Pregled bibliografske jedinice broj: 62564
Paraoxonase genotype distribution in cardiovascular dieseases
Paraoxonase genotype distribution in cardiovascular dieseases // Genes candidats de risque cardio-vasculaire et implications therapeutiques
Nancy, 1999. (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 62564 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Paraoxonase genotype distribution in cardiovascular dieseases
Autori
Topić, Elizabeta ; Ivanišević, Ana-Maria ; Štefanović, Mario ; Nikolić, Vjeran ; Petrač, Dubravko ; Čubrilo-Turek, Mirjana ; Demarin, Vida ; Žuntar, Irena
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Genes candidats de risque cardio-vasculaire et implications therapeutiques
/ - Nancy, 1999
Skup
2eme mini-colloque international de Biologie Prospective:Genes candidats de risque cardio-vasculaire et implications therapeutiques
Mjesto i datum
Nancy, Francuska, 22.03.1999. - 23.03.1999
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
paraoxonase; CVD
Sažetak
Paraoxonase (PON1) genetic polymorphism at codon 192 (glutamine to arginine substitution, genotypes A and B, respectively) has been shown to affect the risk of CVD. The aim of this study was to genotype 44 controls and 100 CVD patients with different diagnosis (coronary artery disease (CAD), myocardial infarction (MI), hypertension and carotid stenosis (CS)) by PCR-RFLP using Alw1 restriction enzyme. Study results showed that out of 44 controls 18/44 (40.9%) were A and 1/44 (2.3%) B homozygotes and 25/44 (56.8%) heterozygotes. Among 31 CAD patients 9/31 (29.0%) were A and 5/31 (16.1%) B homozygotes and 17/31 (54.8%) heterozygotes. In 27 MI patients 8/27 (29.6%) were A and 4/27 (14.8%) B homozygotes and 15/27 (55.6%) heterozygotes. Out of 16 hypertension patients 6/16 (37.5%) were A and 3/16 (18.8%) B homozygotes and 7/16 (43.8%) heterozygotes. Among 26 CS patients 15/26 (57.7%) were A and 2/26 (7.7%) B homozygotes and 9/26 (34.6%) heterozygotes. Genotypes between controls and patients differed significantly (Chi-square test; P=0.002, 0.003, <0.001 and 0.003; for CAD, MI, Hypertension and CS patients, respectively). Allelic frequencies did not differ significantly between controls and patients. Our findings indicate the association between the codon 192 polymorphism of PON1 gene and cardiovascular diseases.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA
Projekti:
134003
Ustanove:
KBC "Sestre Milosrdnice"
Profili:
Mirjana Čubrilo-Turek
(autor)
Mario Štefanović
(autor)
Dubravko Petrač
(autor)
Irena Žuntar
(autor)
Vida Demarin
(autor)
Elizabeta Topić
(autor)