Amador X F, Malaspina D, Sackeim H A, Coleman E A, Kaufmann C A, Hasan A, Gorman J M
Department of Clinical Psychobiology, New York State Psychiatric Institute, NY 10032, USA.
J Neuropsychiatry Clin Neurosci. 1995 Spring;7(2):197-206. doi: 10.1176/jnp.7.2.197.
Increasing evidence suggests that smooth pursuit eye movement (SPEM) dysfunction may serve as an endophenotype or genetic marker of schizophrenia. The authors tested SPEM and visual fixation (VF) in 31 patients with schizophrenia, 33 of their first-degree relatives, and 24 patients with major depressive disorder. A high rate of abnormal VF was found in schizophrenic patients and their first-degree relatives, but not in affective disorder patients with or without psychotic features. Rate of VF abnormality distinguished schizophrenic patients from acutely depressed mood disorder patients; SPEM did not. VF and SPEM performance correlated only moderately, suggesting that the pathophysiologies of these two eye movement abnormalities may be partially independent. Implications for identifying a schizophrenia endophenotype are discussed.
越来越多的证据表明,平稳跟踪眼球运动(SPEM)功能障碍可能是精神分裂症的一种内表型或遗传标记。作者对31例精神分裂症患者、33例其一级亲属以及24例重度抑郁症患者进行了SPEM和视觉注视(VF)测试。在精神分裂症患者及其一级亲属中发现了高比例的异常VF,但在有或无精神病性特征的情感障碍患者中未发现。VF异常率可将精神分裂症患者与急性抑郁情绪障碍患者区分开来;而SPEM则不能。VF和SPEM表现仅呈中度相关,这表明这两种眼球运动异常的病理生理学可能部分独立。文中讨论了对识别精神分裂症内表型的意义。