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Stroke and Cerebrovascular Research
URMC Neurology Research
Scope of Research: Basic Science and Clinical Research
Research goals of the Stroke Unit include 1) expanding our understanding
of the mechanisms of ischemic injury to the brain; 2) improving
acute ischemic stroke treatment; 3) developing more effective
strategies in secondary stroke prevention; and 4) identifying
cost-effective diagnostic testing and treatment.
Clinical stroke research includes:
• Active participation in clinical trials of novel treatment agents
for acute stroke (Activated Protein C), endovascular interventions
in acute stroke, insulin in hyperglycemic patients with intracerebral
hemorrhage, and secondary prevention in patients with insulin resistance,
small vessel ischemic disease or patent forament ovale.
• Identifying predictive factors for the use of transesophagel
echocardiography in acute stroke
• Cost-effectiveness of carotid artery stenting vs endarterectomy
• Characterizing risk of stroke in patients with ventricular-assist
devices
• Utility of telemetry in acute stroke monitoring
• Use of anti-platelet agents following carotid interventions
• Medical vs. surgical management of unruptured brain AVMs
• Genetic study of strokes in siblings
Basic science research includes:
• Investigating the response of the brain to hypoxia and how it
influences cell death during stroke. In particular, we are interested
in the role of Hypoxia-inducible factor 1 alpha in altering cell
death during hypoxia and stroke.
• Collaborative research on putative neuroprotectants in acute
ischemic stroke (Berislav Zlokovic, M.D., Ph.D.)
References
Vangeison, G., Carr, D., Damsker, Jesse M. , Nowak, Romana A.,
Constant, Stephanie L. ,Federoff, HJ and Rempe D. Astrocytic
CD147, which is partially regulated by HIF-1, enhances hypoxia-induced
neuronal death. Journal of Neuroscience (2008); accepted pending
revisions
Vangeison, G., Carr, D., Federoff, HJ and Rempe D. The Good, the Bad, and the Cell-Type Specific Roles of HIF-1? in Neurons and Astrocytes. Journal of Neuroscience (2008); 28(8):1988-1993 View PubMed Reference
Halterman MW, De Jesus, C., Rempe D., Schor, N., and HJ Federoff. c/EBP- ß Inhibits the Adaptive to Pathologic Switch in a Model of Hypoxia-Induced Neuronal Apoptosis. Molecular and Cellular Neuroscience (2008) Jun;38(2):125-37 View PubMed Reference
Rempe, D., Lelli, K., Vangeison, G., Federoff, H. In cultured astrocytes, p53 and MDM2 do not alter hypoxic HIF-1? function regardless of presence of DNA damage. Journal of Biological Chemistry (2007); 82(22):16187-201. View PubMed Reference
Kasner, S E. MD; Lynn, M J. MS; Chimowitz, M I. MB, ChB; Frankel, M R. MD; Howlett-Smith, H RN; Hertzberg, V S. PhD; Chaturvedi, S MD; Levine, S R. MD; Stern, B J. MD; Benesch, C G. MD; Jovin, T G. MD; Sila, C A. MD; Romano, J G. MD; for the Warfarin Aspirin Symptomatic Intracranial Disease (WASID) Trial Investigators. Warfarin vs aspirin for symptomatic intracranial stenosis: Subgroup analyses from WASID. Neurology 2006;67:1275-1278. View PubMed Reference
Kelly A, Thompson JB, Tuttle D, Benesch CG, Holloway RG. Public reporting of quality data for stroke; Is it measuring quality? Stroke (in publication). View PubMed Reference
Curtis Benesch, M.D., M.P.H., Unit Chief
curtis_benesch@urmc.rochester.edu
(585) 275-2530



