Ay Arzu, Alkanli Nevra, Ustundag Sedat
Department of Biophysics, Faculty of Medicine, Trakya University, Edirne, Turkey.
Department of Biophysics, Faculty of Medicine, Haliç University, Istanbul, Turkey.
Biol Trace Elem Res. 2022 May;200(5):2040-2052. doi: 10.1007/s12011-021-02828-6. Epub 2021 Jul 15.
The aim of this study is to investigate the relationship between IL-18 (- 607 C/A), IL-18 (- 137 G/C), and MMP-2 (- 1306 C/T) gene variations and serum trace element levels in patients diagnosed with CRF. Genotype distributions of IL-18 (- 607 C/A, - 137 G/C) gene variations were determined by polymerase chain reaction (PCR) method. PCR-restriction fragment length polymorphism (RFLP) methods were used to determine the MMP-2 (- 1306 C/T) gene variation genotype distributions. Serum trace element levels were determined by atomic absorption spectrophotometer method. A significant difference was found between the CRF patient and healthy control groups in terms of genotype distributions of IL-18 (- 607 C/A) and MMP-2 (- 1306 C/T) gene variations (p < 0.05). The significant difference was found between the patient and control groups in terms of serum copper and zinc levels and copper/zinc ratio (p < 0.05). The significant difference was detected between patient and control groups in terms of copper and zinc levels and copper/zinc ratio according to IL-18 (- 607 C/A), IL-18 (- 137 G/C), and MMP-2 (- 1306 C/T) gene variations and genotype distributions (p < 0.05). In addition, significant difference was determined in terms of serum copper and zinc levels and copper/zinc ratio according to haplotypes of IL-18 (- 607 C/A), IL-18 (- 137 G/C), and MMP-2 (- 1306 C/T) gene variations between patient and control groups (p < 0.05). In conclusion, evaluation of IL-18 (- 607 C/A, - 137 G/C) and MMP-2 (- 1306 C/T) gene variations and serum trace element levels together is extremely important in terms of obtaining important biomarkers in CRF early diagnosis and progression.
本研究旨在探讨白细胞介素-18(IL-18,-607 C/A)、白细胞介素-18(-137 G/C)和基质金属蛋白酶-2(MMP-2,-1306 C/T)基因变异与慢性肾衰竭(CRF)患者血清微量元素水平之间的关系。采用聚合酶链反应(PCR)法测定IL-18(-607 C/A,-137 G/C)基因变异的基因型分布。采用PCR-限制性片段长度多态性(RFLP)方法测定MMP-2(-1306 C/T)基因变异的基因型分布。采用原子吸收分光光度计法测定血清微量元素水平。在IL-18(-607 C/A)和MMP-2(-1306 C/T)基因变异的基因型分布方面,CRF患者与健康对照组之间存在显著差异(p<0.05)。在血清铜、锌水平及铜/锌比值方面,患者组与对照组之间存在显著差异(p<0.05)。根据IL-18(-607 C/A)、IL-18(-137 G/C)和MMP-2(-1306 C/T)基因变异及基因型分布,患者组与对照组在铜、锌水平及铜/锌比值方面存在显著差异(p<0.05)。此外,根据IL-18(-607 C/A)、IL-18(-137 G/C)和MMP-2(-1306 C/T)基因变异的单倍型,患者组与对照组在血清铜、锌水平及铜/锌比值方面也存在显著差异(p<0.05)。总之,综合评估IL-18(-607 C/A,-137 G/C)和MMP-2(-1306 C/T)基因变异及血清微量元素水平,对于在CRF早期诊断和病情进展中获取重要生物标志物极为重要。