A RELAÇAO APO-B/APO-AI, MAS NAO OS POLIMORFISMOS DAS APOLIPOPROTEINAS AI-CIII ASSOCIAM-SE A DOENÇA ARTERIAL CORONARIANA PREMATURA

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A relação apo-B/apo-AI aumentada e fatores de risco clássicos associaram-se à doença arterial coronariana prematura. Polimorfismos no cluster gênico AI-CIII não influenciaram sua ocorrência.
oliveiraizar9.jpg Autor:
Maria cristina De oliveira izar
Columnista Experto de SIIC

Institución:
Universidade Federal de São Paulo


Artículos publicados por Maria cristina De oliveira izar
Recepción del artículo
9 de Marzo, 2006
Aprobación
29 de Marzo, 2006
Primera edición
27 de Junio, 2006
Segunda edición, ampliada y corregida
7 de Junio, 2021

Resumen
Este estudo avaliou associações entre fatores de risco clássicos e emergentes na doença arterial coronariana (DAC) prematura. Métodos: Estudo caso-controle incluiu 112 indivíduos com DAC prematura e 112 controles, pareados por sexo e idade. Lípides e apolipoproteínas (AI e B), marcadores da hemostasia (fibrinogênio, dímero-D, fator de Von Willebrand, fator VII e inibidor do ativador do plasminogênio-1), e polimorfismos do cluster gênico AI-CIII foram examinados em jejum após intervenção nutricional (NCEP III). Resultados: A hipertensão arterial, o diabetes, o fumo pregresso e o antecedente familiar de DAC prematura foram mais prevalentes na DAC prematura (p < 0.001), e esses pacientes apresentaram níveis maiores de colesterol total, LDL-C, triglicérides e de apo-B (p < 0.01) e menores de HDL-C e apo-AI (p < 0.001), além de maior relação apo-B/apo-AI. O fibrinogênio plasmático e o dímero-D (p < 0.02) foram maiores na DAC prematura. Não se observaram associações entre os polimorfismos estudados e a DAC prematura. A chance da DAC prematura associou-se à relação desfavorável apo-B/apo-AI (OR = 23.8), ao diabetes (OR = 6.1), à hipertensão arterial (OR = 3.9), ao fumo pregresso (OR = 3.7) e ao antecedente familiar de DAC prematura (OR = 2.5). Conclusão: Fatores de risco modificáveis associam-se à doença coronariana prematura e ações preventivas ambientais de impacto poderão reduzir os desfechos cardiovasculares nessas populações.

Palabras clave
fatores de risco, lípides, apolipoproteínas, hemostasia, polimorfismos, genética


Artículo completo

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Abstract
This study was aimed to evaluate associations of classic and emergent risk factors and early coronary heart disease (CHD). Methods: A case-control study included 112 individuals with early CHD and 112 controls, paired by age and sex. Lipids and apolipoproteins (AI and B), markers of hemostasis (fibrinogen, D-dimer, von Willebrand factor, factor VII and PAI-1), and polymorphisms of AI-CIII gene cluster were examined in the fasting state after nutrition counseling (NCEP III). Results: Hypertension, diabetes, prior smoking and family history of premature CHD were more prevalent in early CHD (p < 0.001), and these patients presented higher serum total cholesterol, LDL-C, triglycerides, and apo-B (p < 0.01), and lower HDL-C and apo-AI (p < 0.001) than controls. Elevated Apo-B/apo-AI ratio was seen in early CHD, as well. Fibrinogen and D-dimer (p < 0.02) were higher in premature CHD. No associations were found between the studied polymorphisms and early CHD. Risk of early CHD was associated with increased apo-B/apo-AI ratio (OR = 23.8), diabetes (OR = 6.1), hypertension (OR = 3.9), prior smoking (OR = 3.7) and family history of premature CHD (OR = 2.5). Conclusions: Modifiable risk factors are associated with early CHD, and preventive actions to reduce its impact might reduce cardiovascular events in these populations.

Key words
risk factors, lipids, apolipoproteins, hemostasis, polymorphisms, genetics


Clasificación en siicsalud
Artículos originales > Expertos de Iberoamérica >
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Especialidades
Principal: Cardiología
Relacionadas: Bioquímica, Diagnóstico por Laboratorio, Medicina Interna



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Enviar correspondencia a:
Maria Cris de Oliveira Izar, Universidade Federal de São Paulo, 04039-001, Rua Pedro de Toledo 458, Vila Clementino, San Pablo, Brasil
Patrocinio y reconocimiento:
Agradecimentos: Este trabalho recebeu auxílio financeiro da Fapesp (Fundação de Amparo à Pesquisa do Estado de São Paulo), nº 98/02174-4.
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