Bittner Robert A, Linden David E J, Roebroeck Alard, Härtling Fabian, Rotarska-Jagiela Anna, Maurer Konrad, Goebel Rainer, Singer Wolf, Haenschel Corinna
Laboratory for Neurophysiology and Neuroimaging, Department of Psychiatry, Psychosomatic Medicine and Psychotherapy and Brain Imaging Center, University Hospital Frankfurt, Goethe University, Frankfurt am Main, Germany Department of Neurophysiology, Max-Planck-Institute for Brain Research, Frankfurt am Main, Germany Ernst Strüngmann Institute for Neuroscience (ESI) in Cooperation with Max Planck Society, Frankfurt am Main, Germany.
MRC Centre for Neuropsychiatric Genetics and Genomics, Institute of Psychological Medicine and Clinical Neurosciences, School of Medicine School of Psychology, Cardiff University, Cardiff, UK.
Cereb Cortex. 2015 Sep;25(9):2494-506. doi: 10.1093/cercor/bhu050. Epub 2014 Mar 27.
Behavioral evidence indicates that working memory (WM) in schizophrenia is already impaired at the encoding stage. However, the neurophysiological basis of this primary deficit remains poorly understood. Using event-related fMRI, we assessed differences in brain activation and functional connectivity during the encoding, maintenance and retrieval stages of a visual WM task with 3 levels of memory load in 17 adolescents with early-onset schizophrenia (EOS) and 17 matched controls. The amount of information patients could store in WM was reduced at all memory load levels. During encoding, activation in left ventrolateral prefrontal cortex (VLPFC) and extrastriate visual cortex, which in controls positively correlated with the amount of stored information, was reduced in patients. Additionally, patients showed disturbed functional connectivity between prefrontal and visual areas. During retrieval, right inferior VLPFC hyperactivation was correlated with hypoactivation of left VLPFC in patients during encoding. Visual WM encoding is disturbed by a failure to adequately engage a visual-prefrontal network critical for the transfer of perceptual information into WM. Prefrontal hyperactivation appears to be a secondary consequence of this primary deficit. Isolating the component processes of WM can lead to more specific neurophysiological markers for translational efforts seeking to improve the treatment of cognitive dysfunction in schizophrenia.
行为学证据表明,精神分裂症患者的工作记忆(WM)在编码阶段就已受损。然而,这种原发性缺陷的神经生理学基础仍知之甚少。我们使用事件相关功能磁共振成像(fMRI),评估了17名早发性精神分裂症(EOS)青少年和17名匹配对照在视觉WM任务的编码、维持和检索阶段,在3种记忆负荷水平下大脑激活和功能连接的差异。在所有记忆负荷水平下,患者能够存储在WM中的信息量均减少。在编码过程中,左侧腹外侧前额叶皮层(VLPFC)和纹外视觉皮层的激活减少,而在对照组中,这些区域的激活与存储信息量呈正相关。此外,患者前额叶和视觉区域之间的功能连接紊乱。在检索过程中,患者右侧VLPFC的过度激活与编码过程中左侧VLPFC的激活不足相关。视觉WM编码受到干扰,原因是未能充分激活对将感知信息转移到WM至关重要的视觉-前额叶网络。前额叶过度激活似乎是这种原发性缺陷的继发后果。分离WM的组成过程可以为旨在改善精神分裂症认知功能障碍治疗的转化研究带来更具体的神经生理学标志物。