dc.contributor.author
Schmitz-Steinkrüger, Helen
dc.contributor.author
Lange, Catharina
dc.contributor.author
Apostolova, Ivayla
dc.contributor.author
Amthauer, Holger
dc.contributor.author
Lehnert, Wencke
dc.contributor.author
Klutmann, Susanne
dc.contributor.author
Buchert, Ralph
dc.date.accessioned
2020-08-19T12:23:50Z
dc.date.available
2020-08-19T12:23:50Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/28081
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-27831
dc.description.abstract
Background: This study investigated the impact of the size of the normal database on the classification performance of the specific binding ratio (SBR) in dopamine transporter (DAT) SPECT with [123I]FP-CIT in different settings.
Methods: The first subject sample comprised 645 subjects from the Parkinson's Progression Marker Initiative (PPMI), 207 healthy controls (HC), and 438 Parkinson's disease (PD) patients. The second sample comprised 372 patients from clinical routine patient care, 186 with non-neurodegenerative parkinsonian syndrome (PS) and 186 with neurodegenerative PS. Single-photon emission computed tomography (SPECT) images of the clinical sample were reconstructed with two different reconstruction algorithms (filtered backprojection, iterative ordered subsets expectation maximization (OSEM) reconstruction with resolution recovery). The putaminal specific binding ratio (SBR) was computed using an anatomical region of interest (ROI) predefined in standard (MNI) space in the Automated Anatomic Labeling (AAL) atlas or using hottest voxels (HV) analysis in large predefined ROIs. SBR values were transformed to z-scores using mean and standard deviation of the SBR in a normal database of varying sizes (n = 5, 10, 15,…, 50) randomly selected from the HC subjects (PPMI sample) or the patients with non-neurodegenerative PS (clinical sample). Accuracy, sensitivity, and specificity for identifying patients with PD or neurodegenerative PS were determined as performance measures using a predefined fixed cutoff on the z-score. This was repeated for 10,000 randomly selected normal databases, separately for each size of the normal database. Mean and 5th percentile of the performance measures over the 10,000 realizations were computed. Accuracy, sensitivity, and specificity when using the whole set of HC or non-neurodegenerative PS subjects as normal database were used as benchmark.
Results: Mean loss of accuracy of the putamen SBR z-score was below 1% when the normal database included at least 15 subjects, independent of subject sample (PPMI or clinical), reconstruction method (filtered backprojection or OSEM), and ROI method (AAL or HV). However, the variability of the accuracy of the putamen SBR z-score decreased monotonically with increasing size of normal database and was still considerable at size 15. In order to achieve less than 5% "maximum" loss of accuracy (defined by the 5th percentile) in all settings required at least 25 to 30 subjects in the normal database. Reduction of mean and "maximum" loss of accuracy of the putamen SBR z-score by further increasing the size of the normal database was very small beyond size 40.
Conclusions: The results of this study suggest that 25 to 30 is the minimum size of the normal database to reliably achieve good performance of semi-quantitative analysis in dopamine transporter (DAT) SPECT, independent of the algorithm used for image reconstruction and the ROI method used to estimate the putaminal SBR.
en
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
Dopamine transporter
en
dc.subject
Normal database
en
dc.subject
Specific binding ratio
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit
dc.title
Impact of the size of the normal database on the performance of the specific binding ratio in dopamine transporter SPECT
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.articlenumber
34
dcterms.bibliographicCitation.doi
10.1186/s40658-020-00304-z
dcterms.bibliographicCitation.journaltitle
EJNMMI Physics
dcterms.bibliographicCitation.originalpublishername
Springer
dcterms.bibliographicCitation.volume
7
refubium.affiliation
Charité - Universitätsmedizin Berlin
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.bibliographicCitation.pmid
32435936
dcterms.isPartOf.eissn
2197-7364