C626G Polymorphism in the Apoptotic Death Receptor-4 TRAIL Binding Domain Associated with Recurrent Pregnancy Loss: Case-Control Research

Küçük Resim Yok

Tarih

2021

Dergi Başlığı

Dergi ISSN

Cilt Başlığı

Yayıncı

Turkiye Klinikleri

Erişim Hakkı

info:eu-repo/semantics/openAccess

Özet

Objective: Disruption of apoptotic balance in cells during embryonic development can lead to pregnancy losses. In this study, the relationship between unexplained recurrent pregnancy loss (RPL) and apoptotic inducing death receptor-4 (DR-4) gene polymorphisms was investigated. Material and Methods: In this study, genomic DNA was obtained from 70 women diagnosed with RPL and 70 women as a control group. The polymorphisms of rs6557634 G422A in the 3rd exon of the DR-4 gene, rs20575 C626G in the 4th exon and rs20576 A683C in the 5th exon were determined in both groups using the polyme rase chain reaction-restriction fragment length polymorphism method. Results: It was determined that the incidence of C626G polymorphism, which is a missense variant in exon 4 resulting in the change of threo-nine to arginine in the 209th codone in the extracellular TRAIL ligand binding domain of DR-4, increased in RPL cases compared to the con-trols. For the investigated exon 3 and exon 5 polymorphisms, no statistical difference was observed between the RPL and the control group. Conclusion: We conclude that the missense exon 4 polymorphism in the DR-4 gene, which we detected in patients with RPL, may cause pregnancy losses through the invasion of the embryo to the uterus during embryonic development and the disruption of the apoptotic balance in its immunological tolerance. © 2021 by Türkiye Klinikleri.

Açıklama

Anahtar Kelimeler

Apoptosis, Death receptor-4, Polymorphism, Recurrent pregnancy loss, TRAIL

Kaynak

Turkiye Klinikleri Journal of Medical Sciences

WoS Q Değeri

Scopus Q Değeri

Q4

Cilt

41

Sayı

4

Künye