2007
DOI: 10.1111/j.1365-4632.2007.02957.x
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Cytochrome P450 polymorphisms in patients with Behcet's disease

Abstract: We observed that patients with BD presented with a higher prevalence of the heterozygous CYP2C19*2 genotype. Hereditary deficiencies of this enzyme activity may lead to an imbalance between pro- and antioxidant systems, resulting in the formation of excessive reactive oxygen species.

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Cited by 9 publications
(6 citation statements)
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“…Studies on CYP2C19 polymorphisms have also been conducted in a Turkish population. In a study of 106 healthy volunteers, PM frequency was found to be 0.94% [23]. Aynacioglu et al, who found the PM frequency to be~1% [13], reported that the mutation responsible for the PM genotype was CYP2C19*2 and that there was no CYP2C19*3 in any of the individuals in the study.…”
Section: Discussionmentioning
confidence: 94%
“…Studies on CYP2C19 polymorphisms have also been conducted in a Turkish population. In a study of 106 healthy volunteers, PM frequency was found to be 0.94% [23]. Aynacioglu et al, who found the PM frequency to be~1% [13], reported that the mutation responsible for the PM genotype was CYP2C19*2 and that there was no CYP2C19*3 in any of the individuals in the study.…”
Section: Discussionmentioning
confidence: 94%
“…In a study from Turkey, Tursen et al [23] investigated CYP2C9*2 and *3 in 62 patients with BD as compared to 107 healthy controls and found no difference in the frequency of these alleles. No phenotype of CYP2C9, as our test with losartan, was performed and, therefore, the CYP2C9 activity in these 62 patients is unknown.…”
Section: Discussionmentioning
confidence: 99%
“…Bu mutasyon allelerinin enzim kapasitesi hızlı metabolizör olarak da adlandırılan yabanıl tipe göre düşüktür (106). Türk popülasyonunda CYP2C9*2 ve CYP2C9*3 polimorfizminin BH ile ilişkisi araştırılmış ve bir anlamlılık olmadığı kaydedilmiştir (107). CYP2C19'daki mutasyonlar da enzim aktivitesindeki azalma ile ilişkilidir.…”
Section: Biyotransformasyon Enzimleriunclassified