Three-year changes of cortical F-FDG in amnestic vs. non-amnestic sporadic early-onset Alzheimer's disease
Creators
- 1. Department of Neuroradiology, CHU Lille (France)
- 2. Department of Nuclear Medicine, CHU Lille (France)
- 3. Inserm U1171, CHU Lille, University of Lille (France)
- 4. Inserm U1171, CHU Lille, Memory Center, DISTALZ, University of Lille (France)
- 5. Department of Neurology, CHU Lille (France)
- 6. Department of Neuropsychology, CHU Lille (France)
- 7. Siemens Medical Solutions USA, Inc., Molecular Imaging, Knoxville, TN (United States)
Description
To examine and compare longitudinal changes of cortical glucose metabolism in amnestic and non-amnestic sporadic forms of early-onset Alzheimer's disease and assess potential associations with neuropsychological performance over a 3-year period time. Eighty-two participants meeting criteria for early-onset (< 65 years) sporadic form of probable Alzheimer's disease and presenting with a variety of clinical phenotypes (47 amnestic and 35 non-amnestic forms) were included at baseline and followed up for 1.44 ± 1.23 years. All of the participants underwent a work-up at baseline and every year during the follow-up period, which includes clinical examination, neuropsychological testing, genotyping, cerebrospinal fluid biomarker assays, and structural MRI and F-FDG PET. Vertex-wise partial volume-corrected glucose metabolic maps across the entire cortical surface were generated and longitudinally assessed together with the neuropsychological scores using linear mixed-effects modeling as a function of amnestic and non-amnestic sporadic forms of early-onset Alzheimer's disease. Similar evolution patterns of glucose metabolic decline between amnestic and non-amnestic forms were observed in widespread neocortical cortices. However, only non-amnestic forms appeared to have a greater reduction of glucose metabolism in lateral orbitofrontal and bilateral medial temporal cortices associated with more severe declines of neuropsychological performance compared with amnestic forms. Furthermore, results suggest that glucose metabolic decline in amnestic forms would progress along an anterior-to-posterior axis, whereas glucose metabolic decline in non-amnestic forms would progress along a posterior-to-anterior axis. We found differences in spatial distribution and temporal trajectory of glucose metabolic decline between amnestic and non-amnestic early-onset Alzheimer's disease groups, suggesting that one might want to consider treating the two forms of the disease as two separate entities.
Availability note (English)
Available from: http://dx.doi.org/10.1007/s00259-019-04519-wAdditional details
Identifiers
Publishing Information
- Journal Title
- European Journal of Nuclear Medicine and Molecular Imaging
- Journal Volume
- 47
- Journal Issue
- 2
- Journal Page Range
- p. 304-318
- ISSN
- 1619-7070
- CODEN
- EJNMA6
INIS
- Country of Publication
- Germany
- Country of Input or Organization
- Germany
- INIS RN
- 51039222
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- BIOLOGICAL MARKERS; BRAIN; CEREBROSPINAL FLUID; COMPARATIVE EVALUATIONS; FLUORINE 18; FLUORODEOXYGLUCOSE; GLUCOSE; IMAGE PROCESSING; MENTAL DISORDERS; METABOLISM; NERVOUS SYSTEM DISEASES; NMR IMAGING; POSITRON COMPUTED TOMOGRAPHY; RADIOPHARMACEUTICALS; RELAXATION TIME; SPATIAL DISTRIBUTION; TIME DEPENDENCE; UPTAKE; WEIGHTING FUNCTIONS
- Descriptors DEC
- ALDEHYDES; ANTIMETABOLITES; BETA DECAY RADIOISOTOPES; BETA-PLUS DECAY RADIOISOTOPES; BIOLOGICAL MATERIALS; BODY; BODY FLUIDS; CARBOHYDRATES; CENTRAL NERVOUS SYSTEM; COMPUTERIZED TOMOGRAPHY; DIAGNOSTIC TECHNIQUES; DISEASES; DISTRIBUTION; DRUGS; EMISSION COMPUTED TOMOGRAPHY; EVALUATION; FLUORINE ISOTOPES; FUNCTIONS; HEXOSES; HOURS LIVING RADIOISOTOPES; ISOMERIC TRANSITION ISOTOPES; ISOTOPES; LABELLED COMPOUNDS; LIGHT NUCLEI; MATERIALS; MONOSACCHARIDES; NANOSECONDS LIVING RADIOISOTOPES; NERVOUS SYSTEM; NUCLEI; ODD-ODD NUCLEI; ORGANIC COMPOUNDS; ORGANS; PROCESSING; RADIOACTIVE MATERIALS; RADIOISOTOPES; SACCHARIDES; TOMOGRAPHY