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Cholesterol associated genetic risk score and acute coronary syndrome in Czech males.
Hubacek, Jaroslav A; Adamkova, Vera; Lanska, Vera; Stanek, Vladimir; Mrázková, Jolana; Gebauerová, Marie; Kettner, Jiri; Kautzner, Josef; Pitha, Jan.
Afiliação
  • Hubacek JA; Experimental Medicine Centre, Institute for Clinical and Experimental Medicine, IKEM-CEM-LMG, Videnska 1958/9, 140 21, Prague 4, Czech Republic. jahb@ikem.cz.
  • Adamkova V; 3rd Department of Internal Medicine, 1st Faculty of Medicine, Charles University, Prague, Czech Republic. jahb@ikem.cz.
  • Lanska V; Preventive Cardiology Centre, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
  • Stanek V; Information Technology Division, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
  • Mrázková J; Cardiac Centre, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
  • Gebauerová M; Experimental Medicine Centre, Institute for Clinical and Experimental Medicine, IKEM-CEM-LMG, Videnska 1958/9, 140 21, Prague 4, Czech Republic.
  • Kettner J; Cardiac Centre, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
  • Kautzner J; Cardiac Centre, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
  • Pitha J; Cardiac Centre, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
Mol Biol Rep ; 51(1): 164, 2024 Jan 22.
Article em En | MEDLINE | ID: mdl-38252350
ABSTRACT

BACKGROUND:

Despite a general decline in mean levels across populations, LDL-cholesterol levels remain a major risk factor for acute coronary syndrome (ACS). The APOB, LDL-R, CILP, and SORT-1 genes have been shown to contain variants that have significant effects on plasma cholesterol levels. METHODS AND

RESULTS:

We examined polymorphisms within these genes in 1191 controls and 929 patients with ACS. Only rs646776 within SORT-1 was significantly associated with a risk of ACS (P < 0.05, AA vs. + G comparison; OR 1.21; 95% CI 1.01-1.45). With regard to genetic risk score (GRS), the presence of at least 7 alleles associated with elevated cholesterol levels was connected with increased risk (P < 0.01) of ACS (OR 1.26; 95% CI 1.06-1.52). Neither total mortality nor CVD mortality in ACS subjects (follow up-9.84 ± 3.82 years) was associated with the SNPs analysed or cholesterol-associated GRS.

CONCLUSIONS:

We conclude that, based on only a few potent SNPs known to affect plasma cholesterol, GRS has the potential to predict ACS risk, but not ACS associated mortality.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome Coronariana Aguda / Estratificação de Risco Genético Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Humans / Male País/Região como assunto: Europa Idioma: En Revista: Mol Biol Rep Ano de publicação: 2024 Tipo de documento: Article País de afiliação: República Tcheca

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome Coronariana Aguda / Estratificação de Risco Genético Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Humans / Male País/Região como assunto: Europa Idioma: En Revista: Mol Biol Rep Ano de publicação: 2024 Tipo de documento: Article País de afiliação: República Tcheca