Maziade M, Roy M A, Martinez M, Cliche D, Fournier J P, Garneau Y, Nicole L, Montgrain N, Dion C, Ponton A M
Centre de recherche, Université Laval Robert-Giffard, Québec, Canada.
Am J Psychiatry. 1995 Oct;152(10):1458-63. doi: 10.1176/ajp.152.10.1458.
This study aimed to answer the following questions: 1) Can we reliably measure the psychopathologic dimensions of schizophrenia by using a lifetime frame and by rating acute and interepisode periods separately? 2) Can we reproduce in subjects with familial schizophrenia the characteristic three-factor structure of schizophrenic symptoms that has been found previously in general groups of schizophrenic patients? 3) Is the factor structure also present in familial bipolar disorder?
Lifetime measures of psychotic symptoms were taken through a slightly modified version of the Comprehensive Assessment of Symptoms and History for 138 patients with highly familial DSM-III-R schizophrenia (N = 51), bipolar disorder (N = 44), or spectrum disorders (N = 43). Symptoms were rated separately in the acute episodes and in the stabilized interepisode intervals across the patients' lives.
A satisfactory level of reliability was obtained. In this highly familial study group, the positive/negative factorial distinction was replicated, as was a three-factor model similar to that observed in prior general groups of schizophrenic patients. These factors were also present in bipolar affective disorder. The negative, psychoticism, and disorganized factor model applied more to the acute phase of illness than to the stabilized state.
These findings offer an empirical basis for testing biological or genetic variables in relation to negative/positive symptom dimensions, rather than diagnoses. Observations of a shared structure for schizophrenia and bipolar disorder suggest some continuity in the causes of these disorders.
本研究旨在回答以下问题:1)我们能否通过使用终生框架并分别对急性期和发作间期进行评分来可靠地测量精神分裂症的心理病理维度?2)我们能否在家族性精神分裂症患者中重现先前在一般精神分裂症患者群体中发现的精神分裂症症状的特征性三因素结构?3)这种因素结构在家族性双相情感障碍中是否也存在?
通过对138例患有高度家族性DSM-III-R精神分裂症(N = 51)、双相情感障碍(N = 44)或谱系障碍(N = 43)的患者进行症状和病史综合评估的略微修改版本,获取终生精神病症状测量值。在患者一生中的急性发作期和稳定的发作间期分别对症状进行评分。
获得了令人满意的可靠性水平。在这个高度家族性研究组中,阳性/阴性因子区分得到了重复,与先前在一般精神分裂症患者群体中观察到的三因素模型相似的模型也得到了重复。这些因素在双相情感障碍中也存在。阴性、精神病性和紊乱因子模型在疾病急性期比在稳定期更适用。
这些发现为测试与阴性/阳性症状维度相关而非诊断相关的生物学或遗传变量提供了实证基础。对精神分裂症和双相情感障碍共享结构的观察表明这些疾病病因存在一些连续性。