Cerebrospinal fluid levels of biotin in various neurological disorders

Citation
M. Anagnostouli et al., Cerebrospinal fluid levels of biotin in various neurological disorders, ACT NEUR SC, 99(6), 1999, pp. 387-392
Citations number
34
Categorie Soggetti
Neurology,"Neurosciences & Behavoir
Journal title
ACTA NEUROLOGICA SCANDINAVICA
ISSN journal
00016314 → ACNP
Volume
99
Issue
6
Year of publication
1999
Pages
387 - 392
Database
ISI
SICI code
0001-6314(199906)99:6<387:CFLOBI>2.0.ZU;2-V
Abstract
Objectives - To analyse biotin concentrations in human cerebrospinal fluid (CSF) and serum from controls without evidence of nutritional or neurologic al disorders and patients with common neurological disorders. Patients and methods - Cerebrospinal fluid was obtained from patients by lumbar puncture , serum was prepared from freshly drawn whole blood and biotinidase in samp les was inhibited before being analysed for biotin by radioligand assay. Re sults - Assay characteristics were within an acceptable range (intra-and in terassay coefficient of variations were 8.8 and 12.0 respectively, recovery : 91-114% and sensitive, lowest standard concentration 15 ng/l). Significan tly lower values for biotin were found in patients with multiple sclerosis (both CSF and serum) in comparison to the controls. Significantly reduced v alues for cerebrospinal fluid biotin were found in epileptics compared to c ontrols, whereas, in serum the difference was approaching significance. No significant differences were observed in other groups of patients. Conclusi on - There is a significant reduction in cerebrospinal fluid biotin in epil eptics and patients with multiple sclerosis compared to controls. In epilep tics this may be related to competition between biotin and anticonvulsants bearing carbamide ring for absorption. Reduction of biotin levels in patien ts with multiple sclerosis could be attributed to intestinal malabsorption caused by the underlying disease or a biotin-binding immunoglobulin which m ay be involved in multiple sclerosis pathogenesis.