[(11) C]arachidonic acid incorporation measurement in human brain: Optimization for clinical use.
[(11) C]arachidonic acid incorporation measurement in human brain: Optimization for clinical use.
复制标题
DOI:
10.1002/syn.22018
复制
发表时间:
2018-03
期刊:
影响因子:
--
通讯作者:
Sublette ME
中科院分区:
文献类型:
--
作者:
Zanderigo F;Kang Y;Kumar D;Nikolopoulou A;Mozley PD;Kothari PJ;He B;Schlyer D;Rapoport SI;Oquendo MA;Vallabhajosula S;Mann JJ;Sublette ME
Arachidonic acid (AA) is involved in signal transduction, neuroinflammation, and production of eico-sanoid metabolites. The AA brain incorporation coefficient (K*) is quantifiable in vivo using [11C]AA positron emission tomography, although repeatability remains undetermined. We evaluated K* estimates obtained with population-based metabolite correction (PBMC) and image-derived input function (IDIF) in comparison to arterial blood-based estimates, and compared repeatability. Eleven healthy volunteers underwent a [11C]AA scan; five repeated the scan 6 weeks later, simulating a pre- and post-treatment study design. For all scans, arterial blood was sampled to measure [11C] AA plasma radioactivity. Plasma [11C]AA parent fraction was measured in 5 scans. K* was quantified using both blood data and IDIF, corrected for [11C]AA parent fraction using both PBMC (from published values) and individually measured values (when available). K* repeatability was calculated in the test-retest subset. K* estimates based on blood and individual metabolites were highly correlated with estimates using PBMC with arterial input function (r = 0.943) or IDIF (r = 0.918) in the subset with measured metabolites. In the total dataset, using PBMC, IDIF-based estimates were moderately correlated with arterial input function-based estimates (r = 0.712). PBMC and IDIF-based K* estimates were ∼6.4% to ∼11.9% higher, on average, than blood-based estimates. Average K* test-retest absolute percent difference values obtained using blood data or IDIF, assuming PBMC for both, were between 6.7% and 13.9%, comparable to other radiotracers. Our results support the possibility of simplified [11C]AA data acquisition through eliminating arterial blood sampling and metabolite analysis, while retaining comparable repeatability and validity.
登录
查看更多内容
影响因子:
6.3
作者:
Ogden, R. Todd;Ojha, Ashish;Parsey, Ramin V.
通讯作者:
Parsey, Ramin V.
DOI:
10.1007/s00259-015-3149-8
发表时间:
2016-01-01
影响因子:
9.1
作者:
Collste, K.;Forsberg, A.;Cervenka, S.
通讯作者:
Cervenka, S.
影响因子:
4.2
作者:
DEGEORGE, JJ;NORONHA, JG;RAPOPORT, SI
通讯作者:
RAPOPORT, SI
DOI:
10.1016/j.plefa.2007.10.018
发表时间:
2007-11-01
影响因子:
3
作者:
Lae, Ho-Joo;Rao, Jagadeesh S.;Bazinet, Richard P.
通讯作者:
Bazinet, Richard P.
影响因子:
9.8
作者:
Hopkins, WG
通讯作者:
Hopkins, WG