001     151491
005     20230915093952.0
024 7 _ |a 10.1097/RLU.0000000000002960
|2 doi
024 7 _ |a 0363-9762
|2 ISSN
024 7 _ |a 1536-0229
|2 ISSN
024 7 _ |a altmetric:76836603
|2 altmetric
024 7 _ |a pmid:32108697
|2 pmid
037 _ _ |a DZNE-2020-01079
041 _ _ |a English
082 _ _ |a 610
100 1 _ |a Özden, Cansu
|0 P:(DE-HGF)0
|b 0
|e Corresponding author
245 _ _ |a FDG Uptake in the Basal Forebrain as Measured by Digital High-Resolution PET Is a Promising Marker of Basal Forebrain Degeneration in the Lewy Body Disease Spectrum
260 _ _ |a [S.l.]
|c 2020
|b Ovid
264 _ 1 |3 print
|2 Crossref
|b Ovid Technologies (Wolters Kluwer Health)
|c 2020-04-01
336 7 _ |a article
|2 DRIVER
336 7 _ |a Output Types/Journal article
|2 DataCite
336 7 _ |a Journal Article
|b journal
|m journal
|0 PUB:(DE-HGF)16
|s 1600777728_28892
|2 PUB:(DE-HGF)
336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a Journal Article
|0 0
|2 EndNote
520 _ _ |a Purpose Cognitive decline in diseases of the Lewy body spectrum (LBS) is linked to dysfunction/degeneration of the basal forebrain (BF). Assessment of glucose metabolism in the BF by FDG PET is hampered by the small size of the BF and limited spatial resolution of conventional PET. This pilot study tested the feasibility of assessing BF glucose metabolism by high-resolution digital PET (dPET).Patients and Methods The retrospective study included 12 LBS patients (61–86 years, 5 demented). Whole-brain stereotactic normalization to anatomical standard space was followed by local stereotactic normalization of a 7 × 7 × 7-cm3 box around the BF to a custom-made 1 × 1 × 1-mm3 FDG dPET template. FDG uptake was scaled voxelwise to mean FDG uptake in the pons. Scaled FDG uptake in the BF was compared between demented and nondemented LBS patients and tested for correlation with cortical FDG uptake.Results Scaled FDG uptake in the BF was significantly lower in demented compared with nondemented patients (1.14 ± 0.09 vs 1.25 ± 0.06, P = 0.031). Brain-wide voxel-based testing for correlations with scaled FDG uptake in the BF revealed a large cluster comprising medial and ventrolateral frontal cortex, anterior cingulate cortex, insular cortex, and striatum as well as smaller clusters in motor cortex and occipital cortex (P < 0.001, uncorrected).Conclusions These results suggest that dementia-associated BF degeneration in LBS can be sensitively measured as reduced BF FDG uptake on dPET. More accurate delineation of the BF based on individual high-resolution MRI might be useful to make optimal use of improved spatial resolution of dPET and to correct for possible disease- and age-dependent partial volume effects.
536 _ _ |a 344 - Clinical and Health Care Research (POF3-344)
|0 G:(DE-HGF)POF3-344
|c POF3-344
|f POF III
|x 0
536 _ _ |a 345 - Population Studies and Genetics (POF3-345)
|0 G:(DE-HGF)POF3-345
|c POF3-345
|f POF III
|x 1
588 _ _ |a Dataset connected to CrossRef
700 1 _ |a Frings, Lars
|b 1
700 1 _ |a Apostolova, Ivayla
|b 2
700 1 _ |a Lange, Catharina
|0 P:(DE-HGF)0
|b 3
700 1 _ |a Klutmann, Susanne
|b 4
700 1 _ |a Adam, Gerhard
|b 5
700 1 _ |a Bannas, Peter
|b 6
700 1 _ |a Meyer, Philipp T.
|b 7
700 1 _ |a Grothe, Michel J.
|0 P:(DE-2719)2810708
|b 8
|u dzne
700 1 _ |a Buchert, Ralph
|b 9
773 1 8 |a 10.1097/rlu.0000000000002960
|b : Ovid Technologies (Wolters Kluwer Health), 2020-04-01
|n 4
|p 261-266
|3 journal-article
|2 Crossref
|t Clinical Nuclear Medicine
|v 45
|y 2020
|x 0363-9762
773 _ _ |a 10.1097/RLU.0000000000002960
|g Vol. 45, no. 4, p. 261 - 266
|0 PERI:(DE-600)2045053-9
|n 4
|p 261-266
|t Clinical nuclear medicine
|v 45
|y 2020
|x 0363-9762
909 C O |o oai:pub.dzne.de:151491
|p VDB
910 1 _ |a Deutsches Zentrum für Neurodegenerative Erkrankungen
|0 I:(DE-588)1065079516
|k DZNE
|b 8
|6 P:(DE-2719)2810708
913 1 _ |a DE-HGF
|b Forschungsbereich Gesundheit
|l Erkrankungen des Nervensystems
|1 G:(DE-HGF)POF3-340
|0 G:(DE-HGF)POF3-344
|2 G:(DE-HGF)POF3-300
|v Clinical and Health Care Research
|x 0
913 1 _ |a DE-HGF
|b Forschungsbereich Gesundheit
|l Erkrankungen des Nervensystems
|1 G:(DE-HGF)POF3-340
|0 G:(DE-HGF)POF3-345
|2 G:(DE-HGF)POF3-300
|v Population Studies and Genetics
|x 1
914 1 _ |y 2020
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0160
|2 StatID
|b Essential Science Indicators
|d 2020-01-02
915 _ _ |a Allianz-Lizenz
|0 StatID:(DE-HGF)0410
|2 StatID
|d 2022-11-29
|w ger
915 _ _ |a JCR
|0 StatID:(DE-HGF)0100
|2 StatID
|b CLIN NUCL MED : 2021
|d 2022-11-29
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0200
|2 StatID
|b SCOPUS
|d 2022-11-29
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0300
|2 StatID
|b Medline
|d 2022-11-29
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0199
|2 StatID
|b Clarivate Analytics Master Journal List
|d 2022-11-29
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0150
|2 StatID
|b Web of Science Core Collection
|d 2022-11-29
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1110
|2 StatID
|b Current Contents - Clinical Medicine
|d 2022-11-29
915 _ _ |a IF >= 10
|0 StatID:(DE-HGF)9910
|2 StatID
|b CLIN NUCL MED : 2021
|d 2022-11-29
920 1 _ |0 I:(DE-2719)7000008
|k U T4 Researchers - Bonn
|l U T4 Researchers - Bonn
|x 0
920 1 _ |0 I:(DE-2719)1510100
|k Clinical Dementia Research Rostock /Greifswald ; AG Teipel
|l Clinical Dementia Research Rostock /Greifswald
|x 1
980 _ _ |a journal
980 _ _ |a VDB
980 _ _ |a I:(DE-2719)7000008
980 _ _ |a I:(DE-2719)1510100
980 _ _ |a UNRESTRICTED


LibraryCollectionCLSMajorCLSMinorLanguageAuthor
Marc 21