Associations of extracranial carotid atherosclerosis progression with coronary status and risk factors in patients with and without coronary artery disease

Intimal medial thickness of the extracranial carotid arteries (IMT) is related to coronary artery disease (CAD) and CAD risk factors. Few studies have explored the association of risk factors with progression of IMT, and none have evaluated their associations with IMT progression specifically in pat...

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Published inCirculation (New York, N.Y.) Vol. 106; no. 16; pp. 2061 - 2066
Main Authors CROUSE, John R, RONG TANG, ESPELAND, Mark A, TERRY, James G, MORGAN, Timothy, MERCURI, Michele
Format Journal Article
LanguageEnglish
Published Hagerstown, MD Lippincott Williams & Wilkins 15.10.2002
American Heart Association, Inc
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Summary:Intimal medial thickness of the extracranial carotid arteries (IMT) is related to coronary artery disease (CAD) and CAD risk factors. Few studies have explored the association of risk factors with progression of IMT, and none have evaluated their associations with IMT progression specifically in patients with and without CAD. We used coronary angiography to identify 280 patients equally divided between men and women and those with either > or =50% coronary artery stenosis or no CAD. Risk factors were measured at baseline and IMT was measured at baseline and yearly for 3 years in 241 of these individuals. Baseline risk factors and CAD status were related to IMT progression. IMT of patients with CAD progressed 3 times faster than that of patients with no CAD (mean+/-SEM, 33.7+/-7.4 versus 8.9+/-7.1 microm/year; P=0.02), and CAD status and high-density lipoprotein (HDL) cholesterol were independently associated with IMT progression. Male sex, increased waist to hip ratio, cigarette smoking, increased triglycerides, and decreased HDL cholesterol were associated with increased progression in CAD patients. Patients with CAD have more rapid progression of IMT than CAD-free controls, and risk factors are related to progression in them.
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ISSN:0009-7322
1524-4539
DOI:10.1161/01.CIR.0000033833.54884.34