Cadenhead Kristin S, Light Gregory A, Geyer Mark A, McDowell Jennifer E, Braff David L
Department of Psychiatry, University of California, San Diego, La Jolla, 92093-0810, USA.
Am J Psychiatry. 2002 May;159(5):869-71. doi: 10.1176/appi.ajp.159.5.869.
Subjects with schizotypal personality disorder demonstrate deficits in inhibition when assessed on prepulse inhibition, P50 suppression, and antisaccade paradigms. This study determined if distinct subgroups of subjects with schizotypal personality disorder could be identified on the basis of performance on these measures and whether endophenotypes could be defined for future genetic study by using measures of inhibitory function.
Prepulse inhibition, P50 suppression, and antisaccade paradigms were assessed in 21 subjects with schizotypal personality disorder.
Seven subjects with schizotypal personality disorder had deficits on each paradigm; seven had no deficits on any paradigm. P50 and antisaccade deficits were present in five of the same subjects and significantly correlated.
These results suggest that P50 and antisaccade performance reflects a common endophenotype and that prepulse inhibition identifies a separate endophenotype reflecting different neurobiological substrate(s) in subjects with schizotypal personality disorder. This pattern may generalize to schizophrenia spectrum disorder patients.
分裂型人格障碍患者在进行预脉冲抑制、P50抑制和反扫视范式评估时表现出抑制功能缺陷。本研究旨在确定能否根据这些测试的表现识别出分裂型人格障碍患者的不同亚组,以及能否通过使用抑制功能测试来定义内表型,以供未来的基因研究使用。
对21名分裂型人格障碍患者进行预脉冲抑制、P50抑制和反扫视范式评估。
7名分裂型人格障碍患者在每种范式上均有缺陷;7名患者在任何范式上均无缺陷。5名患者同时存在P50和反扫视缺陷,且两者显著相关。
这些结果表明,P50和反扫视表现反映了一种共同的内表型,而预脉冲抑制识别出了一种单独的内表型,反映了分裂型人格障碍患者不同的神经生物学底物。这种模式可能适用于精神分裂症谱系障碍患者。