首页> 外文期刊>Annals of Saudi medicine. >Prevalence of methylenetetrahydrofolate reductase gene polymorphisms (C677T, and A1298C) among Saudi children receiving dental treatment
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Prevalence of methylenetetrahydrofolate reductase gene polymorphisms (C677T, and A1298C) among Saudi children receiving dental treatment

机译:沙特儿童接受牙科治疗的沙特儿童中亚甲基四氢盐还原酶基因多态性(C677T和A1298C)的患病率

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BACKGROUND: Methylenetetrahydrofolate reductase, the encoded by the MTHFR gene, plays a crucial role in converting the amino acid homocysteine to methionine. Two polymorphisms of the MTHFR gene, C677T and A1298C, reportedly reduce enzyme activity, resulting in hyperhomocysteinemia. Patients with C677T and A1298C polymorphisms may be at higher risk for developing abnormal hyperhomocysteinemia, which has been linked to catastrophic neurological including fatal outcomes. OBJECTIVE: Determine the prevalence of the MTHFR gene variants C677T and A1298C among pediatric dental patients treated at King Abdulaziz University Hospital. DESIGN: Cross-sectional. SETTING: Clinics of pediatric dentistry department. SUBJECTS AND METHODS: Healthy Saudi children 6–12 years old with no known allergies were screened for eligibility between May and December 2019. A single investigator collected saliva samples. The MTHFR C677T and A1298C polymorphisms were analyzed using polymerase chain reaction and restriction fragment length polymorphism. MAIN OUTCOME MEASURE: The prevalence of MTHFR gene variants (C677T and A1298C) among the subjects. SAMPLE SIZE: 138. RESULTS: MTHFR C677T polymorphism was present in 36.2% of the sample and 90.0% of children carrying this allele were heterozygotes. MTHFR A1298C polymorphism was present in 91.3% of the sample and 77.0% of the children carrying this allele were heterozygotes. No linkage disequilibrium between MTHFR C677T and MTHFR A1298C was observed within this sample. CONCLUSIONS: Our study found a high frequency of the MTHFR A1298C genotype, which was substantially more abundant than expected based on a Hardy-Weinberg distribution. Therefore, caution is advised in using N 2 O in Saudi children as the increased prevalence of this MTHFR allele may increase the incidence of serious adverse effects among these children. LIMITATIONS: Further studies are recommended with a larger sample size from randomly selected hospitals from different regions of Saudi Arabia. CONFLICT OF INTEREST: None.
机译:背景:MTHFR基因编码的亚甲基四氢溶酯还原酶在将氨基酸同型半胱氨酸转化为甲硫氨酸时起着至关重要的作用。据报道,MTHFR基因,C677T和A1298C的两种多态性,据报道,降低酶活性,导致高管抑制因素。患有C677T和A1298C多态性的患者可能具有较高的风险,以发展异常的过粒细胞血症,这与灾难性神经系统有关,包括致命的结果。目的:确定在Abdulaziz大学医院王牙科患者中患有MTHFR基因变体C677T和A1298C的患病率。设计:横截面。环境:儿科牙科部门的诊所。主题和方法:6-12岁的健康沙特儿童在2019年5月和12月之间没有众所周知的过敏症的资格被筛选。一个调查员收集了唾液样本。使用聚合酶链反应和限制片段长度多态性分析MTHFR C677T和A1298C多态性。主要结果措施:受试者中MTHFR基因变体(C677T和A1298C)的患病率。结果:138。结果:MTHFR C677T多态性存在于36.2%的样品中,90.0%的携带此等位基因的儿童是杂合子。 MTHFR A1298C多态性存在于91.3%的样品中,77.0%的携带此等位基因的儿童是杂合子。在该样品中观察到MTHFR C677T和MTHFR A1298C之间没有连接不平衡。结论:我们的研究发现了MTHFR A1298C基因型的高频率,基于Hardy-Weinberg分布基本上比预期的高度大。因此,在沙特儿童中使用N 2 O建议小心,因为这种MTHFR等位基因的患病率增加可能会增加这些儿童的严重不良影响的发生率。局限性:建议进一步研究,其中来自沙特阿拉伯不同地区的随机选择的医院的更大样本。利益冲突:无。

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