Streeten Elizabeth A, Mohtasebi Yasaman, Konig Manige, Davidoff Lisa, Ryan Kathleen
Department of Endocrinology, Diabetes and Nutrition, University of Maryland Medical Center, Baltimore, Maryland 21201.
St. Vincent Hospital, Indianapolis, Indiana, 46260.
J Clin Endocrinol Metab. 2017 May 1;102(5):1505-1510. doi: 10.1210/jc.2016-3712.
Options for chronic treatment of hypoparathyroidism include calcitriol, recombinant human parathyroid hormone, and high-dose vitamin D (D2). D2 is used in a minority of patients because of fear of prolonged hypercalcemia and renal toxicity. There is a paucity of recent data about D2 use in hypoparathyroidism.
Compare renal function, hypercalcemia, and hypocalcemia in patients with hypoparathyroidism treated chronically with either D2 (D2 group) or calcitriol.
DESIGN, SETTING, AND PATIENTS: A retrospective study of patients with hypoparathyroidism treated at the University of Maryland Hospital. Participants were identified by a billing record search with diagnosis confirmed by chart review. Thirty patients were identified; 16 were treated chronically with D2, 14 with calcitriol. Data were extracted from medical records.
Serum creatinine and calcium, hospitalizations, and emergency department (ED) visits for hypercalcemia and hypocalcemia.
D2 and calcitriol groups were similar in age (58.9 ± 16.7 vs 50.9 ± 22.6 years, P = 0.28), sex, and treatment duration (17.8 ± 14.2 vs 8.5 ± 4.4 years, P = 0.076). Hospitalization or ED visits for hypocalcemia occurred in none of the D2 group vs four of 14 in the calcitriol group (P = 0.03); three in the calcitriol group had multiple ED visits. There were no differences between D2 and calcitriol groups in hospitalizations or ED visits for hypercalcemia, serum creatinine or calcium, or kidney stones.
We found less morbidity from hypocalcemia in hypoparathyroid patients treated chronically with D2 compared with calcitriol and found no difference in renal function or morbidity from hypercalcemia. Treatment with D2 should be considered in patients with hypoparathyroidism, particularly in those who experience recurrent hypocalcemia.
甲状旁腺功能减退症的长期治疗方案包括骨化三醇、重组人甲状旁腺激素和大剂量维生素D(D2)。由于担心长期高钙血症和肾毒性,少数患者使用D2。目前关于甲状旁腺功能减退症患者使用D2的近期数据较少。
比较长期使用D2(D2组)或骨化三醇治疗的甲状旁腺功能减退症患者的肾功能、高钙血症和低钙血症情况。
设计、地点和患者:对马里兰大学医院治疗的甲状旁腺功能减退症患者进行回顾性研究。通过账单记录搜索确定参与者,并通过病历审查确认诊断。共确定30例患者;16例长期使用D2治疗,14例使用骨化三醇治疗。数据从病历中提取。
血清肌酐和钙、住院情况以及因高钙血症和低钙血症而进行的急诊科就诊情况。
D2组和骨化三醇组在年龄(58.9±16.7岁对50.9±22.6岁,P = 0.28)、性别和治疗持续时间(17.8±14.2年对8.5±4.4年,P = 0.076)方面相似。D2组无一例因低钙血症住院或进行急诊科就诊,而骨化三醇组14例中有4例(P = 0.03);骨化三醇组中有3例多次进行急诊科就诊。D2组和骨化三醇组在因高钙血症住院或进行急诊科就诊、血清肌酐或钙以及肾结石方面无差异。
我们发现,与骨化三醇相比,长期使用D2治疗的甲状旁腺功能减退症患者低钙血症的发病率更低,且肾功能或高钙血症的发病率无差异。甲状旁腺功能减退症患者,尤其是那些反复出现低钙血症的患者,应考虑使用D2治疗。