The present cohort study revealed that VAT/TAT elevation was a significant risk factor for progression to severe or critical disease in COVID-19 patients. The significant trends were also observed in the association of the VAT/TAT levels with the future risk of COVID-19 progression. ROC analysis showed the significant superiority of VAT/TAT to BMI for predicting morbidity in COVID-19. The outcomes did not vary by smoking status. This is the first prospective longitudinal study to evaluate the prognostic impact of VAT/TAT on COVID-19.
To the best of our knowledge, there have been only four studies investigating obesity-related radiological biomarkers for prognosis in subjects with COVID-19 [8–11]. They showed the association of VAT with the likelihood of intensive care unit admission or developing pneumonia; however, all of them were designed as retrospective or cross-sectional studies, and the authors were unable to make a causal inference. The present research was unique in controlling for potential confounders to highlight the robustness of the results. Our findings reinforced and ensured the value of intra-abdominal fat mass as an independent risk factor for COVID-19 progression.
VAT/TAT can increase directly on account of VAT overload and/or relatively due to frailty [12]. Independently of coexistent metabolic disorders such as diabetes and cardiovascular disease, excessive adipose tissue increases the risk of SARS-CoV-2 infection via enhancement of viral entry due to hyperexpression of angiotensin-converting enzyme 2 [13, 14], cell surface glucose–regulated protein 78 [15, 16], heparan sulfate proteoglycan [17, 18], and neuropilin-1 [19, 20]. Adipose tissue and its related immune cells also induce an inadequate response and overreaction of the immune system, triggering a cytokine storm [21, 22]. Furthermore, in the obese, the risk for developing a thrombus formation and hemorrhage is elevated due to hyperleptinemia [23], the upregulation of plasminogen activator inhibitor 1 [24], endothelial dysfunction [25], and the impaired bioavailability of vitamin K [26]. On the other hand, frailty has been widely known as a coexisting condition with underweight and high intra-abdominal fat mass [12], causing high vulnerability for dependency and death [27]. A recent multicenter observational cohort study revealed that frailty raised the risk of morbidity and mortality in patients with COVID-19 [28]. Hence, it is reasonable for VAT/TAT, rather than VAT or BMI, to be strongly correlated with unfavorable outcomes in COVID-19, as demonstrated in the present study.
Several studies have indicated that a high BMI, namely, overweight and obesity, is a risk factor for major complications in COVID-19 [5, 6, 29]. In line with the previous report [10], our analysis showed the reliable performance of VAT/TAT, distinct from BMI, as a prognostic factor in COVID-19. The differences in predictive adequacy between VAT/TAT and BMI were likely to be affected by the aforementioned influence of frailty on the prognosis of COVID-19, since frailty is linked to high VAT/TAT and low BMI [12]. The association of frailty with poor prognosis was parallel to that of VAT/TAT, whereas it was inconsistent with the undesirable effect of increased BMI and therefore seemed to have attenuated the trend in the relationship between BMI and disease progression in COVID-19. The current results confirmed the usefulness and importance of VAT/TAT assessment in the field of COVID-19.
The strengths of our study were the highly accurate measurement of intra-abdominal fat deposition based on CT images, the prospective cohort study design to minimize the effects of reverse causation, and the certainty of the findings established through multivariable adjustment and stratified analyses. However, some potential limitations should be noted. First, the value of VAT/TAT was based on a single measurement. Second, VAT/TAT and other radiological biomarkers were estimated using a CT image not at the navel level but at the level of upper pole of the right kidney. These two limitations might have caused misclassification of the VAT/TAT level, which could have weakened the association found in the present study, biasing the results toward a null hypothesis. However, strong correlations were demonstrated between radiological factors at the upper pole of the right kidney and those at the navel level in the present study, consistent with preceding literature [30, 31]. Thus, the value of VAT/TAT at the upper pole of the right kidney, usually available from routinely collected chest CT, appeared comparable to the value at the standard position and is practical for use in daily clinics. Third, we were unable to adjust the effects of intensity or duration of smoking on the prognosis of COVID-19 due to a lack of data concerning the number of pack years of cigarette smoking. However, in a subgroup analysis by smoking status, the association of VAT/TAT with the risk of COVID-19 progression did not differ from the primary results. We therefore speculate that this limitation did not alter our conclusions. Lastly, the sample size was relatively small owing to the study design as single-center analyses. This limitation might have led to overlooking the association between obesity-related biomarkers other than VAT/TAT and the endpoint of interest. To overcome this limitation, a larger-scale cohort study is warranted.