Pediatric Neurology
Volume 12, Issue 2 , Pages 139-145, February 1995

Thyrotropin-releasing hormone in treatment of intractable epilepsy: Neurochemical analysis of CSF monoamine metabolites

  • Yoshihiro Takeuchi, MD

      Affiliations

    • Corresponding Author InformationCommunication should be addressed to: Dr. Takeuchi; Department of Pediatrics, Kyoto Prefectural University of Medicine, Kawaramachi-Hirokoji, Kamikyo-ku; Kyoto 602, Japan.
    • Department of Pediatrics, Kyoto Prefectural University of Medicine, Japan
  • ,
  • Masashi Tominaga, MD

      Affiliations

    • Department of Pediatrics, Kyoto Municipal Hospital, Japan
  • ,
  • Nobuto Mitsufuji, MD

      Affiliations

    • Department of Pediatrics, Kyoto First Red Cross Hospital, Kyoto, Japan
  • ,
  • Ichiro Yamazoe, MD

      Affiliations

    • Department of Pediatrics, Kyoto Prefectural University of Medicine, Japan
  • ,
  • Syouji Kawase, MD

      Affiliations

    • Department of Pediatrics, Kyoto Prefectural University of Medicine, Japan
  • ,
  • Akira Nishimura, MD

      Affiliations

    • Department of Pediatrics, Kyoto Prefectural University of Medicine, Japan
  • ,
  • Satoshi Matsuo, MD

      Affiliations

    • Department of Pediatrics, Kyoto Prefectural University of Medicine, Japan
  • ,
  • Tadashi Sawada, MD

      Affiliations

    • Department of Pediatrics, Kyoto Prefectural University of Medicine, Japan

Received 19 September 1994; accepted 12 December 1994.

Abstract 

The efficacy of thyrotropin-releasing hormone in children with intractable epilepsy was investigated and changes in cerebrospinal fluid monoamine metabolites were analyzed. The 18 patients had either West syndrome (12 patients) or Lennox-Gastaut syndrome (6 patients), which was intractable to antiepileptic drug therapy and to adrenocorticotrophic hormone. Thyrotropin-releasing hormone-tartrate was administered for 4 weeks. Before and after the thyrotropin-releasing hormone administration, cerebrospinal fluid was collected and analyzed for 5-hydroxyindoleacetic acid, kynurenine, homovanillic acid, and 3-methoxy-4-hydroxyphenyl glycol. The patients were classified into 3 groups, based on seizure frequency and electroencephalographic effects: cessation of seizures and seizure discharges (very effective; group A), reduction of seizures and/or seizure discharges (effective; group B), and no changes in frequency of seizures or discharges (not effective; group C). There were 6 patients in group A, 3 in group B, and 9 in group C. There were no significant differences in monoamine metabolites before and after the thyrotropin-releasing hormone therapy. A trial of thyrotropin-releasing hormone for the treatment of intractable epilepsy is warranted and further study is required on the mechanism of the antiepileptic action of thyrotropin-releasing hormone.

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 This study was supported in part by grants from the Mother and Child Health Foundation, and the Ministry of Education, Science and Culture, Japan.

PII: 0887-8994(94)00149-V

Pediatric Neurology
Volume 12, Issue 2 , Pages 139-145, February 1995