The training program in ?Cardiovascular Biomechanics and Imaging? has the primary goal of attracting highly qualified, multi-disciplinary scientists in the area of cardiovascular bioengineering at pre- and post- doctoral levels. This supplement will expand this training to two laboratories involved in cardiovascular biomechanics and imaging in heart defects and cardiovascular pathologies in models of Down syndrome. This additional focus will leverage collaborations with the Linda Crnic Institute for Down Syndrome on the Anschutz Medical Campus at the University of Colorado and will attract more researchers to Down syndrome research. The new portions of this supplement will use human trisomy 21 iPSC lines and Down syndrome mouse models provided by the Crnic Institute for targeted, high-risk, high-reward basic science studies on chromosome 21. These projects will specifically address the NHLBI INCLUDE funding priorities of characterization of differentiation of disease-related tissue types in induced pluripotent stem cells (iPSCs) derived from cells from individuals with Down syndrome and compared to euploid iPSCs, and characterization in animal models of the morphological events occurring in early heart development that give rise to the specific forms of congenital heart disease that are the primary cause of death during the first year of life for infants born with Down syndrome.

Public Health Relevance

This supplement expands the training grant in ?Cardiovascular Biomechanics and Imaging? at the University of Colorado Anschutz Medical Campus to include two additional projects involving Down syndrome. One project will investigate the reasons that infants with Down syndrome have a high rate of heart defects. The other will investigate heart defects and failure in a mouse model of Down syndrome.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Institutional National Research Service Award (T32)
Project #
3T32HL072738-16S1
Application #
9935678
Study Section
Special Emphasis Panel (ZHL1)
Program Officer
Lidman, Karin Fredriksson
Project Start
2003-04-01
Project End
2020-05-31
Budget Start
2019-09-14
Budget End
2020-05-31
Support Year
16
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of Colorado Denver
Department
Biomedical Engineering
Type
Schools of Medicine
DUNS #
041096314
City
Aurora
State
CO
Country
United States
Zip Code
80045
Schäfer, Michal; Kheyfets, Vitaly O; Barker, Alex J et al. (2018) Reduced shear stress and associated aortic deformation in the thoracic aorta of patients with chronic obstructive pulmonary disease. J Vasc Surg 68:246-253
Gates, Phillip E; Gurung, Arati; Mazzaro, Luciano et al. (2018) Measurement of Wall Shear Stress Exerted by Flowing Blood in the Human Carotid Artery: Ultrasound Doppler Velocimetry and Echo Particle Image Velocimetry. Ultrasound Med Biol 44:1392-1401
St Clair, Joshua R; Ramirez, David; Passman, Samantha et al. (2018) Contrast-enhanced ultrasound measurement of pancreatic blood flow dynamics predicts type 1 diabetes progression in preclinical models. Nat Commun 9:1742
Govindarajan, Tina; Shandas, Robin (2017) Shape Memory Polymers Containing Higher Acrylate Content Display Increased Endothelial Cell Attachment. Polymers (Basel) 9:
McClatchey, Penn M; Frisbee, Jefferson C; Reusch, Jane E B (2017) A conceptual framework for predicting and addressing the consequences of disease-related microvascular dysfunction. Microcirculation 24:
Gurung, Arati; Gates, Phillip E; Mazzaro, Luciano et al. (2017) Echo Particle Image Velocimetry for Estimation of Carotid Artery Wall Shear Stress: Repeatability, Reproducibility and Comparison with Phase-Contrast Magnetic Resonance Imaging. Ultrasound Med Biol 43:1618-1627
Mason McClatchey, P; Bauer, Timothy A; Regensteiner, Judith G et al. (2017) Dissociation of local and global skeletal muscle oxygen transport metrics in type 2 diabetes. J Diabetes Complications 31:1311-1317
Mason McClatchey, P; Wu, Fan; Olfert, I Mark et al. (2017) Impaired Tissue Oxygenation in Metabolic Syndrome Requires Increased Microvascular Perfusion Heterogeneity. J Cardiovasc Transl Res 10:69-81
McClatchey, P Mason; Keller, Amy C; Bouchard, Ron et al. (2016) Fully automated software for quantitative measurements of mitochondrial morphology. Mitochondrion 26:58-71
McClatchey, P Mason; Keller, Amy C; Bouchard, Ron et al. (2016) Raw and processed microscope images of fixed cells at baseline and following various experimental perturbations. Data Brief 6:998-1006

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