key: cord-0859624-yak66w80 authors: Amerta, Ghosh; Anjana, Ranjit Mohan; Shanthi Rani, Coimbatore Subramanian; Rani, Saravanan Jeba; Ritesh, Gupta; Alka, Jha; Vimal, Gupta; Atu, Luthra; Suhai, Durrani; Shafi, Kuchay; Koel, Dutta; Kanika, Tyagi; Ranjit, Unnikrishnan; Srivastava, Brijendra Kumar; Ramu, Muthu; Sastry, Nadiminty Ganapathi; Gupta, Prasanna Kumar; Umasankari, Ganesan; Jayashri, Ramamoorthy; Mohan, Viswanathan; Misra, Anoop title: Glycemic parameters in new-onset diabetes during COVID-19 pandemic are more severe than new-onset diabetes before the pandemic: NOD COVID India study date: 2020-12-29 journal: Diabetes Metab Syndr DOI: 10.1016/j.dsx.2020.12.033 sha: 6dc3ce4b285a907b51f2d41668faf79531e73f8b doc_id: 859624 cord_uid: yak66w80 BACKGROUND AND AIMS: It is not known if new onset diabetes during Coronavirus-19 disease (COVID-19; NOD COVID) is phenotypically or biochemically different than new onset diabetes before COVID-19 (NOD). METHODS: All adults diagnosed with new onset diabetes from during the time of COVID-19 were compared with new onset diabetes prior to COVID-19, from two tertiary care hospitals in Chennai and Delhi. RTPCR test for SARS-CoV-2 virus was done as appropriate, and COVID-19 antibody test was done in all other NOD COVID patients. RESULT: A total of 555 patients with new onset diabetes were included in the study (282 NOD and 273 NOD COVID patients). Patients with NOD COVID had higher fasting and post prandial blood glucose and glycated hemoglobin vs. NOD patients. Both the groups had high average body mass index; ∼28 kg/m2. Interestingly, fasting C-peptide levels were significantly higher in the NOD COVID group vs. NOD group. There was no difference in C-peptide or glycemic parameters between the COVID-19 antibody positive and negative NOD COVID cases. CONCLUSION: Individuals who were diagnosed with diabetes during COVID-19 epidemic (NOD COVID) do not significantly differ from those diagnosed before COVID-19 in symptomatology, phenotype, and C-peptide levels but they had more severe glycemia. Diabetes is one of the most important comorbidities significantly contributing to adverse outcomes during the ongoing novel COVID-19 pandemic caused by the novel Severe Acute Respiratory Syndrome-Coronavirus 2 (SARS-CoV-2) (1). Specifically, those with uncontrolled diabetes are at high risk for developing COVID-19 related complications, including acute respiratory distress syndrome and even to increased mortality (2, 3) . In order to slow down the COVID-19 pandemic, a strict lockdown was enforced in It is well-known that viral infections can trigger diabetes. Previously, diabetes has been reported following infections with influenza and dengue viruses in India (5, 6) . Further, islet cell autoimmunity and subsequent type 1 diabetes was reported after infection with H1N1 pandemic influenza virus (7) . Cases of pancreatic damage and new-onset diabetes following COVID-19 (including some with diabetic ketoacidosis and presentation similar to type 1 diabetes) have been reported from India (8) and other countries (9) . Pancreatic beta-cells carry Angiotensin Converting enzyme-2 (ACE 2), a receptor which facilitates entry of SARS-CoV-2 into the cell, followed by damage to the cell and subsequent development of diabetes (10) . We hypothesized that both the COVID-19 pandemic and the response to it (in the form of lockdown) could increase the incidence and severity of diabetes compared to J o u r n a l P r e -p r o o f before the pandemic because of the multiple putative pathophysiological factors discussed above. The present study was undertaken in newly diagnosed adults with type 2 diabetes mellitus (T2DM) from two sites in India, namely Chennai and Delhi, to examine whether diabetes with onset during COVID-19 (NOD COVID) was different from new onset diabetes before COVID-19 (NOD) in terms of clinical and biochemical profile. All adults diagnosed with new onset T2DM from 1 st April till 30 th October 2020 from two tertiary care hospitals in Chennai and Delhi were included in the study. These patients constituted the NOD COVID group. As a comparator group, we selected age-and sex-matched adults diagnosed with new onset T2DM from 1 st September 2019 to 29th February 2020, from the same hospitals. This was the NOD group. A structured questionnaire was used to capture data on symptomatology, family history of diabetes, behavioral habits, anthropometry, and glycemic parameters. These measurements were done at both sites 'in person' for the NOD COVID group and as a telephonic interview for the NOD group. For the NOD COVID group, responses to questions on symptomatology for COVID-19, whether a reverse transcriptase polymerase chain reaction (RTPCR) COVID-19 test was done, or was already carried out previously, and information on hospitalization for COVID-19 including drug usage, specifically use of corticosteroids, were recorded. For all patients of NOD COVID, other than those in whom RTPCR was performed based on symptoms, immunoassay to qualitatively detect antibodies against SARS-CoV-2 i.e. the COVID-19 antibody test was done. The Elecsys Anti-SARS-CoV-2 assay uses a recombinant protein representing the nucleocapsid (N) antigen for the determination of antibodies against SARS-CoV-2 using the Sandwich principle. The test has sensitivity of 100% and specificity of 99.8%-99.9%(11). Institutional review board permission was taken independently at both sites. Informed consent was obtained from all patients before the start of the study. Table 1 shows the characteristics of the two groups of patients. There were no significant differences in the mean age, sex distribution, body mass index (BMI) and family history of diabetes between the NOD and the NOD COVID groups. However, fasting blood glucose, post prandial blood glucose, glycated hemoglobin and fasting C-peptide were found to be significantly higher in the NOD COVID group. These differences held true even after stratifying patients by study site i.e. North India vs. South India ( Table 2 ). There were also no significant differences in the treatment pattern for diabetes between the groups. COVID-19 antibody levels were assessed for 167 patients, North (n = 67) and South (n=100). A total of 44 patients (26.3%) were found to be positive (North, 15/67, 22 .3%, South, 29/100, 29%) probably reflecting higher numbers of COVID-19 cases in Chennai compared to Delhi at the time of the study. In addition, a total of 25 patients self-reported that they had been COVID-19 positive (16 in North India and 9 in South India), of whom confirmed RT-PCR test reports were available 13/16 in North India and 8/9 patients in South India. Table 3 compares the characteristics of patients with NOD based on COVID-19 antibody status. There were no differences in the risk factors for diabetes between COVID-19 antibody positive and negative patients. There were also no differences in the biochemical parameters based on COVID-19 antibody status. As shown in Figure 1 , more patients diagnosed with diabetes during COVID-19 reported symptoms such as weakness, polyuria, polyphagia, headache, giddiness, burning micturition, cough, running nose, sneezing and breathlessness compared to those diagnosed before COVID-19. A higher proportion of NOD COIVID individuals (50.9%) reported increased "stress" levels compared to NOD group (12.8%) ( Figure 2 ). Patients with new onset of diabetes who had a history of having suffered from COVID-19 (self-reported COVID-19 infection) had higher fasting blood glucose, post prandial blood glucose and glycated hemoglobin compared to those without a similar J o u r n a l P r e -p r o o f history. There was also a history of steroid use in 15 patients. However, there were no differences in symptomatology or risk factors of diabetes or other biochemical characteristics between those who reported having had COVID-19 compared to those who did not. Two patients of NOD COVID presented with diabetic ketoacidosis, which later resolved and glycemia was controlled on oral antihyperglycemic drugs after initial insulin therapy. These have been previously reported (8, 12) . This is the first study to have looked at new onset diabetes during the COVID-19 pandemic in India. We show the following: 1. New onset diabetes during COVID-19 (NOD COVID) had worse glycemic parameters and higher C-peptide levels compared to NOD; however, there was no difference in clinical, anthropometric, behavioural, or other biochemical parameters. 2. There was also no difference in the above parameters between NOD COVID and NOD based on COVID-19 antibody levels. 3. There appears to be no major damage to beta cells (as assessed by C-peptide levels) from COVID-19 infection. There could be multiple reasons for higher the magnitude of glycemia in patients with NOD COVID as compared to NOD. The first reason which seems to be apparent from our data is significantly higher levels of stress, although we have not characterised the type of stress in our study. The panic and fear due to the COVID-19, as well as the lockdown, have led to an increase in stress levels across all sections of society. Fear of contracting the virus, of losing loved ones to the disease, of losing one's job and livelihood as well as challenges associated with working from home, have all contributed to this (13) . Stress can precipitate hyperglycemia by different mechanisms: adoption of harmful health behaviors including binge eating and decreased physical activity, dysregulated physiological stress response with outpouring of counterregulatory hormones (such as glucocorticoids) and development of chronic low-grade inflammation (14) . While hyperglycemia resolves with amelioration of stress in many cases, it may persist in some, leading to J o u r n a l P r e -p r o o f development of NOD, progression from pre-diabetes to diabetes or worsening of existing diabetes. A likely explanation relates to changes in dietary and exercise profile during the pandemic and lockdown. However, the direction of these changes depends on the previous lifestyle of patients. Earlier studies from North India have shown a trend of weight gain during the lockdown period. Specifically, carbohydrate consumption and frequency of snacking increased in 21% and 23%, exercise duration was reduced in 42% and weight gain occurred in 19% patients (15) . Even in apparently non-diabetic individuals, weight gain was seen in 40% of the cohort during lockdown, with 16% of the population experiencing a 2.1-5 kg weight increment. (13) (16) . Imbalance in eating habits and increase in weight have also been shown by studies from other parts of India (17) and from other countries as well (18, 19) . In particular, increased snacking during lockdown was correlated with increase in BMI in a UK based study (19) . In this context, it is important to note the higher BMI of patients with NOD COVID-19 (27-28 Kg/m 2 ) in the current study. While obesity most likely predated the onset of COVID-19 in these patients, it is likely that the enforced lifestyle changes during the lockdown accelerated development of diabetes. It is also likely that many of these patients were already having undiagnosed diabetes, or rapidly converted from prediabetes to diabetes during the pandemic, for the same reasons. However, some other studies from south India have shown no major changes (or even improvement) in glycemia and improved eating habits and exercise regimen during the lockdown (20) . These differences likely represent socioeconomic or cultural differences but do emphasize the fact that the adverse effects of lockdown on glycemia are not inevitable. Yet another explanation for the higher magnitude of glycemia among NOD COVID could be delayed diagnosis, either due to difficulty in accessing lab facilities for blood testing or fear of contracting COVID-19 while visiting healthcare facilities. It is also more likely that only individuals with more severe hyperglycemia approached healthcare providers during the pandemic, as suggested by the higher prevalence of various symptoms of hyperglycemia in the NOD COVID group. A recently debated question is whether SARS-CoV-2 could attack and destroy pancreatic beta cells sufficiently to cause hyperglycemia, given that ACE-2 receptors, are present on endocrine pancreas (10) . A direct attack of virus on pancreas is a real possibility, given previously known data of other viruses implicated in the aetiology of type 1 diabetes as discussed earlier. Previous studies on SARS viruses showed that some affected patients developed acute onset diabetes (10) . In a series of 52 patients suffering from COVID-19 pneumonia from China, 9 had mild pancreatic injury. Out of these, 6 had varying degrees of hyperglycemia. The authors stated that this could be due to direct pancreatic injury by SARS-CoV-2 or due to 'harmful immune response" (21) . Pancreatic necrosis ascribed to COVID-19 in a patient with diabetes has been reported from India from our group (12) (22) . It is possible that the 'cytokine storm' as seen in some patients with severe COVID-19 may also cause beta cell apoptosis. Some anecdotal reports have described acute hyperglycemia and diabetic ketoacidosis caused by COVID-19 infection, including two cases reported from India, which are also included in the current study (8) .Interestingly, these cases were initially treated with insulin therapy, but shortly after resolution of ketoacidosis, were controlled on oral antihyperglycemic therapy (12) . However, in our study C-peptide levels were not lower in the NOD COVID group, even in those who were antibody positive for COVID-19 indicating that there was perhaps no major damage to beta cells due to COVID-19 infection. It could be reasonably stated that in our cohort, direct pancreatic damage due to SARS-CoV-2 was seen in only two patients, and even this seems to be transient. The strengths of the study are that it includes a fairly large number of individuals with new onset diabetes from both North and South India. Secondly, we have compared patients diagnosed pre and during COVID-19 epidemic. We have also compared those who were COVID-19 antibody positive and negative. We believe that many of these are described for the first time from India. 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