ICube - CNRS UMR 7357, Neurophysiology, FMTS, University of Strasbourg, France; CEMNIS - Noninvasive Neuromodulation Center, University Hospital Strasbourg, France.
ICube - CNRS UMR 7357, Neurophysiology, FMTS, University of Strasbourg, France.
Prog Neuropsychopharmacol Biol Psychiatry. 2018 Aug 30;86:363-369. doi: 10.1016/j.pnpbp.2018.03.008. Epub 2018 Mar 17.
Schizophrenia as a single liability model was confronted to the multiple psychotic phenotypes model proposed by the Wernicke-Kleist-Leonhard school, focusing on two: periodic catatonia (PC) and cataphasia (C). Both are stable and heritable psychotic phenotypes with no crossed liability and are coming with the buildup of specific residual symptoms: impairment of psychomotricity for PC and a specific disorganization of thought and language in C. Regional cerebral blood flow (rCBF) was used as a biomarker. We attempted to refute the single phenotype model by looking at relevant and specific rCBF anomalies for PC and C, that would exceed anomalies in common relative to controls (CTR), i.e. looking for a double dissociation. Twenty subjects with PC, 9 subjects with C and 27 matched controls had two MRI QUIPSS-II arterial spin labeling sequences converted in rCBF. One SPM analysis was performed for each rCBF measurement and the results were given as the conjunction of both analysis. There was a clear double dissociation of rCBF correlates between PC and C, both being meaningful relative to their residual symptomatology. In PC: rCBF was increased in the left motor and premotor areas. In C: rCBF was decreased bilaterally in the temporo-parietal junctions. Conversely, in both (schizophrenia): rCBF was increased in the left striatum which is known to be an anti-psychotics' effect. This evidence refuts the single schizophrenia model and suggests better natural foundations for PC and C phenotypes. This pleads for further research on them and further research on naturally founded psychotic phenotypes.
Name of the registry: ClinicalTrials.gov Identification: NCT02868879.
精神分裂症作为单一的责任模型与 Wernicke-Kleist-Leonhard 学派提出的多种精神病表型模型相对立,该模型集中于两种:周期性紧张症(PC)和 Cataphasia(C)。这两种都是稳定且可遗传的精神病表型,没有交叉责任,伴随着特定残留症状的积累:PC 损害精神运动,C 出现特定的思维和语言紊乱。区域脑血流(rCBF)被用作生物标志物。我们试图通过观察 PC 和 C 相关且特定的 rCBF 异常来反驳单一表型模型,这些异常将超过相对于对照组(CTR)的常见异常,即寻找双重分离。20 名 PC 患者、9 名 C 患者和 27 名匹配的对照组进行了两次 MRI QUIPSS-II 动脉自旋标记序列转换为 rCBF。对每个 rCBF 测量进行了一次 SPM 分析,结果作为两次分析的联合给出。PC 和 C 之间的 rCBF 相关性存在明显的双重分离,两者相对于其残留症状均具有意义。在 PC 中:左运动和前运动区 rCBF 增加。在 C 中:双侧颞顶交界处 rCBF 减少。相反,在两者(精神分裂症)中:左侧纹状体 rCBF 增加,这是众所周知的抗精神病药物的作用。这一证据反驳了单一的精神分裂症模型,并为 PC 和 C 表型提供了更好的自然基础。这为进一步研究这些表型以及进一步研究基于自然的精神病表型提供了依据。
登记名称:ClinicalTrials.gov 识别号:NCT02868879。