Long-Term Neurologic and Neurocognitive Sequelae Following Pediatric Ebola Virus in Liberia

Overview

Background: Ebola virus disease (EVD) causes fever, vomiting, and diarrhea, and may cause internal bleeding. It is often fatal. EVD may also damage the brain and nervous system. It can cause headaches, tremors, weakness, and other problems. These issues can continue for years after people recover from EVD infection. Researchers want to understand more about how EVD may have affected the brains of people who contracted the disease as children. Objective: To learn more about the long-term effects of EVD on the brain and nervous system in people who had the disease as children. Eligibility: People who were less than 18 years old when they took part in a previous study called the PREVAIL III Natural History of Ebola study. They can be either a survivor of EVD or a close contact. A close contact is someone who had a relationship with a person who survived EVD but never had the disease themself. Design: Participants will have 1 clinic visit. They will undergo several tasks: They will have an exam of their nervous system performed by a neurologist. They will do physical tasks and answer questions about any problems or symptoms since they had EVD. They may have blood drawn. They will have tests of their memory, attention, and thinking skills. For one test, participants will answer questions and solve puzzles using pencil and paper. For another test, they will play 4 different games on an iPad. They will have an interview. A researcher will ask questions about their mood and other symptoms that may affect their brain and nervous system; their past medical diagnoses, symptoms, and experiences; and how they are doing at home, school, or work.

Study Description: The long-term neurological sequelae of Ebola virus disease (EVD) are not well-described, particularly in survivors infected during pediatric age. The 2015 west Africa EVD epidemic had dramatic effect on adults and children and by one year following infection, concerns for neurologic sequelae became apparent. The PREVAIL III (PIII) Ebola Natural History Study in Monrovia, Liberia had a number of substudies, including both an adult Neurology and pediatric Neurology Substudy which were undertaken to better understand the long-term neurologic sequelae of EVD. The adult Neurology Substudy had over five years of follow up visits whereas the original Pediatric Neurology Substudy cohort was composed of a small sample of children seen in 2015 one time under PIII with no subsequent follow ups. Although this pediatric cohort was small, pilot data from this assessment revealed lower cognitive scores in the pediatric EVD survivors compared to controls, as well as worse executive function scores, more complaints of neuropsychiatric symptoms, and worse disability on modified Rankin Scale, among other findings. PIII subsequently closed out between 2020 and 2021. Here we propose a new protocol to observe and study the neurologic and neurocognitive sequelae following Ebola virus exposure at an age below 18. We propose conducting a single in-person neurologic visit including neurologic exam, neurocognitive assessment, and neurologic history and symptom questionnaire to be given to participants at greater than 5-years following exposure. We also plan to do a single blood draw at time of visit to assess for Ebola Virus antibody titers in survivors and close contacts (controls). The participants included in this study will include Ebola survivors and close contacts (controls) that were enrolled in PIII at age less than 18. We hypothesize that some pediatric Ebola survivors will have longterm neurologic sequelae at greater than 5 years post exposure that may be subtle in nature. Included in this study will be one embedded substudy. Longitudinal Pediatric Neuro EVD Substudy: We propose to see the original small cohort of pediatric participants seen in 2015 for a second visit as a longitudinal sub study. In evaluating our longitudinal cohort, we expect that some of the sequelae noted during their initial evaluation may have improved over time, but these survivors still may have persistent neurological sequelae even after over 5 years convalescence from EVD. Objectives: Primary Objective: 1. Pediatric EVD Neuro Follow up Study: To observe and describe the range of neurologic and neurocognitive findings that are present in EVD survivors at greater than 5 years following infection as compared to controls. 2. Longitudinal Pediatric Neuro EVD Substudy (Subset of population): To compare neurologic and neurocognitive findings found in EVD survivors and controls at greater than 5 years following infection to that of the same participants at first visit about 1 year post infection. Secondary Objectives 1. Pediatric EVD Neuro Follow up Study: To characterize serum Zaire Ebola virus (EBOV) specific antibodies in pediatric EVD survivors at greater than 5 years following infection compared to that of controls. 2. Longitudinal Pediatric Neuro EVD Substudy: To characterize serum EBOV specific antibodies in pediatric EVD survivors at greater than 5 years following infection to that of the same participant at first visit about 1 year post infection. Exploratory Objective: Pediatric EVD Neuro Follow up Study 1. To compare EBOV specific antibodies in pediatric EVD survivors with and without neurologic and neurocognitive sequelae. 2. To compare neurologic and neurocognitive findings in pediatric EVD survivors and controls at greater than 5 years post infection to that of adult participants from the PIII adult Neurology sub study. 3. To explore the presence of other serologic markers in pediatric EVD survivors compared to close-contacts (control). Outcomes: Primary Endpoint: 1. Pediatric EVD Neuro Follow up Study: In comparison of EVD survivors at greater than 5 years following infection with close contacts (controls), the prevalence of: * neurological symptoms (as asked on neurologic symptom questionnaire CRF) * physical disability (as assessed through MRS score) * executive function dysfunction (as assessed through executive function assessment questions) * neuropsychiatric symptoms (as indicated on neuropsychiatric symptom portion of CRF) * neurologic exam abnormalities (as found on full neurologic physical exam performed by licensed neurologist during visit) * neurocognitive deficits (as determined by cognitive exam scores on NIH Toolbox exam and ICA-P assessment) 2. Longitudinal Pediatric Neuro EVD Substudy: In comparison of EVD survivors at greater than 5 years following infection to that at first visit about 1 year after infection, the change in: * number of neurological symptoms (as asked on neurologic symptom questionnaire CRF) * Physical disability (as assessed through MRS score) * Executive function dysfunction (as assessed through executive function assessment questions). * number of neuropsychiatric symptoms (as indicated on neuropsychiatric symptom portion of CRF. * persistence of neurologic exam abnormalities (as found on full neurologic physical exam performed by licensed neurologist during visit). * neurocognitive deficits (as determined by cognitive exam scores on NIH Toolbox exam and ICA-P assessment). Secondary Endpoints: 1. Pediatric EVD Neuro Follow up Study: The degree of antibody response in pediatric EVD survivors at greater than 5 years following infection compared to that of close contacts (controls). 2. Longitudinal Pediatric Neuro EVD Substudy: The degree of antibody response in pediatric EVD survivors at greater than 5 years following infection compared to that at about 1 year following infection. Exploratory Endpoints: Pediatric EVD Neuro Follow up Study: 1. In EVD survivors at greater than 5 years post infection, the correlation between serum EBOV specific antibody presence and: * presence of neurological symptoms (as asked on neurologic symptom questionnaire CRF). * presence of physical disability (as assessed through MRS score). * presence of executive function dysfunction (as assessed through executive function assessment questions) * presence of neuropsychiatric symptoms (as indicated on neuropsychiatric symptom portion of CRF) * presence of neurologic exam abnormalities (as found on full neurologic physical exam performed by licensed neurologist during visit). * presence of neurocognitive deficits (as determined by cognitive exam scores on NIH Toolbox exam) 2. In pediatric versus adult EVD survivors at greater than 5 years following infection, the prevalence of: * neurological symptoms (as asked on neurologic symptom questionnaire CRF). * physical disability (as assessed through MRS score) * neuropsychiatric symptoms (as indicated on neuropsychiatric symptom portion of CRF) * neurologic exam abnormalities (as found on full neurologic physical exam performed by licensed neurologist during visit) * neurocognitive deficits (as determined by cognitive exam scores on NIH Toolbox exam). 3. The profile of serologic immune markers in pediatric EVD survivors at greater than 5 years following infection.