he role of inflammation in patients with acute coronary syndromes (ACS) is presently undisputed, supported by histopathological studies of unstable coronary plaque, 1 as well as clinical studies of elevated circulating acute-phase reactants. 2,3 Oxidized low-density lipoprotein (ox-LDL) is generally considered to be a key factor in the genesis of the inflammatory process in atherosclerotic lesions 4,5 and the detection of ox-LDL in human plasma has opened new avenues of the study of its relationship to the atherosclerotic process. [6][7][8][9][10] We developed a sandwich enzyme-linked immunosorbent assay (ELISA) method to measure plasma ox-LDL levels, using a specific anti-ox-LDL monoclonal antibody (DLH3) and an antiCirculation Journal Vol.71, May 2007 apolipoprotein B (apoB) polyclonal antibody. 11,12 DLH3 is specific for ox-LDL because it recognizes oxidized phosphatidylcholines (ox-PC) molecules 11 and does not bind to native, acetylated, malondialdehyde-treated, or glycated low-density lipoprotein (LDL). Using this new and highly sensitive method, we have reported that in patients with acute myocardial infarction (AMI) the plasma levels of ox-LDL are significantly higher than in patients with unstable angina pectoris (UAP) or stable angina pectoris (SAP), or in controls. 7 Recently, we also demonstrated that persistence of an increased plasma level of ox-LDL at discharge is a strong independent predictor of stent restenosis at 6-month follow-up in AMI patients. 10 UAP as a clinical diagnosis incorporates a diverse group of clinical presentations that occupy an intermediate position between the more strictly defined clinical entities of AMI and SAP. A number of previous studies have demonstrated that angiographically the culprit lesions in patients with UAP often appear irregular and contain filling defects likely to represent plaque disruption and/or plaque thrombus. [13][14][15][16] Previous clinical studies have also revealed that angiographically detected complex lesions correlated with higher Braunwald class. 17,18 However, it has also been shown that patients with Braunwald class I occasionally show angiographic evidence of a complex lesion. 17,18 Hence, given the role of ox-LDL in plaque instability in Hiroyuki Itabe, PhD † ; Toru Kataoka, MD; Yoshiki Kobayashi, MD; Anton E. Becker, MD ‡ ; Junichi Yoshikawa, MD † † ; Makiko Ueda, MD** Background Increased levels of oxidized low-density lipoprotein (ox-LDL) are related to plaque instability, so the aim of the present study was to investigate whether there is a relationship between angiographic coronary plaque morphology in patients with unstable angina pectoris (UAP) and the level of ox-LDL.
Methods and ResultsPlasma ox-LDL levels were measured in 149 patients with UAP and in 88 control subjects, using a highly sensitive enzyme-linked immunosorbent assay method. Angiographic morphology of the culprit lesion was classified as either simple or complex based on the Ambrose classification. Plasma ox-LDL levels in patients with Braunwald class III were s...