Pregled bibliografske jedinice broj: 62797
Genetic polymorphism of paraoxonase and the risk of cardiovascular diseases (CVD)
Genetic polymorphism of paraoxonase and the risk of cardiovascular diseases (CVD) // Clin Chem Lab Med 1999;vol 37,Abstracts volume, special supplement / Siest, Gerard (ur.).
Milano: Walter de Gruyter, 1999. (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 62797 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Genetic polymorphism of paraoxonase and the risk of cardiovascular diseases (CVD)
Autori
Ivanišević, Ana-Maria ; Štefanović, Mario ; Topić, Elizabeta ; Nikolić, Vjeran ; Petrač, Dubravko ; Čubrilo-Turek, Mirjana
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Clin Chem Lab Med 1999;vol 37,Abstracts volume, special supplement
/ Siest, Gerard - Milano : Walter de Gruyter, 1999
Skup
IFCC-World Lab, 17th International and 13th European Congress of Clinical Chemistry and Laboratory Medicine
Mjesto i datum
Firenca, Italija, 06.06.1999. - 11.06.1999
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
PON1; cardiovascular diseses
Sažetak
Genetic polymorphism of paraoxonase (PON1) at codon 192 (glutamine to arginine substitution, genotypes A and B, respectively) has been implicated in the risk of CVD. The aim of this study was to evaluate the distribution of PON1 polymorphism in 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 Alw I restriction enzyme. Study results showed that out of 44 controls 40.9% were A and 2.3% B homozygotes and 56.8% heterozygotes. Among 31 CAD patients 29.0% were A and 16.1% B homozygotes and 54.8% heterozygotes. In 27 MI patients 29.6% were A and 14.8% B homozygotes and 55.6% heterozygotes. Out of 16 hypertension patients 37.5% were A and 18.8% B homozygotes and 43.8% heterozygotes. Among 26 CS patients 57.7% were A and 7.7% B homozygotes and 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 that common polymorphism in the PON1 gene may be an independent risk factor for some cardiovascular diseases.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA
Projekti:
134003
Ustanove:
KBC "Sestre Milosrdnice"
Profili:
Mario Štefanović
(autor)
Mirjana Čubrilo-Turek
(autor)
Dubravko Petrač
(autor)
Elizabeta Topić
(autor)