J Clin Invest. 2019 May 20;129(6):2201-2204. doi: 10.1172/JCI128709.
Excessive excretion of oxalate in the urine results in the formation of calcium oxalate crystals and subsequent kidney stone formation. Severe forms of hyperoxaluria, including genetic forms and those that result from ethylene glycol poisoning, can result in end-stage renal disease. Therapeutic interventions are limited and often rely on dietary intervention. In this issue of the JCI, Le Dudal and colleagues demonstrate that the lactate dehydrogenase 5 inhibitor (LDH5) stiripentol reduces urinary oxalate excretion. Importantly, stiripentol treatment of a single individual with primary hyperoxaluria reduced the urinary oxalate excretion. Together, these results support further evaluation of LDH5 as a therapeutic target for hyperoxaluria.
尿中草酸盐排泄过多会导致草酸钙晶体形成,并随后形成肾结石。包括遗传形式和乙二醇中毒引起的严重高草酸尿症会导致终末期肾病。治疗干预措施有限,通常依赖于饮食干预。在本期 JCI 中,Le Dudal 及其同事证明,乳酸脱氢酶 5 抑制剂(LDH5)司替戊醇可减少尿草酸盐排泄。重要的是,司替戊醇治疗一名原发性高草酸尿症患者可降低尿草酸盐排泄。这些结果共同支持进一步评估 LDH5 作为高草酸尿症的治疗靶点。