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Secondary Abnormal CSF Neurotransmitter Metabolite Profiles in a Pediatric Tertiary Care Centre.
van Karnebeek, Clara D M; Dunbar, Mary; Egri, Csilla; Sayson, Bryan; Milea, Janetta; Stockler-Ipsiroglu, Sylvia; Huh, Linda; Connolly, Mary B; Horvath, Gabriella A.
Afiliação
  • van Karnebeek CDM; 1Department of Pediatrics,University of British Columbia,Vancouver,Canada.
  • Dunbar M; 1Department of Pediatrics,University of British Columbia,Vancouver,Canada.
  • Egri C; 7Department of Medicine,University of British Columbia,Vancouver,Canada.
  • Sayson B; 1Department of Pediatrics,University of British Columbia,Vancouver,Canada.
  • Milea J; 8Western Sussex Hospitals NHS Foundation Trust,United Kingdom.
  • Stockler-Ipsiroglu S; 1Department of Pediatrics,University of British Columbia,Vancouver,Canada.
  • Huh L; 1Department of Pediatrics,University of British Columbia,Vancouver,Canada.
  • Connolly MB; 1Department of Pediatrics,University of British Columbia,Vancouver,Canada.
  • Horvath GA; 1Department of Pediatrics,University of British Columbia,Vancouver,Canada.
Can J Neurol Sci ; 45(2): 206-213, 2018 03.
Article em En | MEDLINE | ID: mdl-29506600
ABSTRACT

BACKGROUND:

Secondary neurotransmitter deficiencies have been reported in several reviews. Our primary aim was to assess the relationship among epilepsy, antiseizure medications, and specific neurotransmitter abnormalities. We also evaluated movement disorders and brain abnormalities via magnetic resonance imaging scans in patients with secondary neurotransmitter defects.

METHODS:

This is a retrospective case series of 376 patients who underwent neurotransmitter analysis at BC Children's Hospital between 2009 and 2013, for a variety of neurological presentations. The biochemical genetics laboratory database was interrogated for results of cerebrospinal fluid neurotransmitter analyses. Clinical data for patients with abnormal results were collected from the hospital charts. Statistical analysis included one-way analysis of variance, chi-square, and a two-way contingency table.

RESULTS:

Abnormal neurotransmitter values were identified in 67 (17.8%) patients, two (0.53%) of which were attributable to a congenital neurotransmitter disorder and 11 (16.9%) secondary to other genetic diagnoses. Of 64 patients with secondary abnormal neurotransmitter values, 38 (59%) presented with epilepsy and 20 (31%) with movement disorders. A combination of epilepsy and movement disorder was less frequent.

DISCUSSION:

Acknowledging the limitations of this retrospective chart review, we conclude that, in our cohort, in addition to patients with movement disorders, a considerable number of patients with epilepsy and epileptic encephalopathy also showed secondary neurotransmitter mono-amine abnormalities. There is no clear relation, however, between clinical phenotype and type of neurotransmitter affected. In addition, no association was identified between the type of antiseizure medications and affected neurotransmitter type. We outline the need for prospective studies to further enrich our understanding of the relation between epilepsy and neurotransmitters with a focus on improving treatments and patient outcomes.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neurotransmissores / Centros de Atenção Terciária / Doenças Metabólicas / Anticonvulsivantes Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Child, preschool / Female / Humans / Male Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neurotransmissores / Centros de Atenção Terciária / Doenças Metabólicas / Anticonvulsivantes Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Child, preschool / Female / Humans / Male Idioma: En Ano de publicação: 2018 Tipo de documento: Article