Visuospatial planning in unmedicated major depressive disorder and bipolar disorder: distinct and common neural correlates

重性抑郁障碍 心理学 双相情感障碍 心情 情绪障碍 萧条(经济学) 精神科 执行功能障碍 临床心理学 认知 听力学 神经心理学 医学 焦虑 宏观经济学 经济
作者
Maria M. Rive,Maarten W. J. Koeter,Dick J. Veltman,Aart H. Schene,Henricus G. Ruhé
出处
期刊:Psychological Medicine [Cambridge University Press]
卷期号:46 (11): 2313-2328 被引量:15
标识
DOI:10.1017/s0033291716000933
摘要

Cognitive impairments are an important feature of both remitted and depressed major depressive disorder (MDD) and bipolar disorder (BD). In particular, deficits in executive functioning may hamper everyday functioning. Identifying the neural substrates of impaired executive functioning would improve our understanding of the pathophysiology underlying these disorders, and may eventually aid in discriminating between MDD and BD, which is often difficult during depression and remission. To date, mostly medicated MDD and BD subjects have been investigated, which may have influenced results. Therefore, we investigated executive functioning in medication-free depressed and remitted MDD and BD subjects.We used the Tower of London (ToL) visuospatial planning task to assess behavioural performance and blood oxygen-level dependent responses in 35 healthy controls, 21 remitted MDD, 23 remitted BD, 19 depressed MDD and nine depressed BD subjects.Visuospatial planning per se was associated with increased frontostriatal activity in depressed BD compared to depressed MDD. In addition, post-hoc analyses indicated that visuospatial planning load was associated with increased parietal activity in depressed compared to remitted subjects, and BD compared to MDD subjects. Task performance did not significantly differ between groups.More severely affected, medication-free mood disorder patients require greater parietal activity to perform in visuospatial planning, which may be compensatory to maintain relatively normal performance. State-dependent frontostriatal hyperactivity during planning may be a specific BD characteristic, providing clues for further characterization of differential pathophysiology in MDD v. BD. This could potentially provide a biomarker to aid in the differentiation of these disorders.
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