Araştırma Makalesi
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Kardiyak Sendrom X Hastalarında CYP2J2 Polimorfizminin Belirlenmesi

Yıl 2019, Cilt: 9 Sayı: 2, 79 - 86, 01.08.2019

Öz

ÖZET
Amaç: Tipik anjinaya sahip, invaziv olmayan testlerde iskemi bulgusuna rastlanan ve koroner anjiyografide normal epikardiyal koroner arterlere sahip olan hasta popülasyonu Kardiyak Sendrom X (KSX) olarak tanımlanmaktadır. KSX hastalarında CRP ve diğer inflamatuvar belirteçlerin düzeylerinin artması, hastalığın inflamasyon aracılı bir patogeneze sahip olduğunu gösterir niteliktedir. Sitokrom P450 enzimi olan CYP2J2, koroner arter endoteli, düz kas hücreleri ve kardiyomiyositlerde yüksek düzeylerde eksprese edilen bir hem protein ailesi üyesidir. CYP2J2’nin başlıca görevi, araşidonik asidin; 5,6- 8,9- 11,12- 14,15- olmak üzere 4 farklı çeşit epoksieikozatrienoik asitlere (EET) dönüşümünü sağlamaktır. Bu EET’ler, TNF-α ile uyarılan VCAM-1’in, endotelyal ekspresyonunu azaltarak
inflamatuvar yanıt oluşumunu baskılamakta ve NF-κB’yi de inhibe ederek vasküler duvara lökosit adezyonunu azaltmaktadır. CYP2J2 geni -76G>T polimorfizmi, hücre içerisinde CYP2J2 ve metabolitlerinin ekspresyonunda düşüşe neden olmaktadır. Biz bu çalışmamızda, patofizyolojisinde inflamatuvar süreçlerin etkili olduğu düşünülen KSX hastalığı ile inflamatuvar yolakta rol aldığı bilinen CYP2J2 geni -76G>T polimorfizmi arasındaki bağlantıyı incelemeyi amaçladık. Materyal ve Metot: Ardışık 125 KSX hastası ve 125 sağlıklı bireyden oluşan kontrol grubunu, CYP2J2 geni -76G>T polimorfizmi açısından karşılaştırdık. DNA örneklerinden CYP2J2 geni -76G>T polimorfizminin genotiplemesi gerçek zamanlı PCR metodu kullanılarak yapılmıştır. Bulgular: Hasta ve kontrol gruplarında görülen TT, GT ve GG genotipleri incelendiğinde, istatistiksel olarak anlamlı bir fark gözlenmemiştir (p>0,05). Sonuç: Bu durum KSX hastalığının patogenezinde, inflamasyon artışına neden olan CYP2J2 geni -76G>T polimorfizminin önemli bir rolü olmadığını düşündürmektedir.

Kaynakça

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Toplam 47 adet kaynakça vardır.

Ayrıntılar

Birincil Dil Türkçe
Konular Klinik Tıp Bilimleri
Bölüm Araştırma Makalesi
Yazarlar

Melissa Tatlıdil Akal Bu kişi benim

Burak Önal Bu kişi benim

Deniz Özen Bu kişi benim

Bülent Demir Bu kişi benim

Ahmet Gökhan Akkan Bu kişi benim

Sibel Özyazgan Bu kişi benim

Yayımlanma Tarihi 1 Ağustos 2019
Yayımlandığı Sayı Yıl 2019 Cilt: 9 Sayı: 2

Kaynak Göster

APA Tatlıdil Akal, M., Önal, B., Özen, D., Demir, B., vd. (2019). Kardiyak Sendrom X Hastalarında CYP2J2 Polimorfizminin Belirlenmesi. Kafkas Journal of Medical Sciences, 9(2), 79-86.
AMA Tatlıdil Akal M, Önal B, Özen D, Demir B, Akkan AG, Özyazgan S. Kardiyak Sendrom X Hastalarında CYP2J2 Polimorfizminin Belirlenmesi. KAFKAS TIP BİL DERG. Ağustos 2019;9(2):79-86.
Chicago Tatlıdil Akal, Melissa, Burak Önal, Deniz Özen, Bülent Demir, Ahmet Gökhan Akkan, ve Sibel Özyazgan. “Kardiyak Sendrom X Hastalarında CYP2J2 Polimorfizminin Belirlenmesi”. Kafkas Journal of Medical Sciences 9, sy. 2 (Ağustos 2019): 79-86.
EndNote Tatlıdil Akal M, Önal B, Özen D, Demir B, Akkan AG, Özyazgan S (01 Ağustos 2019) Kardiyak Sendrom X Hastalarında CYP2J2 Polimorfizminin Belirlenmesi. Kafkas Journal of Medical Sciences 9 2 79–86.
IEEE M. Tatlıdil Akal, B. Önal, D. Özen, B. Demir, A. G. Akkan, ve S. Özyazgan, “Kardiyak Sendrom X Hastalarında CYP2J2 Polimorfizminin Belirlenmesi”, KAFKAS TIP BİL DERG, c. 9, sy. 2, ss. 79–86, 2019.
ISNAD Tatlıdil Akal, Melissa vd. “Kardiyak Sendrom X Hastalarında CYP2J2 Polimorfizminin Belirlenmesi”. Kafkas Journal of Medical Sciences 9/2 (Ağustos 2019), 79-86.
JAMA Tatlıdil Akal M, Önal B, Özen D, Demir B, Akkan AG, Özyazgan S. Kardiyak Sendrom X Hastalarında CYP2J2 Polimorfizminin Belirlenmesi. KAFKAS TIP BİL DERG. 2019;9:79–86.
MLA Tatlıdil Akal, Melissa vd. “Kardiyak Sendrom X Hastalarında CYP2J2 Polimorfizminin Belirlenmesi”. Kafkas Journal of Medical Sciences, c. 9, sy. 2, 2019, ss. 79-86.
Vancouver Tatlıdil Akal M, Önal B, Özen D, Demir B, Akkan AG, Özyazgan S. Kardiyak Sendrom X Hastalarında CYP2J2 Polimorfizminin Belirlenmesi. KAFKAS TIP BİL DERG. 2019;9(2):79-86.