TY - JOUR
T1 - Cortical hypoperfusion in Parkinson's disease assessed using arterial spin labeled perfusion MRI
AU - Fernández-Seara, María A.
AU - Mengual, Elisa
AU - Vidorreta, Marta
AU - Aznárez-Sanado, Maite
AU - Loayza, Francis R.
AU - Villagra, Federico
AU - Irigoyen, Jaione
AU - Pastor, María A.
N1 - Funding Information:
This work was supported by the Spanish Ministry of Science and Innovation (grants SAF2008-00678 and RYC-2010-07161 ) and by the Navarra Government Health Department (grant 17/2008 GN Salud). M. Aznárez-Sanado was supported by a grant from the Navarra Government Education Department.
PY - 2012/2/1
Y1 - 2012/2/1
N2 - Alterations in cerebral perfusion and metabolism in Parkinson's disease have been assessed in several studies, using nuclear imaging techniques and more recently magnetic resonance imaging. However, to date there is no consensus in the literature regarding the extent and the magnitude of these alterations. In this work, arterial spin labeled perfusion MRI was employed to quantify absolute cerebral blood flow in a group of early-to-moderate Parkinson's disease patients and age-matched healthy controls. Perfusion comparisons between the two groups showed that Parkinson's disease is characterized by wide-spread cortical hypoperfusion. Subcortically, hypoperfusion was also found in the caudate nucleus. This pattern of hypoperfusion could be related to cognitive dysfunctions that have been previously observed even at the disease early stages. The present results were obtained by means of whole brain voxel-wise comparisons of absolute perfusion values, using statistical parametric mapping, thus avoiding the potentially biased global mean normalization procedure. In addition, this work demonstrates that between-group comparison of relative perfusion values after global mean normalization, introduced artifactual relative perfusion increases, where absolute perfusion was in fact preserved. This has implications for perfusion studies of other brain disorders.
AB - Alterations in cerebral perfusion and metabolism in Parkinson's disease have been assessed in several studies, using nuclear imaging techniques and more recently magnetic resonance imaging. However, to date there is no consensus in the literature regarding the extent and the magnitude of these alterations. In this work, arterial spin labeled perfusion MRI was employed to quantify absolute cerebral blood flow in a group of early-to-moderate Parkinson's disease patients and age-matched healthy controls. Perfusion comparisons between the two groups showed that Parkinson's disease is characterized by wide-spread cortical hypoperfusion. Subcortically, hypoperfusion was also found in the caudate nucleus. This pattern of hypoperfusion could be related to cognitive dysfunctions that have been previously observed even at the disease early stages. The present results were obtained by means of whole brain voxel-wise comparisons of absolute perfusion values, using statistical parametric mapping, thus avoiding the potentially biased global mean normalization procedure. In addition, this work demonstrates that between-group comparison of relative perfusion values after global mean normalization, introduced artifactual relative perfusion increases, where absolute perfusion was in fact preserved. This has implications for perfusion studies of other brain disorders.
KW - Aged
KW - Artifacts
KW - Brain Mapping
KW - Cerebral Arteries
KW - Cerebral Cortex
KW - Cerebrovascular Circulation
KW - Cluster Analysis
KW - Data Interpretation, Statistical
KW - Female
KW - Functional Laterality
KW - Humans
KW - Magnetic Resonance Imaging
KW - Male
KW - Middle Aged
KW - Neuropsychological Tests
KW - Parkinson Disease
KW - Perfusion
KW - Spin Labels
KW - Journal Article
KW - Research Support, Non-U.S. Gov't
KW - Parkinson's disease
KW - Global mean normalization
KW - Arterial spin labeling
UR - http://www.scopus.com/inward/record.url?scp=84855428685&partnerID=8YFLogxK
U2 - 10.1016/j.neuroimage.2011.10.033
DO - 10.1016/j.neuroimage.2011.10.033
M3 - Article
C2 - 22032942
SN - 1053-8119
VL - 59
SP - 2743
EP - 2750
JO - NeuroImage
JF - NeuroImage
IS - 3
ER -