Cinacalcet改善透析治疗继发性甲状旁腺功能亢进患者的促红细胞生成素抵抗。

IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY Current pharmaceutical design Pub Date : 2025-01-14 DOI:10.2174/0113816128321721241118171041
Wenjuan Weng, Yingjuan Li, Yongda Lin, Jiali Wang, Xiutian Chen, Tianbiao Zhou
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引用次数: 0

摘要

慢性肾脏疾病(CKD)是公认的一个主要的全球公共卫生问题。透析是终末期肾病患者的主要治疗方法,可以延长CKD患者的生存期。随着患者存活率的提高,并发症的治疗变得更加重要。CKD-矿物质和骨骼疾病(CKD- mbd)和肾性贫血是CKD患者常见的并发症。Cinacalcet是一种治疗成人透析患者继发性甲状旁腺功能亢进症(SHPT)的拟钙化剂,通过增加钙敏感受体的敏感性来调节甲状旁腺激素的合成和分泌。本回顾性研究评估了cinacalcet在透析患者中的疗效。方法:对47例甲状旁腺激素升高的透析患者进行分析。入选患者在我院门诊定期随访,并定期使用cinacalcet,疗程不少于6个月。结果:在6个月疗效评价期,cinacalcet不仅降低了完整甲状旁腺激素(iPTH, P≤0.05)、血钙(P≤0.01)、Ca×P水平(P≤0.05),而且降低了周促红细胞生成素剂量(P≤0.01)和促红细胞生成素抵抗指数(ERI, P≤0.05)。结论:在控制CKD患者SHPT的同时,cinacalcet可降低EPO抵抗并改善肾性贫血。综上所述,cinacalcet不仅降低了iPTH、血清钙和Ca×P的水平,而且降低了EPO的周剂量和ERI水平。在CKD患者中控制SHPT, cinacalcet也降低ERI和改善肾性贫血。
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Cinacalcet Improves Erythropoietin Resistance in Patients with Secondary Hyperparathyroidism Receiving Dialysis Treatment.

Introduction: Chronic Kidney Disease (CKD) is recognized as a major global public health problem. Dialysis is the mainstay of treatment for patients with end-stage renal disease and can prolong survival in patients with CKD. As patient survival increases, the treatment of complications becomes more important. CKD-mineral and bone disorders (CKD-MBD) and renal anemia are common complications in patients with CKD. Cinacalcet is a calcimimetic for the treatment of Secondary Hyperparathyroidism (SHPT) in adult dialysis patients, which regulates the synthesis and secretion of parathyroid hormone by increasing the sensitivity of calcium-sensitive receptors. This retrospective study evaluated the efficacy of cinacalcet in dialysis patients.

Method: Forty-seven patients on dialysis with elevated parathyroid hormone were included. The selected patients have regular follow-up visits in our outpatient clinic and regular use of cinacalcet for no less than 6 months.

Result: During the 6-month efficacy evaluation phase, cinacalcet not only reduced the levels of the intact parathyroid hormone (iPTH, P ≤ 0.05), serum calcium (P ≤ 0.01), and Ca×P (P ≤ 0.05) but also reduced weekly erythropoietin dosage (P ≤ 0.01) and erythropoietin resistance index (ERI, P ≤ 0.05).

Conclusion: While controlling SHPT in patients with CKD, cinacalcet reduced EPO resistance and improved renal anemia. In conclusion, cinacalcet not only decreased the levels of the iPTH, serum calcium, and Ca×P but also reduced weekly EPO dosage and ERI levels. Controlling SHPT in patients with CKD, cinacalcet also reduced ERI and improved renal anemia.

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来源期刊
CiteScore
6.30
自引率
0.00%
发文量
302
审稿时长
2 months
期刊介绍: Current Pharmaceutical Design publishes timely in-depth reviews and research articles from leading pharmaceutical researchers in the field, covering all aspects of current research in rational drug design. Each issue is devoted to a single major therapeutic area guest edited by an acknowledged authority in the field. Each thematic issue of Current Pharmaceutical Design covers all subject areas of major importance to modern drug design including: medicinal chemistry, pharmacology, drug targets and disease mechanism.
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