Kinetic analysis and test-retest variability of the radioligand [11C](R)-PK11195 binding to TSPO in the human brain - a PET study in control subjects

Background Positron-emission tomography and the radioligand [ 11 C](R)-PK11195 have been used for the imaging of the translocator protein (TSPO) and applied to map microglia cells in the brain in neuropsychiatric disorders. [ 11 C](R)-PK11195 binding has been quantified using reference region approa...

Celý popis

Uloženo v:
Podrobná bibliografie
Vydáno v:EJNMMI research Ročník 2; číslo 1; s. 15
Hlavní autoři: Jučaite, Aurelija, Cselényi, Zsolt, Arvidsson, Annie, Åhlberg, Gabrielle, Julin, Per, Varnäs, Katarina, Stenkrona, Per, Andersson, Jan, Halldin, Christer, Farde, Lars
Médium: Journal Article
Jazyk:angličtina
Vydáno: Berlin/Heidelberg Springer Berlin Heidelberg 01.01.2012
Springer
Témata:
Cardiac Imaging
Imaging
Medicine
Medicine & Public Health
Nuclear Medicine
Oncology
Original Research
Orthopedics
Radiology
positron-emission tomography
C](R)-PK11195
translocator protein
[
peripheral benzodiazepine receptors
ISSN:2191-219X, 2191-219X
On-line přístup:Získat plný text
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo vytvoří štítek k tomuto záznamu!
Popis
Shrnutí:Background Positron-emission tomography and the radioligand [ 11 C](R)-PK11195 have been used for the imaging of the translocator protein (TSPO) and applied to map microglia cells in the brain in neuropsychiatric disorders. [ 11 C](R)-PK11195 binding has been quantified using reference region approaches, with the reference defined anatomically or using unsupervised or supervised clustering algorithms. Kinetic compartment modelling so far has not been presented. In the present test-retest study, we examine the characteristics of [ 11 C](R)-PK11195 binding in detail, using the classical compartment analysis with a metabolite-corrected arterial input function. Methods [ 11 C](R)-PK11195 binding was examined in six control subjects at two separate occasions, 6 weeks apart. Results of one-tissue and two-tissue compartment models (1TCM, 2TCM) were compared using the Akaike criteria and F -statistics. The reproducibility of binding potential ( BP ND ) estimates was evaluated by difference in measurements (error in percent) and intraclass correlation coefficients (ICCs). Results [ 11 C](R)-PK11195 binding could be described by 2TCM which was the preferred model. Measurement error (in percent) indicated good reproducibility in large brain regions (mean error: whole brain 4%, grey matter 5%), but not in smaller subcortical regions (putamen 25%, caudate 55%). The ICC values were moderate to low, highest for the white matter (0.73), whole brain and thalamus (0.57), and cortical grey matter (0.47). Sizeable [ 11 C](R)-PK11195 BP ND could be identified throughout the human brain (range 1.11 to 2.21). Conclusions High intra-subject variability of [ 11 C](R)-PK11195 binding limits longitudinal monitoring of TSPO changes. The interpretation of [ 11 C](R)-PK11195 binding by 2TCM suggests that the presence of specific binding to TSPO cannot be excluded at physiological conditions.
ISSN:2191-219X
2191-219X
DOI:10.1186/2191-219X-2-15