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Polycystic ovary syndrome in patients on antiepileptic drugs

OBJECTIVE: This study aims to discuss the prevalence of polycystic ovary (PCO) and Polycystic ovary syndrome (PCOS) in women with epilepsy (WWE) on valproate (VPA), carbamazepine (CBZ), or phenobarbitone (PB), drug naive WWE and women with bipolar affective disorder (BPAD) on VPA. MATERIALS AND METH...

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Autores principales: Viswanathan, Lakshminarayanapuram G., Satishchandra, Parthasarathy, Bhimani, Bipin C., Reddy, Janardhan YC, Rama Murthy, Batchu S., Subbakrishna, Doddaballapura K., Sinha, Sanjib
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4980956/
https://www.ncbi.nlm.nih.gov/pubmed/27570385
http://dx.doi.org/10.4103/0972-2327.179973
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author Viswanathan, Lakshminarayanapuram G.
Satishchandra, Parthasarathy
Bhimani, Bipin C.
Reddy, Janardhan YC
Rama Murthy, Batchu S.
Subbakrishna, Doddaballapura K.
Sinha, Sanjib
author_facet Viswanathan, Lakshminarayanapuram G.
Satishchandra, Parthasarathy
Bhimani, Bipin C.
Reddy, Janardhan YC
Rama Murthy, Batchu S.
Subbakrishna, Doddaballapura K.
Sinha, Sanjib
author_sort Viswanathan, Lakshminarayanapuram G.
collection PubMed
description OBJECTIVE: This study aims to discuss the prevalence of polycystic ovary (PCO) and Polycystic ovary syndrome (PCOS) in women with epilepsy (WWE) on valproate (VPA), carbamazepine (CBZ), or phenobarbitone (PB), drug naive WWE and women with bipolar affective disorder (BPAD) on VPA. MATERIALS AND METHODS: This prospective study included 190 women aged 18–45 years, who had epilepsy or BPAD (on VPA), and consented for study. Patients were grouped as Group 1 (n = 40): WWE on VPA, Group 2 (n = 50): WWE on CBZ, Group 3 (n = 50): WWE on PB, Group 4 (n = 30): drug naïve WWE, and Group 5 (n = 20): women with BPAD on VPA. All women were interviewed for medical, menstrual, drug and treatment history, nature of epilepsy, and seizure control. Chi-square test and Fisher's exact test were done to compare results between the groups. RESULTS: Fifty-two women (52/190; 27.4%) had menstrual disturbances, in which oligomenorrhea was the most common (55.8%). There was a significant difference in the occurrence of PCOS in patients on VPA versus normal population (P = 0.05) and patients on other antiepileptic drugs (AEDs) (P = 0.02). There was, however, no significant difference in the occurrence of PCO between patients on VPA and the untreated epileptic women. VPA group (Epilepsy + BPAD) had a significantly higher occurrence of obesity than other treatment groups (P = 0.043, OR = 2.11). CONCLUSIONS: The study observed significantly higher occurrence of PCO in patients on VPA compared to other AEDs and the normal population. The importance of proper clinical evaluation before initiating VPA is highlighted.
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spelling pubmed-49809562016-08-26 Polycystic ovary syndrome in patients on antiepileptic drugs Viswanathan, Lakshminarayanapuram G. Satishchandra, Parthasarathy Bhimani, Bipin C. Reddy, Janardhan YC Rama Murthy, Batchu S. Subbakrishna, Doddaballapura K. Sinha, Sanjib Ann Indian Acad Neurol Original Article OBJECTIVE: This study aims to discuss the prevalence of polycystic ovary (PCO) and Polycystic ovary syndrome (PCOS) in women with epilepsy (WWE) on valproate (VPA), carbamazepine (CBZ), or phenobarbitone (PB), drug naive WWE and women with bipolar affective disorder (BPAD) on VPA. MATERIALS AND METHODS: This prospective study included 190 women aged 18–45 years, who had epilepsy or BPAD (on VPA), and consented for study. Patients were grouped as Group 1 (n = 40): WWE on VPA, Group 2 (n = 50): WWE on CBZ, Group 3 (n = 50): WWE on PB, Group 4 (n = 30): drug naïve WWE, and Group 5 (n = 20): women with BPAD on VPA. All women were interviewed for medical, menstrual, drug and treatment history, nature of epilepsy, and seizure control. Chi-square test and Fisher's exact test were done to compare results between the groups. RESULTS: Fifty-two women (52/190; 27.4%) had menstrual disturbances, in which oligomenorrhea was the most common (55.8%). There was a significant difference in the occurrence of PCOS in patients on VPA versus normal population (P = 0.05) and patients on other antiepileptic drugs (AEDs) (P = 0.02). There was, however, no significant difference in the occurrence of PCO between patients on VPA and the untreated epileptic women. VPA group (Epilepsy + BPAD) had a significantly higher occurrence of obesity than other treatment groups (P = 0.043, OR = 2.11). CONCLUSIONS: The study observed significantly higher occurrence of PCO in patients on VPA compared to other AEDs and the normal population. The importance of proper clinical evaluation before initiating VPA is highlighted. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC4980956/ /pubmed/27570385 http://dx.doi.org/10.4103/0972-2327.179973 Text en Copyright: © Annals of Indian Academy of Neurology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Viswanathan, Lakshminarayanapuram G.
Satishchandra, Parthasarathy
Bhimani, Bipin C.
Reddy, Janardhan YC
Rama Murthy, Batchu S.
Subbakrishna, Doddaballapura K.
Sinha, Sanjib
Polycystic ovary syndrome in patients on antiepileptic drugs
title Polycystic ovary syndrome in patients on antiepileptic drugs
title_full Polycystic ovary syndrome in patients on antiepileptic drugs
title_fullStr Polycystic ovary syndrome in patients on antiepileptic drugs
title_full_unstemmed Polycystic ovary syndrome in patients on antiepileptic drugs
title_short Polycystic ovary syndrome in patients on antiepileptic drugs
title_sort polycystic ovary syndrome in patients on antiepileptic drugs
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4980956/
https://www.ncbi.nlm.nih.gov/pubmed/27570385
http://dx.doi.org/10.4103/0972-2327.179973
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