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https://hdl.handle.net/11499/6947
Title: | Insulin-like Growth Factor-I Gene and Insulin-like Growth Factor Binding Protein-3 Polymorphism in Patients with Thyroid Dysfunction | Authors: | Kursunluoglu, R. Turgut, Sebahat Akın, Fulya Bastemir, M. Kaptanoglu, B. Genç, Osman Turgut, Günfer |
Keywords: | Hyperthyroidism Hypothyroidism Insulin like growth factor-I (IGF-I) Insulin-like growth factor binding protein-3 (IGFBP-3) Polymorphism DNA somatomedin binding protein 3 somatomedin C article controlled study DNA isolation DNA polymorphism gene frequency genetic variability human hyperthyroidism hypothyroidism major clinical study polymerase chain reaction thyroid disease Base Sequence Case-Control Studies DNA Primers Humans Insulin-Like Growth Factor Binding Protein 3 Insulin-Like Growth Factor I Polymerase Chain Reaction Polymorphism, Genetic Thyroid Diseases |
Abstract: | Background and Aims: Thyroid hormones have important roles in normal growth and skeletal muscle development. IGF-I is one of the most important growth factors and is needed for the proliferation and development of thyroid cells. It stimulates fibroblasts, follicular and endothelia cells in thyroid gland. It has been shown that thyroid hormones play an important role in the regulation of IGF-I and IGFBP-3. In this study we proposed that IGF-I (CA)19 and IGFBP-3-202 A/C gene polymorphism may affect thyroid functions. For this purpose, frequency of IGF-I (CA)19 and IGFBP-3-202 A/C gene polymorphism in hypo- and hyperthyroid patients and possible role of these polymorphism in thyroid functions were investigated. Methods: This study was performed on 37 volunteer hyperthyroid and 76 hypothyroid patients as well as with 50 healthy subjects as controls. DNA isolation was applied in peripheral blood samples obtained from patients and controls. Required areas were amplified with PCR by using proper primers belonging to these gene areas from the isolated DNA samples. The products were evaluated with visualization by UV gel documentation system. Results: Frequency of IGF-I (CA)19 gene polymorphism among hypothyroidism patients, hyperthyroidism patients and controls were statistically significant (?2 = 11.55, df = 4, p = 0.021). Genotypic variations between hyper- and hypothyroid patients were significant (?2 = 11.39, df = 2, p = 0.003), whereas there was no difference in IGF-I (CA)19 gene polymorphism between the patients and controls. Differences in the IGFBP-3-202 A/C gene polymorphism between controls and hypo- as well as hyperthyroid patients were not significant. But IGFBP-3-202 A/C gene polymorphism genotype frequencies showed a significant difference between hypo- and hyperthyroid patients (?2 = 6.24, df = 2, p = 0.044). Conclusions: These findings suggests that IGF-I (CA)19 and IGFBP-3-202 A/C gene polymorphisms may be a risk factor for hypothyroidism. © 2009 IMSS. | URI: | https://hdl.handle.net/11499/6947 https://doi.org/10.1016/j.arcmed.2008.10.009 |
ISSN: | 0188-4409 |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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