Kolbach-Mandel A M, Mandel N S, Cohen S R, Kleinman J G, Ahmed F, Mandel I C, Wesson J A
Medical College of Wisconsin, 9200 W Wisconsin Avenue, Milwaukee, WI, 53226, USA.
Division of Nephrology, Department of Medicine, Zablocki VA Medical Center, 5000 W. National Avenue, Milwaukee, WI, 53295, USA.
Urolithiasis. 2017 Apr;45(2):139-149. doi: 10.1007/s00240-016-0907-4. Epub 2016 Jul 19.
Drug-related kidney stones are a diagnostic problem, since they contain a large matrix (protein) fraction and are frequently incorrectly identified as matrix stones. A urine proteomics study patient produced a guaifenesin stone during her participation, allowing us to both correctly diagnose her disease and identify proteins critical to this drug stone-forming process. The patient provided three random midday urine samples for proteomics studies; one of which contained stone-like sediment with two distinct fractions. These solids were characterized with optical microscopy and Fourier transform infrared spectroscopy. Immunoblotting and quantitative mass spectrometry were used to quantitatively identify the proteins in urine and stone matrix. Infrared spectroscopy showed that the sediment was 60 % protein and 40 % guaifenesin and its metabolite guaiacol. Of the 156 distinct proteins identified in the proteomic studies, 49 were identified in the two stone-components with approximately 50 % of those proteins also found in this patient's urine. Many proteins observed in this drug-related stone have also been reported in proteomic matrix studies of uric acid and calcium containing stones. More importantly, nine proteins were highly enriched and highly abundant in the stone matrix and 8 were reciprocally depleted in urine, suggesting a critical role for these proteins in guaifenesin stone formation. Accurate stone analysis is critical to proper diagnosis and treatment of kidney stones. Many matrix proteins were common to all stone types, but likely not related to disease mechanism. This protocol defined a small set of proteins that were likely critical to guaifenesin stone formation based on their high enrichment and high abundance in stone matrix, and it should be applied to all stone types.
与药物相关的肾结石是一个诊断难题,因为它们含有大量的基质(蛋白质)成分,并且常常被错误地鉴定为基质结石。一项尿液蛋白质组学研究中的患者在参与研究期间产生了愈创甘油醚结石,这使我们能够正确诊断她的疾病,并确定对这种药物结石形成过程至关重要的蛋白质。该患者提供了三份随机的午间尿液样本用于蛋白质组学研究;其中一份含有结石样沉淀物,有两个不同的部分。这些固体通过光学显微镜和傅里叶变换红外光谱进行表征。免疫印迹和定量质谱用于定量鉴定尿液和结石基质中的蛋白质。红外光谱显示沉淀物中蛋白质占60%,愈创甘油醚及其代谢产物愈创木酚占40%。在蛋白质组学研究中鉴定出的156种不同蛋白质中,有49种在结石的两个成分中被鉴定出来,其中约50%的蛋白质也在该患者的尿液中被发现。在这种与药物相关的结石中观察到的许多蛋白质也在尿酸和含钙结石的蛋白质组基质研究中有所报道。更重要的是,有9种蛋白质在结石基质中高度富集且含量丰富,8种在尿液中相应减少,这表明这些蛋白质在愈创甘油醚结石形成中起关键作用。准确的结石分析对于肾结石的正确诊断和治疗至关重要。许多基质蛋白质在所有结石类型中都很常见,但可能与疾病机制无关。该方案基于在结石基质中的高富集和高丰度定义了一小部分可能对愈创甘油醚结石形成至关重要的蛋白质,并且该方案应适用于所有结石类型。