Academic Unit of Psychiatry, Institute of Life Science, The School of Medicine, Swansea University, Singleton Park, Swansea, SA2 8PP, UK.
Eur Arch Psychiatry Clin Neurosci. 2010 Apr;260(3):249-55. doi: 10.1007/s00406-009-0066-5. Epub 2009 Sep 27.
The pathophysiology of autistic spectrum disorder (ASD) is not fully understood and there are no diagnostic or predictive biomarkers. Proteomic profiling has been used in the past for biomarker research in several non-psychiatric and psychiatric disorders and could provide new insights, potentially presenting a useful tool for generating such biomarkers in autism. Serum protein pre-fractionation with C8-magnetic beads and protein profiling by matrix-assisted laser desorption/ionisation-time of flight-mass spectrometry (MALDI-ToF-MS) were used to identify possible differences in protein profiles in patients and controls. Serum was obtained from 16 patients (aged 8-18) and age-matched controls. Three peaks in the MALDI-ToF-MS significantly differentiated the ASD sample from the control group. Sub-grouping the ASD patients into children with and without comorbid Attention Deficit and Hyperactivity Disorder, ADHD (ASD/ADHD+ patients, n = 9; ASD/ADHD- patients, n = 7), one peak distinguished the ASD/ADHD+ patients from controls and ASD/ADHD- patients. Our results suggest that altered protein levels in peripheral blood of patients with ASD might represent useful biomarkers for this devastating psychiatric disorder.
自闭症谱系障碍(ASD)的病理生理学尚未完全阐明,也没有诊断或预测生物标志物。过去,蛋白质组学分析已被用于几种非精神疾病和精神疾病的生物标志物研究,它可能提供新的见解,为自闭症患者生成此类生物标志物提供潜在的有用工具。使用 C8-磁性珠进行血清蛋白预分级,并用基质辅助激光解吸/电离-飞行时间质谱(MALDI-ToF-MS)进行蛋白质分析,以鉴定患者和对照组之间蛋白图谱的可能差异。从 16 名患者(年龄 8-18 岁)和年龄匹配的对照组中获得血清。MALDI-ToF-MS 中有三个峰可显著区分 ASD 样本和对照组。将 ASD 患者分为伴有和不伴有注意力缺陷多动障碍(ADHD)的儿童亚组(ASD/ADHD+患者,n=9;ASD/ADHD-患者,n=7),一个峰可将 ASD/ADHD+患者与对照组和 ASD/ADHD-患者区分开来。我们的结果表明,ASD 患者外周血中蛋白质水平的改变可能代表这种严重精神疾病的有用生物标志物。