TY - JOUR
T1 - White matter alterations in early Parkinson’s disease: role of motor symptom lateralization
AU - Pelizzari, Laura
AU - Di Tella, Sonia
AU - Laganà, Maria M.
AU - Bergsland, Niels
AU - Rossetto, Federica
AU - Nemni, Raffaello
AU - Baglio, Francesca
PY - 2019
Y1 - 2019
N2 - Introduction: Parkinson’s disease (PD) is a motor disorder that initially presents with unilateral symptoms. Widespread white matter (WM) alterations have been reported since the early stages of the disease. The aim of this study was to investigate WM alterations in right-dominant and left-dominant symptom PD patients (RPD and LPD, respectively) with respect to healthy controls (HC) by diffusion-weighted magnetic resonance imaging (MRI).
Methods: Thirty-eight subjects participated in this study: 12 RPD (median H&Y [IQR] = 1.5 [1.1–2], median UPDRS III [IQR] = 23 [7.8–25]), 9 LPD (median H&Y [IQR] = 1.5 [1–2.5], median UPDRS III [IQR] = 17 [12–22]), and 17 HC. All the participants were scanned on a 1.5-T MRI scanner. Maps of fractional anisotropy (FA), mean diffusivity (MD), axial diffusivity (AD), and radial diffusivity (RD) were computed for all the subjects. Tract-based spatial statistics (TBSS) was performed for each diffusion parameter, to testWM differences between RPD, LPD, and HC (ANCOVA design). Family-wise error (FWE) correction was performed and p values lower than 0.05 were considered significant.
Results: No significant FA and RD differences were observed between RPD, LPD, and HC. Significantly increased MD and AD were observed in RPD with respect to HC within widespreadWMregions, bilaterally. Conversely, no significantWMalterations were detected in LPD.
Conclusion: WM integrity was found to be significantly altered in RPD but not in LPD, suggesting that LPD profile may be associated to more favorable prognosis. Since clinical laterality onset may affect the extent ofWMintegrity changes, it should be taken into account in neuroimaging studies investigating PD.
AB - Introduction: Parkinson’s disease (PD) is a motor disorder that initially presents with unilateral symptoms. Widespread white matter (WM) alterations have been reported since the early stages of the disease. The aim of this study was to investigate WM alterations in right-dominant and left-dominant symptom PD patients (RPD and LPD, respectively) with respect to healthy controls (HC) by diffusion-weighted magnetic resonance imaging (MRI).
Methods: Thirty-eight subjects participated in this study: 12 RPD (median H&Y [IQR] = 1.5 [1.1–2], median UPDRS III [IQR] = 23 [7.8–25]), 9 LPD (median H&Y [IQR] = 1.5 [1–2.5], median UPDRS III [IQR] = 17 [12–22]), and 17 HC. All the participants were scanned on a 1.5-T MRI scanner. Maps of fractional anisotropy (FA), mean diffusivity (MD), axial diffusivity (AD), and radial diffusivity (RD) were computed for all the subjects. Tract-based spatial statistics (TBSS) was performed for each diffusion parameter, to testWM differences between RPD, LPD, and HC (ANCOVA design). Family-wise error (FWE) correction was performed and p values lower than 0.05 were considered significant.
Results: No significant FA and RD differences were observed between RPD, LPD, and HC. Significantly increased MD and AD were observed in RPD with respect to HC within widespreadWMregions, bilaterally. Conversely, no significantWMalterations were detected in LPD.
Conclusion: WM integrity was found to be significantly altered in RPD but not in LPD, suggesting that LPD profile may be associated to more favorable prognosis. Since clinical laterality onset may affect the extent ofWMintegrity changes, it should be taken into account in neuroimaging studies investigating PD.
KW - Parkinson’s disease, White matter, White matter alterations, Diffusion tensor MRI, TBSS, Clinical laterality onset
KW - Parkinson’s disease, White matter, White matter alterations, Diffusion tensor MRI, TBSS, Clinical laterality onset
UR - http://hdl.handle.net/10807/150939
U2 - 10.1007/s10072-019-04084-y
DO - 10.1007/s10072-019-04084-y
M3 - Article
SN - 1590-3478
SP - 357
EP - 364
JO - Neurological Sciences
JF - Neurological Sciences
ER -