The results from the pharmacogenetics studies on 196G A were rather inconclusive. BDNF.14 One of the most investigated genetic variations within the is a 196G A (rs6265) substitution, which results in a valine to methionine substitution at amino acid 66 (Val66Met) in the 5?proregion of the protein.15,16 Conflicting results have been reported regarding the association of this variation with antidepressant treatment.17C19 The objective of this study was to determine the relationship between the Val66Met polymorphism in the BNDF gene and the response to antidepressant treatment among patients with suicide attempts or ideation. Patients and methods Patients The study protocol was approved by the institutional review board of the Chongqing Medical University. Written informed consent was obtained from all participants. A total of 125 Han Chinese patients with depression were recruited from consecutive admissions to the Mental Health Center of Chongqing Medical University Hospital from September 2010 to November 2011. The inclusion criteria included: (1) age 18 or above, (2) meeting DSM-IV and Chinese Classification and Diagnostic Criteria of Mental Disorder 3 (CCMD-3) criteria for depression, (3) not taking antidepressant medication within at least two weeks prior to the study, (4) having a 24-item Hamilton Rating Scale for Depression (HAMD-24) score greater than 20, and a Beck Self-Rating Depression Index (BDI) score greater than 5. Exclusion criteria included substance use disorders, pregnancy, menstruation, and physical and mental disorders that require immediate treatment. Healthy volunteers in the Control group (n=91) were recruited from Chongqing Medical University Hospital and the medical school with matched age and gender, HAMD-24 below 8 and no substance abuse history or mental disorders. All experiments on human subjects ZM-241385 were conducted in accordance with the Declaration of Helsinki. Clinical assessments Demographics, family depression histories, and previous antidepressant treatment courses, including the dose and treatment duration, and suicide attempts were obtained from medical records. The patients were treated with daily SSRI, eg, fluoxetine or paroxetine, or SSRI with low dose atypical antipsychotics, eg, olanzapine daily, for 12 weeks. The clinical assessments were conducted by two experienced psychiatrists using the HAMD-24 and BDI before and at 4, 8, and 12 weeks after the antidepressant treatment. The higher the HAMD-24 or the BDI scores were, the more severe depressive symptoms were reported from patients. The medication adherence was assessed by self-report and pill counting by pharmacists. A regular weekly phone reminder was used to assure adherence. Treatment responders were defined as patients with an at least 50% decrease in the HAMD-24 at week 12, whereas the rest of patients were considered to be non-responders.20,21 Plasma BDNF measurement Samples of 4 mL of blood were collected at the baseline and during follow-up visits at 4, 8, and 12 weeks. The blood samples were then centrifuged to obtain plasma for BDNF measurement and blood cells for genomic DNA extraction. Plasma concentrations of BDNF were measured using the Human BDNF Immunoassay Quantikine? ELISA Kit (R&D Systems GmbH, Wiesbaden-Nordenstadt, Germany). ELISA assays were performed according to the manufacturers instructions. Briefly, the plates were pre-coated with the mouse monoclonal antibody against BDNF. Fifty microliters of standards and samples was added in duplicate, and incubated for 2 hrs. After an addition of BDNF Conjugate and a 1 hr incubation period, wells were washed extensively with washing buffer. Two hundred microliters of the Substrate Solution was added followed by 30 mins incubation. Reaction was stopped by adding 50 L of Stop Solution and absorbance was determined within 30 mins at.The prognostic quality of BDNF concentrations in MDD should be explored prospectively in larger clinical evaluations. Acknowledgments This work was supported by the National Natural Science Foundation Project of China (81671360;), the Special Key Projects of Scientific and Technological Innovation for Peoples Livelihood in ZM-241385 Chongqing (CSTC2017SHMS-ZDYF0128;, CSTC2018JCYJAX0164;), the Medical Research Project of Chongqing Medical Planning Commission (2018QNXM014;, 2017MSXM016;) and the Scientific Research and Cultivation Project of the First Affiliated Hospital of Chongqing Medical University (PYJJ2018-20). for antidepressant treatment in MDD. gene might be associated with the response to antidepressant treatment, particularly selective serotonin reuptake inhibitors (SSRIs), since BDNF plays a significant role in the development of the serotonergic system. The is located on the short arm of chromosome 11p14, and consists of 11 exons; encodes a precursor peptide that is cleaved to form the mature protein BDNF.14 One of the most investigated genetic variations within the is a 196G A (rs6265) substitution, which results in a valine to methionine substitution at amino acid 66 (Val66Met) in the 5?proregion of the protein.15,16 Conflicting results have been reported regarding the association of this variation with antidepressant treatment.17C19 The objective of this study was to determine the relationship between the Val66Met polymorphism in the BNDF gene and the response to antidepressant treatment among patients with suicide attempts or ideation. Patients and methods Patients The study protocol was approved by the institutional review board of the Chongqing Medical University. Written informed consent was obtained from all participants. A total of 125 Han Chinese patients with depression were recruited from consecutive admissions to the Mental Health Center of Chongqing Medical University Hospital from September 2010 to November 2011. The inclusion criteria included: (1) age 18 or above, (2) meeting DSM-IV and Chinese Classification and Diagnostic Criteria of Mental Disorder 3 (CCMD-3) criteria for depression, (3) not taking antidepressant medication within at least two weeks prior to the study, (4) having a 24-item Hamilton Rating Scale for Depression (HAMD-24) score greater than 20, and a Beck Self-Rating Depression Index (BDI) score greater than 5. Exclusion criteria included substance use disorders, pregnancy, menstruation, and physical and mental disorders that require immediate treatment. Healthy volunteers in the Control group (n=91) were recruited from Chongqing Medical University Hospital and the medical school with matched age and gender, HAMD-24 below 8 and no substance abuse history or mental disorders. All experiments on human subjects were conducted in accordance with the Declaration of Helsinki. Clinical assessments Demographics, family depression histories, and previous antidepressant treatment courses, including the dose and treatment duration, and suicide attempts were obtained from medical records. The patients were treated with daily SSRI, eg, fluoxetine or paroxetine, or SSRI with low dose atypical antipsychotics, eg, olanzapine daily, for 12 weeks. The clinical assessments were conducted by two experienced psychiatrists using the HAMD-24 and BDI before and at 4, ZM-241385 8, and 12 weeks after the antidepressant treatment. The higher Rabbit Polyclonal to CBLN4 the HAMD-24 or the BDI scores were, the more serious depressive symptoms had been reported from sufferers. The medicine adherence was evaluated by self-report and tablet keeping track of by pharmacists. A normal weekly mobile phone reminder was utilized to make sure adherence. Treatment responders had been defined as sufferers with an at least 50% reduction in the HAMD-24 at week 12, whereas the others of sufferers were regarded as nonresponders.20,21 Plasma BDNF measurement Examples of 4 mL of bloodstream were collected on the baseline and during follow-up visits at 4, 8, and 12 weeks. The bloodstream samples were after that centrifuged to acquire plasma for BDNF dimension and bloodstream cells for genomic DNA removal. Plasma concentrations of BDNF had been assessed using the Individual BDNF Immunoassay Quantikine? ELISA Package (R&D Systems GmbH, Wiesbaden-Nordenstadt, Germany). ELISA assays had been performed based on the producers instructions. Quickly, the plates had been pre-coated using the mouse monoclonal antibody against BDNF. Fifty microliters of criteria and examples was added in duplicate, and incubated for 2 hrs. After an addition of BDNF Conjugate and a 1 hr incubation period, wells had been washed thoroughly with cleaning buffer. 2 hundred microliters from the Substrate Alternative was added accompanied by 30 mins incubation. Response was stopped with the addition of 50 L of End Alternative and absorbance was driven within 30 mins at 450 nm using an ELISA dish reader. The minimal detectable dosage of BDNF as reported by the product manufacturer was 20 pg/mL. Genotyping Genomic DNA was isolated in the bloodstream cells using regular techniques. BDNF 196G A polymorphism (rs6265) was genotyped with the PCR-RFLP technique.22 PCR amplification was performed with primers (forward 5?-AAA Kitty CCG AGG ACA AGG TG-3? and invert 5?-AGA AGA GGA GGC TCC AAA GG-3?, GenScript, Nanjing, China), 2 X Ha sido Taq Master Combine (CoWin Bioscience Co., Ltd., Beijing, China), and 50C100 ng genomic DNA.