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Mismatch Negativity in First-Episode Schizophrenia: A Meta-Analysis

机译:初发精神分裂症患者的失配阴性:一项荟萃分析

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摘要

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.
机译:与健康对照组(Cohen d> 1.0或更高)相比,慢性精神分裂症患者对畸形刺激的失配阴性(MMN)明显较小,导致MMN可能被用作精神分裂症的生物标志物。但是,文献中关于在首发精神分裂症患者中是否能可靠地降低MMN有一些争论。为了将生物标志物用作精神分裂症的预测标志物,在已知患有该疾病的大多数情况下,尤其是在疾病发作时,应减少使用。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者和精神分裂症首发后12个月内患者的MMN音高或持续时间偏差。总体效果大小显示,首发患者的MMN降低至音高偏差(Cohen d <0.04),中度降低至中度偏差至持续时间偏差(Cohen d = 0.47)。总之,这表明音高偏离型MMN并不是精神分裂症预测的候选生物标志物,而持续时间偏离的MMN可能具有一定的前景,尽管其影响是慢性精神分裂症的三分之一。讨论了研究之间差异的潜在原因。

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