Department of Psychiatry and Neuropsychology, South Limburg Mental Health Research and Teaching Network, EURON, Maastricht University, Maastricht, The Netherlands.
J Clin Psychiatry. 2010 Jun;71(6):764-74. doi: 10.4088/JCP.08m04837yel. Epub 2010 Jan 26.
Neurocognitive functioning may represent an indicator of genetic risk and poor outcome in both schizophrenia and bipolar disorder. In this study, shared and nonshared characteristics in the cognitive domain in both disorders were analyzed to determine to what degree neurocognitive functioning may represent a predictor of the familial vulnerability and poor functioning that schizophrenia spectrum disorders and bipolar disorder share.
Neurocognition, psychopathology, and psychosocial functioning were assessed in samples of patients with a schizophrenia spectrum disorder (n = 345) and bipolar disorder (n = 76) meeting DSM-IV criteria, first-degree relatives of both patient groups (n = 331 and n = 37, respectively), and healthy controls (n = 260 and n = 61, respectively). Multiple regression models were used to investigate the effect of group status on neurocognition and to explore associations between cognition, symptoms, and psychosocial functioning in the 2 groups. The schizophrenia spectrum study sample was recruited between September 2004 and January 2008, and the bipolar study sample was recruited between June 2004 and July 2007.
Cognitive deficits were more severe and more generalized in patients with a schizophrenia spectrum disorder compared to patients with bipolar disorder; cognitive alterations were present in relatives of patients with schizophrenia spectrum disorders but not in relatives of bipolar patients. The association between neurocognitive dysfunction and psychosocial functioning was more generalized in schizophrenia spectrum disorders than in bipolar disorder; for both disorders, associations were only partly mediated by symptoms.
The evidence for cognitive dysfunction as a marker of familial vulnerability is stronger for schizophrenia than for bipolar disorder. Although the presence of multiple cognitive deficits is shared by the 2 groups, the severity of cognitive deficits and its consequences appear to partly differ between schizophrenia and bipolar disorder, which is in line with a model that implies the specific presence of a neurodevelopmental impairment in the former but not in the latter.
神经认知功能可能是精神分裂症和双相情感障碍的遗传风险和不良预后的指标。在这项研究中,分析了两种疾病认知领域的共同和非共同特征,以确定神经认知功能在多大程度上可以预测精神分裂症谱系障碍和双相情感障碍所共有的家族易感性和不良功能。
评估符合 DSM-IV 标准的精神分裂症谱系障碍(n=345)和双相情感障碍(n=76)患者样本、两组患者的一级亲属(分别为 n=331 和 n=37)以及健康对照组(分别为 n=260 和 n=61)的神经认知、精神病理学和心理社会功能。使用多元回归模型来研究组间状态对神经认知的影响,并探索两组认知、症状和心理社会功能之间的关联。精神分裂症谱系研究样本于 2004 年 9 月至 2008 年 1 月招募,双相研究样本于 2004 年 6 月至 2007 年 7 月招募。
与双相情感障碍患者相比,精神分裂症谱系障碍患者的认知缺陷更严重且更广泛;精神分裂症谱系障碍患者的亲属存在认知改变,但双相情感障碍患者的亲属则没有。精神分裂症谱系障碍患者的神经认知功能与心理社会功能之间的关联比双相情感障碍患者更广泛;对于两种疾病,关联部分由症状介导。
认知功能障碍作为家族易感性的标志物,在精神分裂症中比在双相情感障碍中更有证据。尽管两组都存在多种认知缺陷,但认知缺陷的严重程度及其后果在精神分裂症和双相情感障碍之间似乎有所不同,这与一种模式一致,即前者存在特定的神经发育障碍,而后者则没有。