Zhang Qing-biao, Jiang Liang-fu, Kong Ling-yu, Lu Yuan-Jun
Department of Pediatric Internal Medicine II, Linyi People's Hospital, Linyi, Shandong Province, PR China.
Department of Pediatric Surgery I, Linyi People's Hospital, Linyi, Shandong Province, PR China.
Int J Dev Neurosci. 2014 Oct;37:65-8. doi: 10.1016/j.ijdevneu.2014.06.013. Epub 2014 Jun 28.
Brain-derived neurotrophic factor (BDNF) plays a critical role in the pathogenesis of Autism spectrum disorders (ASD). The purpose of this study was to investigate the potential role of BDNF in Chinese children with ASD. Sixty patients (48 male, 12 female) diagnosed with ASD and 60 healthy sex and age control subjects were assessed for serum BDNF content at admission. BDNF were assayed with enzyme-linked immunosorbent assay methods, and severity of ASD was evaluated with the Childhood Autism Rating Scale (CARS) Score. The results indicated that the median serum BDNF levels were significantly (P<0.0001) higher in children with ASD as compared to normal cases [17.6(IQR: 13.7-21.4) ng/ml and 11.5(9.6-13.8) ng/ml, respectively]. Based on the receiver operating characteristic (ROC) curve, the optimal cut-off value of serum BDNF levels as an indicator for auxiliary diagnosis of autism was projected to be 15.0 ng/ml. Further, we found that an increased risk of ASD was associated with BDNF levels >15.0 ng/ml (adjusted OR 10.4, 95% CI: 4.39-29.32) after adjusting for above possible confounders. Our study demonstrated that serum BDNF levels were associated with ASD, and higher levels could be considered as an independent risk factor of ASD.
脑源性神经营养因子(BDNF)在自闭症谱系障碍(ASD)的发病机制中起关键作用。本研究旨在探讨BDNF在中国ASD儿童中的潜在作用。对60例诊断为ASD的患者(48例男性,12例女性)和60例性别与年龄匹配的健康对照者在入院时评估血清BDNF含量。采用酶联免疫吸附测定法检测BDNF,并使用儿童自闭症评定量表(CARS)评分评估ASD的严重程度。结果表明,与正常儿童相比,ASD儿童的血清BDNF中位数水平显著更高(P<0.0001)[分别为17.6(四分位间距:13.7 - 21.4)ng/ml和11.5(9.6 - 13.8)ng/ml]。根据受试者工作特征(ROC)曲线,血清BDNF水平作为自闭症辅助诊断指标的最佳截断值预计为15.0 ng/ml。此外,在调整上述可能的混杂因素后,我们发现BDNF水平>15.0 ng/ml与ASD风险增加相关(调整后的比值比为10.4,95%置信区间:4.39 - 至29.32)。我们的研究表明,血清BDNF水平与ASD相关,较高水平可被视为ASD的独立危险因素。