Glutathione S-transferase polymorphisms and their role in recurrent pregnancy loss: A genetic risk assessment.

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Tác giả: Nejmiye Akkus, Hande Kucuk Kurtulgan

Ngôn ngữ: eng

Ký hiệu phân loại: 343.0542 Military, defense, public property, public finance, tax, commerce (trade), industrial law

Thông tin xuất bản: Turkey : Turkish journal of obstetrics and gynecology , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 693725

OBJECTIVE: The frequency of recurrent pregnancy loss in society is 3-5%. Experts suggest that genetics account for over 80% of unexplained recurrent pregnancy loss. Glutathione S-transferase (GST) enzymes, regulated by GST genes, facilitate the detoxification of a variety of naturally occurring metabolites as well as environmentally derived chemicals. This research aimed to investigate GST gene polymorphisms as a potential risk factor in recurrent pregnancy loss etiology in the Turkish population. MATERIALS AND METHODS: This study involved 107 recurrent pregnancy loss patients who sought treatment at the Sivas Cumhuriyet University Faculty of Medicine, Department of Medical Genetics, along with a control group of 107 individuals who had a successful birth and no previous history of miscarriage. The multiplex polymerase chain reaction and restriction fragment length polymorphism techniques were employed to analyze RESULTS: GSTT1 null genotype (X CONCLUSION: A statistically significant association was observed between the GSTT1 null genotype and the diseased group. Our research demonstrated a substantial increase in the risk of recurrent pregnancy loss in the Turkish population, specifically among individuals with the GSTM1-null genotype. No statistical correlation was found between the
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