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Impairment of executive function in Kenyan children exposed to severe falciparum malaria with neurological involvement
BACKGROUND: Persistent neurocognitive impairments occur in a fifth of children hospitalized with severe falciparum malaria. There is little data on the association between different neurological phenotypes of severe malaria (seizures, impaired consciousness and prostration) and impairments in execut...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4171581/ https://www.ncbi.nlm.nih.gov/pubmed/25224247 http://dx.doi.org/10.1186/1475-2875-13-365 |
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author | Kariuki, Symon M Abubakar, Amina Newton, Charles RJC Kihara, Michael |
author_facet | Kariuki, Symon M Abubakar, Amina Newton, Charles RJC Kihara, Michael |
author_sort | Kariuki, Symon M |
collection | PubMed |
description | BACKGROUND: Persistent neurocognitive impairments occur in a fifth of children hospitalized with severe falciparum malaria. There is little data on the association between different neurological phenotypes of severe malaria (seizures, impaired consciousness and prostration) and impairments in executive function. METHODS: Executive functioning of children exposed to severe malaria with different neurological phenotypes (N = 58) and in those unexposed (N = 56) was examined using neuropsychological tests such as vigilance test, test for everyday attention test for children (TEA-Ch), contingency naming test (CNT) and self-ordered pointing test (SOPT). Linear regression was used to determine the association between neurological phenotypes of severe malaria and executive function performance scores, accounting for potential confounders. RESULTS: Children with complex seizures in severe malaria performed more poorly than unexposed controls in the vigilance (median efficiency scores (interquartile range) = 4.84 (1.28-5.68) vs. 5.84 (4.71-6.42), P = 0.030) and SOPT (mean errors (standard deviation) = 29.50 (8.82) vs. 24.80 (6.50), P = 0.029) tests, but no differences were observed in TEA-Ch and CNT tests. Performance scores for other neurological phenotypes of severe malaria were similar with those of unexposed controls. After accounting for potential confounders, such as child’s age, sex, schooling; maternal age, schooling and economic activity; perinatal factors and history of seizures, complex seizures remained associated with efficiency scores in the vigilance test (beta coefficient (β) (95% confidence interval (CI)) = -0.40 (-0.67, -0.13), P = 0.006) and everyday attention scores of the TEA-Ch test (β (95% CI) = -0.57 (-1.04, -0.10), P = 0.019); the association with SOPT error scores was weak (β (95% CI) = 4.57 (-0.73-9.89), P = 0.089). Combined neurological phenotypes were not significantly associated with executive function performance scores. CONCLUSION: Executive function impairment in children with severe malaria is associated with specific neurological phenotypes, particularly complex seizures. Effective prophylaxis and management of malaria-associated acute seizures may improve executive functioning performance scores of children. |
format | Online Article Text |
id | pubmed-4171581 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41715812014-09-24 Impairment of executive function in Kenyan children exposed to severe falciparum malaria with neurological involvement Kariuki, Symon M Abubakar, Amina Newton, Charles RJC Kihara, Michael Malar J Research BACKGROUND: Persistent neurocognitive impairments occur in a fifth of children hospitalized with severe falciparum malaria. There is little data on the association between different neurological phenotypes of severe malaria (seizures, impaired consciousness and prostration) and impairments in executive function. METHODS: Executive functioning of children exposed to severe malaria with different neurological phenotypes (N = 58) and in those unexposed (N = 56) was examined using neuropsychological tests such as vigilance test, test for everyday attention test for children (TEA-Ch), contingency naming test (CNT) and self-ordered pointing test (SOPT). Linear regression was used to determine the association between neurological phenotypes of severe malaria and executive function performance scores, accounting for potential confounders. RESULTS: Children with complex seizures in severe malaria performed more poorly than unexposed controls in the vigilance (median efficiency scores (interquartile range) = 4.84 (1.28-5.68) vs. 5.84 (4.71-6.42), P = 0.030) and SOPT (mean errors (standard deviation) = 29.50 (8.82) vs. 24.80 (6.50), P = 0.029) tests, but no differences were observed in TEA-Ch and CNT tests. Performance scores for other neurological phenotypes of severe malaria were similar with those of unexposed controls. After accounting for potential confounders, such as child’s age, sex, schooling; maternal age, schooling and economic activity; perinatal factors and history of seizures, complex seizures remained associated with efficiency scores in the vigilance test (beta coefficient (β) (95% confidence interval (CI)) = -0.40 (-0.67, -0.13), P = 0.006) and everyday attention scores of the TEA-Ch test (β (95% CI) = -0.57 (-1.04, -0.10), P = 0.019); the association with SOPT error scores was weak (β (95% CI) = 4.57 (-0.73-9.89), P = 0.089). Combined neurological phenotypes were not significantly associated with executive function performance scores. CONCLUSION: Executive function impairment in children with severe malaria is associated with specific neurological phenotypes, particularly complex seizures. Effective prophylaxis and management of malaria-associated acute seizures may improve executive functioning performance scores of children. BioMed Central 2014-09-16 /pmc/articles/PMC4171581/ /pubmed/25224247 http://dx.doi.org/10.1186/1475-2875-13-365 Text en © Kariuki et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Kariuki, Symon M Abubakar, Amina Newton, Charles RJC Kihara, Michael Impairment of executive function in Kenyan children exposed to severe falciparum malaria with neurological involvement |
title | Impairment of executive function in Kenyan children exposed to severe falciparum malaria with neurological involvement |
title_full | Impairment of executive function in Kenyan children exposed to severe falciparum malaria with neurological involvement |
title_fullStr | Impairment of executive function in Kenyan children exposed to severe falciparum malaria with neurological involvement |
title_full_unstemmed | Impairment of executive function in Kenyan children exposed to severe falciparum malaria with neurological involvement |
title_short | Impairment of executive function in Kenyan children exposed to severe falciparum malaria with neurological involvement |
title_sort | impairment of executive function in kenyan children exposed to severe falciparum malaria with neurological involvement |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4171581/ https://www.ncbi.nlm.nih.gov/pubmed/25224247 http://dx.doi.org/10.1186/1475-2875-13-365 |
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