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Basic visual dysfunction allows classification of patients with schizophrenia with exceptional accuracy

机译:基本的视觉功能障碍可对精神分裂症患者进行准确分类

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Basic visual dysfunctions are commonly reported in schizophrenia; however their value as diagnostic tools remains uncertain. This study reports a novel electrophysiological approach using checkerboard visual evoked potentials (VEP). Sources of spectral resolution VEP-components C1, P1 and N1 were estimated by LORETA, and the band-effects (BSE) on these estimated sources were explored in each subject. BSEs were Z-transformed for each component and relationships with clinical variables were assessed. Clinical effects were evaluated by ROC-curves and predictive values. Forty-eight patients with schizophrenia (SZ) and 55 healthy controls participated in the study. For each of the 48 patients, the three VEP components were localized to both dorsal and ventral brain areas and also deviated from a normal distribution. P1 and N1 deviations were independent of treatment, illness chronicity or gender. Results from LORETA also suggest that deficits in thalamus, posterior cingulum, precuneus, superior parietal and medial occipitotemporal areas were associated with symptom severity. While positive symptoms were more strongly related to sensory processing deficits (P1), negative symptoms were more strongly related to perceptual processing dysfunction (N1). Clinical validation revealed positive and negative predictive values for correctly classifying SZ of 100% and 77%, respectively. Classification in an additional independent sample of 30 SZ corroborated these results. In summary, this novel approach revealed basic visual dysfunctions in all patients with schizophrenia, suggesting these visual dysfunctions represent a promising candidate as a biomarker for schizophrenia.
机译:基本的视觉功能障碍在精神分裂症中常有报道。然而,它们作为诊断工具的价值仍不确定。这项研究报告了一种新的使用棋盘视觉诱发电位(VEP)的电生理方法。 LORETA估计了光谱分辨率VEP成分C1,P1和N1的来源,并在每个主题中探索了这些估计来源的带效应(BSE)。将BSE的每个成分进行Z转换,并评估与临床变量的关系。通过ROC曲线和预测值评估临床效果。共有48位精神分裂症(SZ)患者和55位健康对照参加了这项研究。对于48位患者中的每位患者,三个VEP分量均位于背侧和腹侧大脑区域,并且也偏离正态分布。 P1和N1偏差与治疗,疾病慢性病或性别无关。 LORETA的结果还表明,丘脑,后扣带,前胎,顶叶顶和颞枕内侧区域的缺陷与症状严重程度有关。阳性症状与感觉加工缺陷(P1)密切相关,而阴性症状与感觉加工功能障碍(N1)密切相关。临床验证显示正确分类SZ的阳性和阴性预测值分别为100%和77%。在另外的30 SZ独立样本中进行分类,证实了这些结果。总之,这种新颖的方法揭示了所有精神分裂症患者的基本视觉功能障碍,表明这些视觉功能障碍代表了作为精神分裂症生物标志物的有希望的候选者。

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