Department of Psychiatry, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
Research Affairs, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
Metab Brain Dis. 2018 Aug;33(4):1053-1067. doi: 10.1007/s11011-018-0208-4. Epub 2018 Mar 11.
Deficit schizophrenia is characterized by neurocognitive impairments and changes in the patterning of IgA/IgM responses to plasma tryptophan catabolites (TRYCATs). In the current study, supervised pattern recognition methods, including logistic regression analysis (LRA), Support Vector Machine (SVM), and Soft Independent Modeling of Class Analogy (SIMCA), were used to examine whether deficit schizophrenia is a discrete diagnostic class with respect to Consortium To Establish a Registry for Alzheimer's disease (CERAD) and Cambridge Neuropsychological Test Automated Battery (CANTAB) tests and IgA/IgM responses to noxious (NOX) and generally more protective (PRO) TRYCATs. We recruited patients with (n = 40) and without (n = 40) deficit schizophrenia and healthy volunteers (n = 40). The combined use of TRYCAT and CERAD features strongly segregates deficit from nondeficit schizophrenia and healthy controls. Three out of the top five most important features in LRA, SVM and SIMCA agreed, namely two different NOX/PRO TRYCAT ratios and false memory recall. SIMCA shows that deficit schizophrenia is significantly separated from nondeficit schizophrenia and controls with as top 6 features IgA responses to picolinic acid, IgM responses to 3-OH-kynurenine and kynurenic acid, and impairments in Word List Memory and Verbal Fluency Tests and Mini-Mental State Examination. Nevertheless, nondeficit schizophrenia was not significantly separated from controls. The results show that schizophrenia is not a unitary disease with mere continuous differences in severity of illness between apparent subtypes. Deficit schizophrenia is a qualitatively distinct class defined by neuroimmune (autoimmune responses to TRYCATs) and neurocognitive (episodic and semantic memory) features coupled or not with clinical (negative) symptoms.
缺陷型精神分裂症的特征是神经认知障碍和 IgA/IgM 对血浆色氨酸分解产物(TRYCATs)的反应模式发生变化。在当前的研究中,使用了监督模式识别方法,包括逻辑回归分析(LRA)、支持向量机(SVM)和软独立建模分类分析(SIMCA),以检查缺陷型精神分裂症是否是一个离散的诊断类别,针对 Consortium To Establish a Registry for Alzheimer's disease(CERAD)和 Cambridge Neuropsychological Test Automated Battery(CANTAB)测试以及对有害(NOX)和通常更具保护作用(PRO)TRYCATs 的 IgA/IgM 反应。我们招募了有(n=40)和没有(n=40)缺陷型精神分裂症的患者以及健康志愿者(n=40)。TRYCAT 和 CERAD 特征的联合使用强烈地区分了缺陷型和非缺陷型精神分裂症以及健康对照组。LRA、SVM 和 SIMCA 中的前五个最重要的特征中有三个一致,即两种不同的 NOX/PRO TRYCAT 比值和错误记忆回忆。SIMCA 表明,缺陷型精神分裂症与非缺陷型精神分裂症和对照组明显分离,前 6 个特征包括对吡啶甲酸的 IgA 反应、对 3-羟基犬尿氨酸和犬尿氨酸的 IgM 反应,以及单词列表记忆和言语流畅性测试以及简易精神状态检查的损伤。然而,非缺陷型精神分裂症与对照组没有明显分离。结果表明,精神分裂症不是一种单一的疾病,不同亚型之间只有疾病严重程度的连续差异。缺陷型精神分裂症是一种由神经免疫(对 TRYCATs 的自身免疫反应)和神经认知(情景和语义记忆)特征定义的不同类别,无论是否伴有临床(阴性)症状。