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Increased intrathecal production of apolipoprotein D in multiple sclerosis
M Reindl1, G Knipping, I Wicher
1Department of Neurology, University of Innsbruck, Anichstrasse 35, A-6020, Innsbruck, Austria.
Abstract:
Apolipoprotein D (apoD) is a small glycoprotein responsible for the local transport of small hydrophobic ligands. Within the nervous system, apoD may be an acute phase protein that is upregulated in a variety of neuropathological conditions and is involved in the removal of lipids during nerve cell degeneration and provision of lipids during the regenerative phase. In this study, we measured cerebrospinal fluid (CSF) and serum apoD levels in patients with multiple sclerosis (MS), chronic inflammatory demyelinating polyneuropathy (CIDP), Guillain-Barré Syndrome (GBS), infectious inflammatory neurological diseases (IND) and non-inflammatory neurological diseases (NND). We found that mean CSF apoD levels are significantly increased in patients with CIDP/GBS reflecting an acute blood-nerve barrier leakage. In contrast, MS is characterized by an increased intrathecal apoD release as measured by the apoD index. Thus, the results of our study provide the first evidence of an increased intrathecal production of apoD in MS. Moreover, we demonstrate that mean apoD indices are highest in MS patients at the time of their first clinical exacerbation. CSF apoD levels and apoD indices correlate with MS disease duration but not with disability or age. Finally, we found that corticosteroid treatment resulted in significantly elevated CSF apoD levels.
Insights
Apolipoprotein D (apoD) shows increased levels in cerebrospinal fluid for neurological diseases. Multiple sclerosis (MS) patients exhibit elevated intrathecal apoD production, particularly during initial exacerbations.
Area of Science:
- Neuroscience
- Biochemistry
- Immunology
Background:
- Apolipoprotein D (apoD) is a glycoprotein involved in lipid transport.
- Within the nervous system, apoD may act as an acute phase protein, aiding lipid metabolism during nerve degeneration and regeneration.
- Its role in various neuropathologies is under investigation.
Purpose of the Study:
- To measure cerebrospinal fluid (CSF) and serum apoD levels in patients with multiple sclerosis (MS), chronic inflammatory demyelinating polyneuropathy (CIDP), Guillain-Barré Syndrome (GBS), infectious inflammatory neurological diseases (IND), and non-inflammatory neurological diseases (NND).
- To investigate the diagnostic and prognostic significance of apoD in these neurological conditions, particularly MS.
Main Methods:
- Measurement of apoD levels in CSF and serum from patients with various neurological diseases.
- Calculation of the apoD index to assess intrathecal apoD production.
- Correlation analysis of apoD levels and indices with clinical parameters such as disease duration, disability, age, and exacerbation status.
Main Results:
- Significantly increased CSF apoD levels were observed in CIDP/GBS patients, indicating acute blood-nerve barrier leakage.
- MS patients demonstrated an increased intrathecal apoD release, evidenced by a higher apoD index.
- The apoD index was highest in MS patients during their first clinical exacerbation and correlated with disease duration, but not disability or age.
- Corticosteroid treatment led to significantly elevated CSF apoD levels.
Conclusions:
- This study provides the first evidence of increased intrathecal apoD production in MS.
- Elevated CSF apoD in CIDP/GBS suggests blood-nerve barrier compromise.
- ApoD levels and indices may serve as biomarkers for disease activity and progression in MS and other inflammatory neuropathies.
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Multiple Sclerosis l: Introduction
Increased Intracranial Pressure ll: Pathophysiology

