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Neurology 2000;55:484-490
© 2000 American Academy of Neurology


Articles

Rates of hippocampal atrophy correlate with change in clinical status in aging and AD

C. R. Jack, Jr., MD, R. C. Petersen, MD, PhD, Y. Xu, MD, PhD, P. C. O’Brien, PhD, G. E. Smith, PhD, R. J. Ivnik, PhD, B. F. Boeve, MD, E. G. Tangalos, MD and E. Kokmen, MD

From the Departments of Diagnostic Radiology (Drs. Jack and Xu), Neurology (Drs. Petersen, Boeve, and Kokmen), Health Sciences Research (Dr. O’Brien), Department of Psychiatry and Psychology (Drs. Smith and Ivnik), Department of Internal Medicine (Dr. Tangalos), Mayo Clinic and Foundation, Rochester, MN.

Address correspondence and reprint requests to Dr. Clifford R. Jack Jr, Mayo Clinic, Diagnostic Radiology, 200 First Street SW, Rochester, MN 55905

BACKGROUND: The cognitive continuum in the elderly population can be conceptually divided into those who are functioning normally (control subjects), those with a mild cognitive impairment (MCI), and those with probable AD.

OBJECTIVES: To test the hypothesis that the annualized rates of hippocampal atrophy differ as a function of both baseline and change in clinical group membership (control, MCI, or AD).

METHODS: The authors identified 129 subjects from the Mayo Clinic AD Research Center/AD Patient Registry who met established criteria for normal control subjects, MCI, or probable AD, both at entry and at the time of a subsequent clinical follow-up evaluation 3 ± 1 years later. Each subject underwent an MRI examination of the head at the time of the initial assessment and at follow-up clinical assessment; the annualized percentage change in hippocampal volume was computed. Subjects who were classified as controls or patients with MCI at baseline could either remain cognitively stable or could decline to a lower functioning group over the period of observation.

RESULTS: The annualized rates of hippocampal volume loss for each of the three initial clinical groups decreased progressively in the following order: AD > MC > control. Within the control and MCI groups, those who declined had a significantly greater rate of volume loss than those who remained clinically stable. The mean annualized rates of hippocampal atrophy by follow-up clinical group were: control-stable 1.73%, control-decliner 2.81%, MCI-stable 2.55%, MCI-decliner 3.69%, AD 3.5%.

CONCLUSION: Rates of hippocampal atrophy match both baseline cognitive status and the change in cognitive status over time in elderly persons who lie along the cognitive continuum from normal to MCI to AD.




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NeurologyHome page
D. A. Drachman
Hat size, brain size, intelligence, and dementia: What morphometry can tell us about brain function and disease
Neurology, July 23, 2002; 59(2): 156 - 157.
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Cereb CortexHome page
C. Davatzikos and S. M. Resnick
Degenerative Age Changes in White Matter Connectivity Visualized In Vivo using Magnetic Resonance Imaging
Cereb Cortex, July 1, 2002; 12(7): 767 - 771.
[Abstract] [Full Text] [PDF]


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Proc. Natl. Acad. Sci. USAHome page
A. D. Smith
Imaging the progression of Alzheimer pathology through the brain
PNAS, April 2, 2002; 99(7): 4135 - 4137.
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Proc. Natl. Acad. Sci. USAHome page
R. I. Scahill, J. M. Schott, J. M. Stevens, M. N. Rossor, and N. C. Fox
Mapping the evolution of regional atrophy in Alzheimer's disease: Unbiased analysis of fluid-registered serial MRI
PNAS, April 2, 2002; 99(7): 4703 - 4707.
[Abstract] [Full Text] [PDF]


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Arch NeurolHome page
S. Marquis, M. M. Moore, D. B. Howieson, G. Sexton, H. Payami, J. A. Kaye, and R. Camicioli
Independent Predictors of Cognitive Decline in Healthy Elderly Persons
Arch Neurol, April 1, 2002; 59(4): 601 - 606.
[Abstract] [Full Text] [PDF]


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StrokeHome page
J.C. de la Torre
Alzheimer Disease as a Vascular Disorder: Nosological Evidence
Stroke, April 1, 2002; 33(4): 1152 - 1162.
[Abstract] [Full Text] [PDF]


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Am. J. Neuroradiol.Home page
B. L. Miller
Past Glory and Future Promise: Maximizing and Improving Understanding of Atrophy Patterns in the Diagnosis of Degenerative Dementias
AJNR Am. J. Neuroradiol., January 1, 2002; 23(1): 33 - 34.
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BrainHome page
T. den Heijer, S. E Vermeer, R. Clarke, M. Oudkerk, P. J. Koudstaal, A. Hofman, and M. M. B. Breteler
Homocysteine and brain atrophy on MRI of non-demented elderly
Brain, January 1, 2002; 126(1): 170 - 175.
[Abstract] [Full Text] [PDF]


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Arch NeurolHome page
R. C. Petersen, R. Doody, A. Kurz, R. C. Mohs, J. C. Morris, P. V. Rabins, K. Ritchie, M. Rossor, L. Thal, and B. Winblad
Current Concepts in Mild Cognitive Impairment
Arch Neurol, December 1, 2001; 58(12): 1985 - 1992.
[Abstract] [Full Text] [PDF]


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Arch NeurolHome page
D. Sencakova, N. R. Graff-Radford, F. B. Willis, J. A. Lucas, F. Parfitt, R. H. Cha, P. C. O'Brien, R. C. Petersen, and C. R. Jack Jr
Hippocampal Atrophy Correlates With Clinical Features of Alzheimer Disease in African Americans
Arch Neurol, October 1, 2001; 58(10): 1593 - 1597.
[Abstract] [Full Text] [PDF]


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J Geriatr Psychiatry NeurolHome page
Y.-Y. Hsu, A.-T. Du, N. Schuff, and M. W. Weiner
Magnetic Resonance Imaging and Magnetic Resonance Spectroscopy in Dementias
J Geriatr Psychiatry Neurol, September 1, 2001; 14(3): 145 - 166.
[Abstract] [PDF]


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Proc. Natl. Acad. Sci. USAHome page
M. J. de Leon, A. Convit, O. T. Wolf, C. Y. Tarshish, S. DeSanti, H. Rusinek, W. Tsui, E. Kandil, A. J. Scherer, A. Roche, et al.
Prediction of cognitive decline in normal elderly subjects with 2-[18F]fluoro-2-deoxy-D-glucose/positron-emission tomography (FDG/PET)
PNAS, August 23, 2001; (2001) 191044198.
[Abstract] [Full Text] [PDF]


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Proc. Natl. Acad. Sci. USAHome page
M. J. de Leon, A. Convit, O. T. Wolf, C. Y. Tarshish, S. DeSanti, H. Rusinek, W. Tsui, E. Kandil, A. J. Scherer, A. Roche, et al.
Prediction of cognitive decline in normal elderly subjects with 2-[18F]fluoro-2-deoxy-D-glucose/positron-emission tomography (FDG/PET)
PNAS, September 11, 2001; 98(19): 10966 - 10971.
[Abstract] [Full Text] [PDF]




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