Djordjević Vladimir V, Lazarević Dušan, Ćosić Vladan, Knežević Marinela Z, Djordjević Vidosava B, Stojanović Ivana
Clinic for Mental Health Protection, Clinical Centre Niš, Serbia.
Clinic for Psychiatry, Clinical Centre Niš, Serbia.
J Med Biochem. 2016 Jan;35(1):7-16. doi: 10.1515/jomb-2015-0010. Epub 2015 Dec 30.
Brain-derived neurotrophic factor (BDNF) and nitric oxide (NO) play multiple roles in the developing and adult CNS. Since BDNF and NO metabolisms are dysregulated in schizophrenia, we measured these markers simultaneously in the blood of schizophrenics and assessed their diagnostic accuracy.
Thirty-eight patients with schizophrenia classified according to demographic characteristics, symptomatologyand therapy and 39 age- and gender-matched healthy controls were enrolled. BDNF was determined by the ELISA technique while the concentration of nitrite/nitrate ([Formula: see text]) was measured by the colorimetric method.
Serum BDNF levels were significantly lower (20.38±3.73 ng/mL, P = 1.339E-05), whilst plasma [Formula: see text] concentrations were significantly higher (84.3 (72-121) μmol/L, P=4.357E-08) in patients with schizophrenia than in healthy controls (25.65±4.32 ng/mL; 60.9 (50-76) μmol/L, respectively). The lowest value of BDNF (18.14±3.26 ng/mL) and the highest [Formula: see text] concentration (115.3 (80-138) μmol/L) were found in patients treated with second-generation antipsychotics (SGA). The patients diseased before the age of 24 and the patients suffering for up to one year had significantly lower serum BDNF levels than those diseased after the age of 24 and the patients who were ill longer than one year. Both BDNF and [Formula: see text] showed good diagnostic accuracy, but BDNF had better ROC curve characteristics, especially in patients with negative symptomatology.
BDNF and nitrite/nitrate showed inverse changes in schizophrenic patients. The most pronounced changes were found in patients treated with second-generation antipsychotics. Although BDNF is not specific of schizophrenia, it may be a clinically useful biomarker for the diagnosis of patients expressing predominantly negative symptoms.
脑源性神经营养因子(BDNF)和一氧化氮(NO)在中枢神经系统发育和成年期发挥多种作用。由于精神分裂症患者中BDNF和NO代谢失调,我们同时检测了精神分裂症患者血液中的这些标志物,并评估了它们的诊断准确性。
招募了38例根据人口统计学特征、症状学和治疗方法分类的精神分裂症患者以及39例年龄和性别匹配的健康对照者。采用ELISA技术测定BDNF,采用比色法测定亚硝酸盐/硝酸盐([公式:见原文])浓度。
精神分裂症患者的血清BDNF水平显著降低(20.38±3.73 ng/mL,P = 1.339E - 05),而血浆[公式:见原文]浓度显著升高(84.3(72 - 121)μmol/L,P = 4.357E - 08),健康对照者的血清BDNF水平和血浆[公式:见原文]浓度分别为25.65±4.32 ng/mL和60.9(50 - 76)μmol/L。在接受第二代抗精神病药物(SGA)治疗的患者中,BDNF值最低(18.14±3.26 ng/mL),[公式:见原文]浓度最高(115.3(80 - 138)μmol/L)。发病年龄在2岁以下的患者和患病时间长达1年的患者血清BDNF水平显著低于发病年龄在24岁以上的患者和患病时间超过1年的患者。BDNF和[公式:见原文]均显示出良好的诊断准确性,但BDNF具有更好的ROC曲线特征,尤其是在有阴性症状的患者中。
BDNF和亚硝酸盐/硝酸盐在精神分裂症患者中呈相反变化。在接受第二代抗精神病药物治疗的患者中发现了最明显的变化。虽然BDNF并非精神分裂症所特有,但它可能是诊断以阴性症状为主的患者的一种临床有用的生物标志物。