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Obsessive-Compulsive Symptoms and Their Impacts on Psychosocial Functioning in People with Epilepsy

BACKGROUND AND PURPOSE: Obsessive-compulsive symptoms (OCS) in people with epilepsy (PWE) have not been studied systematically. We evaluated the severity, predictors, and psychosocial impact of OCS in PWE. METHODS: We recruited PWE who visited our epilepsy clinic and age-, gender-, and education-mat...

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Autores principales: Seo, Ji-Hye, Lee, Won-Kee, Park, Sung-Pa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Neurological Association 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4017015/
https://www.ncbi.nlm.nih.gov/pubmed/24829598
http://dx.doi.org/10.3988/jcn.2014.10.2.125
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author Seo, Ji-Hye
Lee, Won-Kee
Park, Sung-Pa
author_facet Seo, Ji-Hye
Lee, Won-Kee
Park, Sung-Pa
author_sort Seo, Ji-Hye
collection PubMed
description BACKGROUND AND PURPOSE: Obsessive-compulsive symptoms (OCS) in people with epilepsy (PWE) have not been studied systematically. We evaluated the severity, predictors, and psychosocial impact of OCS in PWE. METHODS: We recruited PWE who visited our epilepsy clinic and age-, gender-, and education-matched healthy controls. Both PWE and healthy controls completed the Maudsley Obsessional-Compulsive Inventory (MOCI), which measures OCS. PWE also completed the Beck Depression Inventory (BDI) and the Quality of Life in Epilepsy Inventory-31 (QOLIE-31). We examined the severity of OCS in PWE relative to healthy controls. Predictors of OCS and the QOLIE-31 score were measured by regression analyses. A path analysis model was constructed to verify interrelations between the variables. RESULTS: The MOCI total score was significantly higher in PWE than in healthy controls (p=0.002). OCS were found in 20% of eligible patients. The strongest predictor of the MOCI total score was the BDI score (β=0.417, p<0.001), followed by EEG abnormality (β=0.194, p<0.001) and etiology (β=0.107, p=0.031). Epileptic syndrome, the side of the epileptic focus, and action mechanisms of antiepileptic drugs did not affect the MOCI total score. The strongest predictor of the QOLIE-31 overall score was the BDI score (β=-0.569, p<0.001), followed by seizure control (β=-0.163, p<0.001) and the MOCI total score (β=-0.148, p=0.001). The MOCI total score directly affected the QOLIE-31 overall score and also exerted indirect effects on the QOLIE-31 overall score through seizure control and the BDI score. CONCLUSIONS: OCS are more likely to develop in PWE than in healthy people. The development of OCS appears to elicit psychosocial problems directly or indirectly by provoking depression or uncontrolled seizures.
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spelling pubmed-40170152014-05-14 Obsessive-Compulsive Symptoms and Their Impacts on Psychosocial Functioning in People with Epilepsy Seo, Ji-Hye Lee, Won-Kee Park, Sung-Pa J Clin Neurol Original Article BACKGROUND AND PURPOSE: Obsessive-compulsive symptoms (OCS) in people with epilepsy (PWE) have not been studied systematically. We evaluated the severity, predictors, and psychosocial impact of OCS in PWE. METHODS: We recruited PWE who visited our epilepsy clinic and age-, gender-, and education-matched healthy controls. Both PWE and healthy controls completed the Maudsley Obsessional-Compulsive Inventory (MOCI), which measures OCS. PWE also completed the Beck Depression Inventory (BDI) and the Quality of Life in Epilepsy Inventory-31 (QOLIE-31). We examined the severity of OCS in PWE relative to healthy controls. Predictors of OCS and the QOLIE-31 score were measured by regression analyses. A path analysis model was constructed to verify interrelations between the variables. RESULTS: The MOCI total score was significantly higher in PWE than in healthy controls (p=0.002). OCS were found in 20% of eligible patients. The strongest predictor of the MOCI total score was the BDI score (β=0.417, p<0.001), followed by EEG abnormality (β=0.194, p<0.001) and etiology (β=0.107, p=0.031). Epileptic syndrome, the side of the epileptic focus, and action mechanisms of antiepileptic drugs did not affect the MOCI total score. The strongest predictor of the QOLIE-31 overall score was the BDI score (β=-0.569, p<0.001), followed by seizure control (β=-0.163, p<0.001) and the MOCI total score (β=-0.148, p=0.001). The MOCI total score directly affected the QOLIE-31 overall score and also exerted indirect effects on the QOLIE-31 overall score through seizure control and the BDI score. CONCLUSIONS: OCS are more likely to develop in PWE than in healthy people. The development of OCS appears to elicit psychosocial problems directly or indirectly by provoking depression or uncontrolled seizures. Korean Neurological Association 2014-04 2014-04-23 /pmc/articles/PMC4017015/ /pubmed/24829598 http://dx.doi.org/10.3988/jcn.2014.10.2.125 Text en Copyright © 2014 Korean Neurological Association http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Seo, Ji-Hye
Lee, Won-Kee
Park, Sung-Pa
Obsessive-Compulsive Symptoms and Their Impacts on Psychosocial Functioning in People with Epilepsy
title Obsessive-Compulsive Symptoms and Their Impacts on Psychosocial Functioning in People with Epilepsy
title_full Obsessive-Compulsive Symptoms and Their Impacts on Psychosocial Functioning in People with Epilepsy
title_fullStr Obsessive-Compulsive Symptoms and Their Impacts on Psychosocial Functioning in People with Epilepsy
title_full_unstemmed Obsessive-Compulsive Symptoms and Their Impacts on Psychosocial Functioning in People with Epilepsy
title_short Obsessive-Compulsive Symptoms and Their Impacts on Psychosocial Functioning in People with Epilepsy
title_sort obsessive-compulsive symptoms and their impacts on psychosocial functioning in people with epilepsy
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4017015/
https://www.ncbi.nlm.nih.gov/pubmed/24829598
http://dx.doi.org/10.3988/jcn.2014.10.2.125
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