Wisniewski K E, Kaczmarski W, Golabek A A, Kida E
New York State Institute for Basic Research in Developmental Disabilities, Department of Pathological Neurobiology, Staten Island 10314, USA.
Am J Med Genet. 1995 Jun 5;57(2):246-9. doi: 10.1002/ajmg.1320570227.
Using Western blot analysis and the ELISA technique, we showed previously significantly higher levels of subunit c in the urine of individuals with late-infantile neuronal ceroid lipofuscinosis (LINCL) and some patients with juvenile NCL (JNCL) [Wisniewski et al., J. Inherited Metab Dis 17: 205-210, 1994]. In an attempt to develop a diagnostic screening test for NCL based on detection of this biochemical marker in urine, we analyzed, using the blotting technique, urine from 7 infantile NCL (INCL), 17 LINCL, and 19 JNCL cases, 30 obligate heterozygotes, and 60 control cases. This analysis confirmed our former data showing significantly higher levels of subunit c in the urine from all LINCL and some JNCL cases. No false positive results were found. This simple analytical method may serve as a fast, non-invasive screening test for NCL.
我们先前利用蛋白质印迹分析和酶联免疫吸附测定技术发现,晚期婴儿型神经元蜡样脂褐质沉积症(LINCL)患者及部分青少年型神经元蜡样脂褐质沉积症(JNCL)患者尿液中的c亚基水平显著更高[维斯涅夫斯基等人,《遗传代谢病杂志》17: 205 - 210, 1994]。为了基于尿液中这种生化标志物的检测开发一种用于神经元蜡样脂褐质沉积症(NCL)的诊断筛查试验,我们使用印迹技术分析了7例婴儿型NCL(INCL)、17例LINCL、19例JNCL患者、30例 obligate杂合子以及60例对照者的尿液。该分析证实了我们之前的数据,即所有LINCL患者及部分JNCL患者尿液中的c亚基水平显著更高。未发现假阳性结果。这种简单的分析方法可作为一种快速、非侵入性的NCL筛查试验。