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Age-related Contribution of Lp (a) with Coronary Artery Calcification in Patients with Acute Coronary Syndrome: a Potential Role of Metabolic Disorder in Calcified Plaque

DC Field Value Language
dc.contributor.author권혁문-
dc.contributor.author홍범기-
dc.contributor.authorDong Soo Kim-
dc.date.accessioned2018-11-20T11:46:21Z-
dc.date.available2018-11-20T11:46:21Z-
dc.date.issued2003-
dc.identifier.issn0513-5796-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/165648-
dc.description.abstractLp(a) and coronary artery calcification (CAC) have recently been reported as predictors of plaque instability, but this is surrounded by much controversy. We investigated the influence of Lp(a) and CAC compared other acute coronary syndrome (ACS) risk factors. 698 patients diagnosed with at least minimal coronary artery obstructive disease from a coronary angiography were randomly selected using SPSS. Lp(a), other lipid profiles and past histories were checked, and CAC semi quantitatively graded on stored fluoroscopic images. The prevalence of CAC was significantly higher in the ACS than the non-ACS group (38.0% vs. 29.9%, p=0.026). The serum level of Lp(a) (26.89 +/- 30.64 vs. 20.85 +/- 21.63, p < 0.01) and prevalence of positive Lp(a) (> 35 mg/dl) was higher in the ACS group (24% vs. 15.7%, p < 0.01). The risk of ACS was higher in the patients with both CAC and elevated an Lp(a) than in those with only one (OR: 2.16, p=0.009, 95% CI; 1.213 - 3.843 vs. OR: 1.79, p < 0.001, 95% CI; 1.300 - 2.456). The risk of ACS was increased 1.451 times (p=0.040, 95% CI; 1.071- 2.071) in patients with CAC and 1.648 times (p=0.014, 95% CI; 1.107- 2.455) in patients with a Lp(a) > 35 mg/dl. In the younger patients (< 60 years), the Lp(a), but not the CAC, was an independent risk factor for ACS (OR=2.248, p=0.005, 95% CI; 1.281-3.943). In the older patients (> 60 years), CAC, but not the Lp(a), was an independent risk factor (OR=1.775, p=0.021, 95% CI; 1.090 - 2.890). Both the Lp(a) and CAC were risk factors for ACS, and they had a synergistic effect on its development. In the younger Lp(a), and the older CAC, was the more potent risk factor for ACS, respectively.-
dc.description.statementOfResponsibilityopen-
dc.formatapplication/pdf-
dc.languageEnglish-
dc.publisherYonsei University-
dc.relation.isPartOfYONSEI MEDICAL JOURNAL-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAcute Disease-
dc.subject.MESHAge Factors-
dc.subject.MESHAged-
dc.subject.MESHAging/blood*-
dc.subject.MESHCalcinosis/blood-
dc.subject.MESHCalcinosis/complications*-
dc.subject.MESHCoronary Artery Disease/blood-
dc.subject.MESHCoronary Artery Disease/etiology*-
dc.subject.MESHCoronary Vessels/pathology*-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHLipoprotein(a)/blood*-
dc.subject.MESHMale-
dc.subject.MESHMetabolic Diseases/complications-
dc.subject.MESHMiddle Aged-
dc.subject.MESHRisk Factors-
dc.subject.MESHSyndrome-
dc.titleAge-related Contribution of Lp (a) with Coronary Artery Calcification in Patients with Acute Coronary Syndrome: a Potential Role of Metabolic Disorder in Calcified Plaque-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorSung Kee Ryu-
dc.contributor.googleauthorBum Kee Hong-
dc.contributor.googleauthorHyuck Moon Kwon-
dc.contributor.googleauthorWook Jin Chung-
dc.contributor.googleauthorByoung Eun Park-
dc.contributor.googleauthorDong Yeon Kim-
dc.contributor.googleauthorYun Hyeong Cho-
dc.contributor.googleauthorSe Jung Yoon-
dc.contributor.googleauthorYoung Won Yoon-
dc.contributor.googleauthorSeung Yun Cho-
dc.contributor.googleauthorHyun Seung Kim-
dc.identifier.doi10.3349/ymj.2003.44.3.445-
dc.contributor.localIdA00260-
dc.contributor.localIdA04394-
dc.relation.journalcodeJ02813-
dc.identifier.eissn1976-2437-
dc.identifier.pmid12833582-
dc.contributor.alternativeNameKwon, Hyuck Moon-
dc.contributor.alternativeNameHong, Bum Kee-
dc.contributor.affiliatedAuthor권혁문-
dc.contributor.affiliatedAuthor홍범기-
dc.citation.volume44-
dc.citation.number3-
dc.citation.startPage445-
dc.citation.endPage453-
dc.identifier.bibliographicCitationYONSEI MEDICAL JOURNAL, Vol.44(3) : 445-453, 2003-
dc.identifier.rimsid60287-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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