Principle Investigator/Program Director (Last, fv'st, middle): Bumett, John, M.D.This competitive renewal application requests continuous funding (years 34-38) of the Mayo General ClinicalResearch Center. The GCRC integrates inpatient and outpatient activities at two distinct sites: the Saint MarysHospital unit (15,000 sq. ft.) has both inpatient and outpatient activity, and the Charlton Building outpatientGCRC (12,500 sq. R.) is exclusively for outpatients. The Charlton outpatient GCRC is an expansion of ourprogram since the previous grant renewal and was opened in 2000 to meet the increasing demand for outpatientstudies. In addition to the patient care areas, the GCRC has core laboratories, a metabolic kitchen,administrative offices, and conference rooms. A unique feature of the Mayo GCRC is the extensive corelaboratory facilities to perform detailed phenotyping, metabolic measurements, and body compositionmeasurements along with gastrointestinal, chemistry, exercise, sleep, microneurography, and echocardiographystudies. Since the previous site visit, these facilities have been substantially modernized and expanded to includethe addition of microarray and new mass spectrometers for proteomie measurements. We expanded the CDMASprogram to an Informatics and Bioinformaties core, which links various GCRC operations and data handling forGCRC investigators. The inpatient utilization (~80% by NIH grants, 95% A beds) remains stable at about 2,100beds; whereas, the outpatient utilization (-60% by NIH grants, 94% A visits) expanded more than three-fold to18,000 visits per year. There was a more than two-fold increase in NIH grants to 86 grants and more than 200protocols based in the GCRC. The major research activities are related to the following areas: 1) cancertherapies, 2) obesity and diabetes, 3) aging and hormonal secretion, 4) muscle, 5) osteoporosis, 6) vascularphysiology, 7) gastric physiology, 8) mechanisms of incontinence, 9) sleep disorders, 10) autonomic neuropathy,11) age-related valvular calcification, 12) hypertension, 13) vaccine research, and 14) neurodegenerativediseases. We have expanded education and training programs and outlined our vision for continued success ofGCRC as a resource for human research at Mayo.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
5M01RR000585-35
Application #
7023070
Study Section
National Center for Research Resources Initial Review Group (RIRG)
Program Officer
Talbot, Bernard
Project Start
1997-02-01
Project End
2006-09-29
Budget Start
2005-12-01
Budget End
2006-09-29
Support Year
35
Fiscal Year
2006
Total Cost
$3,859,208
Indirect Cost
Name
Mayo Clinic, Rochester
Department
Type
DUNS #
006471700
City
Rochester
State
MN
Country
United States
Zip Code
55905
Yu, Alan S L; Shen, Chengli; Landsittel, Douglas P et al. (2018) Baseline total kidney volume and the rate of kidney growth are associated with chronic kidney disease progression in Autosomal Dominant Polycystic Kidney Disease. Kidney Int 93:691-699
Kamimura, Daisuke; Suzuki, Takeki; Wang, Wanmei et al. (2018) Higher plasma leptin levels are associated with reduced left ventricular mass and left ventricular diastolic stiffness in black women: insights from the Genetic Epidemiology Network of Arteriopathy (GENOA) study. Hypertens Res 41:629-638
Nowak, Kristen L; You, Zhiying; Gitomer, Berenice et al. (2018) Overweight and Obesity Are Predictors of Progression in Early Autosomal Dominant Polycystic Kidney Disease. J Am Soc Nephrol 29:571-578
Tirumanisetty, P; Prichard, D; Fletcher, J G et al. (2018) Normal values for assessment of anal sphincter morphology, anorectal motion, and pelvic organ prolapse with MRI in healthy women. Neurogastroenterol Motil 30:e13314
McKenzie, Katelyn A; El Ters, Mirelle; Torres, Vicente E et al. (2018) Relationship between caffeine intake and autosomal dominant polycystic kidney disease progression: a retrospective analysis using the CRISP cohort. BMC Nephrol 19:378
Dad, Taimur; Abebe, Kaleab Z; Bae, K Ty et al. (2018) Longitudinal Assessment of Left Ventricular Mass in Autosomal Dominant Polycystic Kidney Disease. Kidney Int Rep 3:619-624
Brosnahan, Godela M; Abebe, Kaleab Z; Rahbari-Oskoui, Frederic F et al. (2017) Effect of Statin Therapy on the Progression of Autosomal Dominant Polycystic Kidney Disease. A Secondary Analysis of the HALT PKD Trials. Curr Hypertens Rev 13:109-120
Kamimura, Daisuke; Suzuki, Takeki; Furniss, Anna L et al. (2017) Elevated serum osteoprotegerin is associated with increased left ventricular mass index and myocardial stiffness. J Cardiovasc Med (Hagerstown) 18:954-961
Chung, Jin Ook; Koutsari, Christina; Blachnio-Zabielska, Agnieszka U et al. (2017) Intramyocellular Ceramides: Subcellular Concentrations and Fractional De Novo Synthesis in Postabsorptive Humans. Diabetes 66:2082-2091
West, Nancy A; Lirette, Seth T; Cannon, Victoria A et al. (2017) Adiposity, Change in Adiposity, and Cognitive Decline in Mid- and Late Life. J Am Geriatr Soc 65:1282-1288

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