Type II DM confers a markedly increased risk of cardiovascular disease (CVD) in premenopausal women. One potentially significant contributor to increased CVD risk may be impaired fibrinolysis. Healthy premenopausal women appear to have the greatest fibrinolytic potential. Yet studies that have demonstrated impaired fibrinolysis in diabetic patients have included few women and have not controlled for hormonal status. We postulated that the fibrinolytic response to stasis in premenopausal diabetic women would be more impaired than that of age and weight matched diabetic men. Healthy, sedentary, non-smoking diabetic women, diabetic men and control women with no evidence of CVD were studied. Baseline euglobulin lysis time (ELT) was drawn prior to inflation of a blood pressure cuff to mean arterial pressure. At the end of the cuff induced 15-minute stasis period a repeat ELT was drawn. Women with diabetes demonstrated an impaired response to stasis. Specifically there was a smaller decrease in ELT in diabetic women compared to both diabetic men and control women*, P<0.05 difference between diabetic women and other groups, +, P<0.05 difference pre to post stasis. Data suggests that fibrinolytic impairment is more pronounced in diabetic women than diabetic men. The changes may indicate that premenopausal diabetic women have fibrinolytic potential similar to that of postmenopausal women. Future studies should explore the mechanisms of impairment and the theory that increased CVD risk in premenopausal women with diabetes may be related to this significant impairment fibrinolytic response to stasis.

Project Start
1998-12-01
Project End
1999-11-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
38
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of Colorado Denver
Department
Type
DUNS #
065391526
City
Aurora
State
CO
Country
United States
Zip Code
80045
Millstein, Richard J; Pyle, Laura L; Bergman, Bryan C et al. (2018) Sex-specific differences in insulin resistance in type 1 diabetes: The CACTI cohort. J Diabetes Complications 32:418-423
Martin, Maureen P; Naranbhai, Vivek; Shea, Patrick R et al. (2018) Killer cell immunoglobulin-like receptor 3DL1 variation modifies HLA-B*57 protection against HIV-1. J Clin Invest 128:1903-1912
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
Haas, David W; Bradford, Yuki; Verma, Anurag et al. (2018) Brain neurotransmitter transporter/receptor genomics and efavirenz central nervous system adverse events. Pharmacogenet Genomics 28:179-187
Venuto, Charles S; Lim, Jihoon; Messing, Susan et al. (2018) Inflammation investigated as a source of pharmacokinetic variability of atazanavir in AIDS Clinical Trials Group protocol A5224s. Antivir Ther 23:345-351
Li, Binglan; Verma, Shefali S; Veturi, Yogasudha C et al. (2018) Evaluation of PrediXcan for prioritizing GWAS associations and predicting gene expression. Pac Symp Biocomput 23:448-459
Hayden, Kathleen M; Baker, Laura D; Bray, George et al. (2018) Long-term impact of intensive lifestyle intervention on cognitive function assessed with the National Institutes of Health Toolbox: The Look AHEAD study. Alzheimers Dement (Amst) 10:41-48
Shah, V N; Sippl, R; Joshee, P et al. (2018) Trabecular bone quality is lower in adults with type 1 diabetes and is negatively associated with insulin resistance. Osteoporos Int 29:733-739
Jensen, Thomas; Bjornstad, Petter; Johnson, Richard J et al. (2018) Copeptin and Estimated Insulin Sensitivity in Adults With and Without Type 1 Diabetes: The CACTI Study. Can J Diabetes :
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

Showing the most recent 10 out of 1065 publications