Humanitas Research Hospital, IRCCS, via Manzoni 56, 20089, Rozzano (Milan), Italy.
Department of Biomedical Sciences, Humanitas University, Via Rita Levi Montalcini 4, 20090, Milan, Pieve Emanuele, Italy.
Eur J Nucl Med Mol Imaging. 2021 Sep;48(10):3187-3197. doi: 10.1007/s00259-021-05294-3. Epub 2021 Mar 7.
The present study hypothesised that whole-body [18F]FDG-PET/CT might provide insight into the pathophysiology of long COVID.
We prospectively enrolled 13 adult long COVID patients who complained for at least one persistent symptom for >30 days after infection recovery. A group of 26 melanoma patients with negative PET/CT matched for sex/age was used as controls (2:1 control to case ratio). Qualitative and semi-quantitative analysis of whole-body images was performed. Fisher exact and Mann-Whitney tests were applied to test differences between the two groups. Voxel-based analysis was performed to compare brain metabolism in cases and controls. Cases were further grouped according to prevalent symptoms and analysed accordingly.
In 4/13 long COVID patients, CT images showed lung abnormalities presenting mild [18F]FDG uptake. Many healthy organs/parenchyma SUVs and SUV ratios significantly differed between the two groups (p ≤ 0.05). Long COVID patients exhibited brain hypometabolism in the right parahippocampal gyrus and thalamus (uncorrected p < 0.001 at voxel level). Specific area(s) of hypometabolism characterised patients with persistent anosmia/ageusia, fatigue, and vascular uptake (uncorrected p < 0.005 at voxel level).
[18F]FDG PET/CT acknowledged the multi-organ nature of long COVID, supporting the hypothesis of underlying systemic inflammation. Whole-body images showed increased [18F]FDG uptake in several "target" and "non-target" tissues. We found a typical pattern of brain hypometabolism associated with persistent complaints at the PET time, suggesting a different temporal sequence for brain and whole-body inflammatory changes. This evidence underlined the potential value of whole-body [18F]FDG PET in disclosing the pathophysiology of long COVID.
本研究假设全身 [18F]FDG-PET/CT 可能有助于深入了解长新冠的病理生理学。
我们前瞻性招募了 13 名长新冠成年患者,这些患者在感染康复后至少持续出现 1 种症状超过 30 天。将一组 26 名 PET/CT 阴性的黑色素瘤患者作为对照组(2:1 对照与病例比),这些患者的性别和年龄相匹配。对全身图像进行定性和半定量分析。应用 Fisher 确切检验和 Mann-Whitney 检验比较两组间的差异。对病例和对照组的脑代谢进行基于体素的比较分析。根据常见症状对病例进一步分组,并进行相应分析。
在 13 名长新冠患者中,4 名患者的 CT 图像显示肺部异常,出现轻度 [18F]FDG 摄取。两组之间许多健康器官/实质的 SUV 和 SUV 比值存在显著差异(p ≤ 0.05)。长新冠患者右海马旁回和丘脑出现脑代谢低下(未校正的体素水平 p<0.001)。特定区域的代谢低下特征性地出现在持续嗅觉丧失/味觉丧失、疲劳和血管摄取的患者中(未校正的体素水平 p<0.005)。
[18F]FDG PET/CT 承认长新冠的多器官性质,支持潜在系统性炎症的假说。全身图像显示在多个“靶”和“非靶”组织中出现[18F]FDG 摄取增加。我们发现了一种与 PET 时持续症状相关的典型脑代谢低下模式,提示脑和全身炎症变化的时间顺序不同。这一证据强调了全身 [18F]FDG PET 在揭示长新冠病理生理学方面的潜在价值。