Department of Pediatrics, Maulana Azad Medical College (University of Delhi) and associated Lok Nayak Hospital, Delhi, 110002, India.
Department of Biochemistry, Govind Ballabh Pant Institute of Post Graduate Medical Education & Research, New Delhi, India.
Indian J Pediatr. 2023 May;90(5):450-456. doi: 10.1007/s12098-022-04225-w. Epub 2022 Jun 28.
To compare the change in serum vitamin D levels and to compare the changes in serum levels of calcium, phosphate, alkaline phosphatase and parathyroid hormone in vitamin D supplemented and unsupplemented groups after 3 mo.
In this randomized, parallel group, nonblinded, controlled trial, 40 children, 2-12 y of age with newly diagnosed epilepsy, and vitamin D sufficient status, and started on valproate monotherapy, were randomized into the intervention group (n = 20), which was given daily oral 600 IU vitamin D supplementation, and the control group (n = 20), which was not given any supplementation. Changes in the biochemical parameters was measured in the two groups after 3 mo.
There was a significant reduction in the median (IQR) vitamin D levels in the control group as compared to an increase seen in the intervention group [-6.64 (-8.4, -2.65) vs. 5.66 (1.81, 7.12); p < 0.001]. In the control group, 37.5% children developed vitamin D insufficiency and 12.5% developed deficiency whereas only 5% of the intervention group developed vitamin D insufficiency (p = 0.005). There was a significant decrease in ionized calcium (p = 0.02), increase in serum phosphate (p = 0.02), and alkaline phosphatase level (p = 0.003) in the unsupplemented group as compared to the supplemented group.
Vitamin D supplementation can reduce the valproate-associated decline in vitamin D levels and the negative impact on other markers of bone mineral metabolism.
TCTR20200621002, 19.06.2020, retrospectively registered.
比较血清维生素 D 水平的变化,并比较补充和未补充维生素 D 的两组患者在 3 个月后血清钙、磷、碱性磷酸酶和甲状旁腺激素水平的变化。
在这项随机、平行组、非盲、对照试验中,纳入了 40 名年龄在 2-12 岁、新诊断为癫痫且维生素 D 充足的患儿,他们均开始服用单药丙戊酸钠治疗,并随机分为干预组(n = 20)和对照组(n = 20)。干预组每天口服 600 IU 维生素 D 补充剂,对照组不给予任何补充。在 3 个月后,测量两组患者的生化参数变化。
与干预组维生素 D 水平升高相比,对照组维生素 D 水平中位数(IQR)显著降低[-6.64(-8.4,-2.65)vs. 5.66(1.81,7.12);p < 0.001]。对照组中,37.5%的患儿出现维生素 D 不足,12.5%出现维生素 D 缺乏,而干预组只有 5%的患儿出现维生素 D 不足(p = 0.005)。与补充组相比,未补充组的离子钙(p = 0.02)、血清磷(p = 0.02)和碱性磷酸酶水平(p = 0.003)显著降低。
维生素 D 补充可以减少丙戊酸钠相关的维生素 D 水平下降,并降低其对其他骨矿物质代谢标志物的负面影响。
TCTR20200621002,2020 年 6 月 19 日,回顾性注册。