4.2 Article

Serum proBDNF/BDNF and response to fluvoxamine in drug-naive first-episode major depressive disorder patients

Journal

ANNALS OF GENERAL PSYCHIATRY
Volume 13, Issue -, Pages -

Publisher

BIOMED CENTRAL LTD
DOI: 10.1186/1744-859X-13-19

Keywords

BDNF; proBDNF; Major depressive disorder; Serum; Fluvoxamine

Categories

Funding

  1. Dainippon-Sumitomo Pharma Co.
  2. Tanabe Mitsubishi Pharma Co.
  3. Astellas Pharma Co., Ltd
  4. Grants-in-Aid for Scientific Research [26461728] Funding Source: KAKEN

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Background: We investigated the association between serum proBDNF, a precursor of brain-derived neurotrophic factor (BDNF), and response to fluvoxamine in patients with major depressive disorder (MDD) using the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, Text Revision (DSM-IV-TR): physically healthy and free of current alcohol or drug abuse, comorbid anxiety, or personality disorders. Methods: Fifty-one patients with MDD (M/F, 19: 32; age, 38 +/- 19 years) and 51 healthy controls (M/F, 22: 29; age, 34 +/- 17 years) were studied using DSM-IV-TR: physically healthy and free of current alcohol or drug abuse, comorbid anxiety, or personality disorders. Serum levels of proBDNF and MDNF were measured by sandwich enzyme-linked immunosorbent assay (ELISA). Results: Serum mature BDNF levels in the MDD patients were significantly lower than those in the healthy controls (t = 3.046, p = 0.0018). On the other hand, no difference was found in serum proBDNF between the MDD patients and the healthy controls (t = -0.979, p = 0.833). A trend of negative correlation was found between baseline serum BDNF and baseline scores of the 17 items of the Hamilton Rating Scale for Depression (HAMD17) (r = -0.183, p = 0.071). No correlation was however found between HAMD17 scores and proBDNF at baseline (r = 0.092, p = 0.421). Furthermore, no correlation was observed between baseline HAMD17 scores and baseline proBDNF/BDNF (r = -0.130, p = 0.190). No changes were observed in serum levels of proBDNF and BDNF during the treatment periods. Conclusions: These results suggest that there is no association between serum proBDNF/BDNF and fluvoxamine response in MDD patients at least within 4 weeks of the treatment.

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