Dilation and reduced distensibility of carotid artery in patients with abdominal aortic aneurysms

Background Although patients with abdominal aortic aneurysms (AAA) frequently have coexisting systemic atherosclerosis, the dilatative manifestation of AAA is the opposite of the occlusion characteristic of atherosclerotic disease. It has been suggested that this dilatative disease is caused by an a...

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Veröffentlicht in:The American heart journal 2000-08, Vol.140 (2), p.297-302
Hauptverfasser: Makita, Shinji, Ohira, Atsushi, Tachieda, Rintarou, Itoh, Shigehiro, Moriai, Yoshiteru, Niinuma, Hiroyuki, Nakamura, Motoyuki, Hiramori, Katsuhiko
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Sprache:eng
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Zusammenfassung:Background Although patients with abdominal aortic aneurysms (AAA) frequently have coexisting systemic atherosclerosis, the dilatative manifestation of AAA is the opposite of the occlusion characteristic of atherosclerotic disease. It has been suggested that this dilatative disease is caused by an alteration in connective tissue metabolism in systemic arterial wall. Such a condition might alter systemic arterial diameter and wall behavior. We investigated arterial characteristics in AAA patients, including morphologic changes and wall mechanics in the carotid artery. Methods and Results Atherosclerotic intimal changes such as intima-media thickness (IMT), plaque formation, diameter, and wall elasticity of the carotid artery were determined ultrasonographically in patients with AAA (n = 102) and compared with age-matched patients with the atherosclerotic diseases arteriosclerosis obliterans (ASO, n = 115) and coronary artery disease (CAD, n = 123) and with age-matched healthy control patients (CTL, n = 45). Intimal disease in AAA was significantly milder than in ASO, at the same level as CAD, and more severe than in CTL. Although end-diastolic luminal diameters (mm) in AAA (7.05 ± 1.08), ASO (6.74 ± 0.18), and CAD (6.66 ± 0.83) were significantly higher than in CTL (5.97 ± 0.93), they were also excessively increased compared with the equivalent diameters seen in ASO (P
ISSN:0002-8703
1097-6744
DOI:10.1067/mhj.2000.108000