LIPID PROFILE, HEMOSTATIC VARIABLES AND ANGIOGRAPHICALLY-DEFINED CORONARY-ARTERY DISEASE - A CROSS-SECTIONAL STUDY IN AN IRISH POPULATION

Citation
J. Galvin et al., LIPID PROFILE, HEMOSTATIC VARIABLES AND ANGIOGRAPHICALLY-DEFINED CORONARY-ARTERY DISEASE - A CROSS-SECTIONAL STUDY IN AN IRISH POPULATION, Irish journal of medical science, 165(2), 1996, pp. 129-132
Citations number
20
Categorie Soggetti
Medicine, General & Internal
ISSN journal
00211265
Volume
165
Issue
2
Year of publication
1996
Pages
129 - 132
Database
ISI
SICI code
0021-1265(1996)165:2<129:LPHVAA>2.0.ZU;2-W
Abstract
More than 300 risk factors for coronary artery disease (CAD) have been described. There are important geographical and racial differences in both the prevalence of CAD and of potential risk factors. The purpose of this study was to determine the relationship between both the pres ence and extent of angiographically defined CAD in an Irish population and a spectrum of clinical risk factors, lipid profile and haemostati c variables. On univariate analysis, age, male gender, history of smok ing, history of hypertension, total cholesterol, triglycerides, LDL, C holesterol, the LDL:HDL ratio, apoprotein B-100 and the apoprotein B-1 00:A-II ratio were associated with the presence of CAD. However, in mu ltivariate analysis only age, male gender, a history of smoking and th e apoptrotein B-100:A-II ratio remained significantly associated with the presence of CAD. These same risk factors and apoprotein B-100 were significantly associated with the extent of CAD on multivariate analy sis. In addition, apoprotein B-100 levels appeared to be associated wi th disease extent. When all significant variables associated with the presence or extent of CAD were analysed together in a multivariate mod el, they only accounted for 28% of the variability in the distribution of CAD. Thus, advancing age, male gender, cigarette smoking and apopr otein B-100 appear to be important correlates of the presence and exte nt of CAD in this selected population. However, in individual patients most of the variability in the distribution of occlusive CAD remains unexplained.