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Updated: May 30, 2026

A High Throughput, Multiplexed and Targeted Proteomic CSF Assay to Quantify Neurodegenerative Biomarkers and Apolipoprotein E Isoforms Status
Published on: October 20, 2016
Cerebrospinal fluid apolipoprotein E levels in subacute sclerosing panencephalitis
Deniz Yüksel1, Takashi Ichiyama, Deniz Yilmaz
1Department of Pediatric Neurology, Dr. Sami Ulus Children's Hospital, Ankara, Turkey. drdeniz_yuksel@yahoo.com.tr
Subacute sclerosing panencephalitis (SSPE) shows lower total and ApoE4 levels but higher ApoE3 levels in cerebrospinal fluid. Elevated ApoE3 may help control neurofibrillary tangle formation in SSPE.
Area of Science:
- Neuroscience
- Biochemistry
- Neurology
Background:
- Neurofibrillary tangles (NFTs), composed of hyperphosphorylated tau, are found in some subacute sclerosing panencephalitis (SSPE) cases.
- Apolipoprotein E (Apo E) isoforms interact with tau, potentially regulating tau metabolism and NFT formation.
- ApoE3 binds tau in vitro, inhibiting tau hyperphosphorylation and possibly reducing NFT development.
Purpose of the Study:
- To investigate cerebrospinal fluid (CSF) levels of Apo E isoforms in SSPE patients compared to age-matched controls.
- To explore the potential role of Apo E3 in mitigating NFT formation in SSPE.
Main Methods:
- Cerebrospinal fluid (CSF) samples were collected from SSPE patients (n=37) and healthy controls (n=38).
- Levels of total Apo E, Apo E3, and Apo E4 were quantified in CSF using established methods.
- Statistical analysis was performed to compare Apo E levels between the SSPE and control groups.
Main Results:
- Median levels of total Apo E and Apo E4 were significantly lower in the SSPE group compared to controls (p<0.001 and p=0.002, respectively).
- Median Apo E3 levels were significantly higher in the SSPE group (0.28±0.23 μg/ml) than in the control group (p<0.001).
Conclusions:
- Elevated cerebrospinal fluid ApoE3 levels in SSPE patients may play a protective role by inhibiting NFT formation.
- Further research comparing the long-term clinical course of SSPE cases with varying Apo E3 levels is warranted to understand its role in neuroprotection and disease management.
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