TY - JOUR
T1 - Diffusion-weighted imaging in multiple system atrophy
T2 - A comparison between clinical subtypes
AU - Pellecchia, Maria Teresa
AU - Barone, Paolo Barone
AU - Mollica, Carmine
AU - Salvatore, Elena
AU - Ianniciello, Marta
AU - Longo, Katia
AU - Varrone, Andrea
AU - Vicidomini, Caterina
AU - Picillo, Marina
AU - De Michele, Giuseppe
AU - Filla, Allessandro
AU - Salvatore, Marco
AU - Pappatà, Sabina
PY - 2009/4/15
Y1 - 2009/4/15
N2 - Multiple system atrophy can be classi.ed into two main types, a Parkinsonian (MSA-P) and a cerebellar (MSA-C) variant based on clinical presentation. We obtained diffusion-weighted magnetic resonance imaging (DWI) in 9 MSAP and 12 MSA-C patients and 11 controls, and correlated DWI changes with disease duration and severity. We found that Trace (D) values in the entire and anterior putamen were significantly higher in MSA-P than in MSA-C patients and controls, whereas Trace (D) values in the cerebellum and middle cerebellar peduncle (MCP) were significantly higher in MSA-C than in MSA-P patients and controls. Increased disease duration was significantly correlated with increased Trace (D) values in pons of MSA-P patients, and in cerebellum and MCP of MSA-C patients. Both UMSARS and UPDRS motor scores positively correlated with entire and posterior putaminal Trace (D) values in MSA-P patients. The diffusivity changes parallel phenotypical and pathologic differences between MSA-P and MSA-C patients, suggesting that DWI is a feasible tool for in vivo evaluation of neurodegeneration in MSA. Based on our findings, Trace (D) measurements in the putamen and pons in MSA-P patients and in the cerebellum and MCP in MSA-C patients could serve as quantitative markers for microstructural damage in the course of disease.
AB - Multiple system atrophy can be classi.ed into two main types, a Parkinsonian (MSA-P) and a cerebellar (MSA-C) variant based on clinical presentation. We obtained diffusion-weighted magnetic resonance imaging (DWI) in 9 MSAP and 12 MSA-C patients and 11 controls, and correlated DWI changes with disease duration and severity. We found that Trace (D) values in the entire and anterior putamen were significantly higher in MSA-P than in MSA-C patients and controls, whereas Trace (D) values in the cerebellum and middle cerebellar peduncle (MCP) were significantly higher in MSA-C than in MSA-P patients and controls. Increased disease duration was significantly correlated with increased Trace (D) values in pons of MSA-P patients, and in cerebellum and MCP of MSA-C patients. Both UMSARS and UPDRS motor scores positively correlated with entire and posterior putaminal Trace (D) values in MSA-P patients. The diffusivity changes parallel phenotypical and pathologic differences between MSA-P and MSA-C patients, suggesting that DWI is a feasible tool for in vivo evaluation of neurodegeneration in MSA. Based on our findings, Trace (D) measurements in the putamen and pons in MSA-P patients and in the cerebellum and MCP in MSA-C patients could serve as quantitative markers for microstructural damage in the course of disease.
KW - Diffusion-weighted imaging
KW - Magnetic resonance imaging
KW - MSA subtypes
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U2 - 10.1002/mds.22440
DO - 10.1002/mds.22440
M3 - Article
C2 - 19117367
AN - SCOPUS:67651154396
SN - 0885-3185
VL - 24
SP - 689
EP - 696
JO - Movement Disorders
JF - Movement Disorders
IS - 5
ER -