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首页> 外文期刊>Endocrine practice: official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists >Safety of vitamin D replacement in patients with primary hyperparathyroidism and concomitant vitamin D deficiency
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Safety of vitamin D replacement in patients with primary hyperparathyroidism and concomitant vitamin D deficiency

机译:原发性甲状旁腺功能亢进症并发维生素D缺乏症患者补充维生素D的安全性

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Objective: To evaluat. The safety of vitamin D replacement in patients with vitamin D deficiency and primary hyperparathyroidism.Methods: Retrospective chart review of 35 patients from our endocrine clinic, age 22 to 89 years, diagnosed with primary hyperparathyroidism and vitamin D deficiency, and treated with either 1,000 to 2,000 international units (IU) of vitamin D daily or 50,000 IU of vitamin D weekly for 5 months. Data were collected before and after treatment on serum calcium, 25-hydroxyvitamin D (25-OH D), intact parathyroid hormone (iPTH), phosphorus, alkaline phosphatase, nephrolithiasis, fractures, and osteoporosis.Results: 25-OH D increased significantly, from a baseline of 14.65 ± 6.57 ng/mL to 42.17 ± 12.98 ng/mL after weekly treatment with 50,000 IU of vitamin D (P<.0001), and from 22.42 ± 5.47 ng/mL to 33.33 ± 6.39 ng/mL following daily treatment with 1,000 to 2,000 IU of vitamin D (P<.0001). Pre- and posttreatment unadjusted serum calcium remained stable i. The high-dose group (10.80 ± 0.43 mg/dL vs. 10.72 ± 0.67 mg/dL; P = .47), but decreased slightly i. The low-dose group (10.76 ± 0.58 mg/dL vs. 10.11 ± 0.54 mg/dL; P = .0007). After adjusting for age, sex, vitamin D, and PTH levels. The small calcium difference i. The low-dose group became statistically insignificant. Treatment with either high or low doses of vitamin D did not significantly change iPTH levels. Creatinine remained stable in all patients, and no new cases of nephrolithiasis were reported.Conclusion: Replacing vitamin D in mild primary hyperparathyroidism is safe, effective, and does not increase calcium to dangerous levels.
机译:目的:进行评估。方法:回顾性回顾性分析35例22至89岁我院内分泌诊所诊断为原发性甲状旁腺功能亢进症和维生素D缺乏症并经1,000到10,000例治疗的维生素D缺乏症患者的维生素D补充安全性。每天2,000国际单位(IU)的维生素D或每周50,000 IU的维生素D,持续5个月。治疗前后收集血清钙,25-羟基维生素D(25-OH D),完整的甲状旁腺激素(iPTH),磷,碱性磷酸酶,肾结石,骨折和骨质疏松症的数据。结果:25-OH D显着增加,从每周使用50,000 IU维生素D进行治疗后的基线从14.65±6.57 ng / mL降至42.17±12.98 ng / mL(P <.0001),并且每天之后从22.42±5.47 ng / mL降至33.33±6.39 ng / mL用1,000至2,000 IU的维生素D治疗(P <.0001)。治疗前和治疗后未经调整的血清钙保持稳定。高剂量组(10.80±0.43 mg / dL vs. 10.72±0.67 mg / dL; P = 0.47),但i略有下降。低剂量组(10.76±0.58 mg / dL与10.11±0.54 mg / dL; P = 0.0007)。在调整了年龄,性别,维生素D和PTH水平之后。钙的小差异i。低剂量组在统计学上无意义。高剂量或低剂量维生素D的治疗均未显着改变iPTH水平。肌酐在所有患者中保持稳定,没有新的肾结石病例的报道。结论:在轻度原发性甲状旁腺功能亢进中更换维生素D是安全,有效的,并且不会将钙增加到危险水平。

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