Key result
Metabolic syndrome was associated with a significantly higher maximum standardized uptake value (SUVmax) of visceral adipose tissue compared to participants without metabolic syndrome components (0.74 vs 0.65, p=0.01).
Why the study?
Although visceral adipose tissue inflammatory activity is elevated in metabolic syndrome and linked to atherosclerosis vulnerability, whether VAT glucose uptake reflects systemic inflammation and relates to metabolic syndrome components was unclear.
Does 18F-FDG PET/CT assessment of glucose uptake in visceral adipose tissue correlate with systemic inflammatory status and the number of metabolic syndrome components?
Cross-Sectional (n=203)
Single-blind
No
Does 18F-FDG PET/CT assessment of glucose uptake in visceral adipose tissue correlate with systemic inflammatory status and the number of metabolic syndrome components?
Absolute Event Rate: 0.74% vs 0.65%
p-value: p=0.01
18F-FDG PET/CT assessment of visceral adipose tissue glucose uptake reflects systemic inflammation and correlates with the severity of metabolic syndrome.
May reflect systemic inflammation in metabolic syndrome; hypothesis-generating and leaves open clinical utility of PET assessment.
OBJECTIVE: The inflammatory activity of visceral adipose tissue (VAT) is elevated in metabolic syndrome (MS), and associated with vulnerability to atherosclerosis. Inflammation can be assessed by glucose uptake in atherosclerotic plaques. We investigated whether the glucose uptake of VAT, assessed by 18F-fluorodeoxyglucose positron emission tomography/computed tomography (18F-FDG PET/CT), is associated with systemic inflammatory status, and related to the number of MS components. METHODS: 18F-FDG PET/CT was performed in a total of 203 participants: 59 without MS component; M(0), 92 with one or two MS components; M(1-2), and 52 with MS. Glucose uptake in VAT was evaluated using the mean standardized uptake value (SUVmean) and the maximum SUV (SUVmax). Glucose uptakes of immune-related organs such as the spleen and bone marrow (BM) were evaluated using the SUVmax. RESULTS: VAT SUVmax correlated with high-sensitivity C-reactive protein (hsCRP) and the SUVmax of spleen and BM, which reflect the status of systemic inflammation. Both hsCRP and the SUVmax of the spleen and BM were higher in the MS group than in the M(1-2) or M(0) groups. In VAT, SUVmax increased with increasing number of MS components, while SUVmean decreased. CONCLUSIONS: The SUVmax and SUVmean of VAT assessed by 18F-FDG PET/CT reflected inflammation-driven unique glucose metabolism in the VAT of MS patients, distinct from that of atherosclerotic plaques.
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Pahk et al. (2020) conducted a cross-sectional in Metabolic syndrome (n=203). Metabolic syndrome vs. No metabolic syndrome components was evaluated on Maximum standardized uptake value (SUVmax) of visceral adipose tissue (p=0.01). Metabolic syndrome was associated with a significantly higher maximum standardized uptake value (SUVmax) of visceral adipose tissue compared to participants without metabolic syndrome components (0.74 vs 0.65, p=0.01).
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