VDR BsmI 位点的基因检测及其在骨质疏松症患者合理用药中的作用。

Personalized medicine Pub Date : 2024-01-01 Epub Date: 2024-06-21 DOI:10.1080/17410541.2024.2366152
Yu Huang, Nan Qiu, Yunna Wang, Wanjun Ouyang, Miao Liang
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引用次数: 0

摘要

目的:本文测定 350 例患者 VDR BsmI 基因的多态性分布,并根据检测结果提供骨质疏松症的用药建议。材料与方法:将基因型和等位基因频率与其他人群进行卡方检验。结果:基因型频率为 91.66 bsmI:基因型频率为 91.66 bb、8.72 Bb 和 0.21% BB,等位基因频率为 95.43 b 和 4.57% B,符合哈代-温伯格平衡。这些发现表明,VDR 基因多态性,尤其是 BsmIlocus 处的多态性,在骨骼健康和骨质疏松症治疗中发挥着重要作用。基于基因型的药物选择将不良反应从 14 例减少到 2 例。结论这些发现提高了临床治疗效果,指导骨质疏松症患者合理用药。
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Gene detection of VDR BsmI locus and its approteins, genes and growthplication in rational drug use in patients with osteoporosis.

Aim: This paper determines the polymorphism distribution of the VDR BsmI gene in 350 patients and provides medication recommendations for osteoporosis based on detection results. Materials & methods: Chi-square tests compared genotype and allele frequencies with other populations. Results: Genotype frequencies were 91.66 bb, 8.72 Bb and 0.21% BB, with allelic frequencies of 95.43 b and 4.57% B, adhering to Hardy-Weinberg equilibrium. These findings suggest that VDR gene polymorphisms, particularly at the BsmIlocus, play an essential role in bone health and osteoporosis treatment. Genotype-based drug selection reduced adverse reactions from 14 to two cases. Conclusion: These findings improve clinical treatment efficacy and guide rational drug use for osteoporosis patients.

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