Title of article :
Noninvasive tracking of coronary atherosclerosis by electron beam computed tomography: Rationale and design of the Felodipine Atherosclerosis Prevention Study (FAPS)
Author/Authors :
Wong، نويسنده , , Nathan D. and Teng، نويسنده , , Wang and Abrahamson، نويسنده , , David and Willner، نويسنده , , Richard and Henein، نويسنده , , Nassef and Franklin، نويسنده , , Stanley S. and Kashyap، نويسنده , , Moti L and Rosenzweig، نويسنده , , Bruce and Kukes، نويسنده , , Gary and Detrano، نويسنده , , Robert C.، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 1995
Pages :
4
From page :
1239
To page :
1242
Abstract :
The Felodipine Atherosclerosis Prevention Study is designed to evaluate the efficacy of the calcium antagonist felodipine ER and combined felodipine/simvastatin therapy on retarding the progression or atherosclerosis, estimated by serial changes in coronary calcium evaluated by noninvasive electron beam computed tomography. Subjects include 180 men and women aged 40 to 69 and 50 to 69 years, respectively, with moderate type lla dyslipidemia, with either cardiovascular disease or risk factors. All subjects receive simvastatin lipid-lowering therapy, and are randomized either to felodipine or placebo for a treatment period of 2 years. Monitoring of blood chemistry, measures of lipids and apolipoproteins, blood pressure, evaluation of symptoms, and interim clinical event monitoring are done at routine follow-up visits. Baseline and 2-year follow-up electron beam computed tomography, measuring changes in total calcium score, area, and mass, evaluate the effects of intervention on the progression of calcified atherosclerosis. The results from the Felodipine Atherosclerosis Prevention Study will provide valuable information about the effect of felodipine alone and in combination with simvastatin on progression of calcified atherosclerosis evaluated noninvasively.
Journal title :
American Journal of Cardiology
Serial Year :
1995
Journal title :
American Journal of Cardiology
Record number :
1881807
Link To Document :
بازگشت