This subproject is one of many research subprojects utilizing theresources provided by a Center grant funded by NIH/NCRR. The subproject andinvestigator (PI) may have received primary funding from another NIH source,and thus could be represented in other CRISP entries. The institution listed isfor the Center, which is not necessarily the institution for the investigator.(1) Endothelial nitric oxide synthase (eNOS) polymorphism, plasma homocysteine concetrations, markers of inflammationsuch as ESR and C-reactive protein, and oxidative stress are associated w/structural and functional measures of vascular damage in systemic lupus erythematosus (SLE). (2) Will select those patients w/the highest tertile of carotid intima-media thickness as determined by ultrasound scan and treat them w/pravastatin 40 mg daily for 3 years.
SPECIFIC AIM :1) To test the hypothesis that structural and functional measures of vascular damage are more marked in patients w/SLE than in matched controls and that eNOS polymorphism, plasma homocysteine concentrations, markers of inflammation and oxidative stress are associated w/structural and functional measures of vascular damage.2) To test the hypothesis that it is possible to improve structural and functional measures of vascular damage in patients w/SLE through treatment w/an HMG coenzyme A reductase inhibitor.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
3M01RR000095-47S1
Application #
7731350
Study Section
National Center for Research Resources Initial Review Group (RIRG)
Project Start
2006-12-01
Project End
2007-09-16
Budget Start
2006-12-01
Budget End
2007-09-16
Support Year
47
Fiscal Year
2008
Total Cost
$70
Indirect Cost
Name
Vanderbilt University Medical Center
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
004413456
City
Nashville
State
TN
Country
United States
Zip Code
37212
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