기억장애성 경도인지장애 환자의 양전자방출단층촬영검사에서 아밀로이드 침착이 해마 대사량에 미치는 영향 : 예비연구
Effect of Amyloid Deposition in PET on Hippocampal Metabolism in Amnestic-Mild Cognitive Impairment : Pilot Study
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Objectives:Most studies of hippocampal metabolism(HM) in amnestic mild cognitive impairment(aMCI) gave inconsistent results. Our objective was to evaluate the effect of amyloid-beta(Aβ) status on hippocampal metabolism in aMCI. Methods:Overall, 23 aMCI underwent three-dimensional magnetic resonance imaging(MRI), 18F-fluorodeoxyglucose-positron emission tomography(18FDG-PET) and 18F-Fluorbetaben amyloid positron emission tomography (amyloid-PET). According to Aβ status on amyloid PET, 23 aMCI were classified as either Aβ+aMCI(N=13) or Aβ-aMCI(N= 10). The primary outcome was HM using 18FDG-PET and we investigate the difference on HM between Aβ+aMCI and Aβ-aMCI using analysis of variance(ANOVA) model, after controlling hippocampal volume. Results:We found that HM was more decreased in Aβ+aMCI than Aβ-aMCI. This result was not changed after controlling hippocampal volume. Conclusion:Our findings suggest that Aβ+ is associated with decreased HM, regardless of hippocampal volume, in aMCI.
Abstract
Objectives:Most studies of hippocampal metabolism(HM) in amnestic mild cognitive impairment(aMCI) gave inconsistent results. Our objective was to evaluate the effect of amyloid-beta(Aβ) status on hippocampal metabolism in aMCI. Methods:Overall, 23 aMCI underwent three-dimensional magnetic resonance imaging(MRI), 18F-fluorodeoxyglucose-positron emission tomography(18FDG-PET) and 18F-Fluorbetaben amyloid positron emission tomography (amyloid-PET). According to Aβ status on amyloid PET, 23 aMCI were classified as either Aβ+aMCI(N=13) or Aβ-aMCI(N= 10). The primary outcome was HM using 18FDG-PET and we investigate the difference on HM between Aβ+aMCI and Aβ-aMCI using analysis of variance(ANOVA) model, after controlling hippocampal volume. Results:We found that HM was more decreased in Aβ+aMCI than Aβ-aMCI. This result was not changed after controlling hippocampal volume. Conclusion:Our findings suggest that Aβ+ is associated with decreased HM, regardless of hippocampal volume, in aMCI.
참고문헌 (26)
- Petersen RC, "Mild cognitive impairment", Continuum(Minneap Minn), 22, pp.404~418 (2016)
- Li JQ, "Risk factors for predicting progression from mild cognitive impairment to Alzheimer’s disease : a systematic review and meta-analysis of cohort studies", J Neurol Neurosurg Psychiatry, 87, pp.476~484 (2016)
- Hyman BT, "Perforant pathway changes and the memory impairment of Alzheimer’s disease", Ann Neurol, 20, pp.472~481 (1986)
- Bartsch T, "CA1 neurons in the human hippocampus are critical for autobiographical memory, mental time travel, and autonoetic consciousness", Proc Natl Acad Sci U S A, 108, pp.17562~17567 (2011)
- Pagani M, "MCI patients declining and not-declining at mid-term follow-up : FDG-PET findings", Curr Alzheimer Res, 7, pp.287~294 (2010)
- De Santi S, "Hippocampal formation glucose metabolism and volume losses in MCI and AD", Neurobiol Aging, 22, pp.529~539 (2001)
- Mosconi L, "Reduced hippocampal metabolism in MCI and AD : automated FDG-PET image analysis", Neurology, 64, pp.1860~1867 (2005)
- Mevel K, "Detecting hippocampal hypometabolism in Mild Cognitive Impairment using automatic voxel-based approaches", Neuroimage, 37, pp.18~25 (2007)
- Chételat G, "Direct voxel-based comparison between grey matter hypometabolism and atrophy in Alzheimer's disease", Brain, 131, pp.60~71 (2008)
- Kawachi T, "Comparison of the diagnostic performance of FDG-PET and VBM-MRI in very mild Alzheimer’s disease", Eur J Nucl Med Mol Imaging, 33, pp.801~809 (2006)
- Klunk WE, "Imaging brain amyloid in Alzheimer's disease with Pittsburgh Compound-B", Ann Neurol, 55, pp.306~319 (2004)
- Kang Y, "Seoul neuropsychological screening baterry" (2003), Human Brain Research & Consulting Co
- Petersen RC, "Mild cognitive impairment as a diagnostic entity", J Intern Med, 256, pp.183~194 (2004)
- Baek MJ, "Comparison between the story recall test and the word-list learning test in Korean patients with mild cognitive impairment and early stage of Alzheimer’s disease", J Clin Exp Neuropsychol, 34, pp.396~404 (2012)
- Fischl B, "Measuring the thickness of the human cerebral cortex from magnetic resonance images", Proc Natl Acad Sci U S A, 97, pp.11050~11055 (2000)
- Tzourio-Mazoyer N, "Automated anatomical labeling of activations in SPM using a macroscopic anatomical parcellation of the MNI MRI singlesubject brain", Neuroimage, 15, pp.273~289 (2002)
- (2014)[URL]
- Furst AJ, "Amyloid-beta and glucose metabolism in Alzheimer’s disease", J Alzheimers Dis, 26(Suppl 3), pp.105~116 (2011)
- Carbonell F, "Modulation of glucose metabolism and metabolic connectivity by beta-amyloid", J Cereb Blood Flow Metab, 36, pp.2058~2071 (2016)
- Lowe VJ, "Association of hypometabolism and amyloid levels in aging, normal subjects", Neurology, 82, pp.1959~1967 (2014)
- Hanseeuw BJ, "Decreased hippocampal metabolism in high-amyloid mild cognitive impairment", Alzheimers Dement, 12, pp.1288~1296 (2016)
- Kljajevic V, "Distinct pattern of hypometabolism and atrophy in preclinical and predementia Alzheimer’s disease", Neurobiol Aging, 35, pp.1973~1981 (2014)
- Weiner MW, "Recent publications from the Alzheimer’s disease neuroimaging initiative: reviewing progress toward improved AD clinical trials", Alzheimers Dement, 13, pp.e1~e85 (2017)
- Liu Y, "APOE genotype and neuroimaging markers of Alzheimer's disease : systematic review and meta-analysis", J Neurol Neurosurg Psychiatry, 86, pp.127~134 (2015)
- Elcombe EL, "Hippocampal volume in older adults at risk of cognitive decline: the role of sleep, vascular risk, and depression", J Alzheimers Dis, 44, pp.1279~1290 (2015)
- Rhindress K, "Hippocampal subregion volume changes associated with antipsychotic treatment in first-episode psychosis", Psychol Med, 47, pp.1706~1718 (2017)
