Ogata Hiroaki, Koiwa Fumihiko, Shishido Kanji, Takahashi Keiko, Ito Hidetoshi, Kinugasa Eriko, Taguchi Susumu
Department of Internal Medicine, Showa University Northern Yokohama Hospital, Kanagawa, Japan.
Ther Apher Dial. 2007 Jun;11(3):202-9. doi: 10.1111/j.1744-9987.2007.00422.x.
The purpose of this crossover comparison study is to elucidate the differences between the effects of a novel calcitriol analog, 22-oxacalcitriol, and calcitriol on parathyroid hormone (PTH) and bone mineral metabolism in hemodialysis patients with secondary hyperparathyroidism (SHPT). Twenty-three patients with moderate to severe SHPT were included in a random 2 x 2 crossover trial with two vitamin D analogs (12 weeks for each treatment). Two patients withdrew during the run-in period for personal reasons. Serum electrolyte, bone metabolic marker, intact PTH (iPTH) and whole PTH (wPTH) levels were measured periodically. The primary endpoint measure was a decrease in serum iPTH level, and the secondary outcome measures included changes in serum calcium (Ca), phosphate (P), and metabolic bone marker levels. Both treatments decreased iPTH and wPTH levels by similar degrees. 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. 22-Oxacalcitriol significantly decreased the levels of bone metabolic markers, namely, bone-specific alkaline phosphate, intact osteocalcin, pyridinoline, and cross-linked N-telopeptide of type I collagen, after a 12-week treatment. In contrast, calcitriol did not change any of the levels of bone metabolic markers. The present study showed that 22-oxacalcitriol is equally effective for PTH suppression, and Ca and P metabolism. In addition, 22-oxacalcitriol might have putative actions on bone remodeling independent of its PTH suppression. Further study is necessary to confirm the effects of 22-oxacalcitriol on bone metabolism in SHPT.
本交叉对照研究旨在阐明新型骨化三醇类似物22-氧杂骨化三醇与骨化三醇对继发性甲状旁腺功能亢进(SHPT)血液透析患者甲状旁腺激素(PTH)和骨矿物质代谢影响的差异。23例中重度SHPT患者纳入了一项使用两种维生素D类似物的随机2×2交叉试验(每种治疗12周)。2例患者在导入期因个人原因退出。定期测量血清电解质、骨代谢标志物、完整PTH(iPTH)和总PTH(wPTH)水平。主要终点指标是血清iPTH水平降低,次要结局指标包括血清钙(Ca)、磷(P)和代谢性骨标志物水平的变化。两种治疗使iPTH和wPTH水平降低的程度相似。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。12周治疗后,22-氧杂骨化三醇显著降低了骨代谢标志物的水平,即骨特异性碱性磷酸酶、完整骨钙素、吡啶啉和I型胶原交联N-端肽。相比之下,骨化三醇未改变任何骨代谢标志物水平。本研究表明,22-氧杂骨化三醇在抑制PTH以及Ca和P代谢方面同样有效。此外,22-氧杂骨化三醇可能对骨重塑有独立于其抑制PTH作用的假定作用。有必要进一步研究以证实22-氧杂骨化三醇对SHPT患者骨代谢的影响。