Evaluation of reference tissue models for the analysis of [11C](R)-PK11195 studies

被引:58
作者
Kropholler, Marc A.
Boellaard, Ronald
Schuitemaker, Alie
Folkersma, Hedy
van Berckel, Bart N. M.
Lammertsma, Adriaan A.
机构
[1] VU Univ Med Ctr, Dept Nucl Med & PET Res, NL-1007 MB Amsterdam, Netherlands
[2] VU Univ Med Ctr, Dept Neurol, Amsterdam, Netherlands
[3] VU Univ Med Ctr, Dept Neurosurg, Amsterdam, Netherlands
关键词
microglia; peripheral benzodiazepine receptor; PET (positron emission tomography); PK11195; reference tissue models; tracer kinetic modelling;
D O I
10.1038/sj.jcbfm.9600289
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
[C-11](R)-PK11195 is a marker of activated microglia, which can be used to measure inflammation in neurologic disorders. The purpose of the present study was to define the optimal reference tissue model based on a comparison with a validated plasma input model and using clinical studies and Monte Carlo simulations. Accuracy and reproducibility of reference tissue models were evaluated using Monte Carlo simulations. The effects of noise and variation in specific binding, nonspecific binding and blood volume were evaluated. Dynamic positron emission tomography scans were performed on 13 subjects, and radioactivity in arterial blood was monitored online. In addition, blood samples were taken to generate a metabolite corrected plasma input function. Both a (validated) two-tissue reversible compartment model with K-1/k(2) fixed to whole cortex and various reference tissue models were fitted to the data. Finally, a simplified reference tissue model (SRTM) corrected for nonspecific binding using plasma input data (SRTMpl-corr) was investigated. Correlations between reference tissue models (including SRTMpl-corr) and the plasma input model were calculated. Monte Carlo simulations indicated that low-specific binding results in decreased accuracy and reproducibility. In this respect, the SRTM and SRTMpl-corr performed relatively well. Varying blood volume had no effect on performance. In the clinical evaluation, SRTMpl-corr and SRTM had the highest correlations with the plasma input model (R-2 = 0.82 and 0.78, respectively). SRTMpl-corr is optimal when an arterial plasma input curve is available. Simplified reference tissue model is the best alternative when no plasma input is available.
引用
收藏
页码:1431 / 1441
页数:11
相关论文
共 41 条
[1]   Performance evaluation of the whole-body PET scanner ECAT EXACT HR+ following the IEC standard [J].
Adam, LE ;
Zaers, J ;
Ostertag, H ;
Trojan, H ;
Bellemann, ME ;
Brix, G .
IEEE TRANSACTIONS ON NUCLEAR SCIENCE, 1997, 44 (03) :1172-1179
[2]   [11C](R)-PK11195 positron emission tomography imaging of activated microglia in vivo in Rasmussen's encephalitis [J].
Banati, RB ;
Goerres, GW ;
Myers, R ;
Gunn, RN ;
Turkheimer, FE ;
Kreutzberg, GW ;
Brooks, DJ ;
Jones, T ;
Duncan, JS .
NEUROLOGY, 1999, 53 (09) :2199-2203
[3]   Long-term trans-synaptic glial responses in the human thalamus after peripheral nerve injury [J].
Banati, RB ;
Cagnin, A ;
Brooks, DJ ;
Gunn, RN ;
Myers, R ;
Jones, T ;
Birch, R ;
Anand, P .
NEUROREPORT, 2001, 12 (16) :3439-3442
[4]   PK ('peripheral benzodiazepine') - Binding sites in the CNS indicate early and discrete brain lesions: Microautoradiographic detection of [H-3]PK11195 binding to activated microglia [J].
Banati, RB ;
Myers, R ;
Kreutzberg, GW .
JOURNAL OF NEUROCYTOLOGY, 1997, 26 (02) :77-82
[5]   The peripheral benzodiazepine binding site in the brain in multiple sclerosis -: Quantitative in vivo imaging of microglia as a measure of disease activity [J].
Banati, RB ;
Newcombe, J ;
Gunn, RN ;
Cagnin, A ;
Turkheimer, F ;
Heppner, F ;
Price, G ;
Wegner, F ;
Giovannoni, G ;
Miller, DH ;
Perkin, GD ;
Smith, T ;
Hewson, AK ;
Bydder, G ;
Kreutzberg, GW ;
Jones, T ;
Cuzner, ML ;
Myers, R .
BRAIN, 2000, 123 :2321-2337
[6]   Characteristics of a new fully programmable blood sampling device for monitoring blood radioactivity during PET [J].
Boellaard, R ;
van Lingen, A ;
van Balen, SCM ;
Hoving, BG ;
Lammertsma, AA .
EUROPEAN JOURNAL OF NUCLEAR MEDICINE, 2001, 28 (01) :81-89
[7]  
Brix G, 1997, J NUCL MED, V38, P1614
[8]   In vivo detection of microglial activation in frontotemporal dementia [J].
Cagnin, A ;
Rossor, M ;
Sampson, EL ;
MacKinnon, T ;
Banati, RB .
ANNALS OF NEUROLOGY, 2004, 56 (06) :894-897
[9]   In vivo visualization of activated glia by [11C] (R)-PK11195-PET following herpes encephalitis reveals projected neuronal damage beyond the primary focal lesion [J].
Cagnin, A ;
Myers, R ;
Gunn, RN ;
Lawrence, AD ;
Stevens, T ;
Kreutzberg, GW ;
Jones, T ;
Banati, RB .
BRAIN, 2001, 124 :2014-2027
[10]   In-vivo measurement of activated microglia in dementia [J].
Cagnin, A ;
Brooks, DJ ;
Kennedy, AM ;
Gunn, RN ;
Myers, R ;
Turkheimer, FE ;
Jones, T ;
Banati, RB .
LANCET, 2001, 358 (9280) :461-467