Prostaglandin D synthase concentration in cerebrospinal fluid and serum of patients with neurological disorders

被引:51
作者
Melegos, DN
Freedman, MS
Diamandis, EP
机构
[1] MT SINAI HOSP,DEPT PATHOL & LAB MED,TORONTO,ON M5G 1X5,CANADA
[2] UNIV TORONTO,DEPT CLIN BIOCHEM,TORONTO,ON,CANADA
[3] OTTAWA GEN HOSP,DEPT NEUROL,OTTAWA,ON K1H 8L6,CANADA
来源
PROSTAGLANDINS | 1997年 / 54卷 / 01期
关键词
PGD synthase; beta-trace; cerebrospinal fluid; serum; multiple sclerosis; neurological disorders;
D O I
10.1016/S0090-6980(97)00062-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Prostaglandin D synthase (PGD synthase) or beta-trace protein is a major constituent of human cerebrospinal fluid (CSF) representing similar to 3% of the total CSF protein. We have recently developed a highly specific immunofluorometric assay for PGD synthase, which enabled us to quantify the presence of PGD synthase in fluids and tissues not associated with the CNS. In this report we provide quantitative data of the presence of PGD synthase in CSF and serum from 302 subjects with various neurological diseases and symptoms. PGD synthase levels in CSF are approximately 35-fold higher than those of serum, with a median concentration of 11299 mu g/L. A statistically significant association of PGD synthase concentration in CSF was observed with both patient age and gender. There was no correlation between PGD synthase concentration in serum and patient age or gender. To evaluate the clinical utility of PGD synthase in diagnosing neurological diseases, the distribution pattern of PGD synthase in CSF and serum was examined for each neuropathology of 268 patients whose diagnosis was known. No statistical difference was observed between PGD synthase concentration in the CSF (Ies cases) or the serum (94 cases) of multiple sclerosis afflicted subjects in comparison to all other patients studied. The distribution pattern was also not different for PGD synthase levels in CSF of patients with HIV/AIDS related neuropathies, viral meningitis and fibromyalgia. We conclude that PGD synthase measurement presents no clinical utility in diagnosing neurological disorders in adulthood. PGD synthase may have a physiological and/or pathological role in the developing brain and in neurodegenerative diseases.
引用
收藏
页码:463 / 474
页数:12
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