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1.
Virol Sin ; 39(2): 251-263, 2024 Apr.
Article in English | MEDLINE | ID: mdl-38219860

ABSTRACT

Viral encephalitis continues to be a significant public health concern. In our previous study, we discovered a lower expression of antiviral factors, such as IFN-ß, STING and IFI16, in the brain tissues of patients with Rasmussen's encephalitis (RE), a rare chronic neurological disorder often occurred in children, characterized by unihemispheric brain atrophy. Furthermore, a higher cumulative viral score of human herpes viruses (HHVs) was also found to have a significant positive correlation with the unihemispheric atrophy in RE. Type I IFNs (IFN-I) signaling is essential for innate anti-infection response by binding to IFN-α/ß receptor (IFNAR). In this study, we infected WT mice and IFNAR-deficient A6 mice with herpes simplex virus 1 (HSV-1) via periocular injection to investigate the relationship between IFN-I signaling and HHVs-induced brain lesions. While all mice exhibited typical viral encephalitis lesions in their brains, HSV-induced epilepsy was only observed in A6 mice. The gene expression matrix, functional enrichment analysis and protein-protein interaction network revealed four gene models that were positively related with HSV-induced epilepsy. Additionally, ten key genes with the highest scores were identified. Taken together, these findings indicate that intact IFN-I signaling can effectively limit HHVs induced neural symptoms and brain lesions, thereby confirming the positive correlation between IFN-I signaling repression and brain atrophy in RE and other HHVs encephalitis.


Subject(s)
Brain , Epilepsy , Herpesvirus 1, Human , Interferon Type I , Signal Transduction , Animals , Herpesvirus 1, Human/pathogenicity , Herpesvirus 1, Human/immunology , Interferon Type I/metabolism , Interferon Type I/immunology , Mice , Brain/pathology , Brain/virology , Epilepsy/virology , Epilepsy/pathology , Receptor, Interferon alpha-beta/genetics , Receptor, Interferon alpha-beta/deficiency , Disease Models, Animal , Mice, Knockout , Mice, Inbred C57BL , Female , Protein Interaction Maps , Herpes Simplex/virology , Herpes Simplex/pathology , Herpes Simplex/immunology , Encephalitis, Herpes Simplex/virology , Encephalitis, Herpes Simplex/immunology , Encephalitis, Herpes Simplex/pathology , Humans
2.
Epilepsia ; 62(5): 1193-1207, 2021 05.
Article in English | MEDLINE | ID: mdl-33778951

ABSTRACT

OBJECTIVES: To estimate the overall frequency of epilepsy in children with congenital Zika syndrome (CZS) and describe the profile of seizures and the response rate to anti-epileptic treatment in this group of patients. METHODS: A systematic review and meta-analysis were conducted following the Cochrane Handbook and preferred reporting items for systematic reviews and meta-analyses (PRISMA) guidelines. PubMed/MEDLINE, Scopus, Cochrane Library, SciELO, and LILACS were searched until June 23, 2020. Observational studies that evaluated the frequency of epilepsy in children diagnosed with CZS according to international criteria were included in the study. RESULTS: Fourteen studies evaluating 903 patients diagnosed with CZS were pooled in a meta-analysis. All studies were conducted in Brazil, with reports published between 2016 and 2020, and included children diagnosed with CSZ from 0 to 40 months of age. The overall rate of epilepsy in children diagnosed with CZS was estimated at 60% (95% confidence interval [CI] 0.51-0.68). The studies included in this review show that the frequency of epilepsy in patients with CSZ varies with age, with higher rates in older children. Epileptic spasms was the primary type of seizure observed in this group, followed by focal and generalized crisis. The response rate to anti-epileptic drugs was considerably low, ranging from 20% of seizure control in the first year and 30% in the second year. SIGNIFICANCE: Children with CZS presented a high cumulative incidence of epilepsy episodes with increased severity and a low response to anti-epileptic therapy, which is associated with the extensive damage caused by the Zika virus on the cortical structures of patients.


Subject(s)
Epilepsy/epidemiology , Epilepsy/virology , Zika Virus Infection/congenital , Zika Virus Infection/complications , Child , Humans , Incidence
3.
Arch Virol ; 166(3): 733-753, 2021 Mar.
Article in English | MEDLINE | ID: mdl-33502593

ABSTRACT

The chronic dysfunction of neuronal cells, both central and peripheral, a characteristic of neurological disorders, may be caused by irreversible damage and cell death. In 2016, more than 276 million cases of neurological disorders were reported worldwide. Moreover, neurological disorders are the second leading cause of death. Generally, the etiology of neurological diseases is not fully understood. Recent studies have related the onset of neurological disorders to viral infections, which may cause neurological symptoms or lead to immune responses that trigger these pathological signs. Currently, this relationship is mostly based on epidemiological data on infections and seroprevalence of patients who present with neurological disorders. The number of studies aiming to elucidate the mechanism of action by which viral infections may directly or indirectly contribute to the development of neurological disorders has been increasing over the years but these studies are still scarce. Comprehending the pathogenesis of these diseases and exploring novel theories may favor the development of new strategies for diagnosis and therapy in the future. Therefore, the objective of the present study was to review the main pieces of evidence for the relationship between viral infection and neurological disorders such as Alzheimer's disease, Parkinson's disease, Guillain-Barré syndrome, multiple sclerosis, and epilepsy. Viruses belonging to the families Herpesviridae, Orthomyxoviridae, Flaviviridae, and Retroviridae have been reported to be involved in one or more of these conditions. Also, neurological symptoms and the future impact of infection with SARS-CoV-2, a member of the family Coronaviridae that is responsible for the COVID-19 pandemic that started in late 2019, are reported and discussed.


Subject(s)
COVID-19/pathology , Nervous System Diseases/virology , Viral Tropism/physiology , Alzheimer Disease/virology , COVID-19/virology , Epilepsy/virology , Flaviviridae/metabolism , Guillain-Barre Syndrome/virology , Herpesviridae/metabolism , Humans , Multiple Sclerosis/virology , Nervous System Diseases/pathology , Orthomyxoviridae/metabolism , Parkinson Disease/virology , Retroviridae/metabolism , SARS-CoV-2/metabolism
4.
Seizure ; 83: 89-97, 2020 Dec.
Article in English | MEDLINE | ID: mdl-33120327

ABSTRACT

PURPOSE: Traditional neuropsychological testing carries elevated COVID-19 risk for both examinee and examiner. Here we describe how the pilot study of the Australian Epilepsy Project (AEP) has transitioned to tele-neuropsychology (teleNP), enabling continued safe operations during the pandemic. METHODS: The AEP includes adults (age 18-60) with a first unprovoked seizure, new diagnosis of epilepsy or drug resistant focal epilepsy. Shortly after launching the study, COVID-related restrictions necessitated adaptation to teleNP, including delivery of verbal tasks via videoconference; visual stimulus delivery via document camera; use of web-hosted, computerised assessment; substitution of oral versions for written tests; online delivery of questionnaires; and discontinuation of telehealth incompatible tasks. RESULTS: To date, we have completed 24 teleNP assessments: 18 remotely (participant in own home) and six on-site (participant using equipment at research facility). Five face-to-face assessments were conducted prior to the transition to teleNP. Eight of 408 tests administered via teleNP (1.9 %) have been invalidated, for a variety of reasons (technical, procedural, environmental). Data confirm typical patterns of epilepsy-related deficits (p < .05) affecting processing speed, executive function, language and memory. Questionnaire responses indicate elevated rates of patients at high risk of mood (34 %) and anxiety disorder (38 %). CONCLUSION: Research teleNP assessments reveal a typical pattern of impairments in epilepsy. A range of issues must be considered when introducing teleNP, such as technical and administrative set up, test selection and delivery, and cohort suitability. TeleNP enables large-scale neuropsychological research during periods of social distancing (and beyond), and offers an opportunity to expand the reach and breadth of neuropsychological services.


Subject(s)
COVID-19/virology , Epilepsy/virology , Executive Function/physiology , SARS-CoV-2/metabolism , Telemedicine , Australia , COVID-19/complications , Epilepsy/complications , Humans , Neuropsychological Tests , Neuropsychology/methods , Pilot Projects , Surveys and Questionnaires , Telemedicine/methods
5.
Scand J Immunol ; 92(6): e12984, 2020 Dec.
Article in English | MEDLINE | ID: mdl-33037649

ABSTRACT

Human herpesvirus 6A (HHV-6A) and 6B (HHV-6B) are two closely related viruses that can infect cells of the central nervous system (CNS). The similarities between these viruses have made it difficult to separate them on serological level. The broad term HHV-6 remains when referring to studies where the two species were not distinguished, and as such, the seroprevalence is over 90% in the adult population. HHV-6B has been detected in up to 100% of infants with the primary infection roseola infantum, but less is known about the primary infection of HHV-6A. Both viruses are neurotropic and have capacity to establish lifelong latency in cells of the central nervous system, with potential to reactivate and cause complications later in life. HHV-6A infection has been associated with an increased risk of multiple sclerosis (MS), whereas HHV-6B is indicated to be involved in pathogenesis of epilepsy. These two associations show how neurological diseases might be caused by viral infections, but as suggested here, through completely different molecular mechanisms, in an autoimmune disease, such as MS, by triggering an overreaction of the immune system and in epilepsy by hampering internal cellular functions when the immune system fails to eliminate the virus. Understanding the viral mechanisms of primary infection and reactivation and their spectrum of associated symptoms will aid our ability to diagnose, treat and prevent these severe and chronic diseases. This review explores the role of HHV-6A and HHV-6B specifically in MS and epilepsy, the evidence to date and the future directions of this field.


Subject(s)
Central Nervous System/virology , Epilepsy/virology , Exanthema Subitum/virology , Herpesvirus 6, Human/physiology , Multiple Sclerosis/virology , Animals , Autoimmunity , Epigenesis, Genetic , Epilepsy/immunology , Exanthema Subitum/immunology , Humans , Multiple Sclerosis/immunology , Risk
6.
Seizure ; 83: 1-4, 2020 Dec.
Article in English | MEDLINE | ID: mdl-33075670

ABSTRACT

PURPOSE: Our objective is to describe the most prevalent electroencephalographic findings in COVID-19 hospitalized patients, and to determine possible predictors of mortality including EEG and clinical variables. METHODS: A multicentric prospective observational study in patients with COVID-19 requiring EEG during hospitalization. RESULTS: We found 94 EEG from 62 patients (55 % men, mean age 59.7 ± 17.8 years) were analyzed. Most frequent comorbidity was cardiac (52 %), followed by metabolic (45 %) and CNS disease (39 %). Patients required ICU management by 60 %, with a mortality of 27 % in the whole cohort. The most frequent EEG finding was generalized continuous slow-wave activity (66 %). Epileptic activity was observed in 19 % including non-convulsive status epilepticus, seizures and interictal epileptiform discharges. Periodic patterns were observed in 3 patients (3.2 %). Multivariate analysis found that cancer comorbidity and requiring an EEG during the third week of evolution portended a higher risk of mortality CONCLUSION: We observed that the most prevalent EEG finding in this cohort was generalized continuous slow-wave activity, while epileptic activity was observed in less than 20 % of the cases. Mortality risk factors were comorbidity with cancer and requiring an EEG during the third week of evolution, possibly related to the hyperinflammatory state.


Subject(s)
COVID-19/mortality , Electroencephalography , SARS-CoV-2/pathogenicity , Seizures/physiopathology , Adult , Aged , Aged, 80 and over , COVID-19/diagnosis , COVID-19/physiopathology , Electroencephalography/methods , Epilepsy/physiopathology , Epilepsy/virology , Female , Hospitalization/statistics & numerical data , Humans , Inpatients , Male , Middle Aged , Prognosis , Seizures/virology , Status Epilepticus/mortality , Status Epilepticus/physiopathology , Status Epilepticus/virology
7.
Seizure ; 83: 38-40, 2020 Dec.
Article in English | MEDLINE | ID: mdl-33080483

ABSTRACT

PURPOSE: The COVID-19 pandemic and related lockdown measures drastically changed health care and emergency services utilization. This study evaluated trends in emergency department (ED) access for seizure-related reasons in the first 8 weeks of lockdown in Italy. METHODS: All ED accesses of children (<14 years of age) at two university hospitals, in Turin and Rome, Italy, between January 6, 2020 and April 21, 2020, were examined and compared with the corresponding periods of 2019. RESULTS: During the COVID-19 lockdown period (February 23-April 21, 2020), there was a 72 % decrease in all pediatric ED accesses over the corresponding 2019 period (n = 3,395 vs n = 12,128), with a 38 % decrease in seizure-related accesses (n = 41 vs n = 66). The observed decrease of seizure-related ED accesses was not accompanied by significant changes in age, sex, type of seizure, or hospitalization rate after the ED visit. CONCLUSION: The COVID-19 lockdown was accompanied by a sudden decrease in seizure-related hospital emergency visits. School closure, social distancing, reduced risk of infection, and increased parental supervision are some of the factors that might have contributed to the finding.


Subject(s)
COVID-19/complications , Emergency Service, Hospital/statistics & numerical data , Epilepsy/virology , SARS-CoV-2/pathogenicity , Seizures/physiopathology , Adolescent , Child , Emergency Medical Services/statistics & numerical data , Epilepsy/epidemiology , Hospitalization/statistics & numerical data , Humans , Italy , Seizures/virology
8.
Viruses ; 12(10)2020 09 25.
Article in English | MEDLINE | ID: mdl-32992985

ABSTRACT

Clinical outcomes related to congenital Zika syndrome (CZS) include microcephaly accompanied by specific brain injuries. Among several CZS outcomes that have been described, epilepsy and motor impairments are present in most cases. Pharmacological treatment for seizures resulting from epilepsy is performed with anticonvulsant drugs, which in the long term are related to impairments in the child's neuropsychomotor development. Here, we describe the results from a two-year follow-up of a cohort of children diagnosed with CZS related to the growth of the head circumference and some neurological and motor outcomes, including the pharmacological approach, and its results in the treatment of epileptic seizures. This paper is part of a prospective cohort study carried out in the state of Mato Grosso Sul, Brazil, based on a Zika virus (ZIKV)-exposed child population. Our data were focused on the assessment of head circumference growth and some neurological and motor findings, including the description of seizure conditions and pharmacological management in two periods. Among the 11 children evaluated, 8 had severe microcephaly associated with motor impairment and/or epilepsy. Seven children were diagnosed with epilepsy. Of these, 3 had West syndrome. In four children with other forms of epilepsy, there was no pharmacological control.


Subject(s)
Anticonvulsants/therapeutic use , Epilepsy/drug therapy , Microcephaly/virology , Spasms, Infantile/drug therapy , Zika Virus Infection/pathology , Brazil , Child, Preschool , Epilepsy/virology , Female , Head/anatomy & histology , Humans , Infant , Infant, Newborn , Microcephaly/pathology , Muscle Hypertonia/virology , Nervous System Malformations/virology , Paresis/virology , Pregnancy , Pregnancy Complications, Infectious/virology , Prospective Studies , Reflex, Abnormal/physiology , Spasms, Infantile/virology , Zika Virus/pathogenicity
9.
Eur J Paediatr Neurol ; 29: 128-136, 2020 Nov.
Article in English | MEDLINE | ID: mdl-32868196

ABSTRACT

PURPOSE: Herpes simplex virus encephalitis (HSE) is the most common cause of sporadic viral encephalitis in children and is responsible for epilepsy in approximately half of patients. In addition to medical treatment, epilepsy surgery may be offered to drug-resistant patients but carries a high risk of relapse of herpetic encephalitis. We are reporting our series of patients operated on between 2000 and 2019 with the systematic administration of acyclovir (ACV). RESULTS: Four pediatric patients aged 4.5-12.8 years with drug-resistant epilepsy post-HSE underwent a tailored focal resection following invasive recordings (three patients) and a complete callosotomy (one patient). The total number of the surgical procedures for the four patients was eight, and a systematic administration of ACV as a prophylactic treatment of herpetic encephalitis relapse was done at each step. No patients had a relapse and the ACV was well-tolerated in all the cases. Following surgery two patients are seizure free, the patient who underwent callosotomy is Engel 3 and the fourth patient, in whom a large epileptic zone has contraindicated a second surgery, is Engel 4. CONCLUSIONS: Our series demonstrated the dramatic efficacy of systematic ACV prophylaxis during all cranial surgeries. Moreover, our results on epilepsy, together with those of the literature, encourage more consideration regarding epilepsy surgery in this specific etiology. All types of surgical procedures (curative or palliative) can be offered to the patients, but in the case of focal surgery, due to the poor anatomical limits, invasive recordings are highly recommended.


Subject(s)
Acyclovir/therapeutic use , Antiviral Agents/therapeutic use , Encephalitis, Herpes Simplex/complications , Epilepsy/therapy , Epilepsy/virology , Adolescent , Child , Child, Preschool , Drug Resistant Epilepsy/surgery , Encephalitis, Herpes Simplex/prevention & control , Female , Humans , Male , Secondary Prevention/methods
10.
Neurol Sci ; 41(8): 2005-2011, 2020 Aug.
Article in English | MEDLINE | ID: mdl-32594268

ABSTRACT

People with epilepsy (PWE) are neither more likely to be infected by the coronavirus nor are they more likely to have severe COVID-19 manifestations because they suffer from epilepsy. However, management of COVID-19 in PWE may be more complicated than that in other individuals. Drug-drug interactions could pose significant challenges and cardiac, hepatic, or renal problems, which may happen in patients with severe COVID-19, may require adjustment to antiepileptic drugs (AEDs). In this review, we first summarize the potential drug-drug interactions between AEDs and drugs currently used in the management of COVID-19. We then summarize other challenging issues that may happen in PWE, who have COVID-19 and are receiving treatment.


Subject(s)
Coronavirus Infections/complications , Coronavirus Infections/drug therapy , Drug Interactions , Epilepsy/drug therapy , Epilepsy/virology , Pneumonia, Viral/complications , Pneumonia, Viral/drug therapy , Anticonvulsants/therapeutic use , Betacoronavirus , COVID-19 , Humans , Pandemics , SARS-CoV-2
11.
J Neurovirol ; 26(3): 324-329, 2020 06.
Article in English | MEDLINE | ID: mdl-32418055

ABSTRACT

Coronavirus disease 2019 (COVID-19) was reported at the end of 2019 in China for the first time and has rapidly spread throughout the world as a pandemic. Since COVID-19 causes mild to severe acute respiratory syndrome, most studies in this field have only focused on different aspects of pathogenesis in the respiratory system. However, evidence suggests that COVID-19 may affect the central nervous system (CNS). Given the outbreak of COVID-19, it seems necessary to perform investigations on the possible neurological complications in patients who suffered from COVID-19. Here, we reviewed the evidence of the neuroinvasive potential of coronaviruses and discussed the possible pathogenic processes in CNS infection by COVID-19 to provide a precise insight for future studies.


Subject(s)
Ataxia/epidemiology , Brain Edema/epidemiology , Coronavirus Infections/epidemiology , Encephalitis, Viral/epidemiology , Epilepsy/epidemiology , Multiple Sclerosis/epidemiology , Pandemics , Pneumonia, Viral/epidemiology , Severe Acute Respiratory Syndrome/epidemiology , Ataxia/complications , Ataxia/diagnosis , Ataxia/virology , Betacoronavirus/drug effects , Betacoronavirus/immunology , Betacoronavirus/pathogenicity , Blood-Brain Barrier/pathology , Blood-Brain Barrier/virology , Brain Edema/complications , Brain Edema/diagnosis , Brain Edema/virology , COVID-19 , Central Nervous System/pathology , Central Nervous System/virology , Coronavirus Infections/complications , Coronavirus Infections/diagnosis , Coronavirus Infections/transmission , Encephalitis, Viral/complications , Encephalitis, Viral/diagnosis , Encephalitis, Viral/virology , Epilepsy/complications , Epilepsy/diagnosis , Epilepsy/virology , Humans , Multiple Sclerosis/complications , Multiple Sclerosis/diagnosis , Multiple Sclerosis/virology , Pneumonia, Viral/complications , Pneumonia, Viral/diagnosis , Pneumonia, Viral/transmission , Prevalence , SARS-CoV-2 , Severe Acute Respiratory Syndrome/complications , Severe Acute Respiratory Syndrome/diagnosis , Severe Acute Respiratory Syndrome/transmission
12.
Neurology ; 94(23): 1032-1037, 2020 06 09.
Article in English | MEDLINE | ID: mdl-32327490

ABSTRACT

OBJECTIVES: To provide information on the effect of the coronavirus disease of 2019 (COVID-19) pandemic on people with epilepsy and provide consensus recommendations on how to provide the best possible care for people with epilepsy while avoiding visits to urgent care facilities and hospitalizations during the novel coronavirus pandemic. METHODS: The authors developed consensus statements in 2 sections. The first was "How should we/clinicians modify our clinical care pathway for people with epilepsy during the COVID-19 pandemic?" The second was "What general advice should we give to people with epilepsy during this crisis? The authors individually scored statements on a scale of -10 (strongly disagree) to +10 (strongly agree). Five of 11 recommendations for physicians and 3/5 recommendations for individuals/families were rated by all the authors as 7 or above (strongly agree) on the first round of rating. Subsequently, a teleconference was held where statements for which there was a lack of strong consensus were revised. RESULTS: After revision, all consensus recommendations received a score of 7 or above. The recommendations focus on administration of as much care as possible at home to keep people with epilepsy out of health care facilities, where they are likely to encounter COVID-19 (including strategies for rescue therapy), as well as minimization of risk of seizure exacerbation through adherence, and through ensuring a regular supply of medication. We also provide helpful links to additional helpful information for people with epilepsy and health providers. CONCLUSION: These recommendations may help health care professionals provide optimal care to people with epilepsy during the coronavirus pandemic.


Subject(s)
Coronavirus Infections/complications , Epilepsy/complications , Epilepsy/virology , Pneumonia, Viral/complications , Betacoronavirus , COVID-19 , Humans , Pandemics , SARS-CoV-2
13.
Sci Rep ; 10(1): 6763, 2020 04 21.
Article in English | MEDLINE | ID: mdl-32317689

ABSTRACT

Modulation of brain activity is one of the main mechanisms capable of demonstrating the synchronization dynamics of neural oscillations. In epilepsy, modulation is a key concept since seizures essentially result from neural hypersynchronization and hyperexcitability. In this study, we have introduced a time-dependent index based on the Kullback-Leibler divergence to quantify the effects of phase and frequency modulations of neural oscillations in neonatal mice exhibiting epileptiform activity induced by Zika virus (ZIKV) infection. Through this index, we demonstrate that fast oscillations (gamma and beta 2) are the more susceptible modulated rhythms in terms of phase, during seizures, whereas slow waves (delta and theta) mainly undergo changes in frequency. The index also allowed detection of specific patterns associated with the interdependent modulation of phase and frequency in neural activity. Furthermore, by comparing ZIKV modulations with the general computational model Epileptors, we verify different signatures related to the brain rhythms modulation in phase and frequency. These findings instigate new studies on the effects of ZIKV infection on neuronal networks from electrophysiological activities, and how different mechanisms can trigger epilepsy.


Subject(s)
Brain Waves/physiology , Epilepsy/physiopathology , Neurons/physiology , Zika Virus Infection/virology , Animals , Beta Rhythm/physiology , Brain/pathology , Brain/virology , Disease Models, Animal , Epilepsy/complications , Epilepsy/virology , Gamma Rhythm/physiology , Humans , Mice , Neurons/virology , Zika Virus/pathogenicity , Zika Virus Infection/complications , Zika Virus Infection/physiopathology
14.
J Infect Chemother ; 26(7): 736-740, 2020 Jul.
Article in English | MEDLINE | ID: mdl-32201195

ABSTRACT

BACKGROUND: Febrile neonates and young infants presenting with seizure require immediate evaluation and treatment. Herein we experienced two young infants with parechovirus-A3 (PeV-A3) encephalitis, initially presented with focal seizure suspecting herpes simplex virus (HSV) encephalitis. CASES: We have experienced 2 infantile cases, initially presented with focal seizure. At presentation, HSV encephalitis was strongly suspected and empiric acyclovir therapy was started; however, serum and/or cerebrospinal fluid (CSF) PCR for HSV were negative. Instead, serum and/or CSF PCR for parechovirus-A was positive. PeV-A3 infection was confirmed by genetic sequence analyses. Both cases required multiple anticonvulsant therapy and intensive care for intractable seizure. Diffusion-weighted imaging of brain magnetic resonance imaging (MRI) showed distinct findings; high-intensity lesions in the gray matter of parietal and occipital lobes in Case 1, and bilateral decreased diffusion of the deep white matter and corpus callosum in Case 2. We have followed two cases more than four years; Case 1 developed epilepsy, has been on an anticonvulsant to control her seizure. Case 2 has significant neurodevelopmental delay, unable to stand or communicate with language. CONCLUSIONS: PeV-A3 encephalitis needs to be in differential diagnosis when neonates and young infants present with focal seizure, mimicking HSV encephalitis. Special attention may be necessary in patients with PeV-A3 encephalitis given it could present with intractable seizure with high morbidity in a long-term.


Subject(s)
Encephalitis, Herpes Simplex/diagnosis , Encephalitis, Viral/diagnosis , Parechovirus/isolation & purification , Picornaviridae Infections/diagnosis , Seizures/virology , Brain/diagnostic imaging , DNA, Viral/isolation & purification , Diagnosis, Differential , Diffusion Magnetic Resonance Imaging , Encephalitis, Herpes Simplex/virology , Encephalitis, Viral/cerebrospinal fluid , Encephalitis, Viral/complications , Encephalitis, Viral/virology , Epilepsy/drug therapy , Epilepsy/virology , Female , Humans , Infant , Infant, Premature , Male , Neurodevelopmental Disorders/virology , Parechovirus/genetics , Picornaviridae Infections/cerebrospinal fluid , Picornaviridae Infections/complications , Picornaviridae Infections/virology , Polymerase Chain Reaction , RNA, Viral/blood , RNA, Viral/cerebrospinal fluid , RNA, Viral/isolation & purification , Seizures/blood , Seizures/cerebrospinal fluid , Seizures/diagnosis , Simplexvirus/genetics , Simplexvirus/isolation & purification
15.
Pan Afr Med J ; 37: 177, 2020.
Article in English | MEDLINE | ID: mdl-33447332

ABSTRACT

The coronavirus 19 (COVID-19) disease, which was declared in China in December 2019, very early on became a pandemic, claiming more than 28 million victims worldwide to date. Its impact on the central nervous system is still poorly understood. The objective of this work is to assess the involvement of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) in the aggravation of seizures in children known to have epilepsy and in the epileptogenesis of children hitherto seizure-free. Prior to conducting this work, we had obtained informed consent from patients and parents. We report the cases of three (3) patients, one known epileptic and the other two apparently healthy, who presented a febrile seizure in a context of COVID-19 infection. The aggravation of the epileptic seizure was indicative of a SARS-CoV-2 infection in the first patient, while the seizure occurred after induction of chloroquine sulfate treatment in the 2 other patients. Although our current concern is to limit the spread of the disease to COVID-19, it is crucial to address its possible complications. Notably, the worsening of seizures in children with epilepsy and the occurrence of first seizures in children without epilepsy following drug treatment. Equipping our COVID-19 patient management facilities with electroencephalogram (EEG) equipment could facilitate continuous electroencephalographic monitoring of children for proper management.


Subject(s)
COVID-19/complications , Chloroquine/adverse effects , Epilepsy/virology , Seizures, Febrile/etiology , Adolescent , COVID-19/diagnosis , Child , Chloroquine/administration & dosage , Electroencephalography , Epilepsy/physiopathology , Humans , Male , Seizures, Febrile/virology , COVID-19 Drug Treatment
16.
BMJ Open ; 9(11): e032275, 2019 11 03.
Article in English | MEDLINE | ID: mdl-31685512

ABSTRACT

OBJECTIVE: With the emergence of Zika virus (ZIKV) disease in Central and South America in the mid-2010s and recognition of the teratogenic effects of congenital exposure to ZIKV, there has been a substantial increase in new research published on ZIKV. Our objective is to synthesise the literature on health outcomes associated with ZIKV infection in humans. METHODS: We conducted a systematic review (SR) of SRs following Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines. We searched MEDLINE, Embase, Cochrane and LILACS (Literatura Latino-Americana e do Caribe em Ciências da Saúde) databases from inception to 22 July 2019, and included SRs that reported ZIKV-associated health outcomes. Three independent reviewers selected eligible studies, extracted data and assessed the quality of included SRs using the AMSTAR 2 (A MeaSurement Tool to Assess Systematic Reviews 2) tool. Conflicts were resolved by consensus or consultation with a third reviewer. RESULTS: The search yielded 1382 unique articles, of which 21 SRs met our inclusion criteria. The 21 SRs ranged from descriptive to quantitative data synthesis, including four meta-analyses. The most commonly reported ZIKV-associated manifestations and health outcomes were microcephaly, congenital abnormalities, brain abnormalities, neonatal death and Guillain-Barré syndrome. The included reviews were highly heterogeneous. The overall quality of the SRs was critically low with all studies having more than one critical weakness. CONCLUSION: The evolving nature of the literature on ZIKV-associated health outcomes, together with the critically low quality of existing SRs, demonstrates the need for high-quality SRs to guide patient care and inform policy decision making. PROSPERO REGISTRATION NUMBER: CRD42018091087.


Subject(s)
Pregnancy Complications, Infectious , Zika Virus Infection/complications , Brain/abnormalities , Coinfection , Congenital Abnormalities/virology , Epilepsy/virology , Female , Guillain-Barre Syndrome/virology , Humans , Infant , Infant Mortality , Microcephaly/virology , Pregnancy , Systematic Reviews as Topic
17.
BMC Neurol ; 19(1): 165, 2019 Jul 17.
Article in English | MEDLINE | ID: mdl-31315594

ABSTRACT

BACKGROUND: Nowadays, few surgery analysis has been reported in cases of epilepsy after viral encephalitis(VE). Herein, this study was to evaluate the efficacy of surgery and capability of stereoelectroencephalography (SEEG) in the definition of the epileptogenic zone (EZ) after VE, and also to explore the relationship between the SEEG features and the surgical outcomes. METHODS: We retrospectively analyzed 10 surgically treated patients that identified to suffer from epilepsy secondary to VE using SEEG, and investigated the SEEG features associated with surgical outcomes in these patients. Besides visual analysis, we used the epileptogenicity index (EI), a semi-quantitative and supplementary tool to evaluate the validity of SEEG in the context of VE. RESULTS: Among the 10 operated patients, 3 of them became completely seizure-free. The patients who got totally seizure free or significant improvement, the seizure onset was located either in the antero-mesial temporal structures or focal gyrus; patients who got worthwhile improvement or no improvement, the seizure started from multiple brain lobes. The number of electrodes classified as epileptogenic visually involved were closely correlated with EI positive onses.Anatomic areas defined and shown as EZ on MRI by visual assessment were also defined as epileptogenic by the EI in these cases. CONCLUSION: Apart from exploring the surgical outcome related to epilepsy after VE, we also bring insight into the relationship between the SEEG features and surgical outcome with the application of the supplementary methods.


Subject(s)
Electroencephalography/methods , Encephalitis, Viral/complications , Epilepsy/surgery , Adolescent , Adult , Child , Child, Preschool , Electrodes , Epilepsy/virology , Female , Humans , Infant , Magnetic Resonance Imaging , Male , Middle Aged , Retrospective Studies , Seizures/surgery , Treatment Outcome , Young Adult
18.
Epilepsy Res ; 153: 34-39, 2019 07.
Article in English | MEDLINE | ID: mdl-30953871

ABSTRACT

Infection with Human Herpesvirus-6 (HHV-6) has been associated with different epilepsy syndromes, including febrile seizures and status epilepticus, acute symptomatic seizures secondary to encephalitis and temporal lobe epilepsy. This neurotropic DNA virus is ubiquitous and primary infection occurs in up to 80% of children by age two years. While two viral variants have been identified, HHV-6B is the one that has been primarily linked to disease in humans, including epilepsy. After initial viremia, the virus can establish chronic latency in brain tissue, peripherally in tonsils and salivary glands and infect several different cell lines by binding to the complement regulator CD-46. In this review we will focus on discussing the evidence linking HHV-6 infection to different epilepsy syndromes and analyzing proposed pathogenic mechanisms.


Subject(s)
Epilepsy/complications , Epilepsy/virology , Herpesvirus 6, Human/pathogenicity , Roseolovirus Infections/complications , Herpesvirus 6, Human/genetics , Humans , Roseolovirus Infections/virology
19.
Epilepsy Behav ; 93: 49-55, 2019 04.
Article in English | MEDLINE | ID: mdl-30831402

ABSTRACT

BACKGROUND: The prevalence and incidence of seizures are substantially higher in patients with human immunodeficiency virus (HIV) compared with the general population and is associated with higher mortality rates. Despite this, the condition remains poorly understood, and there is variation in reported epidemiological studies. The aim of this systematic review and meta-analysis was to investigate the risk factors associated with seizures in the population with HIV, explore the source of variations, and describe management plans that can aid clinicians in the acute and long-term treatment of these patients. METHODS: A structured electronic database search of MEDLINE, EMBASE, and Cochrane Library was conducted. Studies were included if they described clinical details of patients with HIV with seizures or epilepsy. We extracted select variables from each included study, and we estimated pooled estimates of the incidence and prevalence of seizures using random-effects meta-analysis of proportions. RESULTS: Information on 6639 cases of patients with HIV was extracted from 9 included studies. These comprised of 2 studies from the United States of America (USA), 3 from Europe, 3 from Asia, and 1 from Africa. The pooled prevalence and incidence rate of seizures in HIV were 62 per 1000 population and 60 per 1000 population respectively. Among those who presented with new-onset seizures, 63% had seizure recurrence. At the time of first seizure, 82.3% had acquired immunodeficiency syndrome (AIDS). Factors that appeared to be linked to seizures in HIV included advanced HIV disease, opportunistic infections particularly toxoplasmosis, and metabolic derangement. Most seizures were effectively controlled by common antiepileptic drugs (AEDs). CONCLUSIONS: The prevalence and incidence of seizures and epilepsy in the population with HIV are substantially higher than the general population. Our results suggest that advanced HIV and opportunistic infections are associated with the majority of the seizures. Early initiation of highly active antiretroviral therapy (HAART), prophylactic use of cotrimoxazole (trimethoprim-sulfamethoxazole) and routine electroencephalogram (EEG) in patients with HIV may reduce seizure incidence and frequency and help in early diagnosis of nonconvulsive seizures in this population. We recommend long-term seizure management with AED, and for patients on HAART, enzyme-inducing AED should be avoided when possible.


Subject(s)
Epilepsy/etiology , HIV Infections/complications , Seizures/etiology , Epilepsy/epidemiology , Epilepsy/virology , Global Health , Humans , Incidence , Prevalence , Risk Factors , Seizures/epidemiology , Seizures/virology
20.
Mol Neurobiol ; 56(3): 1897-1907, 2019 Mar.
Article in English | MEDLINE | ID: mdl-29978423

ABSTRACT

Experimental and clinical findings suggest a crucial role for inflammation in the onset of pediatric seizures; this mechanism is not targeted by conventional antiepileptic drugs and may contribute to refractory epilepsy. Several triggers, including infection with neurotropic viruses such as human herpesvirus 6 (HHV-6), other herpesviruses, and picornaviruses, appear to induce activation of the innate and adaptive immune systems, which results in several neuroinflammatory responses, leading to enhanced neuronal excitability, and ultimately contributing to epileptogenesis. This review discusses the proposed mechanisms by which infection with herpesviruses, and particularly with HHV-6, and ensuing inflammation may lead to seizure generation, and later development of epilepsy. We also examine the evidence that links herpesvirus and picornavirus infections with acute seizures and chronic forms of epilepsy. Understanding the mechanisms by which specific viruses may trigger a cascade of alterations in the CNS ultimately leading to epilepsy appears critical for the development of therapeutic agents that may target the virus or inflammatory mechanisms early and prevent progression of epileptogenesis.


Subject(s)
Epilepsy/etiology , Inflammation/complications , Virus Diseases/complications , Epilepsy/pathology , Epilepsy/virology , Humans
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