2010
DOI: 10.1016/j.clinbiochem.2010.01.013
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Apo(a) phenotyping and long-term prognosis for coronary artery disease

Abstract: Small-sized apo(a) isoforms are an independent risk factor for MACCE in patients with coronary artery disease in follow-up. Lp(a) plasma concentration and apo(a) fibrin-binding were associated, although not significant.

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Cited by 9 publications
(8 citation statements)
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“…Based on previous studies [10,11,27], patients were followed up for about 7 years as a sufficient follow-up period. Information was also obtained for patients who no longer underwent medical care at the hospital.…”
Section: Methodsmentioning
confidence: 99%
“…Based on previous studies [10,11,27], patients were followed up for about 7 years as a sufficient follow-up period. Information was also obtained for patients who no longer underwent medical care at the hospital.…”
Section: Methodsmentioning
confidence: 99%
“…These biothiols play important roles in many biological processes, including the maintenance of reduction-oxidation (redox) homeostasisagainst oxidative stress and the inactivation of toxic compounds [1,[7][8][9][10]. In addition, imbalances inbiothiol metabolism areclosely related to various pathologies such as vascular diseases [11,12], neurodegenerative diseases including Alzheimer's [13]and Parkinson's [14], cancers [15,16], and diabetes mellitus [17,18]. Therefore, the simultaneous determination of multiple biothiols in biological samples is important for clarifying the relationship between the in vivo redox status and these disease states.…”
Section: Introductionmentioning
confidence: 99%
“…Substantial evidence supports the notion that enhanced formation of reactive oxygen and nitrogen species (ROS/RNS) leads to oxidative stress and participates in the pathogenesis of atherosclerosis, peripheral vascular and coronary heart diseases [2]. Oxidative modification of lipids and molecules is considered to be a key event in the pathogenesis of atherosclerosis and atherothrombotic cardiovascular disease [3,4], promoting conversion of low‐density lipoproteins (LDL) [2,5] and apolipoprotein(a) [apo(a)] into more atherogenic forms [6] and adversely affecting levels of asymmetric dimethylarginine (ADMA) [7] and fetuin A [8].…”
Section: Introductionmentioning
confidence: 99%