Haemoglobin oxygen affinity in patients with severe COVID‐19 infection

Severely ill COVID-19 patients have an atypical form of respiratory distress. Acute respiratory distress syndrome (ARDS), while heterogenous, classically presents with severe hypoxia and decreased lung compliance.1 In SARS-CoV-2 coronavirus infection (COVID-19) lung mechanics and compliance are relatively well conserved until late in the disease course. Despite early preservation of lung compliance, the hypoxaemia in COVID-19 is severe and is ultimately the primary mechanism of multiple organ failure and death.2 The underlying pathology is due to COVID-19 entering cells via the ACE2 receptor. This receptor is expressed on many cells including alveolar epithelial cells and vascular endothelium resulting in a profound immune response and widespread endothelial dysfunction.3 We were both interested and concerned to read the report by Liu and Li.4 This in silico study used homology modelling and molecular docking algorithms to predict theoretical interactions between COVID-19 and haemoglobin (Hb). COVID-19 expresses a variety of open reading frame proteins including orf1ab, ORF3a, ORF6, ORF7a, ORF10 and ORF8. Liu and Li4 predict that these ORF proteins can interact with haemoglobin to reduce both oxygen (O2) affinity and total haemoglobin content. They report specifically that their modelling predicts a theoretical interaction between orf1ab, ORF10 and ORF3a and the haem moiety of the beta chain while ORF8 and viral surface glycoproteins can directly target the porphyrin. They assert that their data support the use of chloroquine and hydroxychloroquine as therapeutic agents. However, the methods used by Lui and Li have very recently been criticised — not least of all because they are unsupported by experimental evidence.5 It is unclear what testable physiological consequences might arise from an interaction between viral proteins and Hb but these are presumed to include a generalised loss of Hb and/or a change in O2 affinity. While mild anaemia and decreased Hb content have been reported,6,7 to our knowledge the effect of COVID-19 on O2 affinity has not been investigated. Multiple studies and national guidelines strongly support restrictive transfusion practice in the critically ill as a basic standard of care.8 It is possible that if the haemoglobin molecule was adversely affected by COVID-19, and the O2 affinity curve right-shifted, restrictive transfusion could be potentially harmful. Given the very high mortality of these ventilated COVID-19 patients, we considered evaluation of any effect on the O2 affinity curve as urgent to inform our practice. Physicians caring for patients infected with COVID-19 ordered an Hb O2 affinity assessment in 14 patients (four newly admitted from the emergency department and 10 patients receiving mechanical ventilation in critical care) which we compared to 11 age- and sex-matched controls as part of an audit to assess the utility of this investigation in the management of patients with severe disease (Guys and St Thomas’ Hospital Audit No. 10855; Table I). No extra samples or blood tests were taken from patients — rather relevant samples were identified after a routine full blood count had been reported. O2 saturation curves from control and COVID-19-positive patients are shown in Fig 1. It is clear that there are no differences in O2 affinity or co-operativity between samples from COVID-19 and matched controls. The P50 and Hill Slope values are given in Table I. However, as is common in critically ill patients, there is a substantial anaemia and loss of total haemoglobin. In summary, while the total O2-carrying capacity will certainly be reduced by the anaemia and loss of total haemoglobin, we see no evidence, using standard clinical measures in a small cohort of patients, to suggest that COVID-19 alters haemoglobin O2 affinity and there is no requirement to change our transfusion practice. We are grateful for the help of the Special Haematology and Haematology laboratory staff at Viapath, Guy's & St Thomas's NHS Foundation Trust. MJS is supported by the British Heart Foundation (RG/12/4/29426). The help of Felix Torrance with the curve-fitting equations is gratefully acknowledged. CCS and MJS conceived and designed the study; BJH provided access to Viapath analytical labs and haematology expertise; RA and HK were responsible for patient care; YD and SW analysed blood samples and patient data; MJS analysed the data and wrote the first draft; all authors revised and approved the final submission.

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