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Decreased serum levels of brain-derived neurotrophic factor in schizophrenic patients with deficit syndrome
BACKGROUND: Brain-derived neurotrophic factor (BDNF) is a well-established neurotrophin that plays a role in the pathophysiology of numerous psychiatric disorders. Many studies have investigated the serum BDNF levels in patients with schizophrenia. However, there are restricted data in the literatur...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4386764/ https://www.ncbi.nlm.nih.gov/pubmed/25848285 http://dx.doi.org/10.2147/NDT.S79444 |
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author | Akyol, Esra Soydaş Albayrak, Yakup Beyazyüz, Murat Aksoy, Nurkan Kuloglu, Murat Hashimoto, Kenji |
author_facet | Akyol, Esra Soydaş Albayrak, Yakup Beyazyüz, Murat Aksoy, Nurkan Kuloglu, Murat Hashimoto, Kenji |
author_sort | Akyol, Esra Soydaş |
collection | PubMed |
description | BACKGROUND: Brain-derived neurotrophic factor (BDNF) is a well-established neurotrophin that plays a role in the pathophysiology of numerous psychiatric disorders. Many studies have investigated the serum BDNF levels in patients with schizophrenia. However, there are restricted data in the literature that compare the serum BDNF levels in patients with deficit and nondeficit syndromes. In this study, we aimed to compare the serum BDNF levels between schizophrenic patients with deficit or nondeficit syndrome and healthy controls. METHODS: After fulfilling the inclusion and exclusion criteria, 58 patients with schizophrenia and 36 healthy controls were included in the study. The patients were grouped as deficit syndrome (N=23) and nondeficit syndrome (N=35) according to the Schedule for the Deficit Syndrome. Three groups were compared in terms of the sociodemographic and clinical variants and serum BDNF levels. RESULTS: The groups were similar in terms of age, sex, body mass index, and smoking status. The serum BDNF levels in patients with deficit syndrome were significantly lower than those in healthy controls. In contrast, the serum BDNF levels in patients with nondeficit syndrome were similar to those in healthy controls. CONCLUSION: This study suggests that decreased BDNF levels may play a role in the pathophysiology of schizophrenic patients with deficit syndrome. Nonetheless, additional studies using a larger patient sample size are needed to investigate the serum BDNF levels in schizophrenic patients with deficit syndrome. |
format | Online Article Text |
id | pubmed-4386764 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-43867642015-04-06 Decreased serum levels of brain-derived neurotrophic factor in schizophrenic patients with deficit syndrome Akyol, Esra Soydaş Albayrak, Yakup Beyazyüz, Murat Aksoy, Nurkan Kuloglu, Murat Hashimoto, Kenji Neuropsychiatr Dis Treat Original Research BACKGROUND: Brain-derived neurotrophic factor (BDNF) is a well-established neurotrophin that plays a role in the pathophysiology of numerous psychiatric disorders. Many studies have investigated the serum BDNF levels in patients with schizophrenia. However, there are restricted data in the literature that compare the serum BDNF levels in patients with deficit and nondeficit syndromes. In this study, we aimed to compare the serum BDNF levels between schizophrenic patients with deficit or nondeficit syndrome and healthy controls. METHODS: After fulfilling the inclusion and exclusion criteria, 58 patients with schizophrenia and 36 healthy controls were included in the study. The patients were grouped as deficit syndrome (N=23) and nondeficit syndrome (N=35) according to the Schedule for the Deficit Syndrome. Three groups were compared in terms of the sociodemographic and clinical variants and serum BDNF levels. RESULTS: The groups were similar in terms of age, sex, body mass index, and smoking status. The serum BDNF levels in patients with deficit syndrome were significantly lower than those in healthy controls. In contrast, the serum BDNF levels in patients with nondeficit syndrome were similar to those in healthy controls. CONCLUSION: This study suggests that decreased BDNF levels may play a role in the pathophysiology of schizophrenic patients with deficit syndrome. Nonetheless, additional studies using a larger patient sample size are needed to investigate the serum BDNF levels in schizophrenic patients with deficit syndrome. Dove Medical Press 2015-03-30 /pmc/articles/PMC4386764/ /pubmed/25848285 http://dx.doi.org/10.2147/NDT.S79444 Text en © 2015 Akyol et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Akyol, Esra Soydaş Albayrak, Yakup Beyazyüz, Murat Aksoy, Nurkan Kuloglu, Murat Hashimoto, Kenji Decreased serum levels of brain-derived neurotrophic factor in schizophrenic patients with deficit syndrome |
title | Decreased serum levels of brain-derived neurotrophic factor in schizophrenic patients with deficit syndrome |
title_full | Decreased serum levels of brain-derived neurotrophic factor in schizophrenic patients with deficit syndrome |
title_fullStr | Decreased serum levels of brain-derived neurotrophic factor in schizophrenic patients with deficit syndrome |
title_full_unstemmed | Decreased serum levels of brain-derived neurotrophic factor in schizophrenic patients with deficit syndrome |
title_short | Decreased serum levels of brain-derived neurotrophic factor in schizophrenic patients with deficit syndrome |
title_sort | decreased serum levels of brain-derived neurotrophic factor in schizophrenic patients with deficit syndrome |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4386764/ https://www.ncbi.nlm.nih.gov/pubmed/25848285 http://dx.doi.org/10.2147/NDT.S79444 |
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