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Polymorphisms in two paraoxonase genes pon1 and pon2 in angiographycally assessed cerebrovascular stenosis (CROSBI ID 538173)

Prilog sa skupa u časopisu | sažetak izlaganja sa skupa | međunarodna recenzija

Flegar-Meštrić, Zlata ; Kardum Paro, Mirjana Mariana ; Perkov, Sonja ; Vrhovski-Hebrang, Danijela ; Vidjak, Vinko ; Grdić, Marija ; Juretić, Dubravka ; Barišić, Karmela Polymorphisms in two paraoxonase genes pon1 and pon2 in angiographycally assessed cerebrovascular stenosis // Atherosclerosis (Amsterdam) / Humpries, S.E. (ur.). 2008. str. 245-245

Podaci o odgovornosti

Flegar-Meštrić, Zlata ; Kardum Paro, Mirjana Mariana ; Perkov, Sonja ; Vrhovski-Hebrang, Danijela ; Vidjak, Vinko ; Grdić, Marija ; Juretić, Dubravka ; Barišić, Karmela

engleski

Polymorphisms in two paraoxonase genes pon1 and pon2 in angiographycally assessed cerebrovascular stenosis

Background. Human serum paraoxonase (PON1) is an esterase coded by pon1 gene on chromosome 7 and linked with two additional PON-like genes (pon2 and pon3). Alterations of enzyme anti- atherogenic activity due to polymorphisms in the pon genes my be one of the risk factors for the development of atherosclerosis. Aim. To examine the distribution of polymorphisms of pon1 and pon2 genes in patients with angiografically assessed severe stenosis of cerebral arteries and matched control subjects. Methods. The blood samples were recruited from 40 healthy individuals and 29 patients with >70 % of arterial carotides stenosis. DNA was extracted and used for amplification of the target regions by polymerase chain reaction (PCR). Amplified products were digested with BspPI (Q192R), Hin 1II (L55M), BsrBI (-108C>T) and DdeI (S311C) restriction enzymes and determinated by restriction fragment length polymorphism (RFLP) procedure. Results. Genotype frequencies of pon1 and pon2 genes polymorphisms founded in cases vs. controls were: 15 (0, 52) QQ, 11 (0, 38) QR, 3 (0, 10) RR vs. 23 (0, 58) QQ, 15 (0, 37) QR, 2 (0, 05) RR for Q192R ; 13 (0, 45) LL, 10 (0, 34) LM, 6 (0, 21) MM vs. 16 (0, 40) LL, 18 (0, 45) LM, 6 (0, 15) MM for L55M ; 6 (0, 21) CC, 12 (0, 41) CT ; 11 (0, 38) TT vs. 8 (0, 20) CC, 24 (0, 60) CT, 8 (0, 20) TT for – 108C>T and 1 (0, 03) CC, 8 (0, 28) CS, 20 (0, 69) SS vs. 0 (0, 00) CC, 22 (0, 55) CS, 18 (0, 45) SS for S311C. Conclusions. The results of our study show no significant differences in genotype or allele frequencies between patients with severe stenosis of cerebral arteries and controls.

Human serum paraoxonase (PON1); pon1 gene; pon2 gene; cerebrovascular stenosis

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nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

Podaci o prilogu

245-245.

2008.

nije evidentirano

objavljeno

Podaci o matičnoj publikaciji

Atherosclerosis (Amsterdam)

Humpries, S.E.

Istanbul: ScienceDirekt, Elsevier

0021-9150

Podaci o skupu

77th Congress of the European Atherosclerosis Society

ostalo

26.04.2008-29.04.2008

Istanbul, Turska

Povezanost rada

Kliničke medicinske znanosti, Farmacija

Indeksiranost