key: cord-0812090-m4kmsk95
authors: Wang, Zhenzhou; Du, Zhe; Zhao, Xiujuan; Guo, Fuzheng; Wang, Tianbing; Zhu, Fengxue
title: Determinants of Increased Fibrinogen in COVID-19 Patients With and Without Diabetes and Impaired Fasting Glucose
date: 2021-03-24
journal: Clin Appl Thromb Hemost
DOI: 10.1177/1076029621996445
sha: 91b4b78b4b5c3fd4887f0d2033376ea786aa7719
doc_id: 812090
cord_uid: m4kmsk95

BACKGROUND: To investigate the factors associated with elevated fibrinogen (Fbg) levels in COVID-19 patients with and without diabetes (DM) and impaired fasting glucose (IFG). METHODS: According to whether or not their glucose metabolism was impaired, COVID-19 patients were subdivided into 2 groups: 1) with DM and IFG, 2) control group. Their demographic data, medical history, signs and symptoms, laboratory results, and final clinical results were analyzed retrospectively. RESULTS: 28 patients (16.3%) died during hospitalization, including 21 (29.2%) in group 1 and 7 (7.0%) in group 2 (P < 0.001). Fbg levels in groups 1 and 2 were higher than the normal range, at 5.6 g/L (IQR 4.5–7.2 g/L) and 5.0 g/L (IQR 4.0–6.1 g/L), respectively (P = 0.009). Serum ferritin levels, C-reactive protein (CRP), interleukin-6 (IL-6), IL-8, tumor necrosis factor-α (TNF-α), triglycerides (TG) were significantly increased in group 1 compared to those in the control. TG levels were 1.3 mmol/L in the control, while that in group 1 was 1.8 mmol/L. Multiple linear regression showed that the predicting factors of Fbg in the control group were serum ferritin and CRP, R(2) = 0.295; in group 1, serum ferritin, CRP, and TG, R(2) = 0.473. CONCLUSIONS: Fbg in all COVID-19 patients is related to serum ferritin and CRP involved in inflammation. Furthermore, in COVID-19 patients with insulin resistance, Fbg is linearly positively correlated with TG. This suggests that regulation of TG, insulin resistance, and inflammation may reduce hypercoagulability in COVID-19 patients, especially those with insulin resistance.

Patients with severe coronavirus disease (COVID-19) without other thrombotic risk factors still exhibit various thrombotic events, including microvascular thrombosis, venous thrombosis and pulmonary thromboembolism, and acute arterial thrombosis. 1 COVID-19-associated coagulopathy (CAC) is an acute thrombosis and is an important cause of organ failure and death in patients. 1, 2 The pathogenesis of CAC is still unclear, and many factors, such as severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, inflammation, vascular endothelial injury, coagulation, and fibrinolysis imbalance may be involved. [2] [3] [4] Among these, an increased fibrinogen (Fbg) level has been proven as an important part of CAC. [1] [2] [3] Currently, anticoagulant and fibrinolytic drugs are used in the treatment of CAC. 5, 6 People with diabetes mellitus (DM) are more likely to experience complications and death due to COVID-19. 7, 8 Laboratory tests show that COVID-19 patients with elevated glycosylated hemoglobin (HbA1c) have higher cytokines and Fbg. 9 The aims of this study is to answer these questions: What factors are related to the increase of Fbg in COVID-19 patients? Is there a difference between patients with and without DM? To investigate these questions, we conducted a small retrospective study to provide preliminary insight into the pathogenesis and treatment of CAC.

Overall, 176 patients were diagnosed with COVID-19 in the Wuhan Tongji Hospital wards between February 9 and 28, 2020. Four patients were excluded (2 patients treated with glucocorticoids and immunosuppressants for renal transplantation and chronic systemic lupus erythematosus, one hemolytic anemia patient, and one patient with myelosuppression after leukemia chemotherapy); thus, 172 were included in the study. The enrolled patients were divided into 2 groups: (1) 72 patients in the DM and impaired fasting glucose (IFG) group, (2) 100 patients in the control group. Patients in the control group had normal fasting glycemia without DM history. In the group with DM and IFG, 32 patients (44.4%) had type 2 DM history, 19 (26.4%) were newly diagnosed with DM, and 21 (29.2%) had high fasting glycemia. Patients with DM history received one or more oral hypoglycemic drugs (metformin was most used, followed by acarbose) before admission, and 12 (16.7%) received insulin therapy before admission. DM and IFG diagnosis were based on 2019 WHO diagnostic criteria for DM. 10 HbA1c was not used as a diagnostic criterion because of acute viral infections in the patients. COVID-19 was diagnosed according to the Diagnosis and Treatment Plan for Chinese New Coronavirus Pneumonia (7th Edition) 11 issued by the National Health Commission of the People's Republic of China. The basic demographic characteristics of the patients are provided in Table 1 .

This was a retrospective cohort study. Therefore, data on the patient's characteristics, medical history, symptoms and signs, laboratory test results, and final clinical outcomes were retrieved from the electronic medical record system. Laboratory test results reported white blood cell and lymphocyte count values as minimum values during the entire hospitalization. Conversely, serum ferritin, interleukin (IL), tumor necrosis factor-a (TNF-a), c-reactive protein (CRP), triglyceride (TG), lactate dehydrogenase (LDH), and Fbg levels were reported as maximum values. All laboratory parameters were measured after 8 hours of fasting. All patients were treated according to the "Chinese New Coronavirus Pneumonia Diagnosis and Treatment Plan (7th Edition)" 11 and were followed up until April 6, 2020. The study was approved by the Ethics Committee of Peking University People's Hospital.

Categorical variables were presented as frequencies and percentages, and continuous variables were presented as median and interquartile range (IQR). One-way analysis of variance (ANOVA) was used to calculate the difference between groups for continuous variables that fit the normal distribution, and non-parametric tests were used for non-normally distributed continuous variables. The chi-square test was applied to categorical variables. Multiple linear regression was used to analyze the related factors of Fbg. P < 0.05 was considered There was a statistically significant difference in mortality between the 2 groups (P < 0.001). All the deceased patients were previously treated with mechanical ventilation (Table 1) . Fbg levels in the DM and IFG group and control group were higher than the normal range, at 5.6 g/L (IQR 4.5-7.2 g/L) and 5.0 g/L (IQR 4.0-6.1 g/L), respectively (P ¼ 0.009). TG levels were 1.6 mmol/L (IQR 1.1-2.2 mmol/L) in all patients and 1.3 mmol/L (IQR 0.9-2.0 mmol/L) in the control group. Their median did not exceed the normal range. However, the TG level in the DM and IFG group was 1.8 mmol/L (IQR 1.3-2.4 mmol/L), which not only exceeded the normal range but also increased significantly compared to that in the control group (P ¼ 0.046). Table 2 shows that leukocytes, serum ferritin, CRP, IL-6, IL-8, and TNF-a levels also significantly increased in the DM and IFG group compared to the control, while lymphocytes decreased significantly (P < 0.05).

The correlation analysis between the 2 groups of measurement data and Fbg showed that the related factors of Fbg in the control group were lymphocytes, serum ferritin, CRP, IL-2, and TNF-a, while in the group with DM and IFG were lymphocytes, serum ferritin, CRP, and TG (Table 3) . To solve the problem of multicollinearity among related factors, we included them in multiple linear regression equations. The results showed that the factors influencing Fbg in the control group were serum ferritin and CRP, R 2 ¼ 0.295, while in the DM and IFG group, serum ferritin, CRP, and TG, R 2 ¼ 0.473 (Table 4 ).

Fbg, as an acute phase reactive protein, is involved in coagulation and inflammation. 12, 13 On the other hand, inflammation can lead to a significant increase in the expression of Fbg in the Fasting blood glucose (mmol/L) 4.11-6.05 5.7 (5.1-7.1) 5.2 (4.9-5.6) 7.9 (6.5-11.6) 0.000 Fbg (g/L) 2.0-4.0 5.2 (4.1-6.6) 5.0 (4.0-6.1) 5.6 (4.5-7.2) 0.009 Leukocytes (Â10 9 /L) 3.5-9. liver. 14, 15 That is, inflammation and Fbg drive each other. Improperly elevated Fbg can lead to hypercoagulability and excessive inflammation. 13 Fbg can act as a ligand for the surface receptors (such as VE-cadherin, ICAM-1, a IIb b 3 , a 5 b 1 , a V b 3 , a M b 2 , and a X b 2 ) of leukocytes, vascular endothelial cells, platelets, fibroblasts, and smooth muscle cells. 16 Among them, G protein-coupled protease activated receptors can control the expression of cytokines and chemokines. 16, 17 Our research shows that inflammation-related cytokines and Fbg are elevated in COVID-19 patients, especially in patients with DM and IFG. Multiple regression analysis showed that serum ferritin and CRP related to inflammation affect Fbg levels, and are positively correlated with Fbg. This indicates that in COVID-19 patients, there may also be a mutual driving effect between inflammation and Fbg. Our research shows that in COVID-19 patients with DM and IFG, Fbg is not only related to serum ferritin and CRP involved in inflammation but also positively related to TG. Insulin resistance is one of the important pathophysiological mechanisms of IFG and Type 2 DM, and hypertriglyceridemia is one of the typical features of insulin resistance. 18 Studies on visceral obesity and insulin resistance have shown that TG is degraded by lipoprotein lipase to produce free fatty acids (FFA), which leads to a significant increase of FFA in plasma. FFA can activate the NF-kB pathway and increase the liver expression of various pro-inflammatory cytokines, including TNF-a, IL1b, IL6, and monocyte chemoattractant protein 1 (MCP-1). 19 In addition, elevated plasma FFA can also promote Fbg production and reduce fibrinolytic capacity. 20 Studies have shown that Fbg levels are related to insulin resistance. [19] [20] [21] The use of rosiglitazone in patients with type 2 DM to improve insulin resistance can significantly reduce the level of Fbg. 22 In patients with metabolic syndrome, the application of the lipid-lowering drug fenofibrate not only improves blood lipids but also improves insulin resistance and reduces Fbg. 23 Recently, research by Ehrlich et al suggests that elevated lipid metabolism may underlie aspects of COVID-19 pathogenesis, and fenofibrate can treat COVID-19 by disrupting lipid metabolism. 24 According to sequential organ failure assessment (SOFA) score, the severity of coagulation disorders in patients with COVID-19 seems to be related to the degree of organ dysfunction. 25 We compared the parameters in non-survivors to those in survivors, with significant increases in Fbg, TG, and cytokines in non-survivors (Supplemental Table 1 ). An increased level of Fbg is one of the characteristics of CVC. Friedrich et al showed that even with conventional antithrombotic therapy, Fbg levels peaked at the third week of the disease and remained significantly elevated at the eighth week. 26 The persistently high Fbg level may affect the occurrence of thromboembolic events, especially in diabetic patients with higher Fbg levels. Ranucci et al described the correlation between IL-6 and Fbg levels. 27 Similarly, our study also showed that Fbg in all COVID-19 patients is related to serum ferritin and CRP involved in inflammation. Moreover, to the best of our knowledge, our study is the first to associate hyperfibrinogenemia with elevated TG levels in insulin-resistant COVID-19 patients. Our preliminary research suggests it may be possible to reduce the level of TG to reduce Fbg in such patients while undergoing conventional thrombotic treatment, thereby reducing the risk of thrombosis.

Of course, as a retrospective study with a small sample size, our research has limitations. In particular, we lack indicators to quantitatively assess insulin resistance. Using the triglyceride and glucose (TyG) index as indicators of insulin resistance, the study by Ren et al showed that the TyG index was significantly associated with an increased risk of severe case and mortality of COVID-19, after controlling for potential confounders (OR for severe case, 2.9, P ¼ 0.007; OR for mortality, 2.9, P ¼ 0.016). 28 Unfortunately, their study did not provide data on Fbg and other coagulation related factors. Therefore, we still need to do more research.

Fbg in all COVID-19 patients is related to serum ferritin and CRP involved in inflammation. Furthermore, in COVID-19 patients with insulin resistance, Fbg is linearly positively correlated with TG. This suggests that regulation of TG, insulin resistance, and inflammation may reduce hypercoagulability in COVID-19 patients, especially those with insulin resistance.

The study was approved from by the Ethics Committee of Peking University People's Hospital, and written informed consent was obtained from all participants before enrolment in the study. All procedures were in accordance with the ethical standards of the institutional and/or national research committee and with the Declaration of Helsinki. 

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The authors would like to acknowledge the contribution of the survey team members.

Zhenzhou Wang, Zhe Du, These authors contributed equally. ZD and ZZW designed the study, wrote and revised the manuscript. TBW and FXZ analyzed the data. XJZ and FZG reviewed the manuscript. All authors read and approved the final manuscript.

The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This study was supported by Natural Science Foundation of Beijing municipality (7204321) and Peking University People's Hospital Scientific Research Development Funds (RDY-2019-02).

Fengxue Zhu https://orcid.org/0000-0002-6018-1822

Supplemental material for this article is available online.

The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.