ELECTRONIC POSTER - ismrm
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15:00 4325. Abnormal Iron Content in Deep Grey Matter Structures of MS Patients as a<br />
Function of Age<br />
Charbel Abdo Habib 1 , James Garbern, 1,2 , Manju Liu 1 , Ewart Mark Haacke 1<br />
1 Radiology, Wayne State University, Detroit, MI, United States; 2 Neurology, Wayne State University, Detroit,<br />
MI, United States<br />
Multiple sclerosis (MS) is a disease whose etiology until recently has remained a mystery. A possible explanation for MS has been put<br />
forward by Zamboni et al that it is caused by a chronic cerebrospinal venous insufficiency (CCSVI). In this abstract, we show that the<br />
iron deposition seen by susceptibility weighted imaging (SWI) in MS patients is abnormal compared to normal controls and appears in<br />
areas drained by the medial venous drainage system. This finding is consistent with the CCSVI hypothesis.<br />
Multiple Sclerosis II<br />
Hall B Monday 14:00-16:00 Computer 77<br />
14:00 4326. Deep Gray Matter Atrophy in a Large Sample of Clinically Isolated Syndrome and<br />
Early Relapsing-Remitting Multiple Sclerosis Patients<br />
Niels Bergsland 1 , Michael G. Dwyer 1 , Dana Horakova 2 , Ondrej Dolezal 1 , Zdenek Seidl 3 ,<br />
Manuela Vaneckova 3 , Eva Havrdova 2 , Robert Zivadinov 4<br />
1 University at Buffalo, Buffalo Neuroimaging Analysis Center, Buffalo, NY, United States; 2 Charles<br />
University, Department of Neurology, Prague, Czech Republic; 3 Charles University, Department of Radiology,<br />
Prague, Czech Republic; 4 Neurology, Buffalo Neuroimaging Analysis Center, Buffalo , NY , United States<br />
To quantify deep gray matter (DGM) atrophy in a large sample of clinically isolated syndrome (CIS) patients, early relapsingremitting<br />
(RR) multiple sclerosis (MS) patients, and healthy controls (HC). To investigate the relationship between DGM atrophy and<br />
disability in CIS patients.<br />
14:30 4327. Exploring the Relations Between Emotional Disability and Subcortical Atrophy in<br />
Patients with Multiple Sclerosis<br />
Francesca Bagnato 1 , Clelia Pellicano 1 , Fredric Cantor 1 , Antonio Gallo 1 , Sungyoung<br />
Auh 2 , Mary Ehrmantraut 1 , Iordanis Evangelou 1 , Vasiliki Ikonomidou 1 , Robert Kane 3 ,<br />
Joan Ohayon 1 , Susan Stern 1 , Henry McFarland 1<br />
1 NIB-NINDS-NIH, Bethesda, MD, United States; 2 Clinical Director Office-NINDS-NIH, Bethesda, MD,<br />
United States; 3 VA, Baltimore<br />
Pathophysiological mechanisms underlying the development of depression in patients with multiple sclerosis (MS) remain unknown.<br />
We here demonstrate that atrophy of deep grey matter (GM) structures of the limbic circuit, such as thalamus and hippocampus, may<br />
explain up to 30% of the variance of depression in MS. The relation between depression and GM atrophy holds significant when the<br />
effect of patients’ physical disability is taken into account. The results highlight the role of neurodegeneration in specific brain sites as<br />
an important factor associated with depression in MS patients.<br />
15:00 4328. A Five-Year Serial Longitudinal Study of Deep Gray Matter Atrophy in Patients<br />
with Multiple Sclerosis<br />
Robert Zivadinov 1 , Dana Horakova 2 , Michael G. Dwyer 3 , Deepa Ramasamy 3 , Eva<br />
Havrdova 2 , Zdenek Seidl 4 , Ondrej Dolezal 3 , Sara Hussein 3 , Ellen Carl 3 , Manuela<br />
Vaneckova 4 , Niels Bergsland 3<br />
1 Neurology, Buffalo Neuroimaging Analysis Center, Buffalo , NY , United States; 2 Charles University,<br />
Department of Neurology, Prague, Czech Republic; 3 University at Buffalo, Buffalo Neuroimaging Analysis<br />
Center, Buffalo, NY, United States; 4 Charles University, Department of Radiology, Prague, Czech Republic<br />
To compare the evolution of deep gray matter (DGM) atrophy in early relapsing-remitting (RR) multiple sclerosis (MS) patients and<br />
in normal controls (NC) over 2 years. To investigate the extent of DGM atrophy progression in MS patients over 5 years.<br />
15:30 4329. Relation Between Thalamic Atrophy and Long-Term Disability Progression in<br />
Multiple Sclerosis: A 8-Year Follow Up Study<br />
Maria A. Rocca 1 , Sarlota Mesaros 1 , Elisabetta Pagani 1 , Maria Pia Sormani 1,2 , Vittorio<br />
Martinelli 3 , Giancarlo Comi 3 , Massimo Filippi 1<br />
1 Neuroimaging 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 and University Hospital San Raffaele,<br />
Milan, Italy<br />
We assessed the value of thalamic damage (in terms of atrophy and magnetization transfer ratio-MTR), taken in isolation, and its<br />
short-term changes in predicting accumulation of disability over an 8-year period in 73 patients with relapse-onset multiple sclerosis<br />
(MS). At the end of follow up, 44 patients (60%) showed a significant disability worsening. A multivariable model included baseline<br />
thalamic fraction [p=0.01, odds ratio (OR)=0.62], and average lesion MTR percentage change after 12 months (p=0.04, OR=0.90) as