Dear Editor,

I read with great interest the brief report by Knopp et al. [1] entitled ‘Presenting features of COVID-19 in older people: relationships with frailty, inflammation and mortality.’ The authors described the clinical characteristics and outcomes of older adults diagnosed with COVID-19. Results of particular interest include higher Clinical Frailty Scale (CFS) scores with decreases in C-reactive protein (CRP) (p < 0.01), an age-related increase in mortality (HR 1.1, 95% CI 1.0–1.1, p  < 0.01) but neither sex nor frailty was associated with mortality and a higher likelihood of death with rising CRP or higher neutrophil:lymphocyte ratio. I would like to thank the authors for highlighting the importance of the relationship between frailty, inflammation and mortality, especially during the COVID-19 pandemic. Both frailty and inflammation have been linked to increased mortality, especially in patients with COVID-19 [2]. However, I would like to comment on some of their findings which need more clarity.

First, the authors described recording data on ethnicity. I would like to highlight the fact that studies have found a correlation between the severity of COVID-19 and ethnicity with patients of the black, Asian and minority ethnic (BAME) group being more severely affected by COVID-19 [3]. Risk of death is particularly high for Black African (HR 3.24, 95% CI 2.90–3.62) and Pakistani (HR 3.29, 95% CI 2.96–3.64) groups after adjustment for age and region [3]. Having collected this data, adjustment or an attempt to include it in their results would have been informative to better interpret their findings and compare with other research.

Second, the authors suggest that frailty on the CFS is not associated with increased mortality. Previous studies have shown that there exist an association between frailty on the CFS and mortality in older inpatients with COVID-19 [4]. More specifically, the CFS has been shown to be a useful tool for risk stratification in patients with COVID-19 and has been shown to better predict disease outcomes than age and comorbidity [2]. This highlights the importance of treating their findings with caution and encouraging further research on this relationship.

Third, they also show an inverse relationship between CRP and frailty measured on the CFS. Although the relationship between frailty and inflammation is poorly understood, the literature suggests frailty and pre-frailty are associated with higher inflammatory parameters with frail and pre-frail patients having significantly higher serum levels of CRP and IL-6 than robust patients [5]. Perhaps adjustment for factors exhibiting worsening clinical outcome with increasing frailty, including CRP, are required to find the true association between frailty and increased mortality as previously described [2].