The variability of translocator protein signal in brain and blood of genotyped healthy humans using in vivo 123I-CLINDE SPECT imaging: A test-retest study

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

The variability of translocator protein signal in brain and blood of genotyped healthy humans using in vivo 123I-CLINDE SPECT imaging : A test-retest study. / Feng, Ling; Jensen, Per; Thomsen, Gerda; Dyssegaard, Agnete; Svarer, Claus; Knudsen, Lars V.; Møller, Kirsten; Thomsen, Carsten; Mikkelsen, Jens D.; Guilloteau, Denis; Knudsen, Gitte M.; Pinborg, Lars H.

In: Journal of Nuclear Medicine, Vol. 58, No. 6, 2017, p. 989-995.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Feng, L, Jensen, P, Thomsen, G, Dyssegaard, A, Svarer, C, Knudsen, LV, Møller, K, Thomsen, C, Mikkelsen, JD, Guilloteau, D, Knudsen, GM & Pinborg, LH 2017, 'The variability of translocator protein signal in brain and blood of genotyped healthy humans using in vivo 123I-CLINDE SPECT imaging: A test-retest study', Journal of Nuclear Medicine, vol. 58, no. 6, pp. 989-995. https://doi.org/10.2967/jnumed.116.183202

APA

Feng, L., Jensen, P., Thomsen, G., Dyssegaard, A., Svarer, C., Knudsen, L. V., Møller, K., Thomsen, C., Mikkelsen, J. D., Guilloteau, D., Knudsen, G. M., & Pinborg, L. H. (2017). The variability of translocator protein signal in brain and blood of genotyped healthy humans using in vivo 123I-CLINDE SPECT imaging: A test-retest study. Journal of Nuclear Medicine, 58(6), 989-995. https://doi.org/10.2967/jnumed.116.183202

Vancouver

Feng L, Jensen P, Thomsen G, Dyssegaard A, Svarer C, Knudsen LV et al. The variability of translocator protein signal in brain and blood of genotyped healthy humans using in vivo 123I-CLINDE SPECT imaging: A test-retest study. Journal of Nuclear Medicine. 2017;58(6):989-995. https://doi.org/10.2967/jnumed.116.183202

Author

Feng, Ling ; Jensen, Per ; Thomsen, Gerda ; Dyssegaard, Agnete ; Svarer, Claus ; Knudsen, Lars V. ; Møller, Kirsten ; Thomsen, Carsten ; Mikkelsen, Jens D. ; Guilloteau, Denis ; Knudsen, Gitte M. ; Pinborg, Lars H. / The variability of translocator protein signal in brain and blood of genotyped healthy humans using in vivo 123I-CLINDE SPECT imaging : A test-retest study. In: Journal of Nuclear Medicine. 2017 ; Vol. 58, No. 6. pp. 989-995.

Bibtex

@article{6cab017ad1f849599692b473bda6357c,
title = "The variability of translocator protein signal in brain and blood of genotyped healthy humans using in vivo 123I-CLINDE SPECT imaging: A test-retest study",
abstract = "123I-CLINDE is a radiotracer developed for SPECT and targets the 18-kDa translocator protein (TSPO). TSPO is upregulated in glial cells and used as a measure of neuroinflammation in a variety of central nervous system diseases. The aim of this study was to examine the test-retest variability of 123I-CLINDE binding in healthy subjects. Methods: SPECT scans were acquired over 90 min in 16 healthy controls (9 women, 8 mixed-affinity binders [MABs] and 8 high-affinity binders [HABs] twice with an interval of 35 6 15 d). Arterial input functions were based on individual blood measurements in 8 subjects and a population-based approach in combination with individual whole-blood time-activity curves in the other 8 subjects. Seven brain volumes of interest were extracted and quantified by SUVs and by 2-tissue-compartment modeling for calculation of distribution volumes (VT). Test-retest variability was measured by percentage difference (PD), the absolute PD, intraclass correlation coefficient (ICC), and coefficient of variation. Results: The absolute PD of brain SUV and the VT had similar values. The ICC values were higher for VTs than for brain SUVs, which were both moderate to high; however, lower ICC values were observed when calculated separately for HABs and MABs. Test-retest reproducibility was higher in subjects with immediate centrifugation of blood samples. The population-based method efficiently recovered data with delayed centrifugation. The VT of a 49-y-old male HAB was 7.5 6 1.4 mL/cm3 compared with 4.6 6 1.4 mL/cm3 of a sex-and age-matched MAB. The SUVs of a 49-y-old male HAB and MAB were 1.03 6 0.14 and 0.88 6 0.15 g/mL, respectively. Conclusion: The test-retest reproducibility of 123I-CLINDE is comparable or better than that reported for commonly used PET TSPO tracers. Because of the binding of 123I-CLINDE to blood cells and peripheral tissues, SUV is not a sufficient surrogate of VT from2-tissue-compartmentmodeling. The population-adjusted method has the potential to reduce the complexity of blood analyses of TSPO tracers.",
keywords = "Polymorphism, Secondgeneration TSPO tracer, TSPO imaging, Variability",
author = "Ling Feng and Per Jensen and Gerda Thomsen and Agnete Dyssegaard and Claus Svarer and Knudsen, {Lars V.} and Kirsten M{\o}ller and Carsten Thomsen and Mikkelsen, {Jens D.} and Denis Guilloteau and Knudsen, {Gitte M.} and Pinborg, {Lars H.}",
year = "2017",
doi = "10.2967/jnumed.116.183202",
language = "English",
volume = "58",
pages = "989--995",
journal = "The Journal of Nuclear Medicine",
issn = "0161-5505",
publisher = "Society of Nuclear Medicine",
number = "6",

}

RIS

TY - JOUR

T1 - The variability of translocator protein signal in brain and blood of genotyped healthy humans using in vivo 123I-CLINDE SPECT imaging

T2 - A test-retest study

AU - Feng, Ling

AU - Jensen, Per

AU - Thomsen, Gerda

AU - Dyssegaard, Agnete

AU - Svarer, Claus

AU - Knudsen, Lars V.

AU - Møller, Kirsten

AU - Thomsen, Carsten

AU - Mikkelsen, Jens D.

AU - Guilloteau, Denis

AU - Knudsen, Gitte M.

AU - Pinborg, Lars H.

PY - 2017

Y1 - 2017

N2 - 123I-CLINDE is a radiotracer developed for SPECT and targets the 18-kDa translocator protein (TSPO). TSPO is upregulated in glial cells and used as a measure of neuroinflammation in a variety of central nervous system diseases. The aim of this study was to examine the test-retest variability of 123I-CLINDE binding in healthy subjects. Methods: SPECT scans were acquired over 90 min in 16 healthy controls (9 women, 8 mixed-affinity binders [MABs] and 8 high-affinity binders [HABs] twice with an interval of 35 6 15 d). Arterial input functions were based on individual blood measurements in 8 subjects and a population-based approach in combination with individual whole-blood time-activity curves in the other 8 subjects. Seven brain volumes of interest were extracted and quantified by SUVs and by 2-tissue-compartment modeling for calculation of distribution volumes (VT). Test-retest variability was measured by percentage difference (PD), the absolute PD, intraclass correlation coefficient (ICC), and coefficient of variation. Results: The absolute PD of brain SUV and the VT had similar values. The ICC values were higher for VTs than for brain SUVs, which were both moderate to high; however, lower ICC values were observed when calculated separately for HABs and MABs. Test-retest reproducibility was higher in subjects with immediate centrifugation of blood samples. The population-based method efficiently recovered data with delayed centrifugation. The VT of a 49-y-old male HAB was 7.5 6 1.4 mL/cm3 compared with 4.6 6 1.4 mL/cm3 of a sex-and age-matched MAB. The SUVs of a 49-y-old male HAB and MAB were 1.03 6 0.14 and 0.88 6 0.15 g/mL, respectively. Conclusion: The test-retest reproducibility of 123I-CLINDE is comparable or better than that reported for commonly used PET TSPO tracers. Because of the binding of 123I-CLINDE to blood cells and peripheral tissues, SUV is not a sufficient surrogate of VT from2-tissue-compartmentmodeling. The population-adjusted method has the potential to reduce the complexity of blood analyses of TSPO tracers.

AB - 123I-CLINDE is a radiotracer developed for SPECT and targets the 18-kDa translocator protein (TSPO). TSPO is upregulated in glial cells and used as a measure of neuroinflammation in a variety of central nervous system diseases. The aim of this study was to examine the test-retest variability of 123I-CLINDE binding in healthy subjects. Methods: SPECT scans were acquired over 90 min in 16 healthy controls (9 women, 8 mixed-affinity binders [MABs] and 8 high-affinity binders [HABs] twice with an interval of 35 6 15 d). Arterial input functions were based on individual blood measurements in 8 subjects and a population-based approach in combination with individual whole-blood time-activity curves in the other 8 subjects. Seven brain volumes of interest were extracted and quantified by SUVs and by 2-tissue-compartment modeling for calculation of distribution volumes (VT). Test-retest variability was measured by percentage difference (PD), the absolute PD, intraclass correlation coefficient (ICC), and coefficient of variation. Results: The absolute PD of brain SUV and the VT had similar values. The ICC values were higher for VTs than for brain SUVs, which were both moderate to high; however, lower ICC values were observed when calculated separately for HABs and MABs. Test-retest reproducibility was higher in subjects with immediate centrifugation of blood samples. The population-based method efficiently recovered data with delayed centrifugation. The VT of a 49-y-old male HAB was 7.5 6 1.4 mL/cm3 compared with 4.6 6 1.4 mL/cm3 of a sex-and age-matched MAB. The SUVs of a 49-y-old male HAB and MAB were 1.03 6 0.14 and 0.88 6 0.15 g/mL, respectively. Conclusion: The test-retest reproducibility of 123I-CLINDE is comparable or better than that reported for commonly used PET TSPO tracers. Because of the binding of 123I-CLINDE to blood cells and peripheral tissues, SUV is not a sufficient surrogate of VT from2-tissue-compartmentmodeling. The population-adjusted method has the potential to reduce the complexity of blood analyses of TSPO tracers.

KW - Polymorphism

KW - Secondgeneration TSPO tracer

KW - TSPO imaging

KW - Variability

U2 - 10.2967/jnumed.116.183202

DO - 10.2967/jnumed.116.183202

M3 - Journal article

C2 - 28572290

AN - SCOPUS:85020221596

VL - 58

SP - 989

EP - 995

JO - The Journal of Nuclear Medicine

JF - The Journal of Nuclear Medicine

SN - 0161-5505

IS - 6

ER -

ID: 196913964