Partículas lipoproteicas LpA-I, LpA-I: A-II y LpB en enfermedad coronaria
Background: High density lipoproteins are an heterogeneous population of particles. Two main subpopulations have been identified, one contains Apo A-I and Apo A-II and is denominated LpA-I:A-II and another one contains only Apo A-I and is denominated LpA-I. Aim: To measure the concentrations of thes...
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Sociedad Médica de Santiago
2000
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oai:scielo:S0034-988720000001000022000-05-25Partículas lipoproteicas LpA-I, LpA-I: A-II y LpB en enfermedad coronariaCalvo M,CarlosOlmos C,AlfonsoUlloa M,NataliaBustos A,AlejandraToledo B,LorenaDurán S,DanielNaveas,Rina Coronary disease Cholesterol Lipoproteins Lipoproteins, HDL cholesterol Background: High density lipoproteins are an heterogeneous population of particles. Two main subpopulations have been identified, one contains Apo A-I and Apo A-II and is denominated LpA-I:A-II and another one contains only Apo A-I and is denominated LpA-I. Aim: To measure the concentrations of these particles in patients with stable coronary artery disease. Patients and Methods: Serum lipids, A-I and B apolipoproteins, LpA-I, LpA-I:A-II and LpB particles were measured in 73 men aged 33 to 82 years with angiographically documented coronary artery disease (CAD) and 33 control subjects aged 39 to 76 years. LpA-I, LpA-I:A-II and LpB were measured by a noncompetitive enzyme linked immunoassay using previously characterized monoclonal antibodies against ApoA-I, ApoA-II and apoB. Results: Patients with CAD had significantly higher mean levels of LDL cholesterol than the control group (p= 0.038). The mean concentration of LpA-I particles in patients with CAD was significantly lower (p= 0.031) than in control subjects, while the concentration of LpA-I:A-II particles was significantly higher (p=0.016). The percentage of coronary stenosis correlated negatively with LpA-I and positively with LpA-I:A-II. The best relative risk (RR) indicator in these patients was LDL-cholesterol. The relative risk increases 2.5 fold when LpA-I falls below the cut-off level. Likewise, the relative risk increases 3-fold when LpA-I:A-II raises over the cut-off level. Conclusions: Our findings indicate that the quantification of LpA-I and LpA-I:A-II particles might allow a more accurate evaluation of the CAD risk than HDL cholesterol. LpA-I might represent the antiatherogenic fraction of HDL. (Rev Méd Chile 2000; 128: 9-16)info:eu-repo/semantics/openAccessSociedad Médica de SantiagoRevista médica de Chile v.128 n.1 20002000-01-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872000000100002es10.4067/S0034-98872000000100002 |
institution |
Scielo Chile |
collection |
Scielo Chile |
language |
Spanish / Castilian |
topic |
Coronary disease Cholesterol Lipoproteins Lipoproteins, HDL cholesterol |
spellingShingle |
Coronary disease Cholesterol Lipoproteins Lipoproteins, HDL cholesterol Calvo M,Carlos Olmos C,Alfonso Ulloa M,Natalia Bustos A,Alejandra Toledo B,Lorena Durán S,Daniel Naveas,Rina Partículas lipoproteicas LpA-I, LpA-I: A-II y LpB en enfermedad coronaria |
description |
Background: High density lipoproteins are an heterogeneous population of particles. Two main subpopulations have been identified, one contains Apo A-I and Apo A-II and is denominated LpA-I:A-II and another one contains only Apo A-I and is denominated LpA-I. Aim: To measure the concentrations of these particles in patients with stable coronary artery disease. Patients and Methods: Serum lipids, A-I and B apolipoproteins, LpA-I, LpA-I:A-II and LpB particles were measured in 73 men aged 33 to 82 years with angiographically documented coronary artery disease (CAD) and 33 control subjects aged 39 to 76 years. LpA-I, LpA-I:A-II and LpB were measured by a noncompetitive enzyme linked immunoassay using previously characterized monoclonal antibodies against ApoA-I, ApoA-II and apoB. Results: Patients with CAD had significantly higher mean levels of LDL cholesterol than the control group (p= 0.038). The mean concentration of LpA-I particles in patients with CAD was significantly lower (p= 0.031) than in control subjects, while the concentration of LpA-I:A-II particles was significantly higher (p=0.016). The percentage of coronary stenosis correlated negatively with LpA-I and positively with LpA-I:A-II. The best relative risk (RR) indicator in these patients was LDL-cholesterol. The relative risk increases 2.5 fold when LpA-I falls below the cut-off level. Likewise, the relative risk increases 3-fold when LpA-I:A-II raises over the cut-off level. Conclusions: Our findings indicate that the quantification of LpA-I and LpA-I:A-II particles might allow a more accurate evaluation of the CAD risk than HDL cholesterol. LpA-I might represent the antiatherogenic fraction of HDL. (Rev Méd Chile 2000; 128: 9-16) |
author |
Calvo M,Carlos Olmos C,Alfonso Ulloa M,Natalia Bustos A,Alejandra Toledo B,Lorena Durán S,Daniel Naveas,Rina |
author_facet |
Calvo M,Carlos Olmos C,Alfonso Ulloa M,Natalia Bustos A,Alejandra Toledo B,Lorena Durán S,Daniel Naveas,Rina |
author_sort |
Calvo M,Carlos |
title |
Partículas lipoproteicas LpA-I, LpA-I: A-II y LpB en enfermedad coronaria |
title_short |
Partículas lipoproteicas LpA-I, LpA-I: A-II y LpB en enfermedad coronaria |
title_full |
Partículas lipoproteicas LpA-I, LpA-I: A-II y LpB en enfermedad coronaria |
title_fullStr |
Partículas lipoproteicas LpA-I, LpA-I: A-II y LpB en enfermedad coronaria |
title_full_unstemmed |
Partículas lipoproteicas LpA-I, LpA-I: A-II y LpB en enfermedad coronaria |
title_sort |
partículas lipoproteicas lpa-i, lpa-i: a-ii y lpb en enfermedad coronaria |
publisher |
Sociedad Médica de Santiago |
publishDate |
2000 |
url |
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872000000100002 |
work_keys_str_mv |
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