This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. This long-term observational study continues to examine complications of type 1 diabetes. It examines factors associated with development of kidney, macrovascular, eye and nerve complications of diabetes. Study volunteers first participated in the Diabetes Control and Complications Trial (DCCT), between 1984 and 1993. Visits occur annually, for laboratory and physical assessment. Eye exams, scans for cardiac and circulatory status, and evaluations of cognitive skills are included on an intermittent basis. Over the next two years, more detailed assessments of neurological function will be completed. Numerous articles have been published so far. Notably, this study has introduced a concept called 'metabolic memory' as a possible explanation for differences in the appearance and progression of diabetes complications that are still evident between the original conventional and intensive treatment groups, despite years of nearly equal glucose control since DCCT completion. In an allied study, we obtained DNA, blood and urine chemistry, blood pressure, and body size data from 139 first-degree relatives of the University of Washington DCCT/EDIC subjects. This is being analyzed along with samples collected from relatives at other EDIC clinics. Most of the relatives were seen on the GCRC, but others participated through phone interview and 'remote' lab tests at their local physicians' offices. Data is being studied to see what DNA commonalities, if any, appear among family groups where the DCCT/EDIC subject does or does not have significant complications of diabetes. The relatives were seen on the GCRC between September 2002 and August of 2004

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
5M01RR000037-46
Application #
7379303
Study Section
National Center for Research Resources Initial Review Group (RIRG)
Project Start
2006-04-01
Project End
2007-03-31
Budget Start
2006-04-01
Budget End
2007-03-31
Support Year
46
Fiscal Year
2006
Total Cost
$49,619
Indirect Cost
Name
University of Washington
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
605799469
City
Seattle
State
WA
Country
United States
Zip Code
98195
Courcoulas, Anita P; King, Wendy C; Belle, Steven H et al. (2018) Seven-Year Weight Trajectories and Health Outcomes in the Longitudinal Assessment of Bariatric Surgery (LABS) Study. JAMA Surg 153:427-434
Field, Alison E; Inge, Thomas H; Belle, Steven H et al. (2018) Association of Obesity Subtypes in the Longitudinal Assessment of Bariatric Surgery Study and 3-Year Postoperative Weight Change. Obesity (Silver Spring) 26:1931-1937
O'Rourke, Robert W; Johnson, Geoffrey S; Purnell, Jonathan Q et al. (2018) Serum biomarkers of inflammation and adiposity in the LABS cohort: associations with metabolic disease and surgical outcomes. Int J Obes (Lond) :
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Han, Seung Jin; Boyko, Edward J; Kim, Soo Kyung et al. (2018) Association of Thigh Muscle Mass with Insulin Resistance and Incident Type 2 Diabetes Mellitus in Japanese Americans. Diabetes Metab J 42:488-495
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Purnell, Jonathan Q; Johnson, Geoffrey S; Wahed, Abdus S et al. (2018) Prospective evaluation of insulin and incretin dynamics in obese adults with and without diabetes for 2 years after Roux-en-Y gastric bypass. Diabetologia 61:1142-1154
King, Wendy C; Hinerman, Amanda S; Belle, Steven H et al. (2018) Comparison of the Performance of Common Measures of Weight Regain After Bariatric Surgery for Association With Clinical Outcomes. JAMA 320:1560-1569
Han, Seung Jin; Fujimoto, Wilfred Y; Kahn, Steven E et al. (2018) Change in visceral adiposity is an independent predictor of future arterial pulse pressure. J Hypertens 36:299-305

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