Clinical Uses of 22-Oxacalcitriol

被引:7
作者
Mizobuchi, Masahide [1 ]
Ogata, Hiroaki [2 ]
机构
[1] Showa Univ, Sch Med, Dept Med, Div Nephrol, Tokyo 142, Japan
[2] Showa Univ, Northern Yokohama Hosp, Dept Internal Med, Tokyo, Japan
关键词
Maxacalcitriol; percutaneous VDRA injection therapy; secondary hyperparathyroidism; vitamin D analogs; vitamin D receptor activator; 22-oxacalcitriol; SUPPRESSES PARATHYROID-HORMONE; CHRONIC KIDNEY-DISEASE; SECONDARY HYPERPARATHYROIDISM; VITAMIN-D; MAXACALCITOL INJECTION; HEMODIALYSIS-PATIENTS; NONCALCEMIC ANALOG; BINDING-PROPERTIES; MULTICENTER TRIAL; DIALYSIS PATIENTS;
D O I
10.2174/15701611113119990023
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
22-oxacalcitriol (OCT) is a vitamin D3 analog and a vitamin D receptor activator (VDRA) that is used as a drug for secondary hyperparathyroidism (SHPT) and has been available clinically in Japan since 2000. The pharmacological characteristics of OCT include rapid clearance from the systemic circulation compared to that of calcitriol, good tissue distribution, and relatively long retention in the nucleus in parathyroid cells. In clinical studies, OCT has been shown to decrease the parathyroid hormone (PTH) level with an effect equivalent to that of calcitriol. Other reports show that OCT produces superior improvement of bone metabolism compared to calcitriol. Treatment with ultrasound-guided direct injection of OCT into the parathyroid has also been attempted. In animal studies, OCT does not influence the blood Ca or P level and is less likely to promote progression of calcification in cardiovascular tissue. The influence of VDRAs including OCT on the progression of cardiovascular lesions and survival in SHPT patients requires further studies.
引用
收藏
页码:324 / 328
页数:5
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