Impaired medial temporal repetition suppression is related to failure of parietal deactivation in alzheimer disease

American Journal of Geriatric Psychiatry

Volumn 16, Issue 4, 2008, Pages 283-292

  Pihlajamäsignki, Maija ^a,b,c   Depeau, Kristina M ^a,c   Blacker, Deborah ^c   Sperling, Reisa A ^a,c  

^a MASSACHUSETTS GENERAL HOSPITAL   (United States)

^b UNIVERSITY OF EASTERN FINLAND   (Finland)

^c Department of Psychiatry ^*  (United States)

Author keywords

Alzheimer disease; FMRI; Medial temporal lobe; Memory; Parietal cortex; Repetition suppression

Indexed keywords

AGED; ALZHEIMER DISEASE; ARTICLE; ASSOCIATIVE MEMORY; BRAIN REGION; CLINICAL ARTICLE; COMPARATIVE STUDY; CONTROLLED STUDY; EPISODIC MEMORY; FACE; FEMALE; FUNCTIONAL MAGNETIC RESONANCE IMAGING; HUMAN; MALE; MEMORY; MEMORY DISORDER; NERVE CELL NETWORK; NOMENCLATURE; PARIETAL LOBE; PERFORMANCE; PREFRONTAL CORTEX; RECOGNITION; STIMULUS RESPONSE; TASK PERFORMANCE; TEMPORAL LOBE; BRAIN MAPPING; COGNITION; EDUCATIONAL STATUS; HIPPOCAMPUS; HOSPITALIZATION; NUCLEAR MAGNETIC RESONANCE IMAGING; PATHOLOGY; PATHOPHYSIOLOGY; PHYSIOLOGY; PROSOPAGNOSIA; REFERENCE VALUE;

AGED; AGED, 80 AND OVER; ALZHEIMER DISEASE; BRAIN MAPPING; COGNITION; EDUCATIONAL STATUS; FEMALE; HIPPOCAMPUS; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; PARIETAL LOBE; PROSOPAGNOSIA; REFERENCE VALUES; SEVERITY OF ILLNESS INDEX; TEMPORAL LOBE;

EID: 47249145329     PISSN: 10647481     EISSN: 15457214     Source Type: Journal    
DOI: 10.1097/JGP.0b013e318162a0a9     Document Type: Article

References (37)

1. Ranganath C, Rainer G: Neural mechanisms for detecting and remembering novel events. Nat Rev Neurosci 2003; 4:193-202
2. Hasselmo ME, Stern CE: Mechanisms underlying working memory for novel information. Trends Cogn Sci 2006; 10:487-493
3. Hyman BT, Van Hoesen GW, Damasio AR, et al: Alzheimer's disease: cell-specific pathology isolates the hippocampal formation. Science 1984; 225:1168-1170
4. Braak H, Braak E: Neuropathological staging of Alzheimer-related changes. Acta Neuropathol (Berl) 1991; 82:239-259
5. Selkoe DJ: Alzheimer's disease is a synaptic failure. Science 2002; 298:789-791
6. Rombouts SA, Barkhof F, Veltman DJ, et al: Functional MR imaging in Alzheimer's disease during memory encoding. Am J Neuroradiol 2000; 21:1869-1875
7. Sperling RA, Bates JF, Chua EF, et al: fMRI studies of associative encoding in young and elderly controls and mild Alzheimer's disease. J Neurol Neurosurg Psychiatry 2003; 74:44-50
8. Dickerson BC, Salat DH, Greve DN, et al: Increased hippocampal activation in mild cognitive impairment compared to normal aging and AD. Neurology 2005; 65:404-411
9. Golby A, Silverberg G, Race E, et al: Memory encoding in Alzheimer's disease: an fMRI study of explicit and implicit memory. Brain 2005; 128:773-787
10. Brown MW, Aggleton JP: Recognition memory: what are the roles of the perirhinal cortex and hippocampus? Nat Rev Neurosci 2001; 2:51-61
11. Grill-Spector K, Henson R, Martin A: Repetition and the brain: neural models of stimulus-specific effects. Trends Cogn Sci 2006; 10:14-23
12. Rand-Giovannetti E, Chua EF, Driscoll AE, et al: Hippocampal and neocortical activation during repetitive encoding in older persons. Neurobiol Aging 2006; 27:173-182
13. Johnson SC, Baxter LC, Susskind-Wilder L, et al: Hippocampal adaptation to face repetition in healthy elderly and mild cognitive impairment. Neuropsychologia 2004; 42:980-989
14. Lustig C, Snyder AZ, Bhakta M, et al: Functional deactivations: change with age and dementia of the Alzheimer type. Proc Natl Acad Sci U S A 2003; 100:14504-14509
15. Greicius MD, Srivastava G, Reiss AL, et al: Default-mode network activity distinguishes Alzheimer's disease from healthy aging: evidence from functional MRI. Proc Natl Acad Sci U S A 2004; 101:4637-4642
16. Rombouts SA, Barkhof F, Goekoop R, et al: Altered resting state networks in mild cognitive impairment and mild Alzheimer's disease: an fMRI study. Hum Brain Mapp 2005; 26:231-239
17. Celone KA, Calhoun VD, Dickerson BC, et al: Alterations in memory networks in mild cognitive impairment and Alzheimer's disease: an independent component analysis. J Neurosci 2006; 26:10222-10231
18. Daselaar SM, Prince SE, Cabeza R: When less means more: deactivations during encoding that predict subsequent memory. Neuroimage 2004; 23:921-927
19. Grady CL, Springer MV, Hongwanishkul D, et al: Age-related changes in brain activity across the adult lifespan. J Cogn Neurosci 2006; 18:227-241
20. Morris JC, Ernesto C, Schafer K, et al: Clinical dementia rating training and reliability in multicenter studies: the Alzheimer's Disease Cooperative Study experience. Neurology 1997; 48:1508-1510
21. McKhann G, Drachman D, Folstein M, et al: Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease. Neurology 1984; 34:939-944
22. Sperling RA, Bates J, Cocchiarella A, et al: Encoding novel face-name associations: a functional MRI study. Hum Brain Mapp 2001; 14:129-139
23. Beckmann C, Jenkinson M, Smith SM: General multi-level linear modeling for group analysis in FMRI. Neuroimage 2003; 20:1052-1063
24. Worsley KJ, Evans AC, Marrett S, et al: A three-dimensional statistical analysis for CBF activation studies in human brain. J Cereb Blood Flow Metab 1992; 12:900-918
25. Stern CE, Corkin S, Gonzalez RG, et al: The hippocampal formation participates in novel picture encoding: evidence from functional magnetic resonance imaging. Proc Natl Acad Sci U S A 1996; 93:8660-8665
26. Pihlajamäki M, Tanila H, Hänninen T, et al: Encoding of novel picture pairs activates the perirhinal cortex: an fMRI study. Hippocampus 2003; 13:67-80
27. Small SA, Perera GM, DeLaPaz R, et al: Differential regional dysfunction of the hippocampal formation among elderly with memory decline and Alzheimer's disease. Ann Neurol 1999; 45:466-472
28. Hämäläinen A, Pihlajamäki M, Tanila H, et al: Increased fMRI responses during encoding in mild cognitive impairment. Neurobiol Aging 2006; 28:1889-1903
29. Zorrilla LT, Jeste DV, Brown GG: Functional MRI and novel picture-learning among older patients with chronic schizophrenia: abnormal correlations between recognition memory and medial temporal brain response. Am J Geriatr Psychiatry 2002; 10:52-61
30. Pihlajamäki M, Tanila H, Könönen M, et al: Visual presentation of novel objects and new spatial arrangements of objects differentially activates the medial temporal lobe subareas in humans. Eur J Neurosci 2004; 19:1939-1949
31. Sperling R, Chua E, Cocchiarella A, et al: Putting names to faces: successful encoding of associative memories activates the anterior hippocampal formation. Neuroimage 2003; 20:1400-1410
32. Grön G, Riepe MW: Neural basis for the cognitive continuum in episodic memory from health to Alzheimer disease. Am J Geriatr Psychiatry 2004; 12:648-652
33. Gonsalves BD, Kahn I, Curran T, et al: Memory strength and repetition suppression: multimodal imaging of medial temporal cortical contributions to recognition. Neuron 2005; 47:751-761
34. Kogure D, Matsuda H, Ohnishi T, et al: Longitudinal evaluation of early Alzheimer's disease using brain perfusion SPECT. J Nucl Med 2000; 41:1155-1162
35. Kircher TT, Erb M, Grodd W, et al: Cortical activation during cholinesterase-inhibitor treatment in Alzheimer disease: preliminary findings from a pharmaco-fMRI study. Am J Geriatr Psychiatry 2005; 13:1006-1013
36. Matthews B, Siemers ER, Mozley PD: Imaging-based measures of disease progression in clinical trials of disease-modifying drugs for Alzheimer disease. Am J Geriatr Psychiatry 2003; 11:146-159
37. Herholz K, Salmon E, Perani D, et al: Discrimination between Alzheimer dementia and controls by automated analysis of multicenter FDG PET. Neuroimage 2002; 17:302-316