UCL Centre for Nephrology, Department of Clinical Biochemistry, Royal Free Campus and Hospital, Rowland Hill Street, London, NW3 2PF, UK.
Division of Nephrology, Department of Medical Sciences, Gemelli University Hospital, Catholic University of the Sacred Heart, Rome, Italy.
Urolithiasis. 2017 Dec;45(6):535-543. doi: 10.1007/s00240-016-0954-x. Epub 2016 Dec 16.
While vitamin D (vitD) deficiency is thought to contribute to poor health in a variety of ways and should be corrected, there is still concern about giving vitD supplements to patients with a history of nephrolithiasis. The aim is to study the prevalence of vitD deficiency and the effect on stone risk of cholecalciferol (vitD3) supplementation in a cohort of idiopathic stone formers (ISF). We screened for vitD deficiency and urinary measures of stone risk, comparing vitD deficient (serum 25-OH vitD ≤30 nmol/L; ≤12 ng/mL) with vitD insufficient (31-75 nmol/L; 13-30 ng/mL) or vitD replete (>75 nmol/L; >30 ng/mL); we investigated the effect of giving vitD3 (20,000 IU orally, weekly for 4 months) to 37 of the vitD deficients. Thirty-one percent (142/456) were vitD deficient, 57% (259/456) vitD insufficient, and the rest (12%) vitD replete (55/456). Comparison among the groups showed that baseline 24-h urinary measures related to stone risk expressed as concentration ratios over urine creatinine (Cr), such as U. Calcium/Cr, U. Oxalate/Cr, U. Citrate/Cr, and U. Uric acid/Cr were not significantly different. VitD3 supplementation did significantly increase serum 25-OH vitD levels and U. Phosphate/Cr ratios, as well as reduce serum parathyroid hormone (PTH) concentrations. Following vitD3 supplementation, there was an overall rise in 24-h urine calcium excretion, but it failed to reach statistical significance (p = 0.06). U. Calcium/Cr increased in 22 out of 37 patients (average increase +0.07 mmol/mmol), decreased in 14 (average decrease -0.13 mmol/mmol), and remained unchanged in 1; 6 out of 26 initially normocalciuric ISF developed hypercalciuria; and 6 out of 9 patients who became vitD replete were hypercalciuric after supplementation. It is appropriate to monitor urinary Ca excretion in vitD-supplemented stone formers, because it may reveal underlying hypercalciuria in some treated patients.
虽然维生素 D(vitD)缺乏被认为会以多种方式导致健康状况不佳,并且应该加以纠正,但对于有肾结石病史的患者给予 vitD 补充剂仍存在担忧。目的是研究特发性结石形成者(ISF)中胆钙化醇(vitD3)补充剂的 vitD 缺乏患病率及其对结石风险的影响。我们筛查了 vitD 缺乏症和尿结石风险的测量值,将 vitD 缺乏症(血清 25-OH vitD≤30 nmol/L;≤12 ng/mL)与 vitD 不足症(31-75 nmol/L;13-30 ng/mL)或 vitD 充足症(>75 nmol/L;>30 ng/mL)进行比较;我们调查了给 37 名 vitD 缺乏症患者口服 vitD3(20,000 IU,每周 4 个月)的效果。456 名患者中有 31%(142/456)vitD 缺乏,57%(259/456)vitD 不足,其余 12%(55/456)vitD 充足。组间比较显示,基线 24 小时尿结石风险相关测量值以尿肌酐(Cr)的浓度比表示,如 U.钙/Cr、U.草酸盐/Cr、U.柠檬酸盐/Cr 和 U.尿酸/Cr 无显著差异。vitD3 补充确实显著增加了血清 25-OH vitD 水平和 U.磷酸盐/Cr 比值,并降低了血清甲状旁腺激素(PTH)浓度。vitD3 补充后,24 小时尿钙排泄总体增加,但未达到统计学意义(p=0.06)。37 名患者中有 22 名(平均增加+0.07 mmol/mmol)U.钙/Cr 升高,14 名(平均降低-0.13 mmol/mmol)降低,1 名不变;26 名初始尿钙正常的 ISF 中有 6 名出现高钙尿症;9 名补充后 vitD 充足的患者中有 6 名出现高钙尿症。vitD 补充后的结石形成者监测尿钙排泄是合适的,因为它可能揭示一些治疗患者的潜在高钙尿症。