首页> 美国卫生研究院文献>Diabetes Metabolic Syndrome and Obesity: Targets and Therapy >Vitamin D receptor rs7975232 rs731236 and rs1544410 single nucleotide polymorphisms and 25-hydroxyvitamin D levels in Egyptian children with type 1 diabetes mellitus: effect of vitamin D co-therapy
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Vitamin D receptor rs7975232 rs731236 and rs1544410 single nucleotide polymorphisms and 25-hydroxyvitamin D levels in Egyptian children with type 1 diabetes mellitus: effect of vitamin D co-therapy

机译:埃及1型糖尿病儿童的维生素D受体rs7975232rs731236和rs1544410单核苷酸多态性和25-羟基维生素D水平:维生素D联合疗法的作用

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摘要

>Purpose: We aimed to examine the possible association role of vitamin D and vitamin D receptor (VDR) single nucleotide polymorphisms (SNPs) in type 1 diabetes mellitus (T1DM) development, glycemic control and complications among a cohort of Egyptian children.>Subjects and methods: A prospective case-control study has been conducted on 50 Egyptian children with T1DM who were comparable with 50 controls. Vitamin D and HbA1c were measured. VDR-SNPs [ApaI (rs7975232), TaqI (rs731236) and BsmI (rs1544410)] detection was done by polymerase chain reaction through restriction fragment length polymorphism (PCR-RFLP) technique. Vitamin D supplements were given to the included T1DM children with low vitamin D and reassessments of both HbA1c% and 25(OH)D serum levels were performed in those children three months later.>Results: Eighty percent of the included diabetic patients have poor glycemic control. Vitamin D was deficient in 68% and insufficient in 16% of diabetic patients. Significant improvements in both vitamin D and glycemic status among T1DM children, who have low vitamin D and received vitamin D supplementations. There were significantly negative correlations between serum levels of vitamin D with both HbA1c % (r= –0.358, P˂0.05) and daily insulin dose (r=−0.473, P˂0.05). Compared with controls, T1DM children presented more commonly with ApaI a allele (OR: 2.87; 95%CI: 1.39–5.91, P˂0.05) and BsmI b allele (OR: 4.38; 95%CI: 2.30–8.33, P˂0.05). TaqI t allele wasn’t significantly differing among patients and controls (P˃0.05). Aa+aa and Bb+bb genotypes were significantly higher among T1DM vs the controls (OR: 3.08;, 95%CI: 1.33–7.15, P˂0.05 and OR: 9.33; 95%CI: 3.61–24.17, P˂0.05respectively).>Conclusion: ApaI and BsmI were associated with risk of T1DM development among Egyptian children. Low vitamin D status was frequently occurring among T1DM with significant improvement in the glycemic control of such children when adding vitamin D supplements to the standard insulin therapy.
机译:>目的:我们旨在研究维生素D和维生素D受体(VDR)单核苷酸多态性(SNP)在1型糖尿病(T1DM)发育,血糖控制和人群中并发症中的可能关联作用>受试者和方法:前瞻性病例对照研究已经对50名埃及T1DM儿童进行了前瞻性病例对照研究,这些儿童可与50名对照进行比较。测量维生素D和HbA1c。 VDR-SNP [ApaI(rs7975232),TaqI(rs731236)和BsmI(rs1544410)]检测是通过限制性片段长度多态性(PCR-RFLP)技术通过聚合酶链反应进行的。对所包括的维生素D含量较低的T1DM儿童给予了维生素D补充剂,并在三个月后对这些儿童进行了HbA1c%和25(OH)D血清水平的重新评估。>结果:包括糖尿病患者的血糖控制不佳。维生素D缺乏者占68%,糖尿病患者不足16%。维生素D较低并接受维生素D补充的T1DM儿童的维生素D和血糖状况均有显着改善。血清维生素D与HbA1c%(r = –0.358,P˂0.05)和每日胰岛素剂量(r = -0.473,P˂0.05)之间存在显着的负相关。与对照组相比,T1DM儿童的ApaI等位基因(OR:2.87; 95%CI:1.39–5.91,P˂0.05)和BsmI b等位基因(OR:4.38; 95%CI:2.30–8.33,P˂0.05 )。 TaqI t等位基因在患者和对照组之间无显着差异(P˃0.05)。在T1DM中,Aa + aa和Bb + bb基因型显着高于对照组(OR:3.08; 95%CI:1.33-7.15,P˂0.05和OR:9.33; 95%CI:3.61-24.17,P˂0.05 )。>结论: ApaI和BsmI与埃及儿童T1DM发生的风险有关。当在标准胰岛素治疗中添加维生素D补充剂时,T1DM中维生素D的状态通常较低,对此类儿童的血糖控制有显着改善。

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