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TRADITIONAL POSTER - ismrm

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Poster Sessions<br />

coefficient (ADC) and imaging/histopathological features of vulnerability (thin cap, lipid core, haemorrhage, angiogenesis (CD105 or VEGF) &<br />

inflammation (CD68). Mean (SD) plaque ADC was 1.30 X10-3(0.29) mm2/s. There was no difference in ADC between patients with and without MRI<br />

features of plaque vulnerability. There was a positive trend between ADC & CD105/VEGF, markers of angiogenesis meriting further investigation.<br />

2221. Differing Fractional Anisotropy Changes in Grey Matter and White Matter in Early Ischemic Stroke<br />

Mohamed Mustafa Hirji 1,2 , Ashley D. Harris, 2,3 , Robert K. Kosior, 2,4 , Cheryl R. McCreary, 2,5 , Richard<br />

Frayne 2,5<br />

1 University of Calgary, Calgary, Alberta, Canada; 2 Seaman Family MR Research Centre, Alberta Health Services, Calgary, Alberta,<br />

Canada; 3 School of Psychology & Cardiff University Brain Research Imaging Centre, Cardiff University, Cardiff, Wales, United<br />

Kingdom; 4 Biomedical Engineering, University of Calgary, Calgary, Alberta, Canada; 5 Radiology & Clinical Neurosciences,<br />

University of Calgary, Calgary, Alberta, Canada<br />

We characterise the fractional anisotropy (FA) changes in ischemic stroke. Diffusion tensor images of 13 patients were obtained within 26 hours of stroke<br />

(acutely) and >21 days later (follow-up). FA and eigenvalues were measured in freehand regions of interest (ROIs); anatomically-matched contralateral<br />

ROIs were used for control. Acutely, FA increased in gray matter (GM) but not in white matter (WM); the eigenvalue reductions were unbalanced in GM,<br />

but balanced in WM. At follow-up, FA decreased in both GM and WM with the eigenvalue changes similar in both GM and WM. Our results give insight<br />

into microstructural changes in stroke.<br />

2222. Intensive Blood Pressure Lowering Increases Cerebral Blood Flow in Older Subjects with<br />

Hypertension<br />

Jiabao He 1 , Dinesh Tryambake 1 , Michael J. Firbank 2 , John T. O’Brien 2 , Gary A. Ford 1 , Andrew M.<br />

Blamire 1<br />

1 Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, Tyne and Wear, United Kingdom; 2 Institute for Ageing<br />

and Health, Newcastle University, Newcastle upon Tyne, Tyne and Wear, United Kingdom<br />

CBF determines brain tissue metabolic supply and is compromised in chronic hypertension which alters autoregulatory function. Blood pressure (BP)<br />

lowering therapy has clear clinical benefit but may risk inducing hypoperfusion. Optimal target BP in older subjects with hypertension is unclear, although<br />

guidelines recommend target BP of

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