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Persistent lung and vascular inflammation in mild to moderate COVID-19 survivors detected by ¹⁸F-FDG PET/CT: A quantitative imaging study with implications for cardiovascular risk

2025/11/25 by Shipra Verma, N. Lan, Heidi Espedal +9 · 1 voice · 1 citation
Medicine · #COVID-19 Clinical Research Studies #Long-Term Effects of COVID-19 #Lymphadenopathy Diagnosis and Analysis

paper · pdf · doi:10.1007/s00259-025-07656-7

Abstract

Lingering inflammation after COVID-19 has been proposed as a contributor to long-term cardiovascular risk, yet the link between pulmonary and vascular inflammation remains insufficiently defined. This study aimed to quantify residual lung and vascular inflammation in individuals recovered from mild-to-moderate COVID-19 using ¹⁸F-FDG PET/CT and assess their association. Fifty-nine participants underwent ¹⁸F-FDG PET/CT imaging at a median of 97 days (IQR: 77–112.5) following clinical recovery from COVID-19. Lung inflammation was assessed using standardised uptake value maximum (SUVmax), target-to-background ratio maximum and mean (TBRmax, TBRmean), and total lung glycolysis (TLG) in contracted lung volumes to reduce spill-in from mediastinal structures. Metrics were indexed to blood pool activity (TBR) and lung volume (TLGindex). Vascular inflammation was evaluated using TBRmax values of the thoracic aorta and the most diseased segment (MDS). Results were compared with eight COVID-naive individuals using identical protocols. Compared with controls, individuals post-COVID-19 exhibited significantly elevated SUVmax in both lungs (p < 0.001), TBRmax in the left (p = 0.037) and right (p = 0.010) lungs, and TLG in the left lung (p = 0.018). Measures of vascular inflammation correlated significantly with TBRmax, TBRmean, and TLGindex in both lungs (all p < 0.05), suggesting a parallel inflammatory response. Persistent pulmonary inflammation is evident following mild-to-moderate COVID-19 and is associated with increased vascular inflammation. These findings suggest a mechanistic link between post-infectious lung and vascular inflammation, potentially contributing to elevated cardiovascular risk. ¹⁸F-FDG PET/CT enabled sensitive detection of subclinical inflammation in both compartments, highlighting the value of quantitative PET metrics in elucidating systemic inflammatory response following viral infection. In this study, 59 survivors of mild-to-moderate COVID-19 (median interval from infection to imaging: 97 days, IQR 77–112.5) and eight healthy controls underwent ¹⁸F-FDG PET/CT. COVID-19 participants demonstrated persistently elevated lung uptake metrics (SUVmax, TBRmax, and TLG) together with increased aortic inflammation. Significant correlations between pulmonary and vascular FDG uptake suggest that post-COVID lung inflammation may be linked to systemic vascular responses, providing a potential pathway for increased long-term cardiovascular risk.

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