Luo Jiali,Zhang Jie,Wan Jing,Yu Jinming,Ping Junjiao,Association of the brain-derived neurotrophic factor gene polymorphisms and clinical symptoms in patients with schizophrenia[J].SICHUAN MENTAL HEALTH,2023,36(5):409-415
Association of the brain-derived neurotrophic factor gene polymorphisms and clinical symptoms in patients with schizophrenia
DOI:10.11886/scjsws20230220002
English keywords:Schizophrenia  Brain-derived growth factor  rs11030101  rs2030324  rs6265
Fund projects:广东省医学科研基金研究项目(项目名称:精神分裂症患者DNMTs基因多态性、基因间交互作用及BDNF浓度的关联研究,项目编号:A2021205);中山市医学科研项目(项目名称:首发精神分裂症患者认知功能与血清炎症相关因子及SOCS3水平关联性研究,项目编号:2022J221)
Author NameAffiliationPostcode
Luo Jiali Zhongshan Third People's Hospital Zhongshan 528451 China 528451
Zhang Jie Zhongshan Third People's Hospital Zhongshan 528451 China 528451
Wan Jing Zhongshan Third People's Hospital Zhongshan 528451 China 528451
Yu Jinming Zhongshan Third People's Hospital Zhongshan 528451 China 528451
Ping Junjiao* Zhongshan Third People's Hospital Zhongshan 528451 China 528451
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English abstract:
      Background In relation to neurodevelopmental hypothesis in the etiology of schizophrenia, brain-derived neurotrophic factor (BDNF) as a neurotrophin occupies a relatively dominant position in neuronal development and is a potential biomarker for schizophrenia, and previous studies have suggested that its serum concentration and genetic polymorphisms play a vital role in the pathogenesis of schizophrenia, but this remains controversial.Objective To analyze the difference in BDNF serum concentration between schizophrenic patients and healthy controls, and to explore the correlation of three BDNF single nucleotide polymorphism (SNPs) including rs11030101, rs2030324 and rs6265 with BDNF serum concentration and clinical symptoms in patients with schizophrenia, thus providing references for the clinical treatment of schizophrenia.Methods A case-control study was conducted on 55 patients with schizophrenia who attended the Zhongshan Third People's Hospital from January 2019 to December 2020 and met the Diagnostic and Statistical Manual of Mental Disorders, fifth edition (DSM-5), and 31 healthy controls concurrently recruited from the hospital or general population. Positive and Negative Symptom Scale (PANSS) was utilized to evaluate the psychiatric symptoms of patients with schizophrenia. BDNF serum concentration in all participants was measured using enzyme-linked immunosorbent assay (ELISA), and the genotype distributions of three BDNF SNPs (rs11030101, rs2030324, rs6265) were investigated by polymerase chain reaction sequence-based typing method.Results BDNF serum concentration in patient group was lower than that in control group, with statistical difference (t=-3.804, P<0.01). In terms of clinical symptoms, PANSS total score, excitement/hostility domain score, and depression/anxiety domain score demonstrated statistical difference among patients with different genotypes at SNP rs11030101 (t=2.022, Z=-2.696, -2.467, P<0.05 or 0.01). No statistical difference was noted in BDNF serum concentration in patients with different genotypes at three BDNF SNPs (Z=1.483, F=2.584, 0.417, P>0.05).Conclusion Patients with schizophrenia are found to have low BDNF serum concentration, and the three BDNF SNPs (rs11030101, rs2030324, rs6265) are not associated with BDNF serum concentration, whereas the BDNF rs11030101 polymorphism may contribute to the manifestation of clinical symptoms of excitement/hostility and depression/anxiety in patients with schizophrenia. Furthermore, BDNF serum concentration seems to be more dependent on clinical diagnosis effect rather than genetic polymorphism. [Funded by Guangdong Province Medical Science and Technology Research Fund Project (number, A2021205); Zhongshan Medical Research Program (number, 2022J221)]
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