Deregulatory miRNA-BDNF Network Inferred from Dynamic Expression Changes in Schizophrenia
(1) Background: Brain-derived neurotrophic factor (BDNF) is one of the promising risk genes for schizophrenia (SZ), a disease with prominent dysregulation of miRNA networks. Here, we present a study of miRNA-BDNF co-expression changes in peripheral blood of SZ patients. (2) Methods: The expression l...
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Published in | Brain sciences Vol. 12; no. 2; p. 167 |
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Abstract | (1) Background: Brain-derived neurotrophic factor (BDNF) is one of the promising risk genes for schizophrenia (SZ), a disease with prominent dysregulation of miRNA networks. Here, we present a study of miRNA-BDNF co-expression changes in peripheral blood of SZ patients. (2) Methods: The expression levels of the BDNF mRNA and three validated binding miRNAs—miR-124-3p, miR-132-3p, and miR-206—were quantified in the blood of 48 healthy controls and 32 SZ patients before and after 12 weeks of treatment. The co-expression patterns were evaluated in the three groups. (3) Results: The expression levels of BDNF were significantly downregulated in SZ patients compared to the controls. After the treatment, the expression levels of BDNF were upregulated, while the expression levels of the three miRNAs were downregulated. Co-expression analyses showed positive correlations of this network in the SZ patients, while weak negative correlations were observed in the healthy controls. After the 12-week treatment, the overall correlation between BDNF and the three miRNAs reached the levels comparable to the healthy controls. (4) Conclusions: Our findings suggest the involvement of the miRNA-BDNF network in the onset and treatment of SZ. |
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AbstractList | (1) Background: Brain-derived neurotrophic factor (BDNF) is one of the promising risk genes for schizophrenia (SZ), a disease with prominent dysregulation of miRNA networks. Here, we present a study of miRNA-BDNF co-expression changes in peripheral blood of SZ patients. (2) Methods: The expression levels of the BDNF mRNA and three validated binding miRNAs—miR-124-3p, miR-132-3p, and miR-206—were quantified in the blood of 48 healthy controls and 32 SZ patients before and after 12 weeks of treatment. The co-expression patterns were evaluated in the three groups. (3) Results: The expression levels of BDNF were significantly downregulated in SZ patients compared to the controls. After the treatment, the expression levels of BDNF were upregulated, while the expression levels of the three miRNAs were downregulated. Co-expression analyses showed positive correlations of this network in the SZ patients, while weak negative correlations were observed in the healthy controls. After the 12-week treatment, the overall correlation between BDNF and the three miRNAs reached the levels comparable to the healthy controls. (4) Conclusions: Our findings suggest the involvement of the miRNA-BDNF network in the onset and treatment of SZ. (1) Background: Brain-derived neurotrophic factor (BDNF) is one of the promising risk genes for schizophrenia (SZ), a disease with prominent dysregulation of miRNA networks. Here, we present a study of miRNA-BDNF co-expression changes in peripheral blood of SZ patients. (2) Methods: The expression levels of the BDNF mRNA and three validated binding miRNAs-miR-124-3p, miR-132-3p, and miR-206-were quantified in the blood of 48 healthy controls and 32 SZ patients before and after 12 weeks of treatment. The co-expression patterns were evaluated in the three groups. (3) Results: The expression levels of BDNF were significantly downregulated in SZ patients compared to the controls. After the treatment, the expression levels of BDNF were upregulated, while the expression levels of the three miRNAs were downregulated. Co-expression analyses showed positive correlations of this network in the SZ patients, while weak negative correlations were observed in the healthy controls. After the 12-week treatment, the overall correlation between BDNF and the three miRNAs reached the levels comparable to the healthy controls. (4) Conclusions: Our findings suggest the involvement of the miRNA-BDNF network in the onset and treatment of SZ.(1) Background: Brain-derived neurotrophic factor (BDNF) is one of the promising risk genes for schizophrenia (SZ), a disease with prominent dysregulation of miRNA networks. Here, we present a study of miRNA-BDNF co-expression changes in peripheral blood of SZ patients. (2) Methods: The expression levels of the BDNF mRNA and three validated binding miRNAs-miR-124-3p, miR-132-3p, and miR-206-were quantified in the blood of 48 healthy controls and 32 SZ patients before and after 12 weeks of treatment. The co-expression patterns were evaluated in the three groups. (3) Results: The expression levels of BDNF were significantly downregulated in SZ patients compared to the controls. After the treatment, the expression levels of BDNF were upregulated, while the expression levels of the three miRNAs were downregulated. Co-expression analyses showed positive correlations of this network in the SZ patients, while weak negative correlations were observed in the healthy controls. After the 12-week treatment, the overall correlation between BDNF and the three miRNAs reached the levels comparable to the healthy controls. (4) Conclusions: Our findings suggest the involvement of the miRNA-BDNF network in the onset and treatment of SZ. |
Author | Baranova, Ancha Fu, Xiaoqian Zhang, Fuquan Liu, Yansong |
AuthorAffiliation | 2 School of Systems Biology, George Mason University, Manassas, VA 20110, USA; abaranov@gmu.edu 5 Department of Psychiatry, The Affiliated Brain Hospital of Nanjing Medical University, Nanjing 210029, China 3 Research Centre for Medical Genetics, 115478 Moscow, Russia 4 Institute of Neuropsychiatry, The Affiliated Brain Hospital of Nanjing Medical University, Nanjing 210029, China 1 Department of Clinical Psychology, Suzhou Guangji Hospital, The Affiliated Guangji Hospital of Soochow University, Suzhou 215137, China; a126fuxiaoqian@126.com (X.F.); lysway@126.com (Y.L.) |
AuthorAffiliation_xml | – name: 3 Research Centre for Medical Genetics, 115478 Moscow, Russia – name: 2 School of Systems Biology, George Mason University, Manassas, VA 20110, USA; abaranov@gmu.edu – name: 1 Department of Clinical Psychology, Suzhou Guangji Hospital, The Affiliated Guangji Hospital of Soochow University, Suzhou 215137, China; a126fuxiaoqian@126.com (X.F.); lysway@126.com (Y.L.) – name: 4 Institute of Neuropsychiatry, The Affiliated Brain Hospital of Nanjing Medical University, Nanjing 210029, China – name: 5 Department of Psychiatry, The Affiliated Brain Hospital of Nanjing Medical University, Nanjing 210029, China |
Author_xml | – sequence: 1 givenname: Xiaoqian orcidid: 0000-0003-0753-2168 surname: Fu fullname: Fu, Xiaoqian – sequence: 2 givenname: Yansong surname: Liu fullname: Liu, Yansong – sequence: 3 givenname: Ancha surname: Baranova fullname: Baranova, Ancha – sequence: 4 givenname: Fuquan orcidid: 0000-0003-3204-8191 surname: Zhang fullname: Zhang, Fuquan |
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Snippet | (1) Background: Brain-derived neurotrophic factor (BDNF) is one of the promising risk genes for schizophrenia (SZ), a disease with prominent dysregulation of... |
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SubjectTerms | Brain-derived neurotrophic factor co-expression analyses Communication Disease Gene expression Kinases Mental disorders miR-124-3p miR-132-3p miR-206 miRNA mRNA Patients Peripheral blood Psychiatrists Psychotropic drugs Schizophrenia Suicides & suicide attempts |
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Title | Deregulatory miRNA-BDNF Network Inferred from Dynamic Expression Changes in Schizophrenia |
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