Weinstein D D, Diforio D, Schiffman J, Walker E, Bonsall R
Department of Psychology, Emory University, Atlanta, GA 30322, USA.
Am J Psychiatry. 1999 Apr;156(4):617-23. doi: 10.1176/ajp.156.4.617.
A relationship between schizotypal personality disorder and schizophrenia has been documented in behavioral genetic studies, and there are similarities in the cognitive deficits and brain abnormalities associated with these disorders. Adolescents with schizotypal personality disorder are of particular interest because the postpubertal period is a critical one for the development of a DSM axis I disorder. It is likely that some schizotypal adolescents will remain stable over time, some will improve, and a subgroup will develop schizophrenia. This study tested the hypotheses that, like schizophrenic patients, schizotypal adolescents manifest an elevated rate of minor physical and dermatoglyphic anomalies, both of which suggest prenatal neurodevelopmental abnormalities. Cortisol release is also of interest because of evidence that the hypothalamic-pituitary-adrenal axis may influence the behavioral expression of vulnerability to schizophrenia.
Minor physical anomalies, dermatoglyphic asymmetries, and salivary cortisol levels were measured in three groups of adolescents: 20 with schizotypal personality disorder, 20 with other personality disorders, and 26 with no disorder. Assessments began at noon, and four saliva samples were obtained at hourly intervals.
The schizotypal personality disorder group showed more minor physical anomalies and dermatoglyphic asymmetries than the normal comparison group and higher cortisol levels than both of the other groups. Group differences in cortisol level were most pronounced at the beginning of the evaluation. Cortisol level and age were positively correlated.
The findings support the assumption that schizotypal personality disorder is associated with perturbations in fetal neurodevelopment and, under some circumstances, a heightened cortisol response.
行为遗传学研究已证实分裂型人格障碍与精神分裂症之间存在关联,且与这些障碍相关的认知缺陷和大脑异常存在相似之处。患有分裂型人格障碍的青少年尤其值得关注,因为青春期后期是发展为精神疾病诊断与统计手册(DSM)轴I障碍的关键时期。很可能一些分裂型青少年随时间推移会保持稳定,一些会有所改善,还有一小部分会发展为精神分裂症。本研究检验了以下假设:与精神分裂症患者一样,分裂型青少年表现出较高的轻微身体和皮纹异常发生率,这两者均提示产前神经发育异常。由于有证据表明下丘脑 - 垂体 - 肾上腺轴可能影响对精神分裂症易感性的行为表达,所以皮质醇释放也受到关注。
对三组青少年测量了轻微身体异常、皮纹不对称性和唾液皮质醇水平:20名患有分裂型人格障碍的青少年、20名患有其他人格障碍的青少年和26名无任何障碍的青少年。评估于中午开始,每隔一小时采集四份唾液样本。
与正常对照组相比,分裂型人格障碍组表现出更多的轻微身体异常和皮纹不对称性,且皮质醇水平高于其他两组。皮质醇水平的组间差异在评估开始时最为明显。皮质醇水平与年龄呈正相关。
研究结果支持以下假设,即分裂型人格障碍与胎儿神经发育紊乱有关,并且在某些情况下,与皮质醇反应增强有关。