Microarray Analysis of Human Blood During Electroconvulsive Therapy

نویسندگان

  • Takao Kaneko
  • Tetsufumi Kanazawa
  • Masaki Nishiguchi
  • Hiroki Kikuyama
  • Atsushi Tsutsumi
  • Hiroyuki Uenishi
  • Yasuo Kawabata
  • Seiya Kawashige
  • Yoshitaka Nishizawa
  • Souichiro Maruyama
  • Jun Koh
  • Hiroshi Yoneda
چکیده

INTRODUCTION Electroconvulsive therapy (ECT) is currently regarded as a significant treatment option for intractable psychiatric disorders, such as catatonic schizophrenia or treatment-resistant depression; however, the underlying molecular mechanism for its therapeutic effect remains obscure. METHODS Employing microarray analysis (Human Genome U133 Plus 2.0 Array; Affymetrix, United States) of cDNA derived from the peripheral blood of patients with catatonic schizophrenia (n = 5), we detected a significant change in 145 genes (0.68%) before and after modified ECT (mECT). Moreover, we performed quantitative polymerase chain reaction validation of genes that had previously been suggested to be functionally related to schizophrenia. RESULTS Of 4 genes examined (AKT3, TCF7, PPP3R1, and GADD45B), only TCF7 was increased during the mECT procedure (P = 0.0025). DISCUSSION This study describes the first attempt to uncover the molecular mechanism of mECT using a microarray assay of mRNA derived from peripheral blood, and our results suggest that the TCF family may play a role in the functional mechanism of mECT.

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عنوان ژورنال:

دوره 31  شماره 

صفحات  -

تاریخ انتشار 2015