Neurocognitive profiles in bipolar I and bipolar II disorder:: differences in pattern and magnitude of dysfunction

被引:125
|
作者
Simonsen, Carmen [1 ,2 ]
Sundet, Kjetil [2 ]
Vaskinn, Anja [1 ,3 ]
Birkenaes, Astrid B. [1 ,3 ]
Engh, John A. [1 ,3 ]
Hansen, Charlotte Fredslund [1 ,2 ]
Jonsdottir, Halldora [1 ,3 ]
Ringen, Petter Andreas [1 ,3 ]
Opjordsmoen, Stein [1 ,3 ]
Friis, Svein [1 ,3 ]
Andreassen, Ole A. [1 ,3 ]
机构
[1] Ullevaal Univ Hosp, Dept Psychiat, N-0407 Oslo, Norway
[2] Univ Oslo, Inst Psychol, Oslo, Norway
[3] Univ Oslo, Inst Psychiat, Oslo, Norway
关键词
attention; bipolar disorder; bipolar I; bipolar II; executive function; memory; neurocognitive function;
D O I
10.1111/j.1399-5618.2007.00492.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objectives: Studies on neurocognitive functioning in bipolar disorder, reporting deficits in memory, attention, and executive functioning, have primarily focused on bipolar I disorder. The aim of this study was to examine whether patients with bipolar I and bipolar II disorder have different neurocognitive profiles. Methods: Forty-two patients with bipolar I disorder, 31 patients with bipolar II and 124 healthy controls, from a large ongoing study on psychotic disorders, were included. Neurocognitive function was measured with a comprehensive neuropsychological test battery. Results: The bipolar I group performed significantly poorer than the healthy control group and the bipolar II group on all measures of memory. Compared with the control group, the bipolar I group also had significantly reduced performance on most measures of attention and executive functioning, while the bipolar II group only had a significantly reduced performance on a subset of these measures. On average, 24% of the bipolar I group had clinically significant cognitive impairment (<= 1.5 SD below the control group mean) across measures, compared with 13% of the bipolar II group. Conclusions: Patients with bipolar I and bipolar II disorder in this study have different neurocognitive profiles. Bipolar I patients have more widespread cognitive dysfunction both in pattern and magnitude, and a higher proportion has clinically significant cognitive impairments compared with patients with bipolar II. This may suggest neurobiological differences between the two bipolar subgroups.
引用
收藏
页码:245 / 255
页数:11
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