The Scholar will spend at least 75 percent of his/her effort in sickle cell anemia-related research under the leadership of Dr. Luban, an established clinical investigator who also directs faculty training and mentorship at CNMC. Dr. Luban in conjunction with the physicians and scientist of WACSCC will develop a carefully planned, individualized research training program designed to ensure that the Scholar becomes an independent physician and/or biomedical researcher focused on critical translational and clinical questions related to sickle cell disease. An individualized career development plan (ICDP) (Appendix A) will be developed for the Sickle Cell Scholar and will encompass three major components: core curriculum, laboratory training and translational applications in the clinical setting. The first component is formal course work including a variety of disciplines: statistics, epidemiology, clinical trial design, regulatory aspects of clinical investigation, research ethics, scientific tools of clinical investigation, analytical techniques in clinical investigation, and principles and techniques of biochemistry, molecular biology and molecular genetics. These courses will be provided through the HU (RR010284) and CNMC (RR020359) Clinical Research Centers and the HU Research Scientist Program (R25HL003679) augmented by our joint K30 and associated T32 and K12 programs and by course work at HUSM and CNMC, local universities and through selected programs at NIH The second component provides a highly structured laboratory training program that is designed to provide practical training in biochemistry, molecular biology, genetics and analytic techniques, and in the analysis of clinical and laboratory data that results from bench investigations and clinical investigation implemented at the WACSCC collaborative laboratories and GCRCs. Physician scientists and epidemiologic researchers with interests in health care disparities and care delivery will engage in programs designed to learn methodological approaches to data- based investigations and quantitative research. The third component consists of developing and conducting a clinical project in sickle cell disease. The scholar will design, implement and participate in the conduct of a mentored clinical research project. This part of Scholar's training will ensure that he/she develops the training needed to conduct multidisciplinary clinical research, recognize the difficulties in such studies and develop tools to ensure future success as a clinical researcher or collaborative biomedical researcher. The ultimate goal of the Sickle Cell Scholar program is to inspire young and/or new investigators to devote their career to innovative and productive research that will lead to decreasing the disease burden and stigmata of this disease.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Specialized Center--Cooperative Agreements (U54)
Project #
5U54HL090508-03
Application #
8263399
Study Section
Special Emphasis Panel (ZHL1)
Project Start
Project End
Budget Start
2011-05-01
Budget End
2012-02-29
Support Year
3
Fiscal Year
2011
Total Cost
$97,382
Indirect Cost
Name
Howard University
Department
Type
DUNS #
056282296
City
Washington
State
DC
Country
United States
Zip Code
20059
Tatari-Calderone, Zohreh; Gordish-Dressman, Heather; Fasano, Ross et al. (2016) Protective effect of HLA-DQB1 alleles against alloimmunization in patients with sickle cell disease. Hum Immunol 77:35-40
Glass, Penny; Brennan, Tara; Wang, Jichuan et al. (2013) Neurodevelopmental deficits among infants and toddlers with sickle cell disease. J Dev Behav Pediatr 34:399-405
Luban, Naomi L C; McBride, Eileen; Ford, Jason C et al. (2012) Transfusion medicine problems and solutions for the pediatric hematologist/oncologist. Pediatr Blood Cancer 58:1106-11
Sachdev, Vandana; Kato, Gregory J; Gibbs, J Simon R et al. (2011) Echocardiographic markers of elevated pulmonary pressure and left ventricular diastolic dysfunction are associated with exercise intolerance in adults and adolescents with homozygous sickle cell anemia in the United States and United Kingdom. Circulation 124:1452-60
Kasvosve, Ishmael; Debebe, Zufan; Nekhai, Sergei et al. (2010) Ferroportin (SLC40A1) Q248H mutation is associated with lower circulating plasma tumor necrosis factor-alpha and macrophage migration inhibitory factor concentrations in African children. Clin Chim Acta 411:1248-52
Nouraie, Mehdi; Reading, Noel S; Campbell, Andrew et al. (2010) Association of G6PD with lower haemoglobin concentration but not increased haemolysis in patients with sickle cell anaemia. Br J Haematol 150:218-25
Aliyu, Zakari Y; Suleiman, Aisha; Attah, Ester et al. (2010) NT-proBNP as a marker of cardiopulmonary status in sickle cell anaemia in Africa. Br J Haematol 150:102-7