We report the case of a woman who presented cryptogenic temporal lobe seizures from the age of 43 years. Antiepileptic drug (AED) treatment with carbamazepine was able to control seizures for 1 year, but seizures relapsed and an add-on treatment with lamotrigine was started without achieving seizures control. The patient's medical history was unremarkable except for a mild hirsutism for which she was taking finasteride since 45 years of age. In view of the possible relationship between finasteride, a known inhibitor of neurosteroids synthesis, and patient's seizures exacerbation, we stopped finasteride resulting in prompt recovery of seizures control. It is know that 5α-dihydrosteroids are precursors of powerful positive modulators of γ-aminobutyric acid-A inhibitory currents and exert antiseizure effects in animal epilepsy models. This case supports the hypothesis that endogenous neurosteroids can modulate seizure susceptibility and response to AEDs also in humans, suggesting their possible use as a new therapeutic option.

Temporal lobe epilepsy exacerbation during pharmacological inhibition of endogenous neurosteroid synthesis / Pugnaghi, Matteo; Monti, Giulia; Biagini, Giuseppe; Meletti, Stefano. - In: BMJ CASE REPORT. - ISSN 1757-790X. - ELETTRONICO. - 19:(2013), pp. 1-3. [10.1136/bcr-2012-008204]

Temporal lobe epilepsy exacerbation during pharmacological inhibition of endogenous neurosteroid synthesis

PUGNAGHI, Matteo;MONTI, Giulia;BIAGINI, Giuseppe;MELETTI, Stefano
2013

Abstract

We report the case of a woman who presented cryptogenic temporal lobe seizures from the age of 43 years. Antiepileptic drug (AED) treatment with carbamazepine was able to control seizures for 1 year, but seizures relapsed and an add-on treatment with lamotrigine was started without achieving seizures control. The patient's medical history was unremarkable except for a mild hirsutism for which she was taking finasteride since 45 years of age. In view of the possible relationship between finasteride, a known inhibitor of neurosteroids synthesis, and patient's seizures exacerbation, we stopped finasteride resulting in prompt recovery of seizures control. It is know that 5α-dihydrosteroids are precursors of powerful positive modulators of γ-aminobutyric acid-A inhibitory currents and exert antiseizure effects in animal epilepsy models. This case supports the hypothesis that endogenous neurosteroids can modulate seizure susceptibility and response to AEDs also in humans, suggesting their possible use as a new therapeutic option.
2013
19
1
3
Temporal lobe epilepsy exacerbation during pharmacological inhibition of endogenous neurosteroid synthesis / Pugnaghi, Matteo; Monti, Giulia; Biagini, Giuseppe; Meletti, Stefano. - In: BMJ CASE REPORT. - ISSN 1757-790X. - ELETTRONICO. - 19:(2013), pp. 1-3. [10.1136/bcr-2012-008204]
Pugnaghi, Matteo; Monti, Giulia; Biagini, Giuseppe; Meletti, Stefano
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11380/982608
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