Mittal Vijay A, Hasenkamp Wendy, Sanfilipo Michael, Wieland Susan, Angrist Burton, Rotrosen John, Duncan Erica J
Emory University, Department of Psychology, 235 Dental Building, 1462 Clifton Road, Atlanta, GA 30322, United States.
Schizophr Res. 2007 Aug;94(1-3):37-44. doi: 10.1016/j.schres.2007.04.017. Epub 2007 May 31.
Although several studies have identified abnormal rates of neurological soft signs (NSS) as a manifestation of CNS dysfunction in schizophrenia, differences in sample populations have contributed to a discrepancy in empirical findings. Furthermore, little is known about the potential of NSS to predict a clinical response to antipsychotic medications. The present study tests the associations between NSS and schizophrenia symptomatology and examines NSS as a potential marker for predicting treatment response.
Nineteen unmedicated male schizophrenia patients were treated prospectively with haloperidol for six weeks. The subjects were assessed for pre and post-treatment NSS and schizophrenia symptomatology (Brief Psychiatric Rating Scale, BPRS).
NSS at baseline were significantly associated with baseline symptoms on the Positive, Negative, and Psychological Discomfort BPRS subscales. NSS showed a strong trend toward improvement during six weeks of a prospective haloperidol trial. Hierarchical linear regression analyses indicated that more severe baseline NSS predicted poorer response to haloperidol treatment as measured by post-treatment BPRS Total subscale scores.
NSS at untreated baseline are associated with baseline symptom severity, and elevated NSS are predictive of a smaller degree of improvement in symptoms after antipsychotic treatment. These findings are consistent with the hypothesis that NSS are linked to the neuropathology that underlies schizophrenia symptomatology and course.
尽管多项研究已确定神经软体征(NSS)异常率是精神分裂症中枢神经系统功能障碍的一种表现,但样本群体的差异导致了实证研究结果的不一致。此外,关于NSS预测抗精神病药物临床反应的潜力知之甚少。本研究测试了NSS与精神分裂症症状学之间的关联,并将NSS作为预测治疗反应的潜在标志物进行研究。
19名未接受药物治疗的男性精神分裂症患者接受了为期六周的氟哌啶醇前瞻性治疗。对受试者治疗前后的NSS和精神分裂症症状学(简明精神病评定量表,BPRS)进行评估。
基线时的NSS与BPRS阳性、阴性和心理不适分量表上的基线症状显著相关。在为期六周的氟哌啶醇前瞻性试验中,NSS呈现出明显的改善趋势。分层线性回归分析表明,基线时更严重的NSS预示着以治疗后BPRS总分量表得分衡量的氟哌啶醇治疗反应较差。
未经治疗的基线时的NSS与基线症状严重程度相关,NSS升高预示着抗精神病治疗后症状改善程度较小。这些发现与NSS与精神分裂症症状学和病程潜在的神经病理学相关的假设一致。