Cargando…
The Neurocognitive and MRI Outcomes of West Nile Virus Infection: Preliminary Analysis Using an External Control Group
To understand the long-term neurological outcomes resultant of West Nile virus (WNV) infection, participants from a previously established, prospective WNV cohort were invited to take part in a comprehensive neurologic and neurocognitive examination. Those with an abnormal exam finding were invited...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5880927/ https://www.ncbi.nlm.nih.gov/pubmed/29636722 http://dx.doi.org/10.3389/fneur.2018.00111 |
_version_ | 1783311228038283264 |
---|---|
author | Murray, Kristy O. Nolan, Melissa S. Ronca, Shannon E. Datta, Sushmita Govindarajan, Koushik Narayana, Ponnada A. Salazar, Lucrecia Woods, Steven P. Hasbun, Rodrigo |
author_facet | Murray, Kristy O. Nolan, Melissa S. Ronca, Shannon E. Datta, Sushmita Govindarajan, Koushik Narayana, Ponnada A. Salazar, Lucrecia Woods, Steven P. Hasbun, Rodrigo |
author_sort | Murray, Kristy O. |
collection | PubMed |
description | To understand the long-term neurological outcomes resultant of West Nile virus (WNV) infection, participants from a previously established, prospective WNV cohort were invited to take part in a comprehensive neurologic and neurocognitive examination. Those with an abnormal exam finding were invited for MRI to evaluate cortical thinning and regional brain atrophy following infection. Correlations of presenting clinical syndrome with neurologic and neurocognitive dysfunctions were evaluated, as well as correlations of neurocognitive outcomes with MRI results. From 2002 to 2012, a total of 262 participants with a history of WNV infection were enrolled as research participants in a longitudinal cohort study, and 117 completed comprehensive neurologic and neurocognitive evaluations. Abnormal neurological exam findings were identified in 49% (57/117) of participants, with most abnormalities being unilateral. The most common abnormalities included decreased strength (26%; 30/117), abnormal reflexes (14%; 16/117), and tremors (10%; 12/117). Weakness and decreased reflexes were consistent with lower motor neuron damage in a significant proportion of patients. We observed a 22% overall rate of impairment on the Repeatable Battery for the Assessment of Neuropsychological Status (RBANS), with impairments observed in immediate (31%) and delayed memory (25%). On MRI, participants showed significant cortical thinning as compared to age- and gender-matched controls in both hemispheres, with affected regions primarily occurring in the frontal and limbic cortices. Regional atrophy occurred in the cerebellum, brain stem, thalamus, putamen, and globus pallidus. This study provides valuable new information regarding the neurological outcomes following WNV infection, with MRI evidence of significant cortical thinning and regional atrophy; however, it is important to note that the results may include systemic bias due to the external control group. Considering no effective treatment measures are available, strategies to prevent infection are key. |
format | Online Article Text |
id | pubmed-5880927 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-58809272018-04-10 The Neurocognitive and MRI Outcomes of West Nile Virus Infection: Preliminary Analysis Using an External Control Group Murray, Kristy O. Nolan, Melissa S. Ronca, Shannon E. Datta, Sushmita Govindarajan, Koushik Narayana, Ponnada A. Salazar, Lucrecia Woods, Steven P. Hasbun, Rodrigo Front Neurol Neuroscience To understand the long-term neurological outcomes resultant of West Nile virus (WNV) infection, participants from a previously established, prospective WNV cohort were invited to take part in a comprehensive neurologic and neurocognitive examination. Those with an abnormal exam finding were invited for MRI to evaluate cortical thinning and regional brain atrophy following infection. Correlations of presenting clinical syndrome with neurologic and neurocognitive dysfunctions were evaluated, as well as correlations of neurocognitive outcomes with MRI results. From 2002 to 2012, a total of 262 participants with a history of WNV infection were enrolled as research participants in a longitudinal cohort study, and 117 completed comprehensive neurologic and neurocognitive evaluations. Abnormal neurological exam findings were identified in 49% (57/117) of participants, with most abnormalities being unilateral. The most common abnormalities included decreased strength (26%; 30/117), abnormal reflexes (14%; 16/117), and tremors (10%; 12/117). Weakness and decreased reflexes were consistent with lower motor neuron damage in a significant proportion of patients. We observed a 22% overall rate of impairment on the Repeatable Battery for the Assessment of Neuropsychological Status (RBANS), with impairments observed in immediate (31%) and delayed memory (25%). On MRI, participants showed significant cortical thinning as compared to age- and gender-matched controls in both hemispheres, with affected regions primarily occurring in the frontal and limbic cortices. Regional atrophy occurred in the cerebellum, brain stem, thalamus, putamen, and globus pallidus. This study provides valuable new information regarding the neurological outcomes following WNV infection, with MRI evidence of significant cortical thinning and regional atrophy; however, it is important to note that the results may include systemic bias due to the external control group. Considering no effective treatment measures are available, strategies to prevent infection are key. Frontiers Media S.A. 2018-03-27 /pmc/articles/PMC5880927/ /pubmed/29636722 http://dx.doi.org/10.3389/fneur.2018.00111 Text en Copyright © 2018 Murray, Nolan, Ronca, Datta, Govindarajan, Narayana, Salazar, Woods and Hasbun. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Murray, Kristy O. Nolan, Melissa S. Ronca, Shannon E. Datta, Sushmita Govindarajan, Koushik Narayana, Ponnada A. Salazar, Lucrecia Woods, Steven P. Hasbun, Rodrigo The Neurocognitive and MRI Outcomes of West Nile Virus Infection: Preliminary Analysis Using an External Control Group |
title | The Neurocognitive and MRI Outcomes of West Nile Virus Infection: Preliminary Analysis Using an External Control Group |
title_full | The Neurocognitive and MRI Outcomes of West Nile Virus Infection: Preliminary Analysis Using an External Control Group |
title_fullStr | The Neurocognitive and MRI Outcomes of West Nile Virus Infection: Preliminary Analysis Using an External Control Group |
title_full_unstemmed | The Neurocognitive and MRI Outcomes of West Nile Virus Infection: Preliminary Analysis Using an External Control Group |
title_short | The Neurocognitive and MRI Outcomes of West Nile Virus Infection: Preliminary Analysis Using an External Control Group |
title_sort | neurocognitive and mri outcomes of west nile virus infection: preliminary analysis using an external control group |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5880927/ https://www.ncbi.nlm.nih.gov/pubmed/29636722 http://dx.doi.org/10.3389/fneur.2018.00111 |
work_keys_str_mv | AT murraykristyo theneurocognitiveandmrioutcomesofwestnilevirusinfectionpreliminaryanalysisusinganexternalcontrolgroup AT nolanmelissas theneurocognitiveandmrioutcomesofwestnilevirusinfectionpreliminaryanalysisusinganexternalcontrolgroup AT roncashannone theneurocognitiveandmrioutcomesofwestnilevirusinfectionpreliminaryanalysisusinganexternalcontrolgroup AT dattasushmita theneurocognitiveandmrioutcomesofwestnilevirusinfectionpreliminaryanalysisusinganexternalcontrolgroup AT govindarajankoushik theneurocognitiveandmrioutcomesofwestnilevirusinfectionpreliminaryanalysisusinganexternalcontrolgroup AT narayanaponnadaa theneurocognitiveandmrioutcomesofwestnilevirusinfectionpreliminaryanalysisusinganexternalcontrolgroup AT salazarlucrecia theneurocognitiveandmrioutcomesofwestnilevirusinfectionpreliminaryanalysisusinganexternalcontrolgroup AT woodsstevenp theneurocognitiveandmrioutcomesofwestnilevirusinfectionpreliminaryanalysisusinganexternalcontrolgroup AT hasbunrodrigo theneurocognitiveandmrioutcomesofwestnilevirusinfectionpreliminaryanalysisusinganexternalcontrolgroup AT murraykristyo neurocognitiveandmrioutcomesofwestnilevirusinfectionpreliminaryanalysisusinganexternalcontrolgroup AT nolanmelissas neurocognitiveandmrioutcomesofwestnilevirusinfectionpreliminaryanalysisusinganexternalcontrolgroup AT roncashannone neurocognitiveandmrioutcomesofwestnilevirusinfectionpreliminaryanalysisusinganexternalcontrolgroup AT dattasushmita neurocognitiveandmrioutcomesofwestnilevirusinfectionpreliminaryanalysisusinganexternalcontrolgroup AT govindarajankoushik neurocognitiveandmrioutcomesofwestnilevirusinfectionpreliminaryanalysisusinganexternalcontrolgroup AT narayanaponnadaa neurocognitiveandmrioutcomesofwestnilevirusinfectionpreliminaryanalysisusinganexternalcontrolgroup AT salazarlucrecia neurocognitiveandmrioutcomesofwestnilevirusinfectionpreliminaryanalysisusinganexternalcontrolgroup AT woodsstevenp neurocognitiveandmrioutcomesofwestnilevirusinfectionpreliminaryanalysisusinganexternalcontrolgroup AT hasbunrodrigo neurocognitiveandmrioutcomesofwestnilevirusinfectionpreliminaryanalysisusinganexternalcontrolgroup |