4.5 Article

Spatial working memory dysfunction in minimal hepatic encephalopathy: An ethology and BOLD-fMRI study

期刊

BRAIN RESEARCH
卷 1445, 期 -, 页码 62-72

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.brainres.2012.01.036

关键词

Minimal hepatic encephalopathy; Working memory; N-back; Ethology; Functional magnetic resonance imaging

资金

  1. National Nature Science Foundation of China [81072905]
  2. Nature Science Foundation of Guangdong Province of China [S2011010005019, 10151503102000015]
  3. Science and Technology Planning Project of Guangdong Province of China [2010B031600023, 2009B030801323]
  4. Traditional Chinese Medicine Administration Foundation of Guangdong Province of China [2010058, 20111053]
  5. Shantou Technology Bureau Science Foundation of China (Shantou Government Technology [(2011) 46]

向作者/读者索取更多资源

The term minimal hepatic encephalopathy (MHE) refers to a population of individuals who have no recognizable clinical symptoms but perform abnormally on neuropsychological and neurophysiological tests. Research shows that MHE patients have impairments in cognition affecting their daily lives that should be treated. This study explored the neural basis of spatial working memory impairment in MHE patients using behavioral test and BOLD-fMRI. Twelve normal controls, twelve cirrhosis patients without MHE and twelve MHE patients took part. The memory quotient of the MHE group (Wechsler Memory Scale-Chinese revised: WMS-CR) was lower than the normal control group and the cirrhosis-without-MHE group, and primarily concerned short-term memory and transient memory. Performance accuracy was lower for the MHE group than the control group and the cirrhosis-without-MHE group, and mean reaction time was prolonged. The fMRI data highlighted a neural network consisting of: bilateral prefrontal cortex (PFC), bilateral premotor area (PreMA), supplementary motor area (SMA) and bilateral parietal areas (PA), which was activated in the n-back task. The load effect of BOLD-fMRI response appeared in all regions of interest (ROI) for the normal control group, but only appeared in PreMA and PA, and did not vary with n-back load in PFC or SMA for the MHE group. Activation intensities for all ROIs were higher for the normal control group than the MHE group, especially in 2-back load. In conclusion, these results demonstrate that MHE patients have debilitated spatial working memory, and that impairments of bilateral PFC, PMA, SMA, and PA commonly lead to spatial working memory dysfunction. Furthermore, PFC impairment may form the neural basis of spatial working memory impairment. (C) 2012 Elsevier B.V. All rights reserved.

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