医学
脑脊液
结合珠蛋白
脑积水
发病机制
病理
白蛋白
生物标志物
胱抑素C
载脂蛋白E
神经学
常压脑积水
内科学
疾病
免疫学
痴呆
肌酐
生物
生物化学
外科
精神科
作者
Xianfeng Li,M. Miyajima,Reiko Mineki,Hikari Taka,Kimie Murayama,Hirotaka Arai
出处
期刊:Acta neurochirurgica
[Springer Science+Business Media]
日期:2006-06-05
卷期号:148 (8): 859-864
被引量:58
标识
DOI:10.1007/s00701-006-0787-4
摘要
Background. The pathogenesis of idiopathic normal pressure hydrocephalus (INPH) is unknown, and the syndrome of INPH remains a diagnostic and therapeutic challenge. The present study investigated the disease-specific proteins that aid in the diagnosis and treatment of INPH and thus to study their role in the disease process. Methods. A comparative proteomic analysis was used for clinical screening of cerebrospinal fluid (CSF) proteins in 15 patients with INPH and compared with 12 normal subjects. Furthermore, enzyme linked immunosorbent assay (ELISA) was performed for comparison with CSF proteins between individual INPH patients and controls. Results. Seven proteins and their isoforms, including leucine-rich α-2-glycoprotein (LRG), α1-antichymotrypsin, apolipoprotein D, apolipoprotein J, haptoglobin α1, serum albumin, and α-1-microglobulin/bikunin precursor showed significant changes in CSF of INPH patients compared with controls by proteomic analysis. And significant higher CSF levels of LRG in INPH patients compared with controls were found by ELISA. Conclusions. These results indicate that there are significant differences in the expression of certain proteins in the CSF of patients with INPH and normal subjects. In particular, the CSF level assay of LRG suggests that LRG is a specific biomarker for INPH and has potential use in the diagnosis and indication for CSF shunting.
科研通智能强力驱动
Strongly Powered by AbleSci AI