Pretražite po imenu i prezimenu autora, mentora, urednika, prevoditelja

Napredna pretraga

Pregled bibliografske jedinice broj: 62797

Genetic polymorphism of paraoxonase and the risk of cardiovascular diseases (CVD)


Ivanišević, Ana-Maria; Štefanović, Mario; Topić, Elizabeta; Nikolić, Vjeran; Petrač, Dubravko; Čubrilo-Turek, Mirjana
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"


Citiraj ovu publikaciju:

Ivanišević, Ana-Maria; Štefanović, Mario; Topić, Elizabeta; Nikolić, Vjeran; Petrač, Dubravko; Čubrilo-Turek, Mirjana
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)
Ivanišević, A., Štefanović, M., Topić, E., Nikolić, V., Petrač, D. & Čubrilo-Turek, M. (1999) Genetic polymorphism of paraoxonase and the risk of cardiovascular diseases (CVD). U: Siest, G. (ur.)Clin Chem Lab Med 1999;vol 37,Abstracts volume, special supplement.
@article{article, author = {Ivani\v{s}evi\'{c}, Ana-Maria and \v{S}tefanovi\'{c}, Mario and Topi\'{c}, Elizabeta and Nikoli\'{c}, Vjeran and Petra\v{c}, Dubravko and \v{C}ubrilo-Turek, Mirjana}, editor = {Siest, G.}, year = {1999}, pages = {S132}, keywords = {PON1, cardiovascular diseses}, title = {Genetic polymorphism of paraoxonase and the risk of cardiovascular diseases (CVD)}, keyword = {PON1, cardiovascular diseses}, publisher = {Walter de Gruyter}, publisherplace = {Firenca, Italija} }
@article{article, author = {Ivani\v{s}evi\'{c}, Ana-Maria and \v{S}tefanovi\'{c}, Mario and Topi\'{c}, Elizabeta and Nikoli\'{c}, Vjeran and Petra\v{c}, Dubravko and \v{C}ubrilo-Turek, Mirjana}, editor = {Siest, G.}, year = {1999}, pages = {S132}, keywords = {PON1, cardiovascular diseses}, title = {Genetic polymorphism of paraoxonase and the risk of cardiovascular diseases (CVD)}, keyword = {PON1, cardiovascular diseses}, publisher = {Walter de Gruyter}, publisherplace = {Firenca, Italija} }




Contrast
Increase Font
Decrease Font
Dyslexic Font