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Electronic Posters: Neuroimaging - ismrm

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white matter showed significant and widespread alterations throughout the brain of ALS patients. In the gray matter of the ALS group,<br />

significant differences were found in the left frontal- and left parietal lobes for NAA/Cr, and bilateral frontal lobe for Cho/NAA.<br />

15:30 4261. Brain DT MRI Predicts the Long-Term Clinical Evolution in Amyotrophic Lateral<br />

Sclerosis: A 3.4 Year Follow Up Study<br />

Federica Agosta 1 , Elisabetta Pagani 1 , Melissa Petrolini 1 , Maria Pia Sormani 2 , Domenico<br />

Caputo 3 , Michele Perini 4 , Alessandro Prelle 5 , Fabrizio Salvi 6 , Massimo Filippi 1<br />

1 <strong>Neuroimaging</strong> Research Unit, Institute of Experimental Neurology, Division of Neuroscience, Scientific<br />

Institute and University Hospital San Raffaele, Milan, Italy; 2 Unit of Biostatistics, DISSAL, University of<br />

Genoa, Genoa, Italy; 3 Department of Neurology, Scientific Institute Fondazione Don Gnocchi, Milan, Italy;<br />

4 Department of Neurology, Ospedale di Gallarate, Gallarate, Italy; 5 Dino Ferrari Center, Department of<br />

Neuroscience, University of Milan, Milan, Italy; 6 Department of Neurology, Ospedale di Bellaria, University of<br />

Bologna, Bologna, Italy<br />

We investigated whether corticospinal tract (CST) DT-MRI changes contribute to the prediction of long-term clinical evolution in<br />

patients with amyotrophic laterals sclerosis (ALS). Conventional and DT-MRI were obtained in 24 ALS patients, who were followed<br />

prospectively for 3.4 years. Compared with controls, ALS patients showed increased MD and decreased FA of the CST. Shorter<br />

disease duration and lower CST FA were associated with disability worsening. Bulbar-onset and CST FA were independent predictors<br />

of time to death in ALS patients. More severe DT-MRI abnormalities in the CST predicted a poorer clinical outcome after a 3.4 year<br />

follow up in ALS patients.<br />

Tuesday 13:30-15:30 Computer 73<br />

13:30 4262. Altered Functional Connectivity of the Motor Network in Multiple System Atrophy<br />

Feng Feng 1 , Hui You 1 , Han Wang 2 , Fuling Zheng 1 , Chunling Meng 1 , Jue Wang 3 , Yufeng<br />

Zang 3<br />

1 Radiology, Peking Union Medical College Hospital, Beijing, China; 2 Neurology, Peking Union Medical<br />

College Hospital, Beijing, China; 3 State Key Laboratory of Cognitive Neuroscience and Learning, Beijing<br />

Normal University, Beijing, China<br />

MSA is mainly a sporadic neurodegenerative disease. Besides abnormalities of nigrostriatal pathway, the typical pathological findings<br />

were also described in primary motor and supplementary motor cortices. We hypothesize that there is associated disturbance of<br />

functional connectivity of the motor cortex in MSA patients. To test the hypothesis, resting-state functional MRI was used to measure<br />

the coherent spontaneous fluctuations in the blood oxygenation level¨Cdependent signal. Our results showed regional homogeneity<br />

changes in left precentral gyrus, right precuneus, supramarginal gyrus and middle frontal gyrus, indicating functional connectivity<br />

disturbance of motor-related circuits and left-sided predominance of primary motor cortex involvement.<br />

14:00 4263. The Topographical Distribution of White Matter Damage in Parkinson’s Disease<br />

and Progressive Supranuclear Palsy<br />

Federica Agosta 1 , Sebastiano Galantucci 1 , T Stojkovic 2 , A. Tomic 2 , Igor Petrovic 2 , Giulia<br />

Longoni 1 , Vladimir Kostic 2 , Massimo Filippi 1<br />

1 <strong>Neuroimaging</strong> Research Unit, Institute of Experimental Neurology, Division of Neuroscience, Scientific<br />

Institute and University Hospital San Raffaele, Milan, Italy; 2 Department of Neurology, School of Medicine,<br />

University of Belgrade, Belgrade, Yugoslavia<br />

Using TBSS, we investigated WM changes in 39 Parkinson’s disease (PD) patients, 20 progressive supranuclear palsy (PSP) patients<br />

(10 Richardson’s syndrome [PSP-RS] and 10 PSP-Parkinsonism [PSP-P]), and 26 controls. PSP-RS showed the most pronounced<br />

pattern of decreased FA, including both infratentorial and supratentorial regions, vs. controls and other patient groups. A similar<br />

pattern of FA decrease (except for superior cerebellar peduncle) was found in PSP-P vs. controls and PD (only at a lower<br />

significance). Impaired WM integrity was found in PSP but not in PD. The less prominent WM involvement in PSP-P might be<br />

associated to its favorable clinical status.<br />

14:30 4264. The In-Vivo Topographical Distribution of Brain Tissue Loss Associated with<br />

Depression in Parkinson’s Disease: A Voxel-Based Morphometry Study<br />

Massimo Filippi 1 , Federica Agosta 1 , Igor Petrovic 2 , Sebastiano Galantucci 1 , Vladana<br />

Spica 2 , Milica Jecmenica 2 , Vladimir Kostic 2<br />

1 <strong>Neuroimaging</strong> Research Unit, Institute of Experimental Neurology, Division of Neuroscience, Scientific<br />

Institute and University Hospital San Raffaele, Milan, Italy; 2 Department of Neurology, School of Medicine,<br />

University of Belgrade, Belgrade, Yugoslavia<br />

VBM was used to investigate whether specific patterns of gray (GM) and white matter (WM) loss are associated with depression in 40<br />

patients with Parkinson’s disease (PD). Twenty-four PD were diagnosed as non-depressed (PD-NDep), and 16 as having depression<br />

(PD-Dep). Compared with PD-NDep, PD-NDep showed WM loss in the right anterior cingulum and inferior orbitofrontal (OF)<br />

region. In PD patients, Hamilton rating scale for depression score correlated significantly with right inferior OF WM. The pattern of<br />

brain atrophy in PD-Dep overlaps with the key regions involved in major depressive disorders, suggesting an increased vulnerability<br />

of this neural circuit in PD.

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