Large-scale functional brain network abnormalities in Alzheimer's disease: Insights from functional neuroimaging

被引:0
作者
Dickerson, Bradford C. [1 ,2 ,3 ,4 ,5 ]
Sperling, Reisa A. [1 ,2 ,4 ,5 ]
机构
[1] Harvard Univ, Sch Med, Dept Neurol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Massachusetts Alzheimers Dis Res Ctr, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Frontotemporal Dementia Unit, Boston, MA 02115 USA
[4] Massachusetts Gen Hosp, Athinoula A Martinos Ctr Biomed Imaging, Boston, MA 02114 USA
[5] Brigham & Womens Hosp, Div Cognit & Behav Neurol, Dept Neurol, Boston, MA 02115 USA
关键词
Alzheimer's disease; mild cognitive impairment; functional magnetic resonance imaging; hippocampus; parietal cortex; MILD COGNITIVE IMPAIRMENT; POSITRON-EMISSION-TOMOGRAPHY; APOLIPOPROTEIN-E EPSILON-4; HIPPOCAMPAL ACTIVATION; GENETIC RISK; DEFAULT-MODE; PARIETAL DEACTIVATION; MEMORY DECLINE; WORKING-MEMORY; FMRI EVIDENCE;
D O I
10.1155/2009/610392
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Functional MRI (fMRI) studies of mild cognitive impairment (MCI) and Alzheimer's disease (AD) have begun to reveal abnormalities in large-scale memory and cognitive brain networks. Since the medial temporal lobe (MTL) memory system is a site of very early pathology in AD, a number of studies have focused on this region of the brain. Yet it is clear that other regions of the large-scale episodic memory network are affected early in the disease as well, and fMRI has begun to illuminate functional abnormalities in frontal, temporal, and parietal cortices as well in MCI and AD. Besides predictable hypoactivation of brain regions as they accrue pathology and undergo atrophy, there are also areas of hyperactivation in brain memory and cognitive circuits, possibly representing attempted compensatory activity. Recent fMRI data in MCI and AD are beginning to reveal relationships between abnormalities of functional activity in the MTL memory system and in functionally connected brain regions, such as the precuneus. Additional work with "resting state" fMRI data is illuminating functional-anatomic brain circuits and their disruption by disease. As this work continues to mature, it will likely contribute to our understanding of fundamental memory processes in the human brain and how these are perturbed in memory disorders. We hope these insights will translate into the incorporation of measures of task-related brain function into diagnostic assessment or therapeutic monitoring, which will hopefully one day be useful for demonstrating beneficial effects of treatments being tested in clinical trials.
引用
收藏
页码:63 / 75
页数:13
相关论文
共 113 条
[1]   Longitudinal PET evaluation of cerebral metabolic decline in dementia: A potential outcome measure in Alzheimer's disease treatment studies [J].
Alexander, GE ;
Chen, K ;
Pietrini, P ;
Rapoport, SI ;
Reiman, EM .
AMERICAN JOURNAL OF PSYCHIATRY, 2002, 159 (05) :738-745
[2]  
Alsop DC, 2000, ANN NEUROL, V47, P93, DOI 10.1002/1531-8249(200001)47:1<93::AID-ANA15>3.0.CO
[3]  
2-8
[4]   Prodromal Alzheimer's Disease: Successive Emergence of the Clinical Symptoms [J].
Amieva, Helene ;
Le Goff, Melanie ;
Millet, Xavier ;
Orgogozo, Jean Marc ;
Peres, Karine ;
Barberger-Gateau, Pascale ;
Jacqmin-Gadda, Helene ;
Dartigues, Jean Francois .
ANNALS OF NEUROLOGY, 2008, 64 (05) :492-498
[5]   The Topographical and Neuroanatomical Distribution of Neurofibrillary Tangles and Neuritic Plaques in the Cerebral Cortex of Patients with Alzheimer's Disease [J].
Arnold, Steven E. ;
Hyman, Bradley T. ;
Flory, Jill ;
Damasio, Antonio R. ;
Van Hoesen, Gary W. .
CEREBRAL CORTEX, 1991, 1 (01) :103-116
[6]  
BAKKOUR A, 2008, NEUROLOGY
[7]   Familial risk for Alzheimer's disease alters fMRI activation patterns [J].
Bassett, SS ;
Yousem, DM ;
Cristinzio, C ;
Kusevic, I ;
Yassa, MA ;
Caffo, BS ;
Zeger, SL .
BRAIN, 2006, 129 :1229-1239
[8]   fMRI evidence of compensatory mechanisms in older adults at genetic risk for Alzheimer disease [J].
Bondi, MW ;
Houston, WS ;
Eyler, LT ;
Brown, GG .
NEUROLOGY, 2005, 64 (03) :501-508
[9]   Patterns of brain activation in people at risk for Alzheimer's disease [J].
Bookheimer, SY ;
Strojwas, MH ;
Cohen, MS ;
Saunders, AM ;
Pericak-Vance, MA ;
Mazziotta, JC ;
Small, GW .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 343 (07) :450-456
[10]  
Borghesani P.R., 2007, NEUROBIOL AGING