Retinal electrophysiological results in patients receiving lamotrigine monotherapy
Autor: | Bernard Arnaud, Philippe Derambure, Carl Arndt, Jeremie Husson, Jean Claude Hache, Sabine Defoort-Dhellemmes |
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Přispěvatelé: | Service d'Ophtalmologie [Montpellier], Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier)-Hôpital Guy de Chauliac, Groupe matière condensée et matériaux (GMCM), Université de Rennes 1 (UR1), Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES)-Centre National de la Recherche Scientifique (CNRS), Laboratoire de Neurosciences Fonctionnelles et Pathologies (LNFP), Université de Lille, Droit et Santé-Centre National de la Recherche Scientifique (CNRS), Centre National de la Recherche Scientifique (CNRS)-Université de Rennes 1 (UR1), Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES), Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier)-Hôpital Gui de Chauliac [CHU Montpellier], Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier), Université de Rennes (UR)-Centre National de la Recherche Scientifique (CNRS) |
Jazyk: | angličtina |
Rok vydání: | 2005 |
Předmět: |
Male
genetic structures medicine.medical_treatment MESH: Triazines Visual Acuity MESH: gamma-Aminobutyric Acid MESH: Electroretinography MESH: Visual Acuity Epilepsy 0302 clinical medicine MESH: Child Child Pigment Epithelium of Eye gamma-Aminobutyric Acid MESH: Middle Aged Triazines MESH: Retina Middle Aged MESH: Electrooculography 3. Good health Visual field MESH: Vision Screening Neurology MESH: Vision Disorders Anesthesia MESH: Perimetry Anticonvulsants Female [SDV.NEU]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC] medicine.symptom medicine.drug Adult Phenytoin Adolescent MESH: Pigment Epithelium of Eye Vision Disorders Lamotrigine Retina Central nervous system disease 03 medical and health sciences Vision Screening MESH: Anticonvulsants Blurred vision Electroretinography medicine Humans MESH: Adolescent MESH: Humans business.industry MESH: Adult Carbamazepine medicine.disease eye diseases MESH: Male Electrooculography MESH: Epilepsies Partial Anticonvulsant 030221 ophthalmology & optometry Visual Field Tests Epilepsies Partial Neurology (clinical) sense organs business MESH: Female 030217 neurology & neurosurgery |
Zdroj: | Epilepsia Epilepsia, Wiley, 2005, 46 (7), pp.1055-60. ⟨10.1111/j.1528-1167.2005.43204.x⟩ Epilepsia, 2005, 46 (7), pp.1055-60. ⟨10.1111/j.1528-1167.2005.43204.x⟩ |
ISSN: | 0013-9580 |
DOI: | 10.1111/j.1528-1167.2005.43204.x⟩ |
Popis: | Summary: Purpose: To evaluate the effects on vision in patients receiving lamotrigine (LTG) monotherapy. Methods: Twenty-four consecutive patients taking LTG for partial seizures were referred for a routine ophthalmologic examination including visual acuity testing, tonometry, slit lamp, and fundus examination. Automated kinetic perimetry, electrooculogram (EOG), and electroretinogram were performed after informed consent was obtained. Results: In 18 patients finally included, the clinical ophthalmologic examination showed no abnormality. Four patients complained of blurring; among them, one patient had a visual field constriction in both eyes, which, however, was of unclear clinical significance (poor compliance) and a reduced light/dark ratio of the electrooculogram. One other patient with blurred vision had a reduced EOG, but the visual field was normal. Two patients had a reduced EOG but no visual symptoms. Considering the whole group of patients receiving LTG therapy, the light/dark ratio of the EOG was reduced in a dose-dependent fashion (p < 0.0001). The electroretinogram was normal in all patients. Conclusions: No irreversible visual field impairment in patients treated with LTG was encountered, although a dosedependent retinal toxicity may have been present. The exact cellular mechanism of the electrophysiologic changes in patients taking LTG remain to be explained. Key Words: Lamotrigine—Visual field constriction—Retinal pigment epithelium—Electrooculogram—γ -Aminobutyric acid. Lamotrigine (LTG) is an antiepileptic drug (AED) effective against both partial and generalized seizures, including generalized absence seizures. Among the documented side effects, visual blurring is reported by 23% of the patients treated with LTG (1). Although it is highly improbable that these visual symptoms are all related to a measurable dysfunction, they have never been precisely evaluated by a complete visual, clinical, and electrophysiologic investigation in patients treated with the drug. One published case exists of visual field constriction in a child treated with LTG and valproate (VPA) (2). The only established cellular mechanism of LTG is a sodium-current block (3), a mechanism in common with phenytoin (PHT) and carbamazepine (CBZ) (4). However, different from LTG, PHT and CBZ are ineffective against absence seizures and have never been associated with visual field constriction. Therefore it has been advocated that LTG may have as-yet-uncharacterized cellular actions, which could combine with its sodium channel‐ blocking actions (5). Among other effects, there appears |
Databáze: | OpenAIRE |
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