CTLA-4 (+49A/G) polymorphism and type-1diabetes in Turkish children

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Abstract

Objective: To evaluate the contribution of cytotoxic T-Iymphocyte antigen-4 (CTLA-4)+49A/G polymorphism to the susceptibility to type-1 diabetes (T1D) in Turkish children. Methods: A case-control study was designed to include 91 Turkish children with T1D and 99 healthy controls. CTLA-4 (+99A/G) gene polymorphism typing was done by PCR amplification followed by restriction fragment length polymorphism method. Results: The genotype and allele frequencies of the CTLA-4 (+99A/G) polymorphism in patients with T1D were not different from those in the controls (p>0.05). The allele frequency of G was 36.2% in patients with T1D, and 31.8% in controls (p>0.05). Additionally, this polymorphism was not associated with the clinical and laboratory characteristics of the patients with T1D (p>0.05). Conclusions: Our case-control study suggests that the CTLA-4 (+99A/G) gene polymorphism is not associated with T1D in the Turkish population. © Journal of Clinical Research in Pediatric Endocrinology, Published by Galenos Publishing.

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APA

Çelmeli, F., Türkkahraman, D., Özel, D., Akçurin, S., & Yeǧin, O. (2013). CTLA-4 (+49A/G) polymorphism and type-1diabetes in Turkish children. JCRPE Journal of Clinical Research in Pediatric Endocrinology, 5(1), 40–43. https://doi.org/10.4274/Jcrpe.879

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