Liver standardized uptake value corrected for lean body mass at FDG PET/CT

Effect of FDG uptake time

Alin Chirindel, Krishna C. Alluri, Abdel K. Tahari, Muhammad Chaudhry, Richard L. Wahl, Martin Lodge, Rathan M. Subramaniam

Research output: Contribution to journalArticle

Abstract

Objective: The objective of this study is to establish the magnitude change and interreader reliability of the liver standardized uptake value corrected for lean body mass (SULmean) in dual-time-point imaging at 1 and 2 hours and 1 and 4 hours.

Patients and Methods: Early and delayed FDG PET/CT scans were included for 28 patients (13 men and 15 women) who had normal liver by CT or ultrasound. The average uptake time between the early and delayed scans were 55 minutes (range, 44Y69 minutes) for pancreatic adenocarcinoma patients (n = 19) and 184 minutes (range, 140Y197 minutes) for neurofibromatosis patients (n = 9). A 30-mm-diameter spherical volume of interest was placed within the right lobe of the liver above, below, and at the level of the main portal vein by 2 independent readers. Correlation coefficients, analysis of variance, intraclass correlation coefficient, and Bland-Altman analysis were performed.

Results: The mean liver SULmean was between 1.39 and 1.42 and between 1.28 and 1.3 in early and delayed images, respectively (P = 0.001). There is time-dependent reduction in the mean liver SULmean at 2-hour (7%Y8%) and 4-hour uptake time (15%Y21%) compared with 1-hour uptake time. The correlation coefficient between delayed uptake time and liver SULmean reduction is 0.39 to 0.41 at the upper aspect of the liver. The intraclass correlation coefficient for 2 readers varied between 0.997 and 0.998 and between 0.995 and 0.999 in early and delayed images, respectively (P = 0.001).

Conclusions: There is time-dependent reduction of mean liver SULmean, about 7% to 8% within the clinically relevant FDG uptake time, in the same patient with excellent interreader agreement in early and delayed images within the right lobe of the liver. Therefore, liver SULmean could represent a useful reference parameter in quantitative analysis of dual-phase FDG PET/CT in malignancy or atypical infection/inflammatory disease. Furthermore, it may be suitable as a normalization factor in currently available formulae quantifying therapy response on PET imaging.

Original languageEnglish (US)
Pages (from-to)e17-e22
JournalClinical Nuclear Medicine
Volume40
Issue number1
StatePublished - Jan 14 2015

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Liver
Neurofibromatoses
Portal Vein
Analysis of Variance
Adenocarcinoma
Infection
Neoplasms

Keywords

  • Dual-time imaging
  • FDG PET/CT
  • Interreader agreement
  • SUL<inf>mean</inf>

ASJC Scopus subject areas

  • Radiology Nuclear Medicine and imaging
  • Medicine(all)

Cite this

Chirindel, A., Alluri, K. C., Tahari, A. K., Chaudhry, M., Wahl, R. L., Lodge, M., & Subramaniam, R. M. (2015). Liver standardized uptake value corrected for lean body mass at FDG PET/CT: Effect of FDG uptake time. Clinical Nuclear Medicine, 40(1), e17-e22.

Liver standardized uptake value corrected for lean body mass at FDG PET/CT : Effect of FDG uptake time. / Chirindel, Alin; Alluri, Krishna C.; Tahari, Abdel K.; Chaudhry, Muhammad; Wahl, Richard L.; Lodge, Martin; Subramaniam, Rathan M.

In: Clinical Nuclear Medicine, Vol. 40, No. 1, 14.01.2015, p. e17-e22.

Research output: Contribution to journalArticle

Chirindel, A, Alluri, KC, Tahari, AK, Chaudhry, M, Wahl, RL, Lodge, M & Subramaniam, RM 2015, 'Liver standardized uptake value corrected for lean body mass at FDG PET/CT: Effect of FDG uptake time', Clinical Nuclear Medicine, vol. 40, no. 1, pp. e17-e22.
Chirindel A, Alluri KC, Tahari AK, Chaudhry M, Wahl RL, Lodge M et al. Liver standardized uptake value corrected for lean body mass at FDG PET/CT: Effect of FDG uptake time. Clinical Nuclear Medicine. 2015 Jan 14;40(1):e17-e22.
Chirindel, Alin ; Alluri, Krishna C. ; Tahari, Abdel K. ; Chaudhry, Muhammad ; Wahl, Richard L. ; Lodge, Martin ; Subramaniam, Rathan M. / Liver standardized uptake value corrected for lean body mass at FDG PET/CT : Effect of FDG uptake time. In: Clinical Nuclear Medicine. 2015 ; Vol. 40, No. 1. pp. e17-e22.
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abstract = "Objective: The objective of this study is to establish the magnitude change and interreader reliability of the liver standardized uptake value corrected for lean body mass (SULmean) in dual-time-point imaging at 1 and 2 hours and 1 and 4 hours.Patients and Methods: Early and delayed FDG PET/CT scans were included for 28 patients (13 men and 15 women) who had normal liver by CT or ultrasound. The average uptake time between the early and delayed scans were 55 minutes (range, 44Y69 minutes) for pancreatic adenocarcinoma patients (n = 19) and 184 minutes (range, 140Y197 minutes) for neurofibromatosis patients (n = 9). A 30-mm-diameter spherical volume of interest was placed within the right lobe of the liver above, below, and at the level of the main portal vein by 2 independent readers. Correlation coefficients, analysis of variance, intraclass correlation coefficient, and Bland-Altman analysis were performed.Results: The mean liver SULmean was between 1.39 and 1.42 and between 1.28 and 1.3 in early and delayed images, respectively (P = 0.001). There is time-dependent reduction in the mean liver SULmean at 2-hour (7{\%}Y8{\%}) and 4-hour uptake time (15{\%}Y21{\%}) compared with 1-hour uptake time. The correlation coefficient between delayed uptake time and liver SULmean reduction is 0.39 to 0.41 at the upper aspect of the liver. The intraclass correlation coefficient for 2 readers varied between 0.997 and 0.998 and between 0.995 and 0.999 in early and delayed images, respectively (P = 0.001).Conclusions: There is time-dependent reduction of mean liver SULmean, about 7{\%} to 8{\%} within the clinically relevant FDG uptake time, in the same patient with excellent interreader agreement in early and delayed images within the right lobe of the liver. Therefore, liver SULmean could represent a useful reference parameter in quantitative analysis of dual-phase FDG PET/CT in malignancy or atypical infection/inflammatory disease. Furthermore, it may be suitable as a normalization factor in currently available formulae quantifying therapy response on PET imaging.",
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