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Oxidative stress in patients with clinically mild encephalitis/encephalopathy with a reversible splenial lesion
Rie Miyata1, Naoyuki Tanuma, Masaharu Hayashi
1Department of Pediatrics, Tokyo-Kita Social Insurance Hospital, Kita-ku, Tokyo, Japan. rie88miyata@ybb.ne.jp
Abstract:
We examined oxidative stress markers, tau protein and cytokines in the cerebrospinal fluid (CSF) in six patients with clinically mild encephalitis/encephalopathy with a reversible splenial lesion (MERS). In the CSF, 8-hydroxy-2'-deoxyguanosine (8-OHdG) and hexanoyl-lysine adduct levels increased over the cutoff index in four and one out of six MERS patients, respectively. The CSF IL-6 and IL-10 levels were increased in three out of six patients, two of which had extended lesion of the cerebral white matter. The CSF value of tau protein, marker of the axonal damage, was not increased, and neuron specific enolase (NSE) in the CSF was not increased. The increased 8-OHdG levels in the CSF, DNA oxidative stress marker, in four MERS patients, suggesting involvement of oxidative stress in MERS. MERS is occasionally accompanied with hyponatremia, although our patients lacked hyponatremia. It is possible that the disequilibrium of systemic metabolism including electrolytes may lead to facilitation of oxidative stress and reversible white matter lesion in MERS. The increase of cytokine production seems to be involved in the distribution of lesions in MERS.
Insights
Oxidative stress, indicated by increased 8-hydroxy-2'-deoxyguanosine (8-OHdG) in cerebrospinal fluid (CSF), appears involved in mild encephalitis/encephalopathy with a reversible splenial lesion (MERS). Cytokine increases may also contribute to MERS lesion distribution.
Area of Science:
- Neurology
- Neuroscience
- Biochemistry
Background:
- Mild encephalitis/encephalopathy with a reversible splenial lesion (MERS) is a rare neurological condition.
- The underlying pathophysiology of MERS, particularly the role of oxidative stress and inflammation, remains incompletely understood.
Purpose of the Study:
- To investigate oxidative stress markers, tau protein, and cytokine levels in the cerebrospinal fluid (CSF) of MERS patients.
- To explore the potential relationship between these biomarkers and MERS lesion characteristics.
Main Methods:
- Analysis of CSF samples from six MERS patients.
- Measurement of 8-hydroxy-2 -deoxyguanosine (8-OHdG), hexanoyl-lysine adducts, IL-6, IL-10, tau protein, and neuron-specific enolase (NSE).
Main Results:
- Elevated CSF 8-OHdG levels, a marker of DNA oxidative stress, were found in four out of six MERS patients.
- Increased CSF IL-6 and IL-10 levels were observed in three patients, with two showing extended white matter lesions.
- CSF tau protein and NSE levels, markers of axonal damage, were not elevated.
Conclusions:
- Findings suggest a significant involvement of oxidative stress in the pathogenesis of MERS.
- Elevated cytokine production may play a role in the distribution of white matter lesions in MERS.
- Systemic metabolic imbalances could potentially facilitate oxidative stress and reversible white matter lesions in MERS.
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