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Association of patent foramen ovale with epilepsy: A hospital‐based case–control study

OBJECTIVE: This study aimed to investigate the proportion of patent foramen ovale (PFO) in people with epilepsy (PWE) compared to controls without epilepsy and to assess whether PWEs with and without PFO exhibit distinctive clinical features. METHODS: This is a case–control study conducted in a hosp...

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Detalles Bibliográficos
Autores principales: Tang, Yusha, Ji, Shuming, Li, Hua, Dong, Bosi, Li, Yajiao, Zhu, Chenxing, Chen, Lei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10472407/
https://www.ncbi.nlm.nih.gov/pubmed/37422851
http://dx.doi.org/10.1002/epi4.12787
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author Tang, Yusha
Ji, Shuming
Li, Hua
Dong, Bosi
Li, Yajiao
Zhu, Chenxing
Chen, Lei
author_facet Tang, Yusha
Ji, Shuming
Li, Hua
Dong, Bosi
Li, Yajiao
Zhu, Chenxing
Chen, Lei
author_sort Tang, Yusha
collection PubMed
description OBJECTIVE: This study aimed to investigate the proportion of patent foramen ovale (PFO) in people with epilepsy (PWE) compared to controls without epilepsy and to assess whether PWEs with and without PFO exhibit distinctive clinical features. METHODS: This is a case–control study conducted in a hospital. Contrast transthoracic echocardiography with a venous microbubble bolus and provocative maneuvers (Valsalva and coughing) were used to identify PFO and its right‐to‐left shunt (RLS) among 741 PWEs and 800 controls without epilepsy. The risk of having PFO in PWEs was explored using multiple matching methods and logistic regression with adjusted congenital factors that may affect the occurrence of PFO. RESULTS: The proportion of PFO in PWEs and controls was 39.00% and 24.25%, respectively. After 1:1 propensity score matching, the risk of suffering PFO in PWEs was 1.71 times (OR, 1.71; 95% CI, 1.24–2.36) higher than that in controls. PWEs also had a higher risk of having a high RLS grade (β (epilepsy) = 0.390, P < 0.001). Among clinical characteristics of PWEs, migraine, and drug‐resistant epilepsy showed significantly different distributions between those without RLS and those with RLS grade I to III. PWEs with PFO had higher risk of suffering from migraine and drug‐resistant epilepsy (OR in migraine, 2.54, 95% CI, 1.65–3.95; OR in drug‐resistant epilepsy, 1.47, 95% CI, 1.06–2.03). SIGNIFICANCE: The proportion of PFO was found to be higher in PWE than in controls without epilepsy, especially in patients with drug‐resistant epilepsy, suggesting potential relationship between the two disorders. Large multicentric study will be needed to confirm this finding.
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spelling pubmed-104724072023-09-02 Association of patent foramen ovale with epilepsy: A hospital‐based case–control study Tang, Yusha Ji, Shuming Li, Hua Dong, Bosi Li, Yajiao Zhu, Chenxing Chen, Lei Epilepsia Open Original Articles OBJECTIVE: This study aimed to investigate the proportion of patent foramen ovale (PFO) in people with epilepsy (PWE) compared to controls without epilepsy and to assess whether PWEs with and without PFO exhibit distinctive clinical features. METHODS: This is a case–control study conducted in a hospital. Contrast transthoracic echocardiography with a venous microbubble bolus and provocative maneuvers (Valsalva and coughing) were used to identify PFO and its right‐to‐left shunt (RLS) among 741 PWEs and 800 controls without epilepsy. The risk of having PFO in PWEs was explored using multiple matching methods and logistic regression with adjusted congenital factors that may affect the occurrence of PFO. RESULTS: The proportion of PFO in PWEs and controls was 39.00% and 24.25%, respectively. After 1:1 propensity score matching, the risk of suffering PFO in PWEs was 1.71 times (OR, 1.71; 95% CI, 1.24–2.36) higher than that in controls. PWEs also had a higher risk of having a high RLS grade (β (epilepsy) = 0.390, P < 0.001). Among clinical characteristics of PWEs, migraine, and drug‐resistant epilepsy showed significantly different distributions between those without RLS and those with RLS grade I to III. PWEs with PFO had higher risk of suffering from migraine and drug‐resistant epilepsy (OR in migraine, 2.54, 95% CI, 1.65–3.95; OR in drug‐resistant epilepsy, 1.47, 95% CI, 1.06–2.03). SIGNIFICANCE: The proportion of PFO was found to be higher in PWE than in controls without epilepsy, especially in patients with drug‐resistant epilepsy, suggesting potential relationship between the two disorders. Large multicentric study will be needed to confirm this finding. John Wiley and Sons Inc. 2023-07-16 /pmc/articles/PMC10472407/ /pubmed/37422851 http://dx.doi.org/10.1002/epi4.12787 Text en © 2023 The Authors. Epilepsia Open published by Wiley Periodicals LLC on behalf of International League Against Epilepsy. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Tang, Yusha
Ji, Shuming
Li, Hua
Dong, Bosi
Li, Yajiao
Zhu, Chenxing
Chen, Lei
Association of patent foramen ovale with epilepsy: A hospital‐based case–control study
title Association of patent foramen ovale with epilepsy: A hospital‐based case–control study
title_full Association of patent foramen ovale with epilepsy: A hospital‐based case–control study
title_fullStr Association of patent foramen ovale with epilepsy: A hospital‐based case–control study
title_full_unstemmed Association of patent foramen ovale with epilepsy: A hospital‐based case–control study
title_short Association of patent foramen ovale with epilepsy: A hospital‐based case–control study
title_sort association of patent foramen ovale with epilepsy: a hospital‐based case–control study
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10472407/
https://www.ncbi.nlm.nih.gov/pubmed/37422851
http://dx.doi.org/10.1002/epi4.12787
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