticobasal syndrome (CBS, n = 14), multiple system atrophy (MSA, n = 16: 8 with parkinsonian syndrome, MSA-P; 8 with cerebellar syndrome, MSA-C), progressive supranuclear palsy with a Richardson’s syndrome (PSP-RS, n = 12), variant PSP (n = 18), and APS not otherwise specified (APS-NOS, n = 7).
Results: All brainstem regions were smaller in MSA-C (19?42% volume difference, p < 0.0005) and in both PSP groups (18?33%, p < 0.0005) than in controls. MSA-P showed lower volumes in all regions except the SCP (15?26%, p < 0.0005). The most affected region in MSA-C and MSA-P was the pons (42% and 26%, respectively), while the most affected regions in both the PSP-RS and variant PSP groups were the SCP (33% and 23%, respectively) and midbrain (26% and 24%, respectively). The brainstem was less affected in CBS, but nonetheless, the pons (14%, p < 0.0005), midbrain (14%, p < 0.0005) and medulla (10%, p = 0.001) were significantly smaller in CBS than in controls. The brainstem was unaffected in APS-NOS.
Conclusion: Automated methods can accurately quantify the involvement of brainstem structures in APS. This will be important in future trials with large patient numbers where manual segmentation is unfeasible.
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KEYWORD
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Brainstem, Magnetic resonance imaging, Parkinsonian syndromes
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