University of Florida College of Medicine, Gainesville, Florida.
National Medical Association and Research Group, Gainesville, Florida.
Kidney360. 2020 Sep 3;1(11):1284-1290. doi: 10.34067/KID.0001522020. eCollection 2020 Nov 25.
Hyperoxaluria is typically associated with excessive oxalate intake in the diet, decreased dietary calcium, hyperabsorption of oxalate, or increased endogenous production of oxalate. The disorder spectrum extends from recurrent kidney stones to ESKD. This clinical trial sought to evaluate the effectiveness of an acid stable oxalate decarboxylase (OxDC) to reduce urinary oxalate in healthy subjects on a high-oxalate diet.
In this prospective, double-blind, randomized, placebo-controlled, crossover clinical trial, 33 healthy volunteers were randomized into two crossover sequences separated by a 2-day washout period. A controlled high-oxalate diet (750-800 mg oxalate, 500-550 mg calcium daily) was utilized, and six 24-hour urine collections were measured. Subjects were given approximately 1000 U (micromoles per minute per milligram) of OxDC or placebo with meals three times daily during the 4 days of treatment.
Urinary oxalate significantly decreased with OxDC treatment. The baseline corrected within-subject mean reduction in 24-hour urinary excretion (after OxDC dosing versus high-oxalate baseline preceding treatment) was 12.5 mg or 29% (<0.001). OxDC treatment was effective (>5% reduction) in 31 of 33 subjects (94%). Compared with placebo, OxDC produced a 24% reduction (<0.001) in 24-hour oxalate excretion. Other urinary parameters (creatinine, uric acid, citrate, magnesium, calcium) were not affected by OxDC. No serious adverse events and no product-related adverse events occurred.
An orally administered OxDC is capable of significantly reducing urinary oxalate levels in healthy volunteers on a high-oxalate diet without affecting creatinine clearance, urine creatinine, or other solutes related to supersaturation of calcium oxalate.
Evaluation of Nephure, and the Reduction of Dietary Oxalate, in Healthy Volunteers, NCT03661216.
高草酸尿症通常与饮食中草酸摄入过多、膳食钙减少、草酸过度吸收或内源性草酸生成增加有关。这种疾病谱从复发性肾结石延伸到终末期肾病。本临床试验旨在评估一种酸稳定的草酸脱羧酶(OxDC)在高草酸饮食的健康受试者中降低尿草酸的有效性。
在这项前瞻性、双盲、随机、安慰剂对照、交叉临床试验中,33 名健康志愿者被随机分为两个交叉序列,每个序列之间有 2 天的洗脱期。采用控制的高草酸饮食(750-800mg 草酸,500-550mg 钙/天),测量了 6 次 24 小时尿液收集。在治疗的 4 天中,受试者每天随餐服用约 1000U(每分钟每毫克微摩尔)的 OxDC 或安慰剂,每日 3 次。
尿草酸水平随 OxDC 治疗显著降低。在经过 OxDC 给药与治疗前高草酸饮食基础期之间进行的基础校正的个体内 24 小时尿排泄的平均降低量为 12.5mg 或 29%(<0.001)。33 名受试者中有 31 名(94%)治疗有效(降低>5%)。与安慰剂相比,OxDC 使 24 小时尿草酸排泄量降低了 24%(<0.001)。其他尿参数(肌酐、尿酸、枸橼酸、镁、钙)不受 OxDC 影响。未发生严重不良事件和与产品相关的不良事件。
口服 OxDC 能够显著降低高草酸饮食健康志愿者的尿草酸水平,而不影响肌酐清除率、尿肌酐或与草酸钙过饱和有关的其他溶质。
Nephure 的评估和健康志愿者饮食中草酸的减少,NCT03661216。