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血清磷酸盐水平的变化可预测继发性甲状旁腺功能亢进透析患者对静脉注射骨化三醇治疗的长期反应。

Alterations in serum phosphate levels predict the long-term response to intravenous calcitriol therapy in dialysis patients with secondary hyperparathyroidism.

作者信息

Hosaka Kiyoko, Kazama Junichiro James, Yamamoto Suguru, Ito Yumi, Iino Noriaki, Maruyama Hiroki, Saito Akihiko, Narita Ichiei, Gejyo Fumitake

机构信息

Division of Clinical Nephrology and Rheumatology, Niigata University Graduate School of Medical and Dental Sciences, 1-751 Asahimachi-dori, Niigata, Niigata 951-8510, Japan.

出版信息

J Bone Miner Metab. 2008;26(2):185-90. doi: 10.1007/s00774-007-0809-1. Epub 2008 Feb 27.

Abstract

Calcitriol therapy is a central strategy for the treatment of uremic secondary hyperparathyroidism. Although indiscriminate use of calcitriol may lead to worse outcomes, it is difficult to make a decision to discontinue calcitriol therapy when its parathyroid suppression effect remains unsatisfactory. In this study, intravenous calcitriol was administered to 120 chronic hemodialysis patients. Therapy continued for 48 weeks or until plasma intact parathyroid hormone (iPTH) levels decreased to below 300 pg/ml or until the development of any significant adverse effect. Of the 120 patients, the treatment goal was achieved in 47 patients during the first 4 weeks, in 10 during the next 4 weeks, and in 22 patients thereafter. Logistic regression analysis and stepwise regression analysis revealed that iPTH levels were the only significant predictor of the response to calcitriol therapy at weeks 0 and 4. Besides iPTH, the inorganic phosphate (P) levels were another significant predictor of the ultimate response to calcitriol therapy at week 8. The point of best discrimination for successful treatment was P = 6.0 mg/dl at week 8, or P level at week 8/pretreatment P level = 1.0. In conclusion, the P level at week 8 is a predictor of the response to calcitriol therapy for uremic secondary hyperparathyroidism. Changes in treatment are recommended if patients show unsatisfactory parathyroid suppression with a hyperphosphatemic tendency.

摘要

骨化三醇疗法是治疗尿毒症继发性甲状旁腺功能亢进的核心策略。尽管不加区分地使用骨化三醇可能会导致更差的结果,但当甲状旁腺抑制效果仍不令人满意时,很难决定停止骨化三醇治疗。在本研究中,对120例慢性血液透析患者给予静脉注射骨化三醇。治疗持续48周或直至血浆完整甲状旁腺激素(iPTH)水平降至300 pg/ml以下或直至出现任何显著不良反应。在这120例患者中,47例在最初4周内达到治疗目标,10例在接下来的4周内达到,22例在之后达到。逻辑回归分析和逐步回归分析显示,iPTH水平是第0周和第4周对骨化三醇治疗反应的唯一显著预测因素。除iPTH外,无机磷(P)水平是第8周对骨化三醇治疗最终反应的另一个显著预测因素。成功治疗的最佳区分点是第8周时P = 6.0 mg/dl,或第8周时P水平/治疗前P水平 = 1.0。总之,第8周时的P水平是尿毒症继发性甲状旁腺功能亢进对骨化三醇治疗反应的一个预测因素。如果患者甲状旁腺抑制不令人满意且有高磷血症倾向,建议改变治疗方案。

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