4.5 Article

The effect of hypothyroidism on referential background metabolic activity on 18F-FDG PET/CT

Journal

QUANTITATIVE IMAGING IN MEDICINE AND SURGERY
Volume 11, Issue 8, Pages 3666-+

Publisher

AME PUBL CO
DOI: 10.21037/qims-20-1310

Keywords

2-deoxy-2-[F-18]fluoro-D-glucose (F-18-FDG); positron emission tomography-computed tomography (PET/CT); liver; blood pool; hypothyroidism

Funding

  1. Sichuan Provincial Department of Science and Technology support program [2015SZ0128]
  2. National Key Research and Development Program of China [2016YFC0104300]

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In this study, patients with hypothyroidism showed increased liver and blood-pool (18F)-FDG uptake and decreased muscle F-18-FDG uptake compared to euthyroid individuals. Multivariate analysis indicated serum thyroid-stimulating hormone levels as an important predictor for liver and bloodpool standardized uptake values, while serum free triiodothyronine levels were identified as a predictor for muscle standardized uptake values. These findings underscore the importance of considering thyroid function in metabolic response evaluation using PET/CT.
Background: Background uptake activity is used as a reference to assess treatment response by positron emission tomography-computed tomography (PET/CT) with 2-deoxy-2-[F-18]fluoro-D-glucose (F-18-FDG). Prior studies have reported decreased liver and increased muscle F-18-FDG uptake in patients with hyperthyroidism. We hypothesized that hyperthyroidism and hypothyroidism might have inverse effects on F-18-FDG uptake on PET/CT. Methods: We recruited 36 patients with hypothyroidism and 36 age and gender-matched euthyroid participants. We recorded patient factors and background mean standardized uptake values normalized by lean body mass from the aortic blood pool, liver, and muscle. We compared the patient factors and background standardized uptake values normalized by lean body mass between hypothyroidism patients and the controls. We performed a multivariate analysis to determine the best predictors of the 3 different background standardized uptake values normalized by lean body mass. Results: Patients with hypothyroidism had higher liver standardized uptake values normalized by lean body mass (1.77 +/- 0.33 vs. 1.58 +/- 0.26, P=0.009) and aortic blood-pool standardized uptake values normalized by lean body mass (1.21 +/- 0.22 vs. 1.11 +/- 0.20, P=0.040) than the controls. In contrast, the muscle standardized uptake value normalized by lean body mass (0.50 +/- 0.09 vs. 0.54 +/- 0.09, P=0.044) of the patients with hypothyroidism was lower than that of the controls. The serum level of thyroid-stimulating hormone was an independent predictor of liver standardized uptake values normalized by lean body mass (0=0.356, P<0.001) and bloodpool standardized uptake values normalized by lean body mass (0=0.288, P=0.001). The serum level of free triiodothyronine was an independent predictor of muscle standardized uptake values normalized by lean body mass (0=0.310, P=0.002). Conclusions: PET/CT scans showed that hypothyroidism patients had increased liver and blood-pool (18F)-FDG uptake and decreased skeletal muscle F-18-FDG uptake compared with euthyroid individuals. These alterations should be noted when a metabolic response to cancer treatment on PET/CT is determined.

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