Treatment resistant schizophrenia and neurological soft signs may converge on the same pathology: Evidence from explanatory analysis on clinical, psychopathological, and cognitive variables

被引:29
作者
de Bartolomeis, Andrea [1 ]
Prinzivalli, Emiliano [1 ]
Callovini, Gemma [1 ]
D'Ambrosio, Luigi [1 ]
Altavilla, Benedetta [1 ]
Avagliano, Camilla [1 ]
Iasevoli, Felice [1 ]
机构
[1] Univ Sch Med Federico II, Dept Neurosci, Lab Mol & Translat Psychiat, Sect Psychiat,Unit Treatment Resistant Psychosis, Naples, Italy
关键词
1ST-EPISODE SCHIZOPHRENIA; NEUROPSYCHOLOGICAL PERFORMANCE; ANTIPSYCHOTIC TREATMENT; TREATMENT RESPONSE; NEGATIVE SYMPTOMS; SCALE; ABNORMALITIES; INSTRUMENT; PREDICTORS; REMISSION;
D O I
10.1016/j.pnpbp.2017.09.002
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Here, we investigated neurological soft signs (NSSs) in treatment resistant schizophrenia (TRS) vs treatment responder schizophrenia (SZ) patients. TRS is a severe condition, affecting approximately one-third of schizophrenia patients and representing a relevant clinical challenge. NSSs are neurological abnormalities reportedly described in schizophrenia patients and linked to dysregulated network connections. We explored the possibility that NSSs may be: i) more severe in TRS patients; ii) differentially associated to clinical/cognitive variables in TRS vs SZ; iii) predictive of having TRS. In addition, we evaluated whether diagnosis may mediate NSSs associations with the above-mentioned variables. Consecutive patients with schizophrenia diagnosis underwent stringent assessment for TRS diagnosis. Demographics and clinical variables were recorded. Psychopathology (by Positive and Negative Syndrome Scale, PANSS), cognitive performances, and NSSs (by Neurological Evaluation Scale, NES) were tested. TRS had higher scores than SZ patients in total NES score and in almost all NES subscales, even after correction for duration of illness and antipsychotic dose (ANCOVA, p < 0.05). NSSs significantly correlated with multiple clinical, psychopathological, and cognitive variables (above all: duration of disease and negative symptoms) in TRS but not in SZ patients. Two-way ANOVA showed NSS-x-diagnosis interaction in determining outcomes on multiple cognitive performances, but not in other clinical variables. However, simple main effect analysis detected a significant relationship between high severity NSSs and TRS diagnosis on multiple clinical and cognitive outcomes. Hierarchical regression analysis showed that diagnosis was among a discrete number of predictors yielding significant increases in variance explained on NES total, Sensory Integration and Other Signs subscales' scores. NSSs, together with antipsychotic dose and disease severity, were found to be significantly predictive of TRS diagnosis in a binary logistic regression model. These results suggest a stringent association between NSSs and TRS diagnosis, and may imply that NSSs association with clinical, psychopathological, and cognitive variables may be in part mediated by TRS diagnosis.
引用
收藏
页码:356 / 366
页数:11
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