Clinical and Translational Neuroscience Branch, Intramural Research Program, National Institute of Mental Health, National Institutes of Health, Bethesda, MD.
The Lieber Institute for Brain Development, Johns Hopkins Medical Campus, Baltimore, MD.
Schizophr Bull. 2018 Jan 13;44(1):101-113. doi: 10.1093/schbul/sbx039.
Previous research has identified (1) a "deficit" subtype of schizophrenia characterized by enduring negative symptoms and diminished emotionality and (2) a "distress" subtype associated with high emotionality-including anxiety, depression, and stress sensitivity. Individuals in deficit and distress categories differ sharply in development, clinical course and behavior, and show distinct biological markers, perhaps signaling different etiologies. We tested whether deficit and distress subtypes would emerge from a simple but novel data-driven subgrouping analysis, based on Positive and Negative Syndrome Scale (PANSS) negative and distress symptom dimensions, and whether subgrouping was informative regarding other facets of behavior and brain function. PANSS data, and other assessments, were available for 549 people with schizophrenia diagnoses. Negative and distress symptom composite scores were used as indicators in 2-step cluster analyses, which divided the sample into low symptom (n = 301), distress (n = 121), and deficit (n = 127) subgroups. Relative to the low-symptom group, the deficit and distress subgroups had comparably higher total PANSS symptoms (Ps < .001) and were similarly functionally impaired (eg, global functioning [GAF] Ps < .001), but showed markedly different patterns on symptom, cognitive and personality variables, among others. Initial analyses of functional magnetic resonance imaging (fMRI) data from a 182-participant subset of the full sample also suggested distinct patterns of neural recruitment during working memory. The field seeks more neuroscience-based systems for classifying psychiatric conditions, but these are inescapably behavioral disorders. More effective parsing of clinical and behavioral traits could identify homogeneous target groups for further neural system and molecular studies, helping to integrate clinical and neuroscience approaches.
先前的研究已经确定了(1)一种以持久的阴性症状和情绪减退为特征的精神分裂症“缺陷”亚型,以及(2)一种与高情绪性相关的“痛苦”亚型,包括焦虑、抑郁和压力敏感。在发展、临床过程和行为方面,处于缺陷和痛苦类别的个体差异很大,并且表现出明显的生物学标志物,可能表明不同的病因。我们测试了基于阳性和阴性综合征量表(PANSS)阴性和痛苦症状维度的简单但新颖的数据驱动亚组分析是否会出现缺陷和痛苦亚型,以及亚组分析是否与行为和大脑功能的其他方面有关。PANSS 数据和其他评估可用于 549 名精神分裂症患者。负面和痛苦症状综合得分作为两步聚类分析的指标,该分析将样本分为低症状(n = 301)、痛苦(n = 121)和缺陷(n = 127)亚组。与低症状组相比,缺陷和痛苦亚组的总 PANSS 症状(P <.001)相当高,并且同样存在功能障碍(例如,全球功能[GAF]P <.001),但在症状、认知和人格等方面表现出明显不同的模式。对来自全样本中 182 名参与者子集的功能磁共振成像(fMRI)数据的初步分析也表明,在工作记忆期间,大脑的神经活动模式存在明显差异。该领域正在寻求更多基于神经科学的精神疾病分类系统,但这些系统不可避免地是行为障碍。对临床和行为特征进行更有效的细分,可以为进一步的神经系统和分子研究确定同质的目标群体,从而帮助整合临床和神经科学方法。