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000139144 0247_ $$2doi$$a10.1212/WNL.0000000000003585
000139144 0247_ $$2pmid$$apmid:28062720
000139144 0247_ $$2pmc$$apmc:PMC5304459
000139144 0247_ $$2ISSN$$a0028-3878
000139144 0247_ $$2ISSN$$a1526-632X
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000139144 037__ $$aDZNE-2020-05466
000139144 041__ $$aEnglish
000139144 082__ $$a610
000139144 1001_ $$0P:(DE-2719)2810708$$aGrothe, Michel J$$b0$$eFirst author$$udzne
000139144 245__ $$aMultimodal characterization of older APOE2 carriers reveals selective reduction of amyloid load.
000139144 260__ $$a[S.l.]$$bOvid$$c2017
000139144 264_1 $$2Crossref$$3online$$bOvid Technologies (Wolters Kluwer Health)$$c2017-01-06
000139144 264_1 $$2Crossref$$3print$$bOvid Technologies (Wolters Kluwer Health)$$c2017-02-07
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000139144 3367_ $$2BibTeX$$aARTICLE
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000139144 520__ $$aTo comprehensively assess neurobiological effects of the protective APOE2 allele in the aged brain using a cross-sectional multimodal neuroimaging approach.Multimodal neuroimaging data were obtained from a total of 572 older individuals without dementia (cognitively normal and mild cognitive impairment) enrolled in the Alzheimer's Disease Neuroimaging Initiative and included assessments of regional amyloid load with AV45-PET, glucose metabolism with fluorodeoxyglucose-PET, and gray matter volume with structural MRI. Imaging indexes of APOE2 carriers were contrasted to risk-neutral APOE3 homozygotes, and analyses were controlled for age, sex, education, and clinical diagnosis. Additional models examined genotype-specific effects of age on the imaging markers.In region-of-interest-based analyses, APOE2 carriers had significantly less precuneal amyloid pathology and did not show the typical age-related increase in amyloid load, although the age × genotype interaction was only trend-level significant. In contrast, parietal metabolism and hippocampal volume did not differ between APOE2 and APOE3 genotypes, and both groups showed comparable negative effects of age on these markers. The amyloid specificity of APOE2-related brain changes was corroborated in 2 complementary analyses: spatially unbiased voxel-wise analyses showing widespread reductions in amyloid deposition but no differences in gray matter volume or metabolism and an analysis of CSF-based biomarkers showing a significant effect on amyloid but not on tau pathology.Regarding the range of Alzheimer disease biomarkers considered in the present study, the APOE2 allele appears to have a relatively selective effect on reduced accumulation of amyloid pathology in the aged brain.
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000139144 650_7 $$2NLM Chemicals$$aAmyloid
000139144 650_7 $$2NLM Chemicals$$aApolipoprotein E2
000139144 650_7 $$2NLM Chemicals$$aApolipoprotein E3
000139144 650_7 $$2NLM Chemicals$$aBiomarkers
000139144 650_7 $$2NLM Chemicals$$aRadiopharmaceuticals
000139144 650_7 $$00Z5B2CJX4D$$2NLM Chemicals$$aFluorodeoxyglucose F18
000139144 650_7 $$0IY9XDZ35W2$$2NLM Chemicals$$aGlucose
000139144 650_2 $$2MeSH$$aAged
000139144 650_2 $$2MeSH$$aAging: genetics
000139144 650_2 $$2MeSH$$aAging: metabolism
000139144 650_2 $$2MeSH$$aAging: pathology
000139144 650_2 $$2MeSH$$aAmyloid: metabolism
000139144 650_2 $$2MeSH$$aApolipoprotein E2: genetics
000139144 650_2 $$2MeSH$$aApolipoprotein E3: genetics
000139144 650_2 $$2MeSH$$aBiomarkers: cerebrospinal fluid
000139144 650_2 $$2MeSH$$aBrain: diagnostic imaging
000139144 650_2 $$2MeSH$$aBrain: metabolism
000139144 650_2 $$2MeSH$$aCognitive Dysfunction: diagnostic imaging
000139144 650_2 $$2MeSH$$aCognitive Dysfunction: metabolism
000139144 650_2 $$2MeSH$$aFemale
000139144 650_2 $$2MeSH$$aFluorodeoxyglucose F18
000139144 650_2 $$2MeSH$$aGlucose: metabolism
000139144 650_2 $$2MeSH$$aGray Matter: diagnostic imaging
000139144 650_2 $$2MeSH$$aGray Matter: metabolism
000139144 650_2 $$2MeSH$$aHeterozygote
000139144 650_2 $$2MeSH$$aHumans
000139144 650_2 $$2MeSH$$aMagnetic Resonance Imaging
000139144 650_2 $$2MeSH$$aMale
000139144 650_2 $$2MeSH$$aMultimodal Imaging
000139144 650_2 $$2MeSH$$aNeuroimaging
000139144 650_2 $$2MeSH$$aOrgan Size
000139144 650_2 $$2MeSH$$aPositron-Emission Tomography
000139144 650_2 $$2MeSH$$aRadiopharmaceuticals
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