Association of TCF7L2 rs7903146 Polymorphism with the Risk of Type 2 Diabetes Mellitus (T2DM) Among Kurdish Population in Erbil Province, Iraq
Autor: | Delan Ameen Younus, Suhad Asad Mustafa |
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Rok vydání: | 2020 |
Předmět: |
0301 basic medicine
education.field_of_study medicine.medical_specialty endocrine system diseases business.industry Clinical Biochemistry Population nutritional and metabolic diseases Type 2 Diabetes Mellitus Single-nucleotide polymorphism medicine.disease 03 medical and health sciences 030104 developmental biology 0302 clinical medicine 030220 oncology & carcinogenesis Internal medicine Diabetes mellitus Genotype Genetic predisposition medicine Original Research Article education business TCF7L2 Genotyping |
Zdroj: | Indian J Clin Biochem |
ISSN: | 0974-0422 0970-1915 |
DOI: | 10.1007/s12291-020-00904-7 |
Popis: | The genetic predispositions responsible for developing type 2 diabetes mellitus (T(2)DM) in the Middle East are poorly understood. The rs7903146 single nucleotide polymorphism (SNP) located in transcription factor 7-like-2 (TCF7L2) gene has been recognized to have a vital role in the development of T(2)DM disorder. The current study is the first to have researched the possible association between TCF7L2 rs7903146 SNP and T(2)DM among Kurdish population in Kurdistan region of Iraq. The study included 212 participants, half of them were T(2)DM patients, and the other half were disease-free and normoglycemic controls. Genotyping was performed by using a high throughput cost and time effective tetra-primer amplification refractory mutation system-polymerase chain reaction (Tetra ARMS-PCR) assay. The rs7903146 genotypic frequencies for CC, CT and TT were 24.5%, 69.8%, and 5.7% in T(2)DM group respectively, and for the controls were 45.3%, 50.9%, and 3.8% respectively. The frequency of CT genotype was found significantly higher in the cases when compared to the controls (OR = 2.53, 95% CI 1.40–4.57, P value |
Databáze: | OpenAIRE |
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