Khan Saeed R, Canales Benjamin K
Department of Pathology, Immunology, and Laboratory Medicine, University of Florida, Gainesville, FL, USA.
Department of Urology, University of Florida, Gainesville, FL, USA.
Asian J Urol. 2023 Jul;10(3):246-257. doi: 10.1016/j.ajur.2023.01.008. Epub 2023 Apr 13.
Prevalence of kidney stone disease continues to increase globally with recurrence rates between 30% and 50% despite technological and scientific advances. Reduction in recurrence would improve patient outcomes and reduce cost and stone morbidities. Our objective was to review results of experimental studies performed to determine the efficacy of readily available compounds that can be used to prevent recurrence.
All relevant literature up to October 2020, listed in PubMed is reviewed.
Clinical guidelines endorse the use of evidence-based medications, such as alkaline agents and thiazides, to reduce urinary mineral supersaturation and recurrence. However, there may be additional steps during stone pathogenesis where medications could moderate stone risk. Idiopathic calcium oxalate stones grow attached to Randall's plaques or plugs. Results of clinical and experimental studies suggest involvement of reactive oxygen species and oxidative stress in the formation of both the plaques and plugs. The renin-angiotensin-aldosterone system (RAAS), nicotinamide adenine dinucleotide phosphate (NADPH) oxidase, mitochondria, and NOD-like receptor pyrin domain containing-3 (NLRP3) inflammasome have all been implicated at specific steps during stone pathogenesis in animal models.
In addition to supersaturation-reducing therapies, the use of anti-oxidants, free radical scavengers, and inhibitors of NADPH oxidase, NLRP3 inflammasome, and RAAS may prove beneficial for stone prevention. Compounds such as statins and angiotensin converting enzyme inhibitors are already in use as therapeutics for hypertension and cardio-vascular disease and have previously shown to reduce calcium oxalate nephrolithiasis in rats. Although clinical evidence for their use in stone prevention in humans is limited, experimental data support they be considered along with standard evidence-based medications and clinical expertise when patients are being counselled for stone prevention.
尽管有技术和科学进步,但全球肾结石疾病的患病率仍在持续上升,复发率在30%至50%之间。降低复发率将改善患者预后,降低成本和结石发病率。我们的目的是回顾为确定可用于预防复发的现成化合物的疗效而进行的实验研究结果。
对截至2020年10月在PubMed上列出的所有相关文献进行回顾。
临床指南认可使用循证药物,如碱性药物和噻嗪类药物,以降低尿矿物质过饱和度和复发率。然而,在结石发病机制中可能还有其他步骤,药物可以在这些步骤中降低结石风险。特发性草酸钙结石附着在兰德尔斑或栓子上生长。临床和实验研究结果表明,活性氧和氧化应激参与了斑和栓子的形成。肾素-血管紧张素-醛固酮系统(RAAS)、烟酰胺腺嘌呤二核苷酸磷酸(NADPH)氧化酶、线粒体和含NOD样受体吡啉结构域3(NLRP3)炎性小体在动物模型结石发病机制的特定步骤中均有涉及。
除了降低过饱和度的疗法外,使用抗氧化剂、自由基清除剂以及NADPH氧化酶、NLRP3炎性小体和RAAS的抑制剂可能对结石预防有益。他汀类药物和血管紧张素转换酶抑制剂等化合物已被用作高血压和心血管疾病的治疗药物,此前已证明可降低大鼠草酸钙肾结石的发病率。尽管它们在人类结石预防中应用的临床证据有限,但实验数据支持在为患者提供结石预防咨询时,将它们与标准的循证药物和临床专业知识一起考虑。