Association of single nucleotide genetic polymorphisms of vitamin D receptor and calcium-sensitive receptor with calcium-containing kidney stones in Chinese Dai populations: a prospective multi-center study.

IF 1.8 4区 医学 Q3 UROLOGY & NEPHROLOGY International Urology and Nephrology Pub Date : 2024-11-01 Epub Date: 2024-06-17 DOI:10.1007/s11255-024-04109-2
Ji Li, Kunbin Ke, Baiyu Zhang, Yidao Liu, Jing Bai, Mengyue Wang, Hao Li
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Abstract

Purpose: To evaluate the association between vitamin D receptor (VDRs) and calcium-sensitive receptor (CaSR) gene polymorphisms and calcium-containing kidney stones (CCKS) in Dai populations.

Methods: A total of 160 CCKS patients and 87 healthy controls were included in this study. CCKS was confirmed using urological computed tomography (CT), plain abdominal radiograph, or surgical lithotomy. Stone samples obtained during surgery were analyzed using infrared spectroscopy. Venous blood and 24-h urine samples were collected and analyzed using Sanger sequencing and high-performance liquid chromatography, respectively. Genetic variants in the VDR gene (rs7975232, rs2228570, rs731236, and rs1544410) and CaSR gene (rs7652589, rs1801725, and rs1042636) were identified through sequence analysis.

Results: Analysis of genotype and allele frequencies revealed that the rs7975232 polymorphism in the VDR gene and the rs7652589 allele in the CaSR gene were significantly associated with CCKS. Furthermore, patients carrying the AC and AA genotypes of rs7975232 showed a higher incidence of hypocitraturia compared to those with other genotypes (p < 0.05). The AA and GG genotypes of rs1042636 and the AA genotype of rs7652589 were significantly associated with hypercalciuria (p < 0.05).

Conclusion: CCKS in this study population may be closely related to hypocitraturia caused by the VDR locus rs7975232 polymorphism and hypercalciuria caused by the CaSR locus rs1042636 and rs7652589 polymorphism.

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中国傣族人群维生素 D 受体和钙敏感受体的单核苷酸基因多态性与含钙肾结石的关系:一项前瞻性多中心研究。
目的:评估傣族人群中维生素 D 受体(VDRs)和钙敏感受体(CaSR)基因多态性与含钙肾结石(CCKS)之间的关系:本研究共纳入 160 名 CCKS 患者和 87 名健康对照者。CCKS通过泌尿科计算机断层扫描(CT)、腹部X光平片或手术碎石确认。手术中获得的结石样本通过红外光谱进行分析。采集的静脉血和 24 小时尿液样本分别采用桑格测序法和高效液相色谱法进行分析。通过序列分析确定了 VDR 基因(rs7975232、rs2228570、rs731236 和 rs1544410)和 CaSR 基因(rs7652589、rs1801725 和 rs1042636)的遗传变异:结果:对基因型和等位基因频率的分析表明,VDR基因中的rs7975232多态性和CaSR基因中的rs7652589等位基因与CCKS显著相关。此外,与其他基因型的患者相比,携带 rs7975232 的 AC 和 AA 基因型的患者出现低柠檬酸尿症的几率更高(p 结论:CCKS 在该研究人群中可能存在:本研究人群中的 CCKS 可能与 VDR 基因座 rs7975232 多态性导致的低柠檬酸尿症和 CaSR 基因座 rs1042636 和 rs7652589 多态性导致的高钙尿症密切相关。
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来源期刊
International Urology and Nephrology
International Urology and Nephrology 医学-泌尿学与肾脏学
CiteScore
3.40
自引率
5.00%
发文量
329
审稿时长
1.7 months
期刊介绍: International Urology and Nephrology publishes original papers on a broad range of topics in urology, nephrology and andrology. The journal integrates papers originating from clinical practice.
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