Comper Wayne D, Osicka Tanya M, Jerums George
Department of Biochemistry and Molecular Biology, Monash University, Clayton; and the Endocrine Unit, Austin & Repatriation Medical Center, Heidelberg, Victoria, Australia.
Am J Kidney Dis. 2003 Feb;41(2):336-42. doi: 10.1053/ajkd.2003.50041.
Intact albumin in urine may exist in two forms, immunoreactive and immuno-unreactive. Previous estimates of albuminuria in diabetic urine have only detected immunoreactive forms.
High performance liquid chromatography (HPLC) was used in this study to measure both forms of intact albumin (termed total intact albumin) to provide a more accurate measurement of albuminuria compared with radioimmunoassay (RIA) on 97 fresh urine samples from patients with diabetes. Eighty-six control urine samples from volunteers without diabetes were also tested.
There was no significant difference between the two methods for nondiabetic controls. For diabetic urine samples, 91.6% of samples showed a greater concentration of albumin measured by HPLC than RIA. For normoalbuminuric diabetic samples, HPLC gave a mean albumin excretion rate of 12.5 +/- 4.4 microgram/min (SD), whereas RIA gave a rate of 8.0 +/- 6.7 microgram/min (P = 0.004; N = 28). For microalbuminuric samples, there also was a statistically significant difference: HPLC albumin excretion rate, 82.0 +/- 49.9 microgram/min, and RIA, 49.0 +/- 34.6 microgram/min (P = 0.004; N = 30). Thirty-two urine samples were normoalbuminuric by RIA (albumin, 11.4 +/- 3.9 microgram/min), but in the microalbuminuric range as determined by HPLC (albumin, 38.5 +/- 14.4 microgram/min). For urine samples in the macroalbuminuric range, there was no statistically significant difference between HPLC and RIA. Immuno-unreactive albumin was confirmed as albumin, analyzed by two-dimensional electrophoresis and matrix-assisted laser desorption ionization mass spectrometry.
These studies show that to determine microalbuminuria accurately, there is a need to assess urinary total intact albumin, rather than simply immunoreactive albumin. Am J Kidney Dis 41:336-342.
尿中完整白蛋白可能以两种形式存在,即免疫反应性和非免疫反应性。既往对糖尿病患者尿中白蛋白尿的估计仅检测到免疫反应性形式。
本研究采用高效液相色谱法(HPLC)测量两种形式的完整白蛋白(称为总完整白蛋白),与放射免疫分析法(RIA)相比,以更准确地测量97例糖尿病患者新鲜尿液样本中的白蛋白尿。还检测了86例来自无糖尿病志愿者的对照尿液样本。
对于非糖尿病对照,两种方法之间无显著差异。对于糖尿病尿液样本,91.6%的样本通过HPLC测得的白蛋白浓度高于RIA。对于正常白蛋白尿的糖尿病样本,HPLC测得的平均白蛋白排泄率为12.5±4.4微克/分钟(标准差),而RIA测得的排泄率为8.0±6.7微克/分钟(P = 0.004;N = 28)。对于微量白蛋白尿样本,也存在统计学显著差异:HPLC白蛋白排泄率为82.0±49.9微克/分钟,RIA为49.0±34.6微克/分钟(P = 0.004;N = 30)。32例尿液样本经RIA检测为正常白蛋白尿(白蛋白,11.4±3.9微克/分钟),但经HPLC测定处于微量白蛋白尿范围(白蛋白,38.5±14.4微克/分钟)。对于大量白蛋白尿范围的尿液样本,HPLC和RIA之间无统计学显著差异。通过二维电泳和基质辅助激光解吸电离质谱分析证实非免疫反应性白蛋白为白蛋白。
这些研究表明,要准确测定微量白蛋白尿,需要评估尿中总完整白蛋白,而不仅仅是免疫反应性白蛋白。《美国肾脏病杂志》41:336 - 342。