Association of hypercalciuria with vitamin D supplementation in patients undergoing ketogenic dietary therapy

被引:1
作者
Lee, Myeongseob [1 ]
Lee, Hae In [2 ]
Song, Kyungchul [1 ]
Choi, Han Saem [3 ]
Suh, Junghwan [1 ]
Kim, Se Hee [4 ]
Chae, Hyun Wook [1 ]
Kang, Hoon-Chul [4 ]
Lee, Joon Soo [4 ]
Kim, Heung Dong [4 ]
Kim, Ho-Seong [1 ]
Kwon, Ahreum [1 ]
机构
[1] Yonsei Univ, Severance Childrens Hosp, Endocrine Res Inst, Dept Pediat,Coll Med, Seoul, South Korea
[2] CHA Univ, CHA Gangnam Med Ctr, Dept Pediat, Seoul, South Korea
[3] Catholic Kwandong Univ, Int St Marys Hosp, Dept Pediat, Incheon, South Korea
[4] Yonsei Univ, Severance Childrens Hosp, Dept Pediat, Div Pediat Neurol,Coll Med, Seoul, South Korea
来源
FRONTIERS IN NUTRITION | 2022年 / 9卷
关键词
vitamin D; vitamin D deficiency; ketogenic diet; hypercalciuria; urolithiasis; CALCIUM-ABSORPTION; D DEFICIENCY; 25-HYDROXYVITAMIN-D; MECHANISMS; RISK;
D O I
10.3389/fnut.2022.970467
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
BackgroundKetogenic dietary therapy (KDT) is used as an effective treatment for epilepsy. However, KDT carries the risk of bone health deterioration; therefore, vitamin D supplementation is required. Vitamin D replacement therapy in KDT has not been established because it may be related to hypercalciuria/urolithiasis, which are common adverse effects of KDT. Hence, this study aimed to evaluate the dose-dependent association between vitamin D-3 and hypercalciuria/urolithiasis in patients undergoing KDT and dose optimization for renal complications. Materials and methodsOverall, 140 patients with intractable childhood epilepsy started 3:1 KDT (lipid to non-lipid ratio) at the Severance Children's Hospital from January 2016 to December 2019. Regular visits were recommended after KDT initiation. Participants were assessed for height, weight, serum 25-hydroxyvitamin D (25-OH-D-3) level, parathyroid hormone level, and ratio of urinary excretion of calcium and creatinine (Uca/Ucr). Kidney sonography was conducted annually. Patients who already had urolithiasis and were taking hydrochlorothiazide before KDT, failed to maintain KDT for 3 months, did not visit the pediatric endocrine department regularly, did not take prescribed calcium and vitamin D3 properly, or needed hospitalization for > 1 degrees month because of serious medical illness were excluded. Data from patients who started diuretic agents, e.g., hydrochlorothiazide, were excluded from that point because the excretion of calcium in the urine may be altered in these patients. ResultIn total, 49 patients were included in this study. Uca/Ucr ratio significantly decreased with increasing levels of 25-OH-D-3 (p = 0.027). The odds ratio for hypercalciuria was 0.945 (95% confidence interval, 0.912-0.979; p = 0.002) per 1.0 ng/mL increment in 25-OH-D-3 level. Based on findings of receiver operating characteristic curve analysis and Youden's J statistic, the cut-off 25-OH-D-3 level for preventing hypercalciuria was > 39.1 ng/mL at 6 months. Furthermore, the vitamin D-3 supplementation dose cut-off was > 49.5 IU/kg for hypercalciuria prevention. ConclusionAn inverse relationship between Uca/Ucr ratio and 25-OH-D-3 level was noted, which means that vitamin D supplementation is helpful for preventing hypercalciuria related to KDT. We suggest that the recommended 25-OH-D-3 level is > 40 ng/mL for hypercalciuria prevention and that KDT for children with epilepsy can be optimized by vitamin D-3 supplementation at 50 IU/kg.
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