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2.
Ann Clin Transl Neurol ; 7(9): 1674-1680, 2020 09.
Article in English | MEDLINE | ID: mdl-33325656

ABSTRACT

OBJECTIVE: To study the effects of human herpes virus 6 (HHV-6) on the hippocampal volume in patients with mesial temporal sclerosis (MTS). BACKGROUND: HHV-6 may play an etiologic role in MTS. Previous studies found a possible association with febrile status epilepticus. Several investigators have reported a higher prevalence of HHV-6 in MTS resections compared to other epilepsy etiologies. DESIGN/METHODS: We used FreeSurfer to segment cortical structures and obtain whole hippocampal and subfield volumes in 41 patients with intractable epilepsy. In addition, an investigator blinded to other data traced hippocampi manually on each slice. The main study outcome measure was the asymmetry index (AI) between hippocampal volumes ipsilateral and contralateral to seizure foci compared between HHV-6 positive and negative patients. Viral DNA was isolated from fresh brain tissue obtained at temporal lobectomy. For 25 patients, viral detection was performed using quantitative real-time PCR specific for HHV-6A and HHV-6B. For 16 patients, viral DNA detection was performed using digital droplet PCR specific for HHV-6A and HHV-6B. RESULTS: Twenty-two patients were positive (14 of 25 tested with real-time PCR, and 8 of 16 with digital droplet PCR), and 19 negatives for HHV-6. HHV-6 negative patients had significantly greater AI and lower total hippocampal volume ipsilateral to seizure foci than HHV-6 positive patients. Epilepsy duration and age of onset did not affect results. INTERPRETATION: Our data suggest multiple potential etiologies for MTS. HHV-6 may have a less severe effect on the hippocampus than other etiologies.


Subject(s)
Drug Resistant Epilepsy , Epilepsy, Temporal Lobe , Herpesvirus 6, Human/pathogenicity , Hippocampus/pathology , Adult , Anterior Temporal Lobectomy , DNA, Viral/isolation & purification , Drug Resistant Epilepsy/etiology , Drug Resistant Epilepsy/pathology , Drug Resistant Epilepsy/surgery , Drug Resistant Epilepsy/virology , Epilepsy, Temporal Lobe/etiology , Epilepsy, Temporal Lobe/pathology , Epilepsy, Temporal Lobe/surgery , Epilepsy, Temporal Lobe/virology , Female , Humans , Magnetic Resonance Imaging , Male , Sclerosis/pathology , Single-Blind Method
3.
Epilepsia ; 61(10): e135-e139, 2020 10.
Article in English | MEDLINE | ID: mdl-32944946

ABSTRACT

There have been multiple descriptions of seizures during the acute infectious period in patients with COVID-19. However, there have been no reports of status epilepticus after recovery from COVID-19 infection. Herein, we discuss a patient with refractory status epilepticus 6 weeks after initial infection with COVID-19. Extensive workup demonstrated elevated inflammatory markers, recurrence of a positive nasopharyngeal SARS-CoV-2 polymerase chain reaction, and hippocampal atrophy. Postinfectious inflammation may have triggered refractory status epilepticus in a manner similar to the multisystemic inflammatory syndrome observed in children after COVID-19.


Subject(s)
COVID-19/complications , Inflammation/virology , Status Epilepticus/virology , Aged , Drug Resistant Epilepsy/virology , Female , Humans , SARS-CoV-2 , Syndrome
4.
Epilepsy Res ; 126: 119-25, 2016 10.
Article in English | MEDLINE | ID: mdl-27490897

ABSTRACT

OBJECTS: To investigate the expression of human papillomavirus (HPV)-specific antigen in the brain tissue of patients with Rasmussen's Encephalitis (RE) and its possible link to the clinical manifestation of RE. METHODS: The correlation between RE and HPV antigen expression in brain tissue sections was investigated using immunohistochemical (IHC) staining, pathological examination, MRI and clinical manifestations. RESULTS: HPV antigen expression was elevated in three out of four patients with RE, whereas there were no detectable HPV antigens in six control patients. Significant staining for HPV antigen was located mainly around or in the nucleus and cytoplasm of neurons. Among these RE patients, three with elevated expression of HPV antigens had obvious hemisphere atrophy, whereas the patient with negative staining for HPV antigens had mild atrophy. CONCLUSIONS: Elevated expression of HPV antigens was observed in the brain tissue of RE patients, which may correlate with hemisphere atrophy. Thus, our results may suggest that HPV infection or being a carrier of HPV may play a role in the initiation and progression of RE.


Subject(s)
Antigens, Viral/metabolism , Brain/immunology , Encephalitis/immunology , Papillomaviridae/immunology , Atrophy , Brain/pathology , Brain/surgery , Brain/virology , Cell Nucleus/immunology , Cell Nucleus/pathology , Cell Nucleus/virology , Child , Child, Preschool , Cytoplasm/immunology , Cytoplasm/pathology , Cytoplasm/virology , Drug Resistant Epilepsy/immunology , Drug Resistant Epilepsy/pathology , Drug Resistant Epilepsy/surgery , Drug Resistant Epilepsy/virology , Encephalitis/pathology , Encephalitis/surgery , Encephalitis/virology , Female , Humans , Immunohistochemistry , Infant , Male , Neurons/immunology , Neurons/pathology , Neurons/virology , Papillomavirus Infections/complications , Papillomavirus Infections/immunology , Papillomavirus Infections/pathology , Papillomavirus Infections/virology , Retrospective Studies
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