Suppr超能文献

口服法骨化三醇与静脉注射骨化三醇治疗血液透析继发性甲状旁腺功能亢进患者的比较:一项随机交叉试验。

Comparison of oral falecalcitriol and intravenous calcitriol in hemodialysis patients with secondary hyperparathyroidism: a randomized, crossover trial.

作者信息

Ito H, Ogata H, Yamamoto M, Takahashi K, Shishido K, Takahashi J, Taguchi S, Kinugasa E

机构信息

Department of Internal Medicine, Showa University Northern Yokohama Hospital, Yokohama, Japan.

出版信息

Clin Nephrol. 2009 Jun;71(6):660-8. doi: 10.5414/cnp71660.

Abstract

BACKGROUND

Falecalcitriol is a novel vitamin D analog, which has a greater potential to suppress parathyroid hormone (PTH) and a longer half-life. There are few studies to compare clinical effects of oral falecalcitriol treatment with those of intravenous calcitriol treatment.

METHODS

Twenty-one patients with moderate to severe SHPT were included in a random 2 x 2 crossover trial with the two vitamin D analogs (12 weeks for each treatment). The primary endpoint measure was a decrease in serum intact PTH (iPTH) level, and the secondary outcome measures included changes in serum calcium (Ca), phosphate (P), and metabolic bone marker levels.

RESULTS

Both treatments decreased iPTH and whole PTH (wPTH) levels by similar degrees (iPTH, -200.1 +/- 107.0 with falecalcitriol vs. -200.8 +/- 114.9 pg/ml with calcitriol, p = 0.9895; wPTH, -137.1 +/- 73.1 with falecalcitriol vs. -120.4 +/- 81.1 pg/ml with calcitriol, p = 0.5603). Serum Ca, P, and Ca x P product levels at the end of each treatment were comparable and the frequencies of hypercalcemia and hyperphosphatemia were also similar during each treatment period. Although intravenous calcitriol treatment significantly changed intact osteocalcin and cross-linked N-telopeptide of type I collagen after 12 weeks, oral falecalcitriol treatment did not change any bone metabolic marker level.

CONCLUSION

The present study showed that oral falecalcitriol treatment is effective for PTH suppression, and Ca and P metabolism in hemodialysis patients with moderate to severe SHPT, as well as intravenous calcitriol administration.

摘要

背景

帕立骨化醇是一种新型维生素D类似物,具有更强的抑制甲状旁腺激素(PTH)的潜力和更长的半衰期。很少有研究比较口服帕立骨化醇治疗与静脉注射骨化三醇治疗的临床效果。

方法

21例中重度继发性甲状旁腺功能亢进患者被纳入一项随机2×2交叉试验,接受两种维生素D类似物治疗(每种治疗12周)。主要终点指标是血清完整PTH(iPTH)水平的降低,次要结局指标包括血清钙(Ca)、磷(P)和骨代谢标志物水平的变化。

结果

两种治疗降低iPTH和总PTH(wPTH)水平的程度相似(iPTH,帕立骨化醇治疗组为-200.1±107.0,骨化三醇治疗组为-200.8±114.9 pg/ml,p = 0.9895;wPTH,帕立骨化醇治疗组为-137.1±73.1,骨化三醇治疗组为-120.4±81.1 pg/ml,p = 0.5603)。每种治疗结束时的血清Ca、P和Ca×P乘积水平相当,且每个治疗期间高钙血症和高磷血症的发生率也相似。虽然静脉注射骨化三醇治疗12周后可显著改变骨钙素和I型胶原交联N端肽水平,但口服帕立骨化醇治疗未改变任何骨代谢标志物水平。

结论

本研究表明,口服帕立骨化醇治疗对中重度继发性甲状旁腺功能亢进的血液透析患者抑制PTH以及调节钙磷代谢有效,与静脉注射骨化三醇的效果相当。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验