This is a proposal to continue follow-up of the Wisconsin Diabetes Registry, a unique population-based cohort of 595 individuals enrolled at diagnosis of insulin-dependent diabetes mellitus (IDDM) and closely monitored for up to 5 years. Glycemic control and microvascular status have been described comprehensively from the time of diagnosis for all subjects newly diagnosed with IDDM living in a geographically defined area of central and southern Wisconsin and less than 30 years of age at diagnosis. Such information puts this study in a critical position to make a substantial contribution to the understanding of progression and correlates of long term complications of diabetes. The primary goals in following up this cohort are to: 1) determine incidence and progression of nephropathy, retinopathy and neuropathy 6 to 10 years after diagnosis of diabetes; 2) quantify the relationship between incidence and progression of these complications and longitudinal glycemic control, other medical conditions (e.g., hypertension), familial factors (e.g., parent or sibling hypertension), puberty stage and gender, age at diagnosis of diabetes, selected physiologic and genetic characteristics (e.g., genetic markers, IGF-I); 3) determine how age, gender, endogenous insulin, medical management, self-management and economic status influence glycemic control after 6-10 of diabetes; 4) determine the incidence of acute diabetes-related complications after 6-10 years of diabetes and determine the relationship of this incidence to recent and longitudinal glycemic control. New emphasis in this proposal is placed on factors that may correlate with microvascular complications independent of glycemic control. Microvascular complications are present in the majority of individuals with diabetes within 10 years of diagnosis. This study provides the only large population based cohort that can be evaluated during the interval when microvascular complications are most likely to develop. This study will provide a precise description of the time course in which complications evolve, singly or in synergistic combinations. Only by understanding the evolution of complications and factors that influence their chronology will it be possible to identify characteristics that may identify persons at high risk. Intensive preventive and therapeutic interventions could then be focused on such high risk persons.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK036904-09
Application #
2139917
Study Section
Epidemiology and Disease Control Subcommittee 2 (EDC)
Project Start
1987-05-01
Project End
1997-04-30
Budget Start
1995-05-01
Budget End
1996-04-30
Support Year
9
Fiscal Year
1995
Total Cost
Indirect Cost
Name
University of Wisconsin Madison
Department
Public Health & Prev Medicine
Type
Schools of Medicine
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
Hassan, Lina Saleh; Monson, Rebecca S; Danielson, Kirstie K (2017) Oestradiol levels may differ between premenopausal women, ages 18-50, with type 1 diabetes and matched controls. Diabetes Metab Res Rev 33:
Danielson, K K; Monson, R S; LeCaire, T J (2016) Factors Associated with Higher Pro-Inflammatory Tumor Necrosis Factor-? Levels in Young Women with Type 1 Diabetes. Exp Clin Endocrinol Diabetes 124:140-7
Kujath, Amber S; Quinn, Lauretta; Elliott, Mary E et al. (2015) Oxytocin levels are lower in premenopausal women with type 1 diabetes mellitus compared with matched controls. Diabetes Metab Res Rev 31:102-12
LeCaire, Tamara J; Palta, Mari (2015) Longitudinal Analysis of Adiponectin through 20-Year Type 1 Diabetes Duration. J Diabetes Res 2015:730407
Kujath, Amber S; Quinn, Lauretta; Elliott, Mary E et al. (2015) Different health behaviours and clinical factors associated with bone mineral density and bone turnover in premenopausal women with and without type 1 diabetes. Diabetes Metab Res Rev 31:421-32
Palta, Mari; LeCaire, Tamara J; Sadek-Badawi, Mona et al. (2014) The trajectory of IGF-1 across age and duration of type 1 diabetes. Diabetes Metab Res Rev 30:777-83
LeCaire, Tamara J; Palta, Mari; Klein, Ronald et al. (2013) Assessing progress in retinopathy outcomes in type 1 diabetes: comparing findings from the Wisconsin Diabetes Registry Study and the Wisconsin Epidemiologic Study of Diabetic Retinopathy. Diabetes Care 36:631-7
Palta, Mari; LeCaire, Tamara (2009) Managing type 1 diabetes: trends and outcomes over 20 years in the Wisconsin Diabetes Registry cohort. WMJ 108:231-5
Danielson, K K; Elliott, M E; LeCaire, T et al. (2009) Poor glycemic control is associated with low BMD detected in premenopausal women with type 1 diabetes. Osteoporos Int 20:923-33
Cohen, Robert M; LeCaire, Tamara J; Lindsell, Christopher J et al. (2008) Relationship of prospective GHb to glycated serum proteins in incident diabetic retinopathy: implications of the glycation gap for mechanism of risk prediction. Diabetes Care 31:151-3

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