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How to Construct a Bottom-Up Nomothetic Network Model and Disclose Novel Nosological Classes by Integrating Risk Resilience and Adverse Outcome Pathways with the Phenome of Schizophrenia

机译:如何构建自下而上的预测网络模型,并通过与精神分裂症的缺点集成风险弹性和不良结果途径披露新型衰弱课程

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Current case definitions of schizophrenia (DSM-5, ICD), made through a consensus among experts, are not cross-validated and lack construct reliability validity. The aim of this paper is to explain how to use bottom-up pattern recognition approaches to construct a reliable and replicable nomothetic network reflecting the direct effects of risk resilience (RR) factors, and direct and mediated effects of both RR and adverse outcome pathways (AOPs) on the schizophrenia phenome. This study was conducted using data from 40 healthy controls and 80 patients with schizophrenia. Using partial least squares (PLS) analysis, we found that 39.7% of the variance in the phenomenome (lowered self-reported quality of life) was explained by the unified effects of AOPs (IgA to tryptophan catabolites, LPS, and the paracellular pathway, cytokines, and oxidative stress biomarkers), the cognitome (memory and executive deficits), and symptomatome (negative symptoms, psychosis, hostility, excitation, mannerism, psychomotor retardation, formal thought disorders); 55.8% of the variance in the symptomatome was explained by a single trait extracted from AOPs and the cognitome; and 22.0% of the variance in the latter was explained by the RR (Q192R polymorphism and CMPAase activity, natural IgM, and IgM levels to zonulin). There were significant total effects (direct + mediated) of RR and AOPs on the symptomatome and the phenomenome. In the current study, we built a reliable nomothetic network that reflects the associations between RR, AOPs, and the phenome of schizophrenia and discovered new diagnostic subclasses of schizophrenia based on unified RR, AOPs, and phenome scores.
机译:通过专家之间的共识进行精神分裂症(DSM-5,ICD)的当前情况定义,不会交叉验证和缺乏构建可靠性有效性。本文的目的是解释如何使用自下而上的模式识别方法来构建可靠和可复制的元素网络,反映风险弹性(RR)因子的直接影响,以及RR和不良结果途径的直接和介导的影响( AOPS)在精神分裂症上。本研究使用来自40例健康对照和80例精神分裂症患者进行的。使用部分最小二乘(PLS)分析,发现Abops(IgA对色氨酸分解代谢物,LPS和Paracellular途径的统一效果解释了这一现象数(降低的自我报告质量)的39.7%的差异(降低了自我报告的生活质量)。细胞因子,氧化应激生物标志物),认知体(记忆和行政赤字)和症状(阴性症状,精神病,敌对,刺激,锻炼,精神接受迟缓,正式的思想障碍);从AOP和Cognitome提取的单个性状解释了55.8%的症状差异;通过RR(Q192R多态性和CMPAase活性,天然IgM和IgM水平对Zonulin来解释后者的差异的22.0%。对症状和症状的RR和AOPS存在显着的总效果(直接+介导)。在目前的研究中,我们建立了一种可靠的元素网络,反映了基于统一的RR,AOP和诸如诸如诸如统一的RR,AOP和苯甲酸尼分数的rr,aops和精神分裂症缺点的关联。

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