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Genetic Architecture of Plasma T-PA and PAI-1
This study has been completed.
Study NCT00007410   Information provided by National Heart, Lung, and Blood Institute (NHLBI)
First Received: December 19, 2000   Last Updated: January 18, 2008   History of Changes

December 19, 2000
January 18, 2008
September 2000
July 2006   (final data collection date for primary outcome measure)
 
 
Complete list of historical versions of study NCT00007410 on ClinicalTrials.gov Archive Site
 
 
 
Genetic Architecture of Plasma T-PA and PAI-1
 

To determine the effects of six genes on thrombotic risk factors known to be associated with the development of heart disease.

BACKGROUND:

Abnormalities in the plasminogen activator system have been implicated in the pathogenesis of arterial and cerebral thrombosis. In particular, elevated plasma levels of plasminogen activator inhibitor-1 (PAI-1), tissue-type plasminogen activator (t-PA), and t-PA/PAI-1 complexes have been found to correlate with increased risk of myocardial infarction (MI) and/or stroke. Vascular fibrinolytic balance is, to a large part, determined by the competing effects of t-PA and PAI-1, and reflects a complex interplay between genetic and environmental factors. The present collaboration focuses on the common hypothesis that the association between activation of the renin-angiotensin-aldosterone system (RAAS) and atherothrombotic events derives from an interaction between the RAAS and the fibrinolytic system.

The study is part of an initiative "Thrombosis of the Arterial and Cerebral Vasculature: New Molecular Genetic Concepts for Prevention and Treatment" which was released in April 1999. The objective of the initiative is to establish collaborative teams of closely interacting investigators with diverse, complementary areas of expertise to elucidate the molecular genetic mechanisms of thrombosis in the arterial and cerebral vasculature.

DESIGN NARRATIVE:

The investigators will use two population-based samples of unrelated individuals to address their aims: 1) study subjects in the PREVEND study in Groningen, The Netherlands in whom DNA and plasma samples and clinical data have already been collected and 2) an estimated 2000 unrelated study subjects from Ghana, Africa in whom data need to be collected. The collaborative study focuses on the common hypothesis that the association between activation of the renin-angiotensin-aldosterone system (RAAS) and atherothrombotic events derives from an interaction between the RAAS and the fibrinolytic system.

N/A
Observational
 
  • Cardiovascular Diseases
  • Heart Diseases
  • Thrombosis
  • Atherosclerosis
 
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Completed
 
July 2006
July 2006   (final data collection date for primary outcome measure)

No eligibility criteria

Both
 
No
Contact information is only displayed when the study is recruiting subjects
 
 
NCT00007410
 
959
National Heart, Lung, and Blood Institute (NHLBI)
 
Investigator: Jason Moore Vanderbilt University
National Heart, Lung, and Blood Institute (NHLBI)
January 2008

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP