key: cord-334973-jemeyudi authors: Wu, Dingye; Gao, Song title: Analysis of the lymphocyte count in type 2 diabetic patients with coronavirus disease (COVID-19): A retrospective study in a centralized treatment center date: 2020-07-22 journal: Diabetes Res Clin Pract DOI: 10.1016/j.diabres.2020.108340 sha: doc_id: 334973 cord_uid: jemeyudi Abstract Objective To investigate the characteristics of lymphocytes in type 2 diabetic patients with coronavirus disease (COVID-19). Methods Patients with COVID-19 admitted to hospital in Wuxi, China from January 29 to March 15 were included in the study. Lymphocytes were measured and recorded at admission and during treatment. Hospitalization days, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) nucleic acid positive days, minimal lymphocyte count, and occurrence time were collected and comparatively analyzed. Correlations between minimal lymphocyte count and hospitalization days as well as SARS-CoV-2 nucleic acid positive days were analyzed. Results A total of 63 patients were included in the study, with 16 in the diabetic group and 47 in the non-diabetic group. After adjusting for potential confounding factors, we observed lower minimal lymphocyte count (0.67 ± 0.36*109/L vs. 1.30 ± 0.54*109/L, adjusted P = 0.001), earlier occurrence of the minimal lymphocyte count (2.68 ± 2.33 days vs. 5.29 ± 4.95 days, adjusted P = 0.042), and longer hospitalization time (20.44 ± 5.24 days vs. 17.11 ± 4.78 days, adjusted P = 0.047) in the diabetic group than in the non-diabetic group. There was a negative correlation between minimal lymphocyte count and hospitalization days (R = -0.600, P < 0.05) as well as SARS-CoV-2 nucleic acid positive days (R = -0.420, P < 0.05). Conclusions The diabetic group with COVID-19 had lower lymphocyte count, reached the minimal count faster, and had longer hospital stays than the non-diabetic group. Hospitalization days and SARS-CoV-2 nucleic acid positive days were negatively correlated with the minimal lymphocyte count. The coronavirus disease December last year has gradually spread throughout the world. At present, it has caused tens of thousands of deaths, and there are no special antiviral drugs to treat it. Depending on the region, 20-50% of patients affected by the COVID-19 pandemic had diabetes [1] . According to related reports, patients with diabetes are more prone to disease progression than those without diabetes [2, 3] ; however, the mechanism is not yet clear. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causes a reduction in the lymphocyte count of COVID-19 patients [4, 5] . This study aims to analyze the characteristics of lymphocyte count in COVID-19 patients with type 2 diabetes mellitus (T2DM). Adult COVID-19 patients admitted to the Fifth People's Hospital of Wuxi City in China from January 29 to March 15 were included. Age >14 years and diagnosis of COVID-19 (for the criteria, refer to the diagnosis and treatment plan for the COVID-19 in China -Trial Version 7; see the supplementary file for details). Patients with blood diseases, AIDS, and T1DM; patients without incomplete data. Data pertaining to gender, age, T2DM status, body mass index (BMI), systolic blood pressure (SBP), and diastolic blood pressure (DBP) were obtained at the time of admission. Data on alanine aminotransferase (ALT), aspartate aminotransferase (AST), creatinine (Cr), and fasting glucose were obtained the next morning after admission. White blood cell count (WBC), C-reactive protein (CRP) and Lymphocytes were measured at admission and during treatment. Data on maximal and minimal WBC, maximal CRP, minimal lymphocyte count and emergence time, hospitalization days, and SARS-CoV-2 nucleic acid positive days were recorded during hospitalization. According to our medical practice, each patient's WBC count, lymphocyte count, and CRP were measured and recorded at admission and during treatment. . SARS-CoV-2 nucleic acid tests with nose and throat swabs were conducted daily 7 days after admission. Viral nucleic acid tests were stopped after detection of negative results on 2 consecutive days. SARS-CoV-2 nucleic acid positive days refers to the time from the first to the last positive results. This study used retrospective case notes, so the requirement for ethical approval was deemed unnecessary. Patients were divided into diabetes and non-diabetes groups. The differences in general conditions such as gender, age, BMI, SBP, DBP, ALT, AST, and Cr were observed between the two groups. The differences in maximal and minimal WBC count, maximal CRP level, time and value of the minimal lymphocyte count, hospitalization days, and SARS-CoV-2 nucleic acid positive days between the two groups were analyzed. Correlations between minimal lymphocyte count and hospitalization days as well as SARS-CoV-2 nucleic acid positive days were analyzed. IBM SPSS statistics 23 software was used for statistical analysis. Continuous variables with normal distribution were presented as mean ± standard deviation (M±SD), and differences between the two groups were determined by one-way ANOVA test. Continuous variables with nonnormal distribution were presented as median with inter-quartile range (IQR), and differences between the two groups were determined by a rank test. In addition, a multiple linear regression model was used to analyze the effect of diabetes on minimal lymphocyte count and its emergence time, patient's hospitalization days, and SARS-CoV-2 nucleic acid positive days by adjusting for potential confounding factors including age; gender; BMI; SBP; DBP; and ALT, AST, and Cr levels. Categorical variables were described as number or rate, and differences between the two groups were determined by a Chi-square test. The correlation between the two groups was observed using a scatter chart. When linear correlation between two continuous variables was observed, Pearson's product-moment correlation coefficient was used. P <0.05 was considered to be statistically significant for all tests. Of the 66 patients reviewed, three patients were excluded from the study due to lack of data. No patient was excluded from the study due to blood disease, AIDS, or T1DM. Thus, the final study population included 63 people, of whom 16 were in the diabetes group and 47 in the non-diabetes group. There was no significant difference between the two groups in terms of gender; age; BMI; SBP; DBP; and ALT, AST, and Cr levels. There was no significant difference between the two groups in maximal and minimal Table 1 . The scatter plot shows that hospitalization days (R = -0.600, P <0.05, Figure 1 ) and SARS-CoV-2 nucleic acid positive days (R = -0.420, P <0.05, Figure 2 ) are correlated with minimal lymphocyte count. This single center, observational, retrospective study of patients with COVID-19 showed that, patients with T2DM have higher CRP, lower level and more rapid decline in lymphocyte count, and longer hospitalization time than those without T2DM. Patients' age and lymphocyte count were negatively correlated. Hospitalization days and SARS-CoV-2 nucleic acid positive days were negatively correlated with minimal lymphocyte count. Lymphocytes are divided into T lymphocytes, B lymphocytes, and natural killer lymphocytes. When a virus infects the human body, it binds to the receptor, enters the cell through the ligand, replicates the itself, and produces MHC-I molecules and MHC-II molecules in the cell; it is recognized by CD4 + T cells and CD8 + T cells after presenting the antigen, and this activates cellular immunity and humoral immunity, which help eliminate the virus [6, 7] . Virus clearance depends on the body's normal immune function, and the patient's lymphocyte count and function are critical factors. However, after viral infections, lymphocyte counts often decline. The possible causes include the consumption of lymphocytes after virus invasion, the direct killing of lymphocytes by the virus, apoptosis of lymphocytes [8] , and the suppression of immune function by the virus. Bo Diao et al. reported a decrease in T-lymphocyte count in patients with COVID-19 [9] . Li Xinmin's research on patients with SARS showed that the absolute counts of T lymphocytes, T4 cells, and T8 cells were significantly reduced, suggesting that the T cell immune function of patients with SARS is weakened [10] . Liu et al. found [16] counts. Fan Wang [11] observed that patients with COVID-19 had significantly low counts of total lymphocytes (P < 0.0001), CD4+ T cells, patients with COVID-19 is weakened too. Several recent studies have also found that peripheral blood lymphocyte count in patients with COVID-19 is reduced [4, 5, 9] . Pathological examination of the spleen showed degeneration and necrosis, and reduction in lymphocytes [12] , which indirectly reflected lymphocyte depletion or immunosuppression. Our study found a decrease in lymphocyte count in patients with COVID-19, and the lower the lymphocyte count, the longer SARS-CoV-2 nucleic acid positive days and hospitalization days. It is suggested that the decrease in lymphocytes is one of the characteristics of COVID-19, and lymphocytes play an important role in the virus clearance in COVID-19 patients. A meta-analysis [13] showed that lymphopenia on admission was associated with poor outcomes in patients with COVID-19. According to some studies [14] [8, 15] , decreased lymphocyte count is a characteristic of severe COVID-19. Among the patients enrolled, the median time of onset to RT-PCR turning negative was 14 (IQR, [10] [11] [12] [13] [14] [15] [16] [17] [18] [19] [20] days. In groups with rapid virus clearance, high counts of T cells, CD4+ T cells, CD8+ T cells, and B cells were observed. In our study, we found that SARS-CoV-2 nucleic acid positive days were negative correlated with the minimal lymphocyte count. Patients with T2DM often experience immune impairment. Bailin et al. found that CD4+ and CD8+ T lymphocyte counts are lower in diabetic patients than in non-diabetic patients [17] . According to a Japanese research [18] , CD3+CD56+ T cell% (4.1 +/-1.9%) of patients with pancreatic DM was lower than that (6.0 +/-3.0%) of normal subjects (p < 0.05). CD3+CD56+ T cells have cytotoxic activity and it is likely that this activity is similar to that of NK cells. These results suggest that a decrease in peripheral CD3+CD56+ T cell% is a factor reflecting weak host defense to infectious diseases in cases of pancreatic DM. The SARS-CoV-2 merges with target cells with the help of angiotensin converting enzyme 2 (ACE2), which is expressed by epithelial cells of the lung, intestine, and kidney [19] . Studies have shown that the expression of ACE2 in diabetic patients is significantly increased, and it seems that they are more likely to be infected with COVID-19 [20] . Yoshikawa et al. found through animal experiments that the overexpression of ACE2 reduces the activity of the T lymphocytes against SARS-CoV and impairs the immune function [21] . Gupta et al. found that diabetes enhances the severity of COVID-19 and several factors may be responsible for this [22] : (1) Hyperglycemia and possibly hypoglycemia; (2) immune defects especially impaired T-cell response; and (3) associated comorbidities like obesity, heart diseases, and kidney diseases. According to Muniyappa et al., diminished T cell function could be one of the reasons [8] . In our study, we found that diabetic patients showed a faster decline in lymphocyte count, lower minimal lymphocyte count, higher maximal CRP, and longer hospital stay than non-diabetic patients. Although there were no deaths in our study, many other studies have confirmed that diabetes is a risk factor for COVID-19 complications and increased mortality [2, 3, 5] . There is no specific treatment for COVID-19 now, and virus clearance is related to lymphocytes and immune function, so we can provide patients with symptomatic and support treatment, wait for the recovery of their lymphocyte count and immune function, and wait for virus clearance. Avoiding drugs that impair lymphocyte and immune function may be beneficial. Our study has some limitations. The number of COVID-19 cases was small. There were no deaths in our study. The relationship between lymphocyte count and mortality was not observed. We did not obtain data of lymphocyte subsets and could not analyze the decline in specific types of lymphocytes. This research was a retrospective study, and there may be some unknown confounding factors in the study. Basic research and further clinical research are still needed to determine whether the mechanism of lymphocyte count decline in patients with COVID-19 has a synergistic effect with immune function abnormalities caused by diabetes. In summary, COVID-19 patients with T2DM experience a faster decline in lymphocyte count, have lower lymphocyte count, and longer hospital stay than non-diabetic patients. The lower the lymphocyte count, the longer the hospitalization time and viral nucleic acid positive days. 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BMI, body mass index; SBP, systolic blood pressure WBC, white blood cell Multivariable regression model was used to adjust for potential confounding factors including age, gender Multivariable regression model was used to adjust for potential confounding factors including age, gender This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors. All authors declare no conflict of interest.