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      Diabetes mellitus and SARS-CoV-2-related mortality: the impact of acute hyperglycemic crises and some further considerations

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          Abstract

          Dear Editor, We have read with great interest the recently published systematic review and meta-analysis authored by Wu et al. [1], demonstrating that the presence of diabetes mellitus (DM) increases the odds for mortality in the context of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection by 75%. Unfortunately, as the authors clearly state in their limitations section, lack of access to data regarding diabetes type, diabetes medications and complications did not permit further subgroup analyses that could be extremely useful [1]. We would like to emphasize on another aspect of SARS-CoV-2 infection among patients with DM, the triggering of acute hyperglycemic crises, either diabetic ketoacidosis (DKA) or hyperosmolar hyperglycemic state (HHS). In a recently published case series, Hoe Chan et al. described the presentation and clinical course of 6 patients with DM who developed DKA and HHS in the context of SARS-CoV-2 infection [2]. Notably, 4 out of 6 patients required mechanical ventilation, while the same proportion of patients died due to disease [2]. According to recent evidence, patients with DM and SARS-CoV-2-related ketosis are older, with a greater prevalence of coronary artery disease and hypertension, while they also have greater in-hospital stay, compared to non-diabetic patients that develop SARS-CoV-2-related ketosis [3]. In some cases, SARS-CoV-2-induced DKA may even be the first clinical presentation of undiagnosed DM [4]. Based on the knowledge that patients with DM feature greater odds for death due to infection compared to non-diabetic patients, it may be deduced that the complication with an acute hyperglycemic crisis will further worsen overall prognosis [1]. However, according to a recent retrospective analysis from the UK, patients with DM who develop DKA due to disease are more likely to survive compared to those patients that are not complicated by an acute hyperglycemic crisis [5]. The questions that inevitably arise are whether underlying antidiabetic treatment has a real impact on the occurrence of either DKA or HHS and if the type of diabetes really plays a role for the development of an acute hyperglycemic crisis. For example, there is increased concern regarding the risk of DKA with the continuation of the use of sodium-glucose-co-transporter 2 inhibitors during illness, or the risk of dehydration with the use of metformin or glucagon-like peptide-1 receptor agonists, which could eventually lead to DKA/HHS. Therefore, it would be interesting to know in future, large, observational studies the proportion of patients that developed DKA/HHS in the context of SARS-CoV-2 infection, the underlying treatment and the outcome of disease. Such studies could provide us with useful insights into clinical practice, which could eventually lead to optimization of treatment strategy either to infected patients or to patients being at high risk of infection, both in in-hospital and in outpatient setting.

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          Most cited references5

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          COVID ‐19 infection may cause ketosis and ketoacidosis

          Abstract The present study included 658 hospitalized patients with confirmed COVID‐19. Forty‐two (6.4%) out of 658 patients presented with ketosis on admission with no obvious fever or diarrhoea. They had a median (interquartile range [IQR]) age of 47.0 (38.0–70.3) years, and 16 (38.1%) were men. Patients with ketosis were younger (median age 47.0 vs. 58.0 years; P = 0.003) and had a greater prevalence of fatigue (31.0% vs. 10.6%; P < 0.001), diabetes (35.7% vs. 18.5%; P = 0.007) and digestive disorders (31.0% vs. 12.0%; P < 0.001). They had a longer median (IQR) length of hospital stay (19.0 [12.8–33.3] vs. 16.0 [10.0–24.0] days; P < 0.001) and a higher mortality rate (21.4% vs. 8.9%; P = 0.017). Three (20.0%) out of the 15 patients with diabetic ketosis developed acidosis, five patients (26.7%) with diabetic ketosis died, and one of these (25.0%) presented with acidosis. Two (7.4%) and four (14.3%) of the 27 non‐diabetic ketotic patients developed severe acidosis and died, respectively, and one (25.0%) of these presented with acidosis. This suggests that COVID‐19 infection caused ketosis or ketoacidosis, and induced diabetic ketoacidosis for those with diabetes. Ketosis increased the length of hospital stay and mortality. Meanwhile, diabetes increased the length of hospital stay for patients with ketosis but had no effect on their mortality.
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            Diabetic ketoacidosis precipitated by Covid-19 in a patient with newly diagnosed diabetes mellitus

            1 Introduction There is scarce data on diabetic ketoacidosis (DKA) in Covid-19 infection. We report a case of DKA precipitated by Covid-19 in a patient with newly diagnosed diabetes mellitus. A 37 year-old, previously healthy man presented with 1 week history of fever, vomiting, polydipsia and polyuria. On admission, his temperature was 38.5°C. He was haemodynamically stable but mildly tachycardic. He did not display Kussmaul’s breathing and did not require supplemental oxygen. His body mass index was 22.6 kg/m2 with no evidence of insulin resistance. Given positive contact history, he was tested and confirmed to be infected with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Laboratory investigations (Table 1 ) were significant for hyperglycemia, high anion gap metabolic acidosis and ketonemia, confirming the diagnosis of DKA. Table 1 Laboratory results Investigation Result Reference Range Venous glucose (mmol/L) 39.7 - Arterial blood gaspH (mmHg)Bicarbonate (mmol/L)pCO2 (mmHg) 7.281225 7.25 – 7.3522 – 2835 - 45 Sodium (mmol/L) 128 135 - 145 Chloride (mmol/L) 86 95 - 110 Anion gap 30 8 – 16 Ketones (mmol/L) 6.4 < 0.6 Creatinine (umol/L) 95 67 – 112 Glycated haemoglobin (%) 14.2 - He received 6 litres of intravenous fluids and intravenous insulin infusion in the first 24 hours. Serum electrolytes were closely monitored. DKA resolved the following day and he was transitioned to subcutaneous insulin therapy. DKA occurs as a result of insulin deficiency and increased counterregulatory responses, which favour the production of ketones. The interactions between SARS-CoV-2 and the renin-angiotensin-aldosterone system (RAAS) might provide another mechanism in the pathophysiology of DKA. Angiotensin-converting enzyme 2 (ACE2), a key enzyme in the RAAS, catalyzes the conversion of angiotensin II to angiotensin (1-7)[1]. ACE2 is highly expressed in the lungs, pancreas and serves as the entry point for SARS-CoV-2[1]. After endocytosis of the virus complex, ACE2 expression is downregulated[2]. There are 2 implications of these interactions. Firstly, entry of SARS-CoV-2 into pancreatic islet cells may directly aggravate beta cell injury[3]. Secondly, downregulation of ACE2 after viral entry can lead to unopposed angiotensin II, which may impede insulin secretion[4]. These 2 factors might have contributed to the acute worsening of pancreatic beta cell function and precipitated DKA in this patient. In addition, the relationship between SARS-CoV-2 and the RAAS can complicate DKA management. Excessive fluid resuscitation may potentiate acute respiratory distress syndrome as angiotensin II increases pulmonary vascular permeability and worsens damage to lung parenchyma[5]. Furthermore, angiotensin II stimulates aldosterone secretion, potentiating the risk of hypokalemia, which may necessitate more potassium supplementation in order to continue intravenous insulin to suppress ketogenesis. In conclusion, it is possible that SARS-CoV-2 may aggravate pancreatic beta cell function and precipitate DKA. Further studies will help delineate the pathophysiology. We also highlight the pertinent clinical considerations in the concurrent management of two life-threatening conditions – DKA and Covid-19. The authors do not have any financial associations or conflicts of interests to disclose. Funding: None. Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
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              Diabetes increases the mortality of patients with COVID-19: a meta-analysis

              Aims Nowadays, the ongoing pandemic of COVID-19 caused by the novel coronavirus Syndrome-Coronavirus-2 (SARS-CoV-2) is an emerging, rapidly evolving situation. Complications such as hypertension, diabetes, COPD, cardiovascular disease, and cerebrovascular disease are major risk factors for patients with COVID-19. Methods No meta-analysis has explored if or not diabetes related to mortality of patients with COVID-19. Therefore, this meta-analysis first aims to explore the possible clinical mortality between diabetes and COVID-19, analyze if diabetes patients infected with SARS-CoV-2 are exposed to the worst clinical prognostic risk, and to evaluate the reliability of the evidence. Results Our results showed a close relationship between diabetes and mortality of COVID-19, with a pooled OR of 1.75 (95% CI 1.31–2.36; P = 0.0002). The pooled data were calculated with the fixed effects model (FEM) as no heterogeneity appeared in the studies. Sensitivity analysis showed that after omitting any single study or converting a random effect model to FEM, the main results still held. Conclusions Our meta-analysis showed that diabetes increases the mortality of patients with COVID-19. These results indicated the disturbance of blood glucose in the COVID-19 patients. More importantly, this meta-analysis grades the reliability of evidence for further basic and clinical research into the diabetes dysfunction in COVID-19 patients.
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                Author and article information

                Contributors
                dipatoulias@gmail.com
                Journal
                Acta Diabetol
                Acta Diabetol
                Acta Diabetologica
                Springer Milan (Milan )
                0940-5429
                1432-5233
                20 August 2020
                : 1-2
                Affiliations
                [1 ]GRID grid.4793.9, ISNI 0000000109457005, Second Propedeutic Department of Internal Medicine, General Hospital “Hippokration”, , Aristotle University of Thessaloniki, ; Konstantinoupoleos 49, 54642 Thessaloniki, Greece
                [2 ]GRID grid.4793.9, ISNI 0000000109457005, Third Department of Cardiology, General Hospital “Hippokration”, , Aristotle University of Thessaloniki, ; Thessaloniki, Greece
                [3 ]GRID grid.253615.6, ISNI 0000 0004 1936 9510, Veterans Affairs Medical Center, , George Washington University, ; Washington, DC USA
                Author notes

                Managed by Massimo Federici.

                Author information
                http://orcid.org/0000-0002-6899-684X
                Article
                1593
                10.1007/s00592-020-01593-7
                7438670
                20f93fc0-1e92-4ad2-8c4a-531efeeb4b7b
                © Springer-Verlag Italia S.r.l., part of Springer Nature 2020

                This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.

                History
                : 4 July 2020
                : 5 August 2020
                Categories
                Letter to the Editor

                Endocrinology & Diabetes
                Endocrinology & Diabetes

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