急性胰腺炎患者尿和血清中免疫反应性阴离子和阳离子胰蛋白酶原的不同模式。

U Petersson, S Appelros, A Borgström
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引用次数: 27

摘要

背景:急性胰腺炎(AP)导致血清中胰蛋白酶原(T)同工酶浓度升高。尿中免疫反应性阴离子胰蛋白酶原(irAT/u)在AP中升高,最近被认为是一种快速诊断工具和严重程度预测因子。这些结果尚未得到其他研究小组的证实,irAT/u也未得到进一步的表征。尿中免疫反应性阳离子胰蛋白酶原浓度(irCT/u)和AP中血清irAT/irCT比值尚未广泛检测。方法:对50例AP患者和41例非AP患者尿液和血清中的irAT和irCT水平进行了研究。严重程度根据亚特兰大分级进行评估。采用凝胶过滤法对irAT/u进行表征。结果:凝胶过滤仅显示尿中有AT。在AP/非AP和轻度/重度疾病(p = 0.0012)之间,irAT/u有极显著差异(p < 0.0001)。结论:AP患者血清irAT/irCT比值由正常的0.8变为1.3。结论:AP患者尿液中有irAT和微量irCT。AP患者的irAT/ u高于其他急性腹部疾病(非AP),重度AP患者高于轻度AP。血清irAT (irAT/s)比例高于重度AP患者的irCT/s,但不区分轻、重度AP。在一些非AP病例中,irAT/u的水平很高,而在AP病例中,irAT/u的范围很广,这使得该测试的临床价值值得怀疑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Different patterns in immunoreactive anionic and cationic trypsinogen in urine and serum in human acute pancreatitis.

Background: Acute pancreatitis (AP) results in elevated concentrations of trypsinogen (T) isoenzymes in serum. Immunoreactive anionic trypsinogen in urin (irAT/u) is elevated in AP, and has recently been proposed as a rapid diagnostic instrument and severity predictor. These results have not been confirmed by other groups, and irAT/u has not been further characterized. The concentration of immunoreactive cationic trypsinogen in urine (irCT/u) and the serum irAT/irCT ratio in AP have not been extensively examined.

Methods: Levels of irAT and irCT were studied in urine and serum from 50 AP patients and in urine from 41 non-AP patients. Severity was assessed according to the Atlanta classification. irAT/u was characterized by gel filtration.

Results: Gel filtration revealed only AT in the urine. Highly significant differences in irAT/u were seen between AP/non-AP (p < 0.0001) and mild/severe disease (p = 0.0012). The irAT/irCT ratio in serum changed from normal 0.8 to 1.3 in AP.

Conclusions: IrAT and only traces of irCT were found in the urine in AP. IrAT/u was higher in AP than in other acute abdominal disorders (non-AP) and also higher in severe than in mild AP. IrAT in serum (irAT/s) increased proportionally more than irCT/s in AP, but did not discriminate mild from severe forms. High levels of irAT/u in some non-AP cases and a wide range in AP cases make the clinical value of the test questionable.

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