Dujardin K, Duhamel A, Becquet E, Grunberg C, Defebvre L, Destee A
CHRU de Lille, Clinique Neurologique, Neurologie A, Hôpital R. Salengro, 59037 Lille Cedex, France.
J Neurol Neurosurg Psychiatry. 1999 Sep;67(3):323-8. doi: 10.1136/jnnp.67.3.323.
To investigate the cognitive profile of first degree relatives of patients with familial Parkinson's disease to determine whether these subjects presented signs of neuropsychological dysfunction compared with healthy controls. Results of recent genetic and neuroimaging studies suggest a genetic contribution to the aetiology of Parkinson's disease and underline the interest in identifying preclinical signs of the disease.
A battery of tests evaluating executive function was administered to 41 first degree relatives of patients with well documented familial Parkinson's disease and 39 healthy controls. A factorial discriminant analysis allowed isolation of a subgroup of 15 first degree relatives who could be considered as impaired compared with the healthy controls. Among these 15 "deviant" relatives, nine performed globally worse than the control subjects on all tasks. The six other subjects had mean or even high scores on all task variables, except on those highly correlated with the discriminant score of the factorial discriminant analysis.
Among the first degree relatives of patients with familial Parkinson's disease, some manifested executive dysfunction comparable with that typically associated with the disease. Such impairment could represent a preclinical form of Parkinson's disease.
研究家族性帕金森病患者一级亲属的认知特征,以确定与健康对照相比,这些受试者是否存在神经心理功能障碍的迹象。近期的遗传学和神经影像学研究结果表明帕金森病的病因有遗传因素参与,并凸显了识别该疾病临床前体征的重要性。
对41名有明确家族性帕金森病记录的患者的一级亲属和39名健康对照进行了一系列评估执行功能的测试。通过因子判别分析,分离出15名一级亲属组成的亚组,与健康对照相比,这些亲属可被视为存在功能受损。在这15名“异常”亲属中,9名在所有任务上的整体表现均比对照受试者差。另外6名受试者在所有任务变量上的得分平均甚至较高,但与因子判别分析的判别得分高度相关的变量除外。
在家族性帕金森病患者的一级亲属中,一些人表现出与该疾病通常相关的执行功能障碍。这种损害可能代表帕金森病的临床前形式。