Association of Blood Glucose Control and Outcomes in Patients with COVID-19 and Pre-existing Type 2 Diabetes
Cell Metabolism, June 2020, Volume 31, Issue 6, Pages 1068-1077.e3
Type 2 diabetes (T2D) is a major comorbidity of COVID-19. However, the impact of blood glucose (BG) control on the degree of required medical interventions and on mortality in patients with COVID-19 and T2D remains uncertain. Thus, we performed a retrospective, multi-centered study of 7,337 cases of COVID-19 in Hubei Province, China, among which 952 had pre-existing T2D. We found that subjects with T2D required more medical interventions and had a significantly higher mortality (7.8% versus 2.7%; adjusted hazard ratio [HR], 1.49) and multiple organ injury than the non-diabetic individuals. Further, we found that well-controlled BG (glycemic variability within 3.9 to 10.0 mmol/L) was associated with markedly lower mortality compared to individuals with poorly controlled BG (upper limit of glycemic variability exceeding 10.0 mmol/L) (adjusted HR, 0.14) during hospitalization. These findings provide clinical evidence correlating improved glycemic control with better outcomes in patients with COVID-19 and pre-existing T2D.
A cohort of 7,337 COVID-19 patients with or without diabetes was retrospectively studied
Diabetes status increased the need for medical interventions during COVID-19
Diabetes status increased the mortality risk of patients with COVID-19
Well-controlled blood glucose correlated with improved outcomes in infected patients
Type 2 diabetes (T2D) correlates with a worse outcome for COVID-19. Here, Zhu et al. show that among ∼7,300 cases of COVID-19, T2D is associated with a higher death rate, but diabetics with better controlled blood glucose die at a lower rate than diabetics with poorly controlled blood glucose.
Keywords: COVID-19, SARS-CoV-2, diabetes mellitus, blood glucose control, mortality.
Context and Significance
Although type 2 diabetes (T2D) is a major comorbidity of novel coronavirus disease 2019 (COVID-19), the impact of blood glucose control on the degree of medical interventions required and on all-cause mortality of patients with COVID-19 and pre-existing T2D remains unclear. Here, Zhu et al. report that among ∼7,300 individuals with COVID-19 (among which nearly 1,000 had T2D) in Hubei Province, China, those with T2D had significantly increased medical interventions and mortality risk. But among the patients with T2D, those with well-controlled blood glucose regulation (upper limit ≤ 10 mmol/L) fared much better than those with poorly controlled blood glucose (upper limit > 10 mmol/L). These findings provide clinical evidence correlating more proper blood glucose control with improved outcomes in patients with COVID-19.
The novel coronavirus disease 2019 (COVID-19) is caused by infection from the newly emerged, highly contagious coronavirus SARS-CoV-2 ( Wu and McGoogan, 2020 ). SARS-CoV-2 mainly invades the respiratory tract and lungs, leading to a new type of coronavirus pneumonia ( Zhu et al., 2020 ). The severe cases of COVID-19 can rapidly progress to acute respiratory distress syndrome (ARDS), septic shock, and multiple organ dysfunction syndrome (MODS) ( Guan et al., 2020 ). Elderly individuals, along with those with pre-existing conditions, such as hypertension, cancer, cardiovascular diseases, diabetes mellitus, and acute kidney injury, have a demonstrated higher risk for developing more severe cases of COVID-19, as well as suffering a higher risk of mortality ( Wang et al., 2020; Zhang et al., 2020b; Zhou et al., 2020 ). The collision between the two global pandemics of COVID-19 and type 2 diabetes (T2D) has led to the grim reality that T2D is already the second most common comorbidity of COVID-19 ( Zhou et al., 2020 ). However, current evidence implicating T2D in worse COVID-19 prognosis has mostly come from relatively limited-sized cohorts ( Deng and Peng, 2020; Zhang et al., 2020a; Zhou et al., 2020 ). Thus, the clinical features of patients with T2D infected by SARS-CoV-2 remain to be comprehensively clarified in a large-scale analysis, which is needed to more efficiently and precisely manage the treatment of such patients.
It has been well established that patients with diabetes are more susceptible to infections in general and exhibit worse prognosis once infected compared to the non-diabetic population ( Kumar Nathella and Babu, 2017; Xu et al., 2019 ). Such a higher susceptibility has also been previously observed for other coronaviral epidemics. For example, in patients with severe acute respiratory syndrome (SARS), pre-existing T2D was independently associated with poor outcomes. The percentage of known T2D history was significantly higher among patients who succumbed to SARS than who survived ( Booth et al., 2003; Yang et al., 2006 ). Further, epidemiological studies also indicate that T2D was the primary comorbidity associated with severe or lethal MERS-CoV infections ( Alqahtani et al., 2018 ). And with regard to the current COVID-19 pandemic, several recent studies, though with limited participants, have already suggested that T2D is a common comorbidity and constitutes a higher proportion of patients with severe and ICU-admitted cases of COVID-19 than patients with mild symptoms ( Deng and Peng, 2020; Wang et al., 2020; Zhang et al., 2020a; Zhou et al., 2020 ). These associations between diabetes and worse outcome in viral infections are not unexpected as hyperglycemia is detrimental to the control of viremia and inflammation, aggravating morbidity and mortality in a variety of patients ( Forbes et al., 2018 ). However, an overly rigid glucose control may increase the risk of severe hypoglycemia, which can also lead to an increased mortality ( Rodriguez-Gutierrez et al., 2019 ). Consequently, previous clinical trials examining the effects of glucose control on mortality have yielded conflicting results ( Forbes et al., 2018; Van den Berghe et al., 2006 ). For individuals with COVID-19 and pre-existing T2D, a key challenge for clinicians is to improve outcomes in the face of uncertainty regarding the degree of glycemic management that should be maintained and any effects this might have on the benefits and risks of overall treatment. Thus, detailed analyses of data from such patients is needed that links plasma glucose levels with clinic outcomes, including mortality.
In this report, we performed a retrospective longitudinal, multi-centered study from a cohort of 7,337 confirmed COVID-19 cases enrolled among 19 hospitals in Hubei Province, China, focusing on the association between plasma glucose levels and clinic outcomes in COVID-19 patients with T2D. In addition to a significant association between diabetic status and higher mortality rate in patients with COVID-19 and pre-existing T2D versus non-diabetic subjects with COVID-19, our study indicated that well-controlled glycemia was associated with a markedly improved outcome of patients with COVID-19 and pre-existing T2D.
Results and Discussion
Clinical Characteristics of Patients with COVID-19 and Pre-existing T2D upon Admission
Clinic characteristics were collected from a total of 7,337 participants out of 9,663 confirmed cases of COVID-19, including 952 subjects with pre-existing T2D (n = 510 male, 53.6%) and 6,385 non-diabetic cases (n = 2,967 male, 46.5%) ( Figure 1 ). Of the initial 9,663 cases enrolled, 2,326 patients with COVID-19 were excluded from the study, including 1,013 patients younger than 18 or older than 75 years old, 872 patients without complete medical records, 13 patients with acute myocardial infarction, 5 patients with acute coronary syndrome, 8 patients with acute pulmonary embolism, 10 patients with acute stroke, 11 patients with acute severe pancreatitis, 9 patients with cirrhosis, 37 patients with above stage 3 chronic renal insufficiency, 7 patients with severe congestive heart failure, 104 patients with pregnancy, 227 patients with malignancy, 7 patients with type 1 diabetes, 2 patients with a history of gestational diabetes, and 1 patient with drug-induced diabetes. From the final cohort of 7,337 COVID-19 patients analyzed, the prevalence of T2D was 13.0%, which was similar to the nationwide prevalence of T2D in China (about 10.9%) ( Wang et al., 2017 ). The median ages were 62 (55–68) and 53 (40–63) in the diabetic and non-diabetic groups, respectively ( [CR] ). The median body mass index (BMI) in patients with or without T2D was 24.7 (22.0–26.4) and 23.4 (21.0–26.0), respectively. The median duration from the first symptom to admission was 10 days (6–19) for both groups. The major symptoms for both groups were fever (71.8%), cough (63.5%), fatigue (32.3%), and dyspnea (16.1%), similar to the general population of patients ( Chen et al., 2020; Guan et al., 2020; Huang et al., 2020; Wang et al., 2020 ). Patients with T2D reported significantly higher incidences of fatigue (38.0% versus 31.4%) and dyspnea (20.5% versus 15.4%) compared to the non-diabetic group. Pre-existing hypertension (53.4% versus 19.7%), coronary heart disease (CHD; 13.7% versus 3.7%), cerebrovascular disease (5.6% versus 1.5%), and chronic kidney disease (4.9% versus 1.3%) had higher frequencies in the T2D group compared to the non-diabetic group. Chest CT scans indicated that the incidence of bilateral lung lesion was higher (88.1% versus 80.4%) in the diabetic group compared to non-diabetic patients.
While heart rate and respiratory rates did not show differences between the diabetic and the non-diabetic groups, systolic blood pressure was modestly higher in the diabetic group (130 mmHg [120–142] versus 126 mmHg [120–136]). Lab findings showed that blood glucose (BG) level was much higher in the diabetic group compared to the non-diabetic group, as expected (8.3 mmol/L [6.2–12.4] versus 5.2 mmol/L [4.7–6.1]), with higher levels of HbA1c (7.9% [6.8%–9.5%] versus 6.1% [5.7%–6.6%]). Patients with T2D had a significantly higher incidence of lymphopenia (44.5% versus 32.6%), and higher ratio of elevation of leukocyte (11.3% versus 6.6%) and neutrophil (17.2% versus 9.9%) counts in peripheral blood, relative to the non-diabetic individuals. At the same time, elevated serum markers, indicating inflammation (C-reactive protein, CRP [57.0% versus 42.4%] and procalcitonin [33.3% versus 20.3%]), decreased kidney function (creatinine [12.0% versus 5.0%]), and increased coagulation status (D-dimer [50.5% versus 33.3%]), were found more frequently in the T2D group than in the non-diabetic group. Furthermore, SpO2 lower than 95% occurred more frequently in the diabetic group versus the non-diabetic group (18.8% versus 13.2%) on admission.
Patients with COVID-19 and Pre-existing T2D Require More Intensive In-Hospital Treatment
The patients with pre-existing T2D received significantly more intensive integrated treatments to manage their symptoms of COVID-19 than the non-diabetic subjects. The former group registered a higher need for antibiotics (61.3% versus 56.9%), antifungal drugs (2.5% versus 1.2%), systemic corticosteroids (29.4% versus 22.8%), immunoglobin (23.0% versus 17.7%), anti-hypertensive drug (45.1% versus 21.1%), and even vasoactive drugs (7.7% versus 2.2%). Oxygen inhalation (76.9% versus 61.2%), noninvasive ventilation (10.2% versus 3.9%), and invasive ventilation (3.6% versus 0.7%) were also applied significantly more frequently to the individuals with T2D compared to the patients without T2D ( [CR] ).
T2D Is Correlated with a Higher Risk of All-Cause Mortality and Detrimental Comorbidities in Patients with COVID-19
During the 28-day follow-up period, we performed a retrospective longitudinal analysis on various parameters starting from the time of admission to the hospital for each patient in the study. We noticed that, despite having received more aggressive treatment against COVID-19 and the comorbidities, the diabetic group had greater incidences of decreased lymphocyte counts and increased neutrophil counts, as well as higher levels of serum interleukin-6 (IL-6), CRP, and lactic dehydrogenase (LDH), accompanied by higher BG levels, compared to the non-diabetic group. The BG level was also significantly associated with comorbid hypertension, CHD, the incidences of decreased lymphocyte count, and elevated neutrophil count and the levels of serum CRP and creatinine in the entire cohort ( [CR] ).
During the 28-day follow-up period starting from admission, the in-hospital death rate was significantly higher in patients with pre-existing T2D relative to the non-diabetic individuals (7.8% versus 2.7%, p < 0.001) ( [CR] ). The crude HR of the 28-day all-cause mortality in the diabetic group versus non-diabetic individuals was 2.90 (95% CI, 2.21–3.81; p < 0.001) ( [CR] ). After adjusting for age, gender, and hospital site on admission, the HR of the all-cause mortality between these two groups was 1.70 (95% CI, 1.29–2.24; p < 0.001) ( [CR] ). We further adjusted for the severity of COVID-19 and found that the HR of the all-cause mortality between these two groups was 1.49 (95% CI, 1.13–1.96; p = 0.005) ( [CR] ; [CR] ). We here did not adjust for comorbidities closely related to T2D, including hypertension, CHD, cerebrovascular disease, and chronic kidney disease, as these diseases often co-exist with T2D.
Furthermore, the individuals with T2D had a greater occurrence of ARDS (16.9% versus 7.2%), acute heart injury (7.3% versus 3.0%), acute kidney injury (3.9% versus 0.8%), septic shock (3.8% versus 1.0%), and disseminated intravascular coagulation (DIC) (0.5% versus 0.2%) than the non-diabetic group ( [CR] ). Mixed-effect Cox analysis indicated T2D was significantly correlated with the occurrence of ARDS, acute kidney injury, and septic shock with respective adjusted HRs of 1.44 (95% CI, 1.20–1.73), 3.01 (95% CI, 1.94–4.68), and 1.95 (95% CI, 1.18–3.20), after adjusting for age, gender, and severity of COVID-19 among the patients ( [CR] ). Our current study was based on the largest diabetic COVID-19 cohort so far analyzed, and the results were unequivocal to implicate diabetes mellitus in higher risk of death and other detrimental outcomes of COVID-19. Notably, care must be taken in interpreting the significant difference in outcomes between diabetic and non-diabetic patients with COVID-19, since there were notable differences in the covariate distributions between the two groups.
The pathophysiological mechanisms underlying the impact of T2D on COVID-19 progression remain to be fully investigated. In patients with diabetes, pulmonary dysfunction involving lung volume, pulmonary diffusing capacity, control of ventilation, bronchomotor tone, and neuroadrenergic bronchial innervation have been reported ( Fuso et al., 2019 ), which may account for the propensity of poor outcomes in patients with COVID-19 and T2D. At the same time, a dysregulated immune response caused by T2D is likely also responsible for the increased disease severity of COVID-19 in patients with T2D as a higher ratio of lymphopenia and increased levels of neutrophils, serum CRP, and IL-6 were observed in the patients with COVID-19 and pre-existing T2D in our study. These findings dovetail with immune dysregulation observed in other coronavirus infection-triggered pneumonia ( Kulcsar et al., 2019 ). In an experimental model of MERS, diabetic mice had lower numbers of inflammatory monocytes and macrophages and CD4 + T cells, which was accompanied by lower levels of Ccl2 and Cxcl10 expression ( Kulcsar et al., 2019 ). Furthermore, T2D is associated with activation of the renin-angiotensin system in different tissues ( Candido et al., 2002 ). Considering SARS-CoV-2 utilizes angiotensin-converting enzyme 2 (ACE2) to bind and gain entry to infected cells ( Hoffmann et al., 2020; Lu et al., 2020 ) and reduces the expression of ACE2 ( Kuba et al., 2005 ), overactivation of the renin-angiotensin system may also contribute to the increased adverse risk in patients with COVID-19 and diabetes. In this respect, application of renin-angiotensin system inhibitors may have therapeutic effect in patients with COVID-19 and pre-existing T2D.
Differential Glucose Control Is Associated with Different Outcomes in Patients with COVID-19 and Pre-existing T2D
Among the cohort with COVID-19 and T2D, there were 282 individuals with well-controlled BG (136 males, 48.2%) and 528 individuals with poorly controlled BG (298 males, 56.4%). The median BG level was much lower in the well-controlled BG group than the poorly controlled BG group (6.4 mmol/L [5.2–7.5] versus 10.9 mmol/L [7.6–14.3]) ( [CR] ), and the levels of HbA1C in these two groups were 7.3% (6.6%–8.2%) and 8.1% (7.2%–10.1%), respectively. The patients from the well-controlled BG group also had significantly lower incidences of lymphopenia (30.5% versus 49.6%), lower rates of increased counts of leukocyte (6.3% versus 12.2%) and neutrophil (10.7% versus 19.4%), and elevated serum CRP (47.5% versus 59.5%) and procalcitonin (24.2% versus 35.0%). The same pattern was observed for elevated aspartate transaminase (AST) (11.3% versus 20.4%) and D-dimer (37.6% versus 55.4%) ( Table 1 ). Notably, fewer individuals from the well-controlled group had SpO2 lower than 95% compared to the poorly controlled group (12.6% versus 22.7%). But other parameters between the two groups were not significantly different. In particular, these two groups had a median age of 62 (55–67) and 63 (56–68), respectively ( Table 1 ). The difference of the median BMI between patients with well-controlled BG or poorly controlled BG was modest (25.0 [23.9–26.4] versus 23.2 [21.0–24.9], respectively).
|Well Controlled (n = 282)||Poorly Controlled (n = 528)||SD||Well Controlled (n = 250)||Poorly Controlled (n = 250)||SD|
|Clinical Characteristics on Admission|
|Age, median (IQR)||62 (55–67)||63 (56–68)||−0.094||62 (55–67)||63 (54–68)||0.008|
|Male gender, n (%)||136 (48.2%)||298 (56.4%)||−0.165||126 (50.4%)||126 (50.4%)||0.000|
|Female gender, n (%)||146 (51.8%)||230 (43.6%)||0.165||124 (49.6%)||124 (49.6%)||0.000|
|Heart rate, median (IQR), bpm||84.0 (77.0–95.0)||85.0 (76.3–97.0)||−0.103||84.0 (76.5–93.5)||83.0 (76.0–96.0)||−0.048|
|Respiratory rate, median (IQR), bpm||20.0 (18.0–20.0)||20.0 (19.0–21.0)||−0.180||20.0 (18.0–20.0)||20.0 (19.0–21.0)||0.008|
|SBP, median (IQR), mmHg||130.0 (120.0–142.0)||130.0 (120.0–142.0)||0.073||130.0 (120.0–142.0)||130.0 (120.0–142.0)||0.085|
|DBP, median (IQR), mmHg||80.0 (73.0–89.0)||80.0 (72.0–86.0)||0.074||80.0 (73.0–86.5)||80.0 (72.0–86.0)||0.025|
|Symptom onset to admission, median (IQR), day||13.0 (7.0–23.0)||10.0 (6.0–17.0)||0.261||12.0 (7.0–20.0)||10.0 (6.0–18.8)||0.177|
|Fever, n (%)||182 (64.5%)||381 (72.2%)||−0.164||166 (66.4%)||171 (68.4%)||−0.043|
|Cough, n (%)||169 (59.9%)||350 (66.3%)||−0.132||155 (62.0%)||153 (61.2%)||0.016|
|Fatigue, n (%)||90 (31.9%)||218 (41.3%)||−0.196||87 (34.8%)||90 (36.0%)||−0.025|
|Dyspnea, n (%)||48 (17.0%)||117 (22.2%)||−0.130||44 (17.6%)||39 (15.6%)||0.054|
|Comorbidities on Admission|
|Hypertension, n (%)||156 (55.3%)||282 (53.4%)||0.038||136 (54.4%)||135 (54.0%)||0.008|
|Coronary heart disease, n (%)||42 (14.9%)||68 (12.9%)||0.058||39 (15.6%)||32 (12.8%)||0.080|
|Chronic liver disease, n (%)||5 (1.8%)||10 (1.9%)||−0.009||4 (1.6%)||4 (1.6%)||0.000|
|Cerebrovascular diseases, n (%)||18 (6.4%)||27 (5.1%)||0.055||18 (7.2%)||15 (6.0%)||0.048|
|Chronic renal diseases, n (%)||17 (6.0%)||17 (3.2%)||0.134||13 (5.2%)||9 (3.6%)||0.078|
|COPD, n (%)||4 (1.4%)||8 (1.5%)||−0.008||4 (1.6%)||3 (1.2%)||0.034|
|Chest CT on Admission|
|Unilateral lesion, n/N (%)||25/266 (9.4%)||22/468 (4.7%)||0.184||19/239 (8.0%)||18/212 (8.5%)||−0.020|
|Bilateral lesions, n/N (%)||230/266 (86.5%)||425/468 (90.8%)||−0.137||210/239 (87.9%)||184/212 (86.8%)||0.032|
|Laboratory Examination on Admission|
|Leukocyte count > 9.5, 10ˆ9/L, n/N (%)||17/272 (6.3%)||61/500 (12.2%)||−0.207||15/242 (6.2%)||18/231 (7.8%)||−0.063|
|Neutrophil count > 6.3, 10ˆ9/L, n/N (%)||29/272 (10.7%)||97/500 (19.4%)||−0.246||28/242 (11.6%)||24/231 (10.4%)||0.038|
|Lymphocyte count < 1.1, 10ˆ9/L, n/N (%)||83/272 (30.5%)||248/500 (49.6%)||−0.397||81/242 (33.5%)||85/231 (36.8%)||−0.070|
|C-reactive protein increase > ULN a , n/N (%)||103/217 (47.5%)||209/351 (59.5%)||−0.244||97/195 (49.7%)||78/166 (47.0%)||0.055|
|Procalcitonin level increase > ULN a , n/N (%)||51/211 (24.2%)||143/409 (35.0%)||−0.238||48/188 (25.5%)||40/180 (22.2%)||0.078|
|ALT increase > 40 U/L, n/N (%)||31/266 (11.7%)||80/476 (16.8%)||−0.148||27/235 (11.5%)||22/219 (10.1%)||0.047|
|AST increase > 40 U/L, n/N (%)||30/266 (11.3%)||97/476 (20.4%)||−0.251||30/235 (12.8%)||25/219 (11.4%)||0.041|
|Creatinine > ULN a , n/N (%)||20/267 (7.5%)||68/498 (13.7%)||−0.201||20/237 (8.4%)||15/231 (6.5%)||0.074|
|D-dimer > ULN a , n/N (%)||88/234 (37.6%)||252/455 (55.4%)||−0.362||83/208 (39.9%)||91/206 (44.2%)||−0.087|
|K + < 3.5 mmol/L, n/N (%)||38/266 (14.3%)||73/496 (14.7%)||−0.012||36/235 (15.3%)||32/228 (14.0%)||0.036|
|LDL-c, mmol/L, median (IQR)||2.5 (1.9–3.0)||2.4 (1.9–2.9)||0.043||2.4 (1.9–3.0)||2.4 (1.9–2.9)||−0.020|
|SpO2, <95%, n/N (%)||26/206 (12.6%)||94/414 (22.7%)||−0.267||26/182 (14.3%)||27/189 (14.3%)||0.000|
|Blood glucose, mmol/L, median (IQR)||6.4 (5.2–7.5)||10.9 (7.6–14.3)||−1.312||6.4 (5.2–7.4)||10.6 (7.4–13.7)||−1.329|
Other clinical manifestations, including chest CT imaging and the incidences of major comorbidities, were similar between the two groups on admission. Even so, the patients with COVID-19 and T2D with well-controlled BG acquired significantly less integrated treatments than those with poorly controlled BG. There was a significantly lower frequency of pharmacological therapy in the well-controlled BG group versus the poorly controlled group, including the usage of antivirals (62.8% versus 71.2%), antibiotics (53.2% versus 66.5%), antifungal drugs (0.4% versus 2.8%), systemic corticosteroids (20.2% versus 34.9%), immunoglobin (15.3% versus 26.5%), and vasoactive drugs (2.5% versus 8.9%). The incidences of oxygen inhalation (70.2% versus 83.5%), noninvasive ventilation (4.6% versus 11.9%), invasive ventilation (0.0% versus 4.2%), and extracorporeal membrane oxygenation (0.0% versus 0.8%) were lower in the well-controlled group than in the poorly controlled group ( Table 2 ).
|Management||Total (N = 810)||Well Controlled (n = 282)||Poorly Controlled (n = 528)||p Value b|
|Traditional Chinese medicine (%)||650 (80.3%)||235 (83.3%)||415 (78.6%)||0.129|
|Antiviral drug, n (%)||553 (68.3%)||177 (62.8%)||376 (71.2%)||0.017|
|Antibiotics drug, n (%)||501 (61.9%)||150 (53.2%)||351 (66.5%)||<0.001|
|Systemic corticosteroids, n (%)||241 (29.8%)||57 (20.2%)||184 (34.9%)||<0.001|
|Immunoglobin, n (%)||183 (22.6%)||43 (15.3%)||140 (26.5%)||<0.001|
|Anti-hypertensive drug, n (%)||380 (46.9%)||128 (45.4%)||252 (47.7%)||0.575|
|Lipid-lowering drug, n (%)||126 (15.6%)||40 (14.2%)||86 (16.3%)||0.493|
|Vasoactive drug, n (%)||54 (6.7%)||7 (2.5%)||47 (8.9%)||0.001|
|Antifungal medications, n (%)||16 (2.0%)||1 (0.4%)||15 (2.8%)||0.031|
|Metformin, n (%)||278 (34.3%)||76 (27.0%)||202 (38.3%)||0.002|
|Sulfonylurea, n (%)||106 (13.1%)||22 (7.8%)||84 (15.9%)||0.002|
|DPP-4 inhibitor, n (%)||55 (6.8%)||11 (3.9%)||44 (8.3%)||0.025|
|Insulin, n (%)||328 (40.5%)||40 (14.2%)||288 (54.6%)||<0.001|
|Alpha-glucosidase inhibitor, n (%)||337 (41.6%)||90 (31.9%)||247 (46.8%)||<0.001|
|Trizaolidinedione, n (%)||9 (1.1%)||2 (0.7%)||7 (1.3%)||0.508|
|Meglitide||35 (4.3%)||7 (2.5%)||28 (5.3%)||0.089|
|Oxygen inhalation, n (%)||639 (78.9%)||198 (70.2%)||441 (83.5%)||<0.001|
|Noninvasive ventilation, n (%) a||76 (9.4%)||13 (4.6%)||63 (11.9%)||0.001|
|Invasive ventilation, n (%) a||22 (2.7%)||0 (0.0%)||22 (4.2%)||0.001|
|Renal replacement therapy, n (%)||15 (1.9%)||5 (1.8%)||10 (1.9%)||1.000|
|Extracorporeal membrane oxygenation, n (%) a||4 (0.5%)||0 (0.0%)||4 (0.8%)||0.304|
Well-Controlled Blood Glucose Is Correlated with Reduced Risk of All-Cause Mortality and Detrimental Complications in Patients with COVID-19 and Pre-existing T2D
Correlated with persistent lower BG levels, the well-controlled group had higher lymphocyte counts, lower neutrophil counts, and lower serum levels of IL-6, CRP, and LDH throughout the 28-day observation period starting from the time of hospital admission ( Figure 2 ). We further noticed that the in-hospital death rate was significantly lower (1.1% versus 11.0%) in the well-controlled group relative to the poorly controlled group ( [CR] ). The crude HR for the 28-day all-cause mortality between the two groups was 0.09 (95% CI, 0.03–0.30; p < 0.001) ( [CR] ). After adjusting for age, gender, the severity of COVID-19, comorbidities, and site effect, the HR of the all-cause mortality in the well-controlled BG group versus the poorly controlled BG group was 0.13 (95% CI, 0.04–0.44; p < 0.001) ( [CR] ). The E-value for the point estimate was 14.87 with upper limit of CI at 3.97. Further, relative to the poorly controlled BG control, the patients from the well-controlled BG group developed less frequent occurrences of ARDS (7.1% versus 21.4%), acute heart injury (1.4% versus 9.9%), acute kidney injury (0.7% versus 3.8%), septic shock (0.0% versus 4.7%), and DIC (0.0% versus 0.6%) ( [CR] ). After adjusting for age, gender, the severity of COVID-19, site effect, and comorbidities, the respective HRs of ARDS and acute heart injury were 0.41 (95% CI, 0.25–0.66, p < 0.001) and 0.21 (95% CI, 0.07–0.59, p = 0.003) between the well-controlled BG group and poorly controlled BG group ( [CR] ).
A propensity score-matched (PSM) analysis was further performed to avoid confounding variables that could have interfered with the association between BG levels and all-cause mortality. Due to the lack of reliable indicators for the severity of T2D, we specifically included T2D-related comorbidities for matching since comorbidities are closely related to the severity of T2D. These comorbidities included hypertension, cardiovascular disease, cerebrovascular disease, chronic liver disease, and chronic kidney injury. We were able to match 250 patients from the well-controlled BG group to 250 patients from the poorly controlled BG group at a ratio of 1:1, and these 500 individuals were included in the PSM analysis ( Figure 1 ). By applying mixed-effect Cox model using the hospital site as a random effect and adjusting imbalanced durations from symptom onset to admission, the results consistently and significantly demonstrated a lower risk of all-cause mortality in the patients from the well-controlled BG group (adjusted HR, 0.14; 95% CI, 0.03–0.60; p = 0.008) compared to those from the poorly controlled BG group ( Figure 3 ; Tables 3 and [CR] ), although stronger integrated treatment was applied to the poorly controlled BG group ( [CR] ). The robustness of the association between glycemic variability and mortality was further assessed with additional sensitivity analyses by using different matching variables. The results in these sensitivity analyses were similar to the above analysis with HRs of 0.17 (95% CI, 0.05–0.61; p = 0.006) in the first sensitivity analysis and of 0.16 (95% CI, 0.05–0.58; p = 0.005) in the second analysis ( [CR] ). In the PSM analysis, the respective adjusted HRs of ARDS, acute heart injury, and acute kidney injury were 0.47 (95% CI, 0.27–0.83, p = 0.009), 0.24 (95% CI, 0.08–0.71, p = 0.010), and 0.12 (95% CI, 0.01–0.96, p = 0.046) between the well-controlled BG group and poorly controlled BG group ( Table 3 ).
|Well-Controlled versus Poorly Controlled||Unmatched||Matched b|
|Crude||Adjusted a||Adjusted c|
|HR (95% CI)||p Value d||HR (95% CI)||p Value d||HR (95% CI)||p Value d|
|All-cause mortality||0.09 (0.03,0.30)||<0.001||0.13 (0.04,0.44)||<0.001||0.14 (0.03,0.60)||0.008|
|ARDS||0.31 (0.19,0.50)||<0.001||0.41 (0.25,0.66)||<0.001||0.47 (0.27,0.83)||0.009|
|Acute kidney injury||0.19 (0.04,0.80)||0.024||0.22 (0.05,1.03)||0.055||0.12 (0.01,0.96)||0.046|
|Acute heart injury||0.14 (0.05,0.39)||<0.001||0.21 (0.07,0.59)||0.003||0.24 (0.08,0.71)||0.010|
a In mixed-effect Cox model, adjusted variables for comparing BG well-controlled and BG poorly controlled cohorts included age, gender, indicators of the severity of COVID-19, and comorbidities (hypertension, coronary heart disease, cerebrovascular diseases, chronic liver diseases, and chronic renal diseases)
b In the propensity score-matched model, age, gender, hospital sites, indicators of the severity of COVID-19, comorbidities (hypertension, coronary heart disease, cerebral vascular disease, chronic liver disease, and chronic renal diseases), and incidence of increased creatinine were matched
Glycemic variability has been shown to be an important indicator and a possible risk predictor for death and other complications in individuals with T2D ( Forbes et al., 2018 ). The impact of hyperglycemia on the pathogenesis of viral-induced respiratory diseases remains unclear. Elevated BG level has been reported to increase the glucose concentration in airway epithelial secretion ( Philips et al., 2003 ), which may disrupt the defensive capacity of airway epithelia. On the other hand, too rigid glucose control increases the risk of severe hypoglycemia, which can also result in an increased mortality ( Rodriguez-Gutierrez et al., 2019 ). In this study, we found that compared to individuals with well-controlled BG, poor glycemic control in patients with COVID-19 and pre-existing T2D was associated with worse outcome, involving increased need for medical interventions, multi-organ injuries, and higher mortalities. In contrast to such patients, in those with glycemic variability between 3.9 and 10.0 mmol/L there was a significant association with reduced medical interventions, major organ injuries, and all-cause mortality. The findings here provide direct evidence supporting the recent suggestions for clinical management of T2D during COVID-19 ( Bornstein et al., 2020 ).
In conclusion, T2D is an important risk factor for COVID-19 progression and adverse endpoints, and well-controlled BG, maintaining glycemic variability within 3.9 to 10.0 mmol/L, is associated with a significant reduction in the composite adverse outcomes and death. These findings provide critical insights into the clinical characteristics of patients with COVID-19 and pre-existing T2D and the possible avenues to improving their disease outcomes.
Limitations of Study
Due to the retrospective nature of the study and the unprecedented scale of the COVID-19 pandemic, this study has several limitations. First, all data were obtained from patient cohorts admitted in the 19 hospitals in Hubei Province, China. Therefore, the effect of BG control may be different among patients with COVID-19 and pre-existing T2D in the outpatient setting or in ethnically or geographically diverse populations. Second, we were not able to retrieve the pre-hospital status of T2D from the current cohort due to the urgent circumstance of the COVID-19 pandemic. The status of pre-hospital T2D could be significantly associated with numerous clinical parameters, which are known independent risk factors for the poor outcomes of COVID-19, including cardiovascular abnormalities and immunological dysfunction. While we performed PSM analysis to support the independent association of T2D with COVID-19 pathology, the influence from these cofounders cannot be fully excluded. Also, given this lack of pre-hospital data, it was not possible for us to access if BG levels changed as result of COVID-19 progression and/or severity. Third, the number of the patients with T2D and well-controlled BG in this study was modest and might not be powered sufficiently to reflect the overall complexity of the general population. Therefore, large-scale prospective cohort studies will be required in ethnically and geographically diverse cohorts to better understand the association and importance of BG control in the disease progression of COVID-19. Fourth, given the retrospective nature of the study, it was not possible for us to determine if active management of BG levels to a more normal range could ameliorate COVID-19 severity or adverse outcomes. Finally, individuals with type 1 diabetes were excluded from our analysis as there were too few of them in the initial cohort, but it is possible that blood glucose control may also affect their outcomes during COVID-19.
Key Resources Table
|REAGENT or RESOURCE||SOURCE||IDENTIFIER|
|Software and Algorithms|
|R-3.6.3||R Foundation for Statistical Computing||https://www.r-project.org/|
|Graphpad Prism 8||Graphpad||https://www.graphpad.com/|
|SPSS statistics 23.0||IBM Corporation||http://www.spss.com.hk/software/statistics/|
|Adobe illustrator CC 2019||Adobe company||https://www.adobe.com/cn|
|Coxme-2.2.16||Therneau and Pankratz, 2003||https://cran.r-project.org/web/packages/coxme/index.html|
|MatchIt-3.0.2||Ho et al., 2007||https://cran.r-project.org/web/packages/MatchIt/|
Further information and requests for resources and reagents should be directed to the Lead Contact, Hongliang Li ( firstname.lastname@example.org ).
The study did not generate any new reagents or materials.
Data and Code Availability
Data related to the findings of this study will be available from the corresponding author upon reasonable request. The research team will provide an email address for communication once the data are approved to be shared with others. The proposal with detailed aims, statistical plan, and other information/materials may be required to guarantee the rationality of requirement and the security of the data. The patient-level data, but without names and other identifiers, will be shared after review and approval of the submitted proposal and any related requested materials.
Study Design and Participants
This was a multi-centered, retrospective cohort study and the study protocol was approved by the Institution Ethic Committee of Renmin Hospital of Wuhan University and Zhongnan Hospital of Wuhan University. The study design was also individually approved by each collaborating hospital or their institutional ethics boards. Given the urgency of the COVID-19 pandemic, the informed consent forms were waived by the ethics boards of the hospitals.
The study subjects included patients with COVID-19 diagnosed between December 30 th , 2019 and March 20 th , 2020. COVID-19 was diagnosed based on chest computed tomography (CT) manifestations and/or reverse transcription-polymerase chain reaction (RT-PCR) following the criteria of the New Coronavirus Pneumonia Prevention and Control Program (5th edition) published by the National Health Commission of China and WHO interim guidance ( National Health Commission of China, 2020; World Health Organization, 2020; Zhang et al., 2020b ). A total of 9,663 patients with COVID-19 were initially screened for the study. Data from individuals, however, were excluded if the subjects were younger than 18 or older than 75 or had incomplete medical records (e.g., transfer to any other hospital), acute lethal organ injury (e.g., acute myocardial infarction, acute coronary syndrome, acute pulmonary embolism, or acute stroke), decompensated or end stage of chronic organ dysfunction (e.g., decompensated cirrhosis, decompensated chronic renal insufficiency, severe congestive heart failure), pregnancy, type 1 diabetes, getational diabetes, or malignancy. For further study, the remaining cohort (n = 7,337) was categorized into diabetic (n = 952) and non-diabetic (n = 6,385) groups, according to the clinical diagnosis and/or medical history on admission ( Figure 1 ).
The medical records of patients were analyzed by an integrated research team, including physicians, data scientists and statisticians. After deidentification process by removing the personal information (e.g., name and ID) of the participants and designating using a coding system, the basic information, epidemiological records, clinical manifestations, laboratory findings, radiographic characteristics from CT, treatments and outcomes during hospitalization were recorded. Major clinical symptoms (i.e., fever, cough, fatigue, dyspnea and comorbidities) were collected. The laboratory findings included routine blood test, fasting blood glucose (BG) and 2 h postprandial BG (2 hPG), C-reactive protein (CRP), procalcitonin, D-dimer, and serum indicators for liver injury, kidney injury and heart dysfunction. An experienced physician team reviewed, interpreted and double-checked all data to guarantee the accuracy.
The date of disease onset was defined as the day when the first symptom of COVID-19 was noticed. Severe cases were defined according to whether the patients had indication of respiratory rate > 30 breaths/min, or SpO2 ≤ 93% on room air, or PaO2/FiO2 ≤ 300 mmHg. T2D status was designated based on the patient’s medical history and guideline for the prevention and control of T2D in China (2017) ( Chinese Diabetes Society, 2018 ). The timing and frequency of obtaining the fasting and 2-h postprandial BG (2 hPG) varied between individuals, depending on the necessity related to the severity of the comorbid T2D. Severe T2D status accordingly obtained more frequent BG surveillances. Glycemic variability was defined as the range between the lowest fasting BG (FBG) and 2 hPG level during the observation period. Well-controlled BG was defined when glycemic variability ranged from 3.9 to 10.0 mmol/L since the normal range of fasting BG is 3.9 - 6.1 mmol/L and lower than 10 mmol/L is the targeting level of 2 hPG in DM management according to the guideline for the prevention and control of T2D in China (2017) ( Chinese Diabetes Society, 2018 ). Poorly-controlled BG was defined when the lowest fasting BG was above or equal 3.9 mmol/L and the highest 2 hPG level exceeded 10.0 mmol/L during the observation window.
Hypertension was diagnosed when systolic blood pressure is equal or above to 140 mm Hg and/or diastolic blood pressure is equal or above 90 mm Hg. ARDS and septic shock were defined following WHO interim guideline for “clinical management of severe acute respiratory infection when novel coronavirus (2019-nCoV) infection is suspected.” Cardiac injury was defined when the serum level of cardiac injury biomarkers (cardiac troponin I [cTNI], cardiac troponin T [cTNT], or high sensitivity cardiac troponin I [hs-cTNI]] were higher than the upper limit of normal (ULN). Acute liver injury was defined when an acutely increased level of serum alanine aminotransferase (ALT) and serum alkaline phosphatase (ALP) of upper limit of normal (ULN) was observed ( Marrone et al., 2017 ). Acute kidney injury was indicated by the value of serum creatinine level when it reached or exceeded 26.5 μmmol/L within 48 h ( Kellum et al., 2012 ). Disseminated intravascular coagulation (DIC) was diagnosed according to the criteria published by the International Society on Thrombosis and Hemostasis (ISTH) ( Gando et al., 2013 ). The primary endpoint of the study was 28-day all-cause death in COVID-19 patients. The secondary endpoints were occurrence of ARDS, septic shock, acute cardiac injury, acute kidney injury, or DIC.
Propensity Score-Matched Analysis
The variables potentially confounding the association between BG and the outcomes of COVID-19 were addressed using the propensity score-matching (PSM) method ( Waljee et al., 2013 ). PSM requires a complete set of variables for every patient, randomly missing values of 10 selected parameters from noninvasive tests were therefore imputed. The non-parameter imputation method missForest was applied and the estimation of the imputation error was 4.08%. The bootstrapped cross validation was further applied and repeated 10 times for evaluating imputation performance on the training data after 10% more parameters were randomly introduced. The missForest method yielded 4.11% (IQR 1.91%–5.44%) differences between the datasets before and after parameters were introduced. The algorithm of the PSM is as follows:
Logistic(P) = Ln[P/(1-P)] = β0 + β1X1 + β2X2 + …+ βkXk p = e(β0 + β1X1 + β2X2 + …+ βkXk)/1+e(β0 + β1X1 + β2X2 + …+ βkXk). The P in this formula is the predicted probability of glucose control procedure, and the beta value before each variable is the regression coefficient of that variable.
The variables potentially confounding the association between BG and the outcomes of COVID-19 were addressed using the PSM method. When evaluating the association of glucose control level and outcomes, the PSM cohorts were identified by balancing age, gender, fever, cough, dyspnea, CT-diagnosed lung lesions, SpO2, breath frequency, incidence of increased leukocyte count, ALT, AST, D-dimer, creatinine, CRP, procalcitonin and decreased of lymphocyte count, as well as comorbidities (hypertension, coronary artery disease, cerebrovascular disease, chronic liver diseases and chronic renal disease). The propensity score, a predicted probability of glucose change contributed by the above variables, were estimated based on multivariable logistic regression model. The matching ratio was at 1:1 for well-controlled BG versus poorly-controlled BG during the entire hospitalization. Exact matching with a caliper size of 0.05 was applied for all matching pairs according to the propensity scores. Evaluation of the balance between covariates was conducted by estimating standardized differences before and after matching. Only those with small absolute value less than 0.1 were considered qualified balancing.
The robustness of the association between BG level and all-cause mortality was assessed by analyzing E-value in the Mixed-effect Cox proportional hazards model to address unmeasured confounders using the methodology of VanderWeele and Ding ( Haneuse et al., 2019; Mathur et al., 2018; VanderWeele and Ding, 2017 ). Two sensitivity analyses were performed to evaluate the robustness of propensity score-matched cohort analyses, among all pairs.
Quantification and Statistical Analysis
All statistical analysis was performed using R-3.6.3 (R Foundation for Statistical Computing, Vienna, Austria) and SPSS Statistics (version 23.0, IBM, Armonk, NY, USA). Data with continuous variables were presented as median and interquartile range (IQR), and data with categorical variables were presented as frequency rates and percentage (%). Comparison between 2 groups was analyzed using Student’s t tests (normally distributed) or Mann-Whitney U test (nonnormally distributed) for continuous variables. Comparison of categorical variables was analyzed by Fisher’s exact test or χ2 test. Generalized linear model (GLM) was performed to evaluate correlation between the median of blood glucose and factors related to viral infection or glycemic control in patients with diabetes. The risk for composite endpoints and corresponding hazard ratio (HR) were analyzed using Cox proportional hazard model and mixed-effect Cox model. The cumulative rates of death were plotted by applying Kaplan-Meier method. A difference with a two-side α less than 0.05 was considered statistically significant.
This work was supported by grants from the National Key R&D Program of China ( 2016YFF0101504 to Z.-G.S.), the National Natural Science Foundation of China ( 81630011 to Haomiao Li, 81970364 to Z.-G.S., 81970070 to X.-J.Z., 81970011 to P.Z., and 81870171 to J.C.), the Major Research Plan of the National Natural Science Foundation of China ( 91639304 to Haomiao Li), the Hubei Science and Technology Support Project ( 2019BFC582 , 2018BEC473 , and 2017BEC001 to Haomiao Li), and Medical Flight Plan of Wuhan University .
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