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Published on: October 20, 2016
14-3-3 protein detection in the cerebrospinal fluid of patients with influenza-associated encephalopathy
Katsunori Fujii1, Yuzo Tanabe, Hideki Uchikawa
1Department of Pediatrics, Graduate School of Medicine, Chiba University, and the Division of Neurology, Chiba Children's Hospital, Japan. kfujii@faculty.chiba-u.jp
Insights
Influenza-associated encephalopathy in children is hard to diagnose. Detecting 14-3-3 brain proteins in cerebrospinal fluid offers a rapid diagnostic marker for this serious influenza complication.
Area of Science:
- Neuroscience
- Infectious Diseases
- Biochemistry
Background:
- Influenza-associated encephalopathy (IAE) presents with neurological symptoms in children following influenza infection.
- The underlying pathophysiology of IAE remains poorly understood.
- Current diagnostic methods may not be rapid enough for timely intervention.
Observation:
- This study investigated the presence of 14-3-3 proteins in the cerebrospinal fluid (CSF) of pediatric patients.
- CSF samples were analyzed from patients with IAE, influenza without encephalopathy, and other encephalopathies.
- Immunoblotting was used to detect acidic brain proteins, specifically 14-3-3 isoforms.
Findings:
- 14-3-3 proteins were detected in 100% of patients with influenza-associated encephalopathy.
- No 14-3-3 proteins were found in patients with influenza alone or other encephalopathies.
- Multiple 14-3-3 isoforms (beta, gamma, epsilon, xi, theta) were identified in the CSF of IAE patients.
Implications:
- Elevated 14-3-3 proteins in CSF suggest significant neuronal damage in IAE.
- CSF 14-3-3 protein detection can serve as a rapid diagnostic marker for influenza-associated encephalopathy.
- This finding may lead to earlier diagnosis and improved management strategies for children with IAE.
Abstract:
Influenza-associated encephalopathy is characterized by high fever, convulsions, and loss of consciousness associated with influenza infection in children, but its pathophysiology remains to be clarified. We examined 14-3-3 proteins, which are acidic brain proteins, in cerebrospinal fluid by immunoblotting in four patients with influenza-associated encephalopathy, four patients with influenza without encephalopathy, and four patients with another encephalopathy. Interestingly, we detected 14-3-3 proteins in all four patients with influenza-associated encephalopathy (100%) but not in any of the other patients. 14-3-3 isoforms, including beta, gamma, epsilon, xi, and theta, were found in the cerebrospinal fluid of the patients with influenza-associated encephalopathy, suggesting extensive damage to the brain. We conclude that 14-3-3 proteins in cerebrospinal fluid are highly detectable in influenza-associated encephalopathy and thus can be used as a rapid diagnostic marker.
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