Haigh Sarah M, Coffman Brian A, Salisbury Dean F
Western Psychiatric Institute and Clinic, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA
Western Psychiatric Institute and Clinic, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Clin EEG Neurosci. 2017 Jan;48(1):3-10. doi: 10.1177/1550059416645980. Epub 2016 May 11.
Mismatch negativity (MMN) to deviant stimuli is robustly smaller in individuals with chronic schizophrenia compared with healthy controls (Cohen's d > 1.0 or more), leading to the possibility of MMN being used as a biomarker for schizophrenia. However, there is some debate in the literature as to whether MMN is reliably reduced in first-episode schizophrenia patients. For the biomarker to be used as a predictive marker for schizophrenia, it should be reduced in the majority of cases known to have the disease, particularly at disease onset. We conducted a meta-analysis on the fourteen studies that measured MMN to pitch or duration deviants in healthy controls and patients within 12 months of their first episode of schizophrenia. The overall effect size showed no MMN reduction in first-episode patients to pitch-deviants (Cohen's d < 0.04), and a small-to-medium reduction to duration-deviants (Cohen's d = 0.47). Together, this indicates that pitch-deviant MMN is not a candidate biomarker for schizophrenia prediction, while duration-deviant MMN may hold some promise, albeit nearly a third as large an effect as in chronic schizophrenia. Potential causes for discrepancies between studies are discussed.
与健康对照组相比,慢性精神分裂症患者对偏差刺激的失配负波(MMN)显著更小(科恩d值>1.0或更高),这使得MMN有可能作为精神分裂症的生物标志物。然而,文献中对于首发精神分裂症患者的MMN是否确实降低存在一些争议。要将该生物标志物用作精神分裂症的预测指标,在已知患有该疾病的大多数病例中,尤其是在疾病发作时,它应该降低。我们对14项研究进行了荟萃分析,这些研究测量了健康对照组以及首发精神分裂症患者在发病12个月内对音高或时长偏差的MMN。总体效应量显示,首发患者对音高偏差的MMN没有降低(科恩d值<0.04),对时长偏差的MMN有小到中等程度的降低(科恩d值 = 0.47)。综合来看,这表明音高偏差的MMN不是精神分裂症预测的候选生物标志物,而时长偏差的MMN可能有一定前景,尽管其效应大小几乎只有慢性精神分裂症的三分之一。文中讨论了研究之间存在差异的潜在原因。