Literature DB >> 20031502

Electroencephalographic changes in pyridoxine-dependant epilepsy: new observations.

Georges Naasan1, Mohamad Yabroudi, Amal Rahi, Mohamad A Mikati.   

Abstract

OBJECTIVE: Pyridoxine-dependent epilepsy (PDE) is a rare disease, of which the EEG manifestations are only partially characterised. We report our observations of EEG recordings in four patients with PDE.
MATERIALS AND METHODS: EEG tracings from four patients fulfilling the clinical criteria for PDE were reviewed. Relative to the time of treatment with pyridoxine, EEG recordings were available before treatment in two patients (at ages four and 10 months), immediately after treatment in two patients and during long-term follow-up with treatment in all four patients.
RESULTS: Pre-pyridoxine interictal EEG findings included: diffuse slowing, bilateral independent multifocal epileptiform discharges, generalized bursts of polyspike slow waves and focal or generalized sharp waves. In addition, the EEG was often asymmetrical and included: generalized semi-rhythmic sharp and slow waves, a burst suppression pattern and continuous generalized spike and slow waves. In one patient, who was followed subsequently, a decrease in multifocal spikes and sharp waves and permanent cessation of clinical seizures, within 10 minutes of concurrent reduction of spikes in the pre-existing generalized spike slow wave pattern, was observed immediately after pyridoxine treatment. However, despite the clinical response in this patient we observed persistent generalized burst suppression for four days, and fluctuation of the EEG with diffuse slowing on day four and transient exacerbation of discharges with continuous spike slow waves on day 22. This was followed by intermittent sharp waves at eight and 20 months, mild slowing at 31 months and normal EEG at 43 months. Long-term EEG findings in the other three patients receiving pyridoxine ranged between normal and intermittent multifocal sharp waves.
CONCLUSION: Our data confirm previous observations and provide the following new findings: (1) the presence of burst suppression pattern after cessation of seizures can occur for up to five days after initiation of pyridoxine and should not exclude the diagnosis of PDE, (2) possible fluctuation and even transient worsening of electrographic discharges were observed for up to three weeks after initiation of pyridoxine and (3) the abnormal EEG can persist for up to 43 months before normalizing (range 1-43 months) and in other cases in which it continues to be abnormal it may still improve after increasing the dose of pyridoxine.

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Year:  2009        PMID: 20031502     DOI: 10.1684/epd.2009.0280

Source DB:  PubMed          Journal:  Epileptic Disord        ISSN: 1294-9361            Impact factor:   1.819


  6 in total

1.  A novel mouse model for pyridoxine-dependent epilepsy due to antiquitin deficiency.

Authors:  Hilal H Al-Shekaili; Terri L Petkau; Izabella Pena; Tess C Lengyell; Nanda M Verhoeven-Duif; Jolita Ciapaite; Marjolein Bosma; Martijn van Faassen; Ido P Kema; Gabriella Horvath; Colin Ross; Elizabeth M Simpson; Jan M Friedman; Clara van Karnebeek; Blair R Leavitt
Journal:  Hum Mol Genet       Date:  2020-11-25       Impact factor: 6.150

2.  Systemic Manifestations in Pyridox(am)ine 5'-Phosphate Oxidase Deficiency.

Authors:  Réjean M Guerriero; Archana A Patel; Brian Walsh; Fiona M Baumer; Ankoor S Shah; Jurriaan M Peters; Lance H Rodan; Pankaj B Agrawal; Phillip L Pearl; Masanori Takeoka
Journal:  Pediatr Neurol       Date:  2017-06-03       Impact factor: 3.372

3.  A Rare Case of Pyridoxine-dependent Seizures in Infancy.

Authors:  V S S Yerramilli Murty; M S S Kishore; Manisha R Patel
Journal:  J Clin Neonatol       Date:  2013-01

4.  Pyridoxine-Dependent Epilepsy in Zebrafish Caused by Aldh7a1 Deficiency.

Authors:  Izabella A Pena; Yann Roussel; Kate Daniel; Kevin Mongeon; Devon Johnstone; Hellen Weinschutz Mendes; Marjolein Bosma; Vishal Saxena; Nathalie Lepage; Pranesh Chakraborty; David A Dyment; Clara D M van Karnebeek; Nanda Verhoeven-Duif; Tuan Vu Bui; Kym M Boycott; Marc Ekker; Alex MacKenzie
Journal:  Genetics       Date:  2017-10-23       Impact factor: 4.562

5.  PLPBP mutations cause variable phenotypes of developmental and epileptic encephalopathy.

Authors:  Hiroshi Shiraku; Mitsuko Nakashima; Saoko Takeshita; Chai-Soon Khoo; Muzhirah Haniffa; Gaik-Siew Ch'ng; Kazuma Takada; Keisuke Nakajima; Masayasu Ohta; Tohru Okanishi; Sotaro Kanai; Ayataka Fujimoto; Hirotomo Saitsu; Naomichi Matsumoto; Mitsuhiro Kato
Journal:  Epilepsia Open       Date:  2018-11-01

6.  Clinical diagnosis, treatment, and ALDH7A1 mutations in pyridoxine-dependent epilepsy in three Chinese infants.

Authors:  Zhixian Yang; Xiaoling Yang; Ye Wu; Jingmin Wang; Yuehua Zhang; Hui Xiong; Yuwu Jiang; Jiong Qin
Journal:  PLoS One       Date:  2014-03-24       Impact factor: 3.240

  6 in total

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