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Sökning: onr:"swepub:oai:DiVA.org:uu-357431" > Spatial normalizati...

LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00004839naa a2200481 4500
001oai:DiVA.org:uu-357431
003SwePub
008180816s2019 | |||||||||||000 ||eng|
009oai:prod.swepub.kib.ki.se:140216467
024a https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-3574312 URI
024a https://doi.org/10.2967/jnumed.118.2078112 DOI
024a http://kipublications.ki.se/Default.aspx?queryparsed=id:1402164672 URI
040 a (SwePub)uud (SwePub)ki
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Lilja, Johanu Uppsala universitet,Radiologi,Hermes Medical Solutions, Stockholm, Sweden4 aut0 (Swepub:uu)johli248
2451 0a Spatial normalization of 18F-Flutemetamol PET images using an adaptive principal-component template
264 c 2018-06-14
264 1b Society of Nuclear Medicine,c 2019
338 a electronic2 rdacarrier
520 a Though currently approved for visual assessment only, there is evidence to suggest that quantification of amyloid-β (Aβ) PET images may reduce interreader variability and aid in the monitoring of treatment effects in clinical trials. Quantification typically involves a regional atlas in standard space, requiring PET images to be spatially normalized. Different uptake patterns in Aβ-positive and Aβ-negative subjects, however, make spatial normalization challenging. In this study, we proposed a method to spatially normalize 18F-flutemetamol images using a synthetic template based on principal-component images to overcome these challenges.Methods: 18F-flutemetamol PET and corresponding MR images from a phase II trial (n = 70), including subjects ranging from Aβ-negative to Aβ-positive, were spatially normalized to standard space using an MR-driven registration method (SPM12). 18F-flutemetamol images were then intensity-normalized using the pons as a reference region. Principal-component images were calculated from the intensity-normalized images. A linear combination of the first 2 principal-component images was then used to model a synthetic template spanning the whole range from Aβ-negative to Aβ-positive. The synthetic template was then incorporated into our registration method, by which the optimal template was calculated as part of the registration process, providing a PET-only–driven registration method. Evaluation of the method was done in 2 steps. First, coregistered gray matter masks generated using SPM12 were spatially normalized using the PET- and MR-driven methods, respectively. The spatially normalized gray matter masks were then visually inspected and quantified. Second, to quantitatively compare the 2 registration methods, additional data from an ongoing study were spatially normalized using both methods, with correlation analysis done on the resulting cortical SUV ratios.Results: All scans were successfully spatially normalized using the proposed method with no manual adjustments performed. Both visual and quantitative comparison between the PET- and MR-driven methods showed high agreement in cortical regions. 18F-flutemetamol quantification showed strong agreement between the SUV ratios for the PET- and MR-driven methods (R2 = 0.996; pons reference region).Conclusion: The principal-component template registration method allows for robust and accurate registration of 18F-flutemetamol images to a standardized template space, without the need for an MR image.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicinx Radiologi och bildbehandling0 (SwePub)302082 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Clinical Medicinex Radiology, Nuclear Medicine and Medical Imaging0 (SwePub)302082 hsv//eng
653 a Alzheimer disease
653 a amyloid-beta
653 a PET
653 a F-18-flutemetamol
653 a adaptive template
700a Leuzy, Antoine4 aut
700a Chiotis, Konstantinosu Karolinska Institutet4 aut
700a Savitcheva, Irina4 aut
700a Sörensen, Jensu Uppsala universitet,Radiologi4 aut0 (Swepub:uu)jenssore
700a Nordberg, Agnetau Karolinska Institutet4 aut
710a Uppsala universitetb Radiologi4 org
773t Journal of Nuclear Medicined : Society of Nuclear Medicineg 60:2, s. 285-291q 60:2<285-291x 0161-5505x 1535-5667x 2159-662X
856u https://doi.org/10.2967/jnumed.118.207811y Fulltext
856u https://uu.diva-portal.org/smash/get/diva2:1239371/FULLTEXT01.pdfx primaryx Raw objecty fulltext:print
856u http://jnm.snmjournals.org/content/60/2/285.full.pdf
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-357431
8564 8u https://doi.org/10.2967/jnumed.118.207811
8564 8u http://kipublications.ki.se/Default.aspx?queryparsed=id:140216467

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