Sethi K, Diamond L H
Nephron. 1981;27(4-5):265-70. doi: 10.1159/000182065.
Nephrotoxicity was evaluated in 37 patients receiving aminoglycosides by serial urinary measurements of the low-molecular weight protein beta 2-microglobulin (beta 2m) and the proximal tubular enzymes N-acetyl-glucosaminidase and beta-glucuronidase. Clinical nephrotoxicity, with a rise in serum creatinine greater than 20% of the baseline value, was diagnosed in 15 of 30 evaluable patients. The laboratory diagnosis of nephrotoxicity, defined as a two-fold increase in beta 2m, N-acetylglucosaminidase and beta-glucuronidase, was confirmed in 11/15 patients. Additionally, there were 3 patients in whom there was definitive laboratory nephrotoxicity in the absence of a rise in serum creatinine. The laboratory diagnosis of nephrotoxicity could be made 4.1--5.5 days prior to significant elevation in serum creatinine. The data suggest that beta 2m and enzyme studies are predictors of nephrotoxicity.
通过对37例接受氨基糖苷类药物治疗患者的尿液进行连续检测,测量低分子量蛋白β2-微球蛋白(β2m)以及近端肾小管酶N-乙酰氨基葡萄糖苷酶和β-葡萄糖醛酸酶,对肾毒性进行了评估。在30例可评估患者中,有15例被诊断为临床肾毒性,即血清肌酐升高超过基线值的20%。11/15的患者证实了肾毒性的实验室诊断,其定义为β2m、N-乙酰氨基葡萄糖苷酶和β-葡萄糖醛酸酶升高两倍。此外,有3例患者在血清肌酐未升高的情况下存在明确的实验室肾毒性。肾毒性的实验室诊断可在血清肌酐显著升高前4.1 - 5.5天做出。数据表明,β2m和酶学研究是肾毒性的预测指标。