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Topiramate is more effective than acetazolamide at lowering intracranial pressure

BACKGROUND: The management of idiopathic intracranial hypertension focuses on reducing intracranial pressure to preserve vision and reduce headaches. There is sparse evidence to support the use of some of the drugs commonly used to manage idiopathic intracranial hypertension, therefore we propose to...

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Autores principales: Scotton, William J, Botfield, Hannah F, Westgate, Connar SJ, Mitchell, James L, Yiangou, Andreas, Uldall, Maria S, Jensen, Rigmor H, Sinclair, Alex J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6376637/
https://www.ncbi.nlm.nih.gov/pubmed/29898611
http://dx.doi.org/10.1177/0333102418776455
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author Scotton, William J
Botfield, Hannah F
Westgate, Connar SJ
Mitchell, James L
Yiangou, Andreas
Uldall, Maria S
Jensen, Rigmor H
Sinclair, Alex J
author_facet Scotton, William J
Botfield, Hannah F
Westgate, Connar SJ
Mitchell, James L
Yiangou, Andreas
Uldall, Maria S
Jensen, Rigmor H
Sinclair, Alex J
author_sort Scotton, William J
collection PubMed
description BACKGROUND: The management of idiopathic intracranial hypertension focuses on reducing intracranial pressure to preserve vision and reduce headaches. There is sparse evidence to support the use of some of the drugs commonly used to manage idiopathic intracranial hypertension, therefore we propose to evaluate the efficacy of these drugs at lowering intracranial pressure in healthy rats. METHODS: We measured intracranial pressure in female rats before and after subcutaneous administration of acetazolamide, topiramate, furosemide, amiloride and octreotide at clinical doses (equivalent to a single human dose) and high doses (equivalent to a human daily dose). In addition, we measured intracranial pressure after oral administration of acetazolamide and topiramate. RESULTS: At clinical and high doses, subcutaneous administration of topiramate lowered intracranial pressure by 32% (p = 0.0009) and 21% (p = 0.015) respectively. There was no significant reduction in intracranial pressure noted with acetazolamide, furosemide, amiloride or octreotide at any dose. Oral administration of topiramate significantly lowered intracranial pressure by 22% (p = 0.018), compared to 5% reduction with acetazolamide (p = >0.999). CONCLUSION: Our in vivo studies demonstrated that both subcutaneous and oral administration of topiramate significantly lowers intracranial pressure. Other drugs tested, including acetazolamide, did not significantly reduce intracranial pressure. Future clinical trials evaluating the efficacy and side effects of topiramate in idiopathic intracranial hypertension patients would be of interest.
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spelling pubmed-63766372019-03-16 Topiramate is more effective than acetazolamide at lowering intracranial pressure Scotton, William J Botfield, Hannah F Westgate, Connar SJ Mitchell, James L Yiangou, Andreas Uldall, Maria S Jensen, Rigmor H Sinclair, Alex J Cephalalgia Original Articles BACKGROUND: The management of idiopathic intracranial hypertension focuses on reducing intracranial pressure to preserve vision and reduce headaches. There is sparse evidence to support the use of some of the drugs commonly used to manage idiopathic intracranial hypertension, therefore we propose to evaluate the efficacy of these drugs at lowering intracranial pressure in healthy rats. METHODS: We measured intracranial pressure in female rats before and after subcutaneous administration of acetazolamide, topiramate, furosemide, amiloride and octreotide at clinical doses (equivalent to a single human dose) and high doses (equivalent to a human daily dose). In addition, we measured intracranial pressure after oral administration of acetazolamide and topiramate. RESULTS: At clinical and high doses, subcutaneous administration of topiramate lowered intracranial pressure by 32% (p = 0.0009) and 21% (p = 0.015) respectively. There was no significant reduction in intracranial pressure noted with acetazolamide, furosemide, amiloride or octreotide at any dose. Oral administration of topiramate significantly lowered intracranial pressure by 22% (p = 0.018), compared to 5% reduction with acetazolamide (p = >0.999). CONCLUSION: Our in vivo studies demonstrated that both subcutaneous and oral administration of topiramate significantly lowers intracranial pressure. Other drugs tested, including acetazolamide, did not significantly reduce intracranial pressure. Future clinical trials evaluating the efficacy and side effects of topiramate in idiopathic intracranial hypertension patients would be of interest. SAGE Publications 2018-06-13 2019-02 /pmc/articles/PMC6376637/ /pubmed/29898611 http://dx.doi.org/10.1177/0333102418776455 Text en © International Headache Society 2018 http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution 4.0 License (http://www.creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Articles
Scotton, William J
Botfield, Hannah F
Westgate, Connar SJ
Mitchell, James L
Yiangou, Andreas
Uldall, Maria S
Jensen, Rigmor H
Sinclair, Alex J
Topiramate is more effective than acetazolamide at lowering intracranial pressure
title Topiramate is more effective than acetazolamide at lowering intracranial pressure
title_full Topiramate is more effective than acetazolamide at lowering intracranial pressure
title_fullStr Topiramate is more effective than acetazolamide at lowering intracranial pressure
title_full_unstemmed Topiramate is more effective than acetazolamide at lowering intracranial pressure
title_short Topiramate is more effective than acetazolamide at lowering intracranial pressure
title_sort topiramate is more effective than acetazolamide at lowering intracranial pressure
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6376637/
https://www.ncbi.nlm.nih.gov/pubmed/29898611
http://dx.doi.org/10.1177/0333102418776455
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