Division of Critical Care Medicine, Department of Emergency Medicine-Critical Care Medicine (EM-CCM), Shuang Ho Hospital, Taipei Medical University, New Taipei City 23561, Taiwan.
Graduate Institute of Clinical Medicine, College of Medicine, Taipei Medical University, Taipei 11031, Taiwan.
Nutrients. 2016 Nov 5;8(11):708. doi: 10.3390/nu8110708.
Active Vitamin D analogues are used clinically for prevention and treatment of secondary hyperparathyroidism (SHPT) in hemodialysis (HD) patients. Nutritional vitamin D supplementation is used for additional local parathyroid (PTH) suppression, with lower incidence of hypercalcemia and hyperphosphatemia. This study evaluates the possible beneficial effects of combined vitamin D treatment (paricalcitol and cholecalciferol).
Sixty HD patients with serum parathyroid hormone (iPTH) >300 pg/mL were enrolled. All patients administered 2 mcg/day of paricalcitol and were randomly allocated into control group (placebo) or study group (cholecalciferol) for 16 weeks. Serum 25(OH)D₃, iPTH and human cathelicidin (hCAP-18) were measured at baseline and during follow-up.
iPTH levels decreased in the study group appropriately and were more significantly decreased at 16 weeks. Study group had significantly increased 25(OH)D₃ levels. In addition, the study group had significantly increased serum hCAP-18 levels compared with control group. Correlation analysis showed a significant correlation between the percentage increase in serum hCAP-18 and 25(OH)D₃ levels.
Cholecalciferol, in combination with paricalcitol, additively lowers the iPTH levels in a significant number of patients after 16 weeks of supplementation. A dose of 5000 IU/week of cholecalciferol could maintain serum 25(OH)D₃ levels above 30 ng/dL as early as 8 weeks after beginning supplementation. Doubling of serum cathelicidin levels were noted after 16 weeks of cholecalciferol supplementation in 40% of study patients.
活性维生素 D 类似物在临床上用于预防和治疗血液透析(HD)患者的继发性甲状旁腺功能亢进症(SHPT)。营养性维生素 D 补充剂用于额外的局部甲状旁腺(PTH)抑制,其发生高钙血症和高磷血症的几率较低。本研究评估了联合维生素 D 治疗(帕立骨化醇和胆钙化醇)的可能有益效果。
纳入了 60 例血清甲状旁腺激素(iPTH)>300pg/mL 的 HD 患者。所有患者均给予 2 mcg/天的帕立骨化醇,并随机分为对照组(安慰剂)或研究组(胆钙化醇),治疗 16 周。在基线和随访期间测量血清 25(OH)D₃、iPTH 和人杀菌/通透性增强蛋白-18(hCAP-18)。
研究组 iPTH 水平适当下降,在 16 周时下降更明显。研究组 25(OH)D₃水平显著升高。此外,与对照组相比,研究组血清 hCAP-18 水平显著升高。相关性分析显示,血清 hCAP-18 水平与 25(OH)D₃水平的百分比增加呈显著相关。
胆钙化醇与帕立骨化醇联合使用,在补充 16 周后,可显著降低大量患者的 iPTH 水平。每周 5000IU 胆钙化醇剂量可在开始补充后 8 周内将血清 25(OH)D₃水平维持在 30ng/dL 以上。在胆钙化醇补充 16 周后,40%的研究患者的血清 cathelicidin 水平增加了一倍。