The Academic Award in Vascular Disease will be used to develop a comprehensive clinical, training, and research program in systemiC and pulmonary vascular diseases at the Center for Vascular Diseases, University of Colorado Health Sciences Center. The mission of the Center will be to provide comprehensive evaluation, and medical and surgical treatment, of patients with peripheral arterial disease, severe pulmonary hypertension, thrombophlebitis, hypercoagulable states, chronic venous disease, cerebrovascular disease and vasospastic diseases. Laboratory support will include sophisticated clinical vascular laboratories, heart catheter laboratories, MRI imaging to assess the systemic and pulmonary circulations, and a coagulation laboratory. An extensive patient registry has been established to monitor the clinical characteristics and status of all patients with vascular diseases in the University system. The Center will provide specialized training for medical students, surgical and medical house staff, graduate students, and Pulmonary and Cardiology fellows. The Center will support two dedicated vascular fellows each year for specialized clinical and research training. Clinical research will focus on the development of exercise rehabilitation and new drug therapies for claudication. Basic vascular biology research will address the role of disordered cell proliferation in the pathogenesis of severe pulmonary hypertension, as well as the mechanisms of the regulation of pulmonary vascular tone. The effects of ischemia on skeletal muscle metabolism and mitochondrial gene expression will also be evaluated. These clinical, training and research programs will be highly integrated, with weekly clinical specialty conferences to coordinate patient care, and a monthly vascular grand rounds as a focus for the training and research activities. Thus, this Center for Vascular Disease will provide a unique mechanism for the integration of clinical care in vascular diseases, the education of clinician/scientists in systemic and pulmonary vascular diseases, and for clinical and basic vascular biology research.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Academic/Teacher Award (ATA) (K07)
Project #
5K07HL002825-02
Application #
2210629
Study Section
Special Emphasis Panel (ZHL1-CCT-L (M1))
Project Start
1993-07-23
Project End
1998-06-30
Budget Start
1994-07-01
Budget End
1995-06-30
Support Year
2
Fiscal Year
1994
Total Cost
Indirect Cost
Name
University of Colorado Denver
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
065391526
City
Aurora
State
CO
Country
United States
Zip Code
80045
Brass, E P; Hiatt, W R (2000) Acquired skeletal muscle metabolic myopathy in atherosclerotic peripheral arterial disease. Vasc Med 5:55-9
Burke, T J; Falk, S; Conger, J D et al. (1999) Hemolysate-mediated renal vasoconstriction and hypersensitization. Ren Fail 21:23-33
Bhat, H K; Hiatt, W R; Hoppel, C L et al. (1999) Skeletal muscle mitochondrial DNA injury in patients with unilateral peripheral arterial disease. Circulation 99:807-12
Voelkel, N F; Allard, J D; Anderson, S M et al. (1999) cGMP and cAMP cause pulmonary vasoconstriction in the presence of hemolysate. J Appl Physiol 86:1715-20
Badesch, D B; Zamora, M; Fullerton, D et al. (1998) Pulmonary capillaritis: a possible histologic form of acute pulmonary allograft rejection. J Heart Lung Transplant 17:415-22
Badesch, D B; Zamora, M R; Jones, S et al. (1995) Independent ventilation and ECMO for severe unilateral pulmonary edema after SLT for primary pulmonary hypertension. Chest 107:1766-70
Minkler, P E; Brass, E P; Hiatt, W R et al. (1995) Quantification of carnitine, acetylcarnitine, and total carnitine in tissues by high-performance liquid chromatography: the effect of exercise on carnitine homeostasis in man. Anal Biochem 231:315-22
Abraham, W T; Raynolds, M V; Gottschall, B et al. (1995) Importance of angiotensin-converting enzyme in pulmonary hypertension. Cardiology 86 Suppl 1:9-15