Drapier Dominique, Surguladze Simon, Marshall Nicolette, Schulze Katja, Fern Adele, Hall Mei-Hua, Walshe Muriel, Murray Robin M, McDonald Colm
Section of Neuroscience and Emotion, Psychological Medicine and Psychiatry, King's College London Institute of Psychiatry, London, United Kingdom.
Biol Psychiatry. 2008 Sep 15;64(6):513-20. doi: 10.1016/j.biopsych.2008.04.038. Epub 2008 Jun 20.
There is evidence that patients with bipolar disorder have working memory deficits even during periods of euthymia. The neural basis of such deficits and its relationship with genetic risk remain unclear. We utilized functional magnetic resonance imaging (fMRI) to investigate neural activity in samples of bipolar disorder patients and their unaffected first-degree relatives while performing working memory tasks of increasing difficulty.
Twenty remitted bipolar I disorder patients, 20 of their unaffected first-degree relatives, and 20 healthy volunteers were recruited and successfully completed scanning. Subjects participated in fMRI scans consisting of an n-back working memory task with three stages of increasing difficulty (1-back, 2-back, and 3-back), alternating with a baseline attention task. Groups were analyzed separately to produce brain activation maps, and a group-by-task analysis of variance (ANOVA) with post hoc comparisons was completed.
Patients performed more poorly online than control subjects and relatives on the 2-back and 3-back tasks. The group-by-task ANOVA demonstrated a significantly altered region of neural activity involving a cluster located in the left frontal pole/ventrolateral gyrus. Post hoc analyses demonstrated that this cluster was accounted for by significantly greater activation in relatives compared with control subjects for the 2-back task. Patients demonstrated a trend to significantly greater activation than control subjects in the same cluster during 1-back performance.
Left prefrontal hyperactivation during working memory is associated with genetic liability for bipolar disorder and represents a potential neurobiological endophenotype for the illness.
有证据表明,双相情感障碍患者即使在心境正常期间也存在工作记忆缺陷。这种缺陷的神经基础及其与遗传风险的关系尚不清楚。我们利用功能磁共振成像(fMRI)来研究双相情感障碍患者及其未受影响的一级亲属在执行难度逐渐增加的工作记忆任务时的神经活动。
招募了20名缓解期的双相I型障碍患者、20名他们未受影响的一级亲属和20名健康志愿者,并成功完成扫描。受试者参与了fMRI扫描,扫描包括一个n-back工作记忆任务,该任务有三个难度逐渐增加的阶段(1-back、2-back和3-back),与一个基线注意力任务交替进行。对各组分别进行分析以生成脑激活图,并完成了一项任务分组方差分析(ANOVA)及事后比较。
在2-back和3-back任务中,患者在在线表现上比对照组受试者和亲属更差。任务分组方差分析显示,神经活动区域有显著改变,涉及位于左额极/腹外侧回的一个簇。事后分析表明,在2-back任务中,与对照组受试者相比,亲属在该簇中的激活明显更强,从而解释了该簇的情况。在1-back任务表现期间,患者在同一簇中的激活比对照组受试者有显著更强的趋势。
工作记忆期间左前额叶过度激活与双相情感障碍的遗传易感性相关,代表了该疾病潜在的神经生物学内表型。