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1.
Mol Biol Rep ; 42(8): 1289-93, 2015 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-25809277

RESUMO

Myocardial infarction (MI) is the leading cause of death in industrialized countries. All the traditional risk factors for MI are responsible for approximately 50% of cases of MI cases. Attention therefore has recently focused on genetic variants that are not associated with conventional risk factors. One of them is the marker rs6922269, which has been suggested as a risk factor for development of MI in Western populations. We analyzed the relationship between rs6922269 variant on MTHFD1L gene and (i) risk of the acute coronary syndrome (ACS) in the Czech population and (ii) mortality in 7 years follow up. Rs6922269 (G>A) variant was analyzed (CR 99.3% for patients and 98.0% for controls) by PCR-RFLP in consecutively examined 1614 men and 503 women with ACS (age below 65 years) and in population-based controls--1191 men and 1368 women (aged up to 65 years). ANOVA and Chi square were used for statistical analysis. The genotype frequencies were almost identical (P=0.87) in the ACS patients and in controls and no differences were observed, if males (P=0.73) and females (P=0.93) were analysed separately. In addition, rs6922269 polymorphism was not associated with the classical risk factors (dyslipidemia, hypertension, obesity, smoking, diabetes) in control population. Cardiovascular mortality was significantly higher in males, carriers of the AA genotype (P<0.001, OR 2.52, 95% CI 1.40-4.55, for AA vs. +G). We conclude, that rs6922269 variant at MTHFD1L gene could be an important prognostic factor for cardiovascular mortality in patients after ACS.


Assuntos
Síndrome Coronariana Aguda/mortalidade , Aminoidrolases/genética , Formiato-Tetra-Hidrofolato Ligase/genética , Metilenotetra-Hidrofolato Desidrogenase (NADP)/genética , Complexos Multienzimáticos/genética , Infarto do Miocárdio/mortalidade , Polimorfismo de Nucleotídeo Único , Síndrome Coronariana Aguda/genética , Adulto , Idoso , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Infarto do Miocárdio/epidemiologia , Infarto do Miocárdio/genética , Polimorfismo de Fragmento de Restrição , Fatores de Risco
2.
Folia Biol (Praha) ; 58(5): 203-8, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-23249639

RESUMO

Myocardial infarction (MI) is the leading cause of death in industrialized countries. All the classical risk factors for MI are responsible for approximately 50 % of MI cases. Attention has therefore recently been attracted to those genetic variants that are not associated with conventional risk factors. One of them is the marker rs10757274 in the "genefree" zone on chromosome 9, which has been repeatedly recognized as a risk factor for development of MI in Western populations. We analysed the relationship between the rs10757274 variant on chromosome 9 and risk of the acute coronary syndrome (ACS) in Czech population. The rs10757274 (A > G) variant was successfully analysed (CR = 99.4 % for patients and 98.4 % for controls) by PCR-RFLP in consecutively examined 1,046 men and 281 women with ACS (age below 65 years) and in population-based controls - 1,162 men and 1,355 women (aged up to 65 years). ANOVA and χ2 were used for statistical analysis. We confirmed that GG homozygotes are more frequent (codominant model of analysis) among patients with myocardial infarction than in the control group both in men (28.5 % vs. 22.0 %, P = 0.0001, OR 1.73, 95 % CI 1.36-2.19) and women (32.0 % vs. 24.6 %, P = 0.02, OR 1.62, 95 % CI 1.13-2.34). However, rs10757274 polymorphism was not associated with the classical risk factors either in control population or in ACS patients. We conclude that the rs10757274 variant at 9p23.1 is an important genetic risk factor for ACS development in the Czech population.


Assuntos
Síndrome Coronariana Aguda/genética , Cromossomos Humanos Par 9/genética , Estudos de Associação Genética , Predisposição Genética para Doença , Adulto , Idoso , Estudos de Casos e Controles , República Tcheca , Feminino , Frequência do Gene/genética , Marcadores Genéticos , Humanos , Masculino , Pessoa de Meia-Idade , Modelos Genéticos , Polimorfismo de Nucleotídeo Único/genética , Reprodutibilidade dos Testes , Fatores de Risco
3.
Vnitr Lek ; 58(4): 319-21, 2012 Apr.
Artigo em Tcheco | MEDLINE | ID: mdl-22559808

RESUMO

The case demonstrates how significant the effects of addictive drugs are for human organism, which may cause serious acute changes in the function of cardiovascular system and can end in permanent heart damage.


Assuntos
Estimulantes do Sistema Nervoso Central/intoxicação , Metanfetamina/intoxicação , Infarto do Miocárdio/induzido quimicamente , Transtornos Relacionados ao Uso de Substâncias/complicações , Adulto , Trombose Coronária/induzido quimicamente , Feminino , Humanos , Drogas Ilícitas/intoxicação
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