Long-term prognosis of juvenile myoclonic epilepsy: A systematic review searching for sex differences

نویسندگان

چکیده

PurposeJuvenile myoclonic epilepsy (JME), like other forms of idiopathic generalized epilepsy, shows a marked female predominance. However, few studies have specifically addressed the role sex in its long-term prognosis. We performed systematic review literature relevant to JME prognosis, focusing on sex-based differences prognostic factors and outcome.MethodsA comprehensive search PubMed Scopus databases was performed, considering all articles up April 2020 which prognosis had been explored outcome or were specified.ResultsWe included 25 published between 1984 2020. Sex by 21 studies, but only three reported different outcomes male vs patients. All found be associated with later response antiseizure medications, worse seizure control, higher risk relapse their entire study samples, Eight possible predictors outcome: prolonged epileptiform EEG runs presence eye closure sensitivity, both more frequent women, possibly linked poorer as praxis induction asymmetric changes, instead common men. Valproate use, men, better outcome.ConclusionMost do not highlight some specificities emerge, especially regard particular reflex traits abnormalities. Finally, may condition therapeutic choices, thus impact outcome.

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

O11: Juvenile Myoclonic Epilepsy as A Spectrum Disorder

لطفاً به چکیده انگلیسی مراجعه شود.

متن کامل

Prognosis of juvenile myoclonic epilepsy is related to endophenotypes

PURPOSE To investigate if phenotypic variations have prognostic implications in juvenile myoclonic epilepsy (JME). METHODS Sixty-five consecutive JME patients had video-EEG recording and were followed for at least three years. Reflex traits were defined as seizures and/or EEG discharges induction by eye-closure, photic stimulation, language, praxis or calculation. Patients had psychiatric eva...

متن کامل

Juvenile myoclonic epilepsy.

2. In treatment of juvenile myoclonic epilepsy, the following is true except: a. Phenobarbitone is an effective treatment for generalized tonic seizures and myoclonic seizures b. Lamotrigine exaggerates myoclonic seizures in 50% of patients c. Levetiracetam has potent antimyoclonic effects d. Life long treatment with a proper AED is recommended for juvenile myoclonic epilepsy e. Pregabalin is a...

متن کامل

[Juvenile myoclonic epilepsy].

CONCLUSION We conclude that despite inevitable variability the clinical picture of JME is characteristic. It is easy to diagnose JME if one thinks of it while the history should be thoroughly analyzed. An EEG recording during sleep confirms the diagnosis. An early diagnosis of JME permits adequate prognosis of the subsequent course of epilepsy, and adequate therapy brings remission in most of t...

متن کامل

Juvenile myoclonic epilepsy.

Juvenile myoclonus epilepsy (JME) is a common epileptic syndrome, the etiology of which is genetically determined. Its onset occurs from 6 through 22 years of age, and affected patients present with myoclonic jerks, often associated with generalized tonic-clonic seizures - the most common association - and absence seizures. JME is non-progressive, and there are no abnormalities on clinical exam...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: Seizure-european Journal of Epilepsy

سال: 2021

ISSN: ['1532-2688', '1059-1311']

DOI: https://doi.org/10.1016/j.seizure.2021.01.005