Document Detail


Serum matrix metalloproteinase-2 levels indicate blood-CSF barrier damage in patients with infectious meningitis.
MedLine Citation:
PMID:  18185989     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
OBJECTIVE: Protein components in cerebrospinal fluid (CSF) are maintained at a specific concentration by a dynamic gradient between the capillary and intrathecal spaces via the blood-cerebrospinal fluid barrier (BCB) in the brain and spinal cord. Permeability to proteins increases when there is structural damage to the BCB. Matrix metalloproteinase-2 (MMP-2; gelatinase A) has been shown to degrade type IV collagen, a major component of the cellular basement membrane. We analyzed alpha2 macroglobulin (alpha2M) indices and evaluated the relationship between alpha2M, as an indicator of BCB permeability, and MMP-2, which degrades the extra-cellular matrix in patients with infectious meningitis. MATERIALS AND METHODS: Albumin levels in CSF or serum were determined by turbidimetric immunoassay, or bromcresol green assay, respectively. alpha2M levels in CSF or serum were measured with enzyme-linked immunosorbent assay, or laser-nephelometry, respectively. Serum MMP-2 levels were determined by enzyme immuno assay. We calculated the alpha2M index, i.e. the ratio of alpha2M (CSF / serum) to albumin (CSF / serum; alpha2M in CSF / alpha2M in serum x albumin in serum / albumin in CSF). RESULTS: alpha2M indices were significantly increased in infectious meningitis compared to healthy controls (p < 0.05). They were highest in bacterial meningitis, and there was a significant difference between viral or mycotic and bacterial meningitis (p < 0.05). Serum MMP-2 levels were increased in infectious meningitis, being highest in bacterial meningitis, where they were significantly different from healthy controls (p < 0.05). There was a significant positive correlation between serum MMP-2 levels and alpha2M indices (r = 0.64, p < 0.0001). CONCLUSION: Markedly increased levels of serum MMP-2 in infectious, especially bacterial, meningitis may reflect the degree of damage to the BCB.
Authors:
Yuhsaku Kanoh; Tadashi Ohara; Motonari Kanoh; Tohru Akahoshi
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Publication Detail:
Type:  Journal Article     Date:  2008-01-10
Journal Detail:
Title:  Inflammation     Volume:  31     ISSN:  0360-3997     ISO Abbreviation:  Inflammation     Publication Date:  2008 Apr 
Date Detail:
Created Date:  2008-03-13     Completed Date:  2008-05-29     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  7600105     Medline TA:  Inflammation     Country:  United States    
Other Details:
Languages:  eng     Pagination:  99-104     Citation Subset:  IM    
Affiliation:
Department of Laboratory Medicine, Kitasato University School of Medicine, 1-15-1 Kitasato, Sagamihara, Kanagawa 228-8555, Japan. kanoh@med.kitasato-u.ac.jp
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MeSH Terms
Descriptor/Qualifier:
Biological Markers / blood,  cerebrospinal fluid
Blood-Brain Barrier / metabolism*,  pathology
Capillary Permeability
Case-Control Studies
Enzyme-Linked Immunosorbent Assay
Humans
Matrix Metalloproteinase 2 / blood*
Meningitis, Bacterial / cerebrospinal fluid,  enzymology*,  pathology
Meningitis, Fungal / cerebrospinal fluid,  enzymology*,  pathology
Meningitis, Viral / cerebrospinal fluid,  enzymology*,  pathology
Nephelometry and Turbidimetry
Serum Albumin / cerebrospinal fluid
Up-Regulation
alpha-Macroglobulins / cerebrospinal fluid*
Chemical
Reg. No./Substance:
0/Biological Markers; 0/Serum Albumin; 0/alpha-Macroglobulins; EC 3.4.24.24/MMP2 protein, human; EC 3.4.24.24/Matrix Metalloproteinase 2

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