Functional MRI study of memory-related brain regions in patients with depressive disorder

被引:53
作者
Werner, Natalie S. [1 ,2 ]
Meindl, Thomas [3 ]
Materne, Julia [2 ]
Engel, Rolf R. [2 ]
Huber, Dorothea [4 ,5 ]
Riedel, Michael [2 ]
Reiser, Maximilian [3 ]
Hennig-Fast, Kristina [1 ,2 ]
机构
[1] Univ Munich, Dept Psychol, D-80802 Munich, Germany
[2] Univ Munich, Clin Psychiat & Psychotherapy, D-80802 Munich, Germany
[3] Univ Munich, Inst Clin Radiol, D-80802 Munich, Germany
[4] Tech Univ Munich, Clin Psychosomat Med & Psychotherapy, D-8000 Munich, Germany
[5] Municipal Clin Munich, Clin Psychosomat Med & Psychotherapy, Munich, Germany
关键词
Depression; Associative learning; Memory; Hippocampus; fMRI; POSITRON-EMISSION-TOMOGRAPHY; RECURRENT MAJOR DEPRESSION; HIPPOCAMPAL VOLUME; UNIPOLAR DEPRESSION; LOBE DYSFUNCTION; METAANALYSIS; RETRIEVAL; SYSTEM; DAMAGE; ABNORMALITIES;
D O I
10.1016/j.jad.2009.03.003
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Structural imaging studies of patients suffering from depressive disorder have revealed reduced hippocampal volume in the majority of cases. The present study aimed specifically at investigating the hippocampal function in unipolar depression using functional magnetic resonance imaging (fMRI). Methods: Eleven unipolar depressed patients and eleven healthy control participants matched for age, gender and years of education underwent an associative learning paradigm during fMRI scanning. In the encoding condition of the paradigm, participants had to learn face-profession pairs. These pairs had to be remembered in the retrieval condition. Results: Hippocampal activity did not differ between depressive patients and control participants during encoding or retrieval. However, during encoding, depressive patients showed increased activity in the left parahippocampal gyrus and decreased activity in frontal and parietal regions. Retrieval of the associative pairs also yielded decreased activation patterns in depressive patients in frontal and parietal areas. Limitations: The present findings may be limited by the small sample size of participants. Additionally the comparatively young age of the depressive sample could indicate a comparatively shorter duration of illness, and thereby less salient measurable hippocampal abnormalities. Conclusion: The current study suggests that depression is associated with modified memory-related brain function. In particular the parahippocampal gyrus, the prefrontal cortex and parietal regions show functional alterations during associative learning. These structures as well as their interrelationships may play an important role in the pathogenesis of depressive disorder. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:124 / 131
页数:8
相关论文
共 58 条
[1]   HPA axis dysfunction in unmedicated major depressive disorder and its normalization by pharmacotherapy correlates with alteration of neural activity in prefrontal cortex and limbic/paralimbic regions [J].
Aihara, Masako ;
Ida, Itsuro ;
Yuuki, Naoya ;
Oshima, Akihiko ;
Kurnano, Hiroshi ;
Takahashi, Keisuke ;
Fukuda, Masato ;
Oriuchi, Noboru ;
Endo, Keigo ;
Matsuda, Hiroshi ;
Mikuni, Masahiko .
PSYCHIATRY RESEARCH-NEUROIMAGING, 2007, 155 (03) :245-256
[2]   Gender-linked brain injury in experimental stroke [J].
Alkayed, NJ ;
Harukuni, I ;
Kimes, AS ;
London, ED ;
Traystman, RJ ;
Hurn, PD .
STROKE, 1998, 29 (01) :159-165
[3]  
[Anonymous], 1997, SKID
[4]   Cognitive performance in tests sensitive to frontal lobe dysfunction in the elderly depressed [J].
Beats, BC ;
Sahakian, BJ ;
Levy, R .
PSYCHOLOGICAL MEDICINE, 1996, 26 (03) :591-603
[5]  
Beblo T., 1999, COGN NEUROPSYCHIATRY, V4, P333
[6]   THE ANATOMY OF MELANCHOLIA - FOCAL ABNORMALITIES OF CEREBRAL BLOOD-FLOW IN MAJOR DEPRESSION [J].
BENCH, CJ ;
FRISTON, KJ ;
BROWN, RG ;
SCOTT, LC ;
FRACKOWIAK, RSJ ;
DOLAN, RJ .
PSYCHOLOGICAL MEDICINE, 1992, 22 (03) :607-615
[7]  
BENES FM, 1994, ARCH GEN PSYCHIAT, V51, P477
[8]  
BONHILLA L, 2003, BRAIN IMAGING, V14, P1291
[9]   Hippocampal volume reduction in major depression [J].
Bremner, JD ;
Narayan, M ;
Anderson, ER ;
Staib, LH ;
Miller, HL ;
Charney, DS .
AMERICAN JOURNAL OF PSYCHIATRY, 2000, 157 (01) :115-117
[10]   Men may be more vulnerable to seizure-associated brain damage [J].
Briellmann, RS ;
Berkovic, SF ;
Jackson, GD .
NEUROLOGY, 2000, 55 (10) :1479-1485