Oknina L B, Wild-Wall N, Oades R D, Juran S A, Röpcke B, Pfueller U, Weisbrod M, Chan E, Chen E Y H
Institute of Higher Nervous Activity and Neurophysiology, Burdenco Neurosurgery Institute, Moscow, Russia.
Schizophr Res. 2005 Jul 1;76(1):25-41. doi: 10.1016/j.schres.2004.10.003. Epub 2004 Nov 11.
Mismatch negativity (MMN) is an event-related potential measure of auditory change detection. It is widely reported to be smaller in patients with schizophrenia and may not improve along with otherwise successful clinical treatment. The main aim of this report is to explore ways of measuring and presenting four features of frequency-deviant MMN dipole sources (dipole moment, peak latency, brain location and orientation) and to relate these to the processes of psychopathology and illness progression. Data from early onset patients (EOS) at the start of the illness in adolescence, and others who had their first break in adolescence 15 years ago (S-15Y) were compared with two groups of age-matched healthy controls (C-EOS, C-15Y). A four-source model fitted the MMN waveform recorded from all four groups, whether MMN amplitude was more (EOS) or less (S-15Y) reduced. The locations were in the left superior temporal and anterior cingulate gyri, right superior temporal and inferior/mid frontal cortices. Dipole latencies confirmed a bottom-up sequence of processing and dipole moments were larger in the temporal lobes and on the left. Patients showed small dipole location changes that were more marked in the S-15Y than the EOS group (more rostral for the left anterior cingulate, more caudal for the right mid-frontal dipole) consistent with illness progression. The modelling of MMN dipole sources on brain atlas and anatomical images suggests that there is a degree of dissociation during illness between small progressive anatomical changes and some functional recovery indexed by scalp recordings from patients with an onset in adolescence 15 years before compared to adolescents in their first episode.
失匹配负波(MMN)是一种用于听觉变化检测的事件相关电位指标。广泛报道称,精神分裂症患者的MMN较小,且可能不会随着其他方面成功的临床治疗而改善。本报告的主要目的是探索测量和呈现频率偏差MMN偶极子源的四个特征(偶极矩、峰潜伏期、脑区位置和方向)的方法,并将这些特征与精神病理学和疾病进展过程联系起来。将青春期发病初期的早发性患者(EOS)以及15年前在青春期首次发病的患者(S - 15Y)的数据与两组年龄匹配的健康对照(C - EOS、C - 15Y)进行比较。无论MMN波幅降低得更多(EOS)还是更少(S - 15Y),一个四源模型都能拟合从所有四组记录到的MMN波形。这些位置位于左侧颞上回和前扣带回、右侧颞上回以及额中/下回皮质。偶极子潜伏期证实了自下而上的处理顺序,且颞叶和左侧的偶极矩更大。患者表现出偶极子位置的微小变化,在S - 15Y组比EOS组更明显(左侧前扣带回更靠前,右侧额中偶极子更靠后),这与疾病进展一致。在脑图谱和解剖图像上对MMN偶极子源进行建模表明,与15年前青春期发病的患者相比,青春期首次发作的青少年患者在疾病过程中,微小的渐进性解剖变化与头皮记录所显示的一些功能恢复之间存在一定程度的分离。