Russ G R, Horgan B A, Mathew T H, Brown H, Mills L, Kirkland J A
Clin Nephrol. 1982 Sep;18(3):148-53.
Patients with analgesic nephropathy are at risk from uro-epithelial malignancy. Enhanced secretion of beta 2-microglobulin occurs from epithelial cancer cells. In order to find a screening test for malignancy in analgesic nephropathy, urinary levels of this protein were measured in patients with analgesic nephropathy with urine cytological abnormalities and were compared to a control group with glomerulonephritis. Mean fractional excretion of beta 2-microglobulin was higher (8.61 +/- 1.76 SEM) in patients with analgesic nephropathy than in those with glomerulonephritis (1.13 +/- 0.76) (P less than 0.025). Those patients with analgesic nephropathy who had malignant cells in the urine had higher mean fractional excretion (18.56 +/- 5.77) than those with only atypical cells (8.5 +/- 2.0) (P less than 0.05) who in turn had higher mean values than those with normal cytology (2.12 +/- 0.62) (P less than 0.0025). It is suggested that the increased beta 2-microglobulin excretion in analgesic nephropathy is due to secretion from abnormal urothelial cells as well as reduced tubular catabolism. Beta 2-microglobulin may be of use as a screening test for malignancy in analgesic nephropathy.
镇痛剂肾病患者有发生尿路上皮恶性肿瘤的风险。上皮癌细胞会增强β2-微球蛋白的分泌。为了找到一种用于筛查镇痛剂肾病患者恶性肿瘤的检测方法,对有尿液细胞学异常的镇痛剂肾病患者的尿中该蛋白水平进行了测量,并与一组肾小球肾炎患者进行了比较。镇痛剂肾病患者的β2-微球蛋白平均分数排泄率(8.61±1.76标准误)高于肾小球肾炎患者(1.13±0.76)(P<0.025)。尿液中有恶性细胞的镇痛剂肾病患者的平均分数排泄率(18.56±5.77)高于仅有非典型细胞的患者(8.5±2.0)(P<0.05),而仅有非典型细胞的患者的平均值又高于细胞学正常的患者(2.12±0.62)(P<0.0025)。提示镇痛剂肾病患者β2-微球蛋白排泄增加是由于异常尿路上皮细胞的分泌以及肾小管分解代谢减少所致。β2-微球蛋白可能用作镇痛剂肾病患者恶性肿瘤的筛查检测方法。