Evaluation of Prognostic Values of Tissue Plasminogen Activator and Plasminogen Activator Inhibitor-1 in Crimean-Congo Hemorrhagic Fever Patients

AUTHORS

Yunus Gurbuz 1 , Baris Ozturk 2 , * , Emin Ediz Tutuncu 1 , Irfan Sencan 1 , Gonul Cicek Senturk 1 , Fatma Aybala Altay 1

1 Infectious Diseases and Clinical Microbiology Clinics, Diskapi Yildirim Beyazit Training and Research Hospital, Ministry of Health, Ankara, Turkey

2 Infectious Diseases and Clinical Microbiology Clinics, Ulucanlar Training and Research Hospital, Ministry of Health, Ankara, Turkey

How to Cite: Gurbuz Y, Ozturk B, Tutuncu E E, Sencan I, Cicek Senturk G, et al. Evaluation of Prognostic Values of Tissue Plasminogen Activator and Plasminogen Activator Inhibitor-1 in Crimean-Congo Hemorrhagic Fever Patients, Jundishapur J Microbiol. 2015 ; 8(10):e26514. doi: 10.5812/jjm.26514.

ARTICLE INFORMATION

Jundishapur Journal of Microbiology: 8 (10); e26514
Published Online: October 20, 2015
Article Type: Research Article
Received: January 7, 2015
Revised: May 20, 2015
Accepted: July 7, 2015
Crossmark

Crossmark

CHEKING

READ FULL TEXT
Abstract

Background: Crimean-Congo hemorrhagic fever (CCHF) is a widespread disease in Turkey, and was responsible for many deaths in endemic regions during the last decade. The pathogenesis of the disease is not fully understood yet.

Objectives: In this study we aimed to determine the levels of tissue plasminogen activator (tPA) and Plasminogen activator inhibitor-1 (PAI-1) as predictors of prognosis in CCHF.

Patients and Methods: Patients who were diagnosed by the polymerase chain reaction (PCR) and IgM positivity in the reference laboratory were included in this study. Tissue Plasminogen activator and PAI-1 levels were measured by the enzyme linked immunosorbent assay (ELISA) using a commercial kit (human t-PA ELISA and human PAL-1 ELISA; BioVendor research and diagnostic products, BioVendor-Laboratorni medicina a.s., Brno, Czech Republic).

Results: A total of 46 patients participated in this study. The significant differences between recovering patients and the patients who died, regarding Aspartate aminotransferase (AST), Creatine Phosphokinase (CPK), Lactate Dehydrogenase (LDH), Prothrombin Time (PT), activated Partial Thromboplastin time (aPTT), and thrombocyte and fibrinogen levels, were consistent with many clinical studies in the literature. The fatal cases were found to have higher tPA and PAI-1 levels in contrast to the patients who completely recovered.

Conclusions: We think that these findings may help the progress of understanding of CCHF pathogenesis.

Keywords

Crimean-Congo Hemorrhagic Fever Tissue Plasminogen Activator Plasminogen Activator Inhibitor-1

Copyright © 2015, Ahvaz Jundishapur University of Medical Sciences. This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.

1. Background

Crimean-Congo hemorrhagic fever (CCHF) is a fatal viral infection, which has been endemic in Turkey since 2002 (1). The disease is also endemic in Kosava, Albania, Bulgaria, Greece, Iran, Pakistan, Afghanistan, the Russian Federation, Kazakhstan, Tajikistan, Georgia, Maruritania, Kenya, Senegal and South Africa (2). The CCHF virus has been found in many species including horses, donkeys, goats, cattle, sheep, and pigs, yet human beings are the only known host of CCHF virus, in which the disease is manifested (3). The CCHF viruses are transmitted to humans by Hyalomma genus ticks, particularly by Hyalomma marginatum marginatum. The dominant tick species in Turkey were found to be H. marginatum in humans, cattle and sheep (4).

The CCHF virus antigens were also found in Hyalomma excavatum, Haemaphysalis parva and Boophilus annulatus ticks collected from cattle and Rhipicephalus bursa ticks from sheep (4). Crimean-Congo hemorrhagic fever is an acute viral hemorrhagic disease with a mortality rate of 3 to 30% (5). The signs and symptoms of the disease include headache, fatigue, muscle aches, abdominal pain, nausea, vomiting, diarrhea, hemorrhage and high fever. The pathogenesis of CCHF is not fully understood. It is thought that vascular endothelial damage might play an important role in the pathogenesis of CCHF (6). The patients may exhibit rapid deteriorations in biochemical and hematologic parameters (3). Fatal cases usually develop disseminated intravascular coagulation (DIC) and multi-organ failures (7). Many studies have suggested that cytokine and adhesion molecules can be used as predictive markers in severe cases (7-11). Hyperfibrinolysis and disordered balance of fibrinolysis are proposed steps in the etiology of multi-organ failure in severe viral hemorrhagic fevers (12-14).

2. Objectives

In this study our aim was to determine the levels of tissue Plasminogen activator (tPA) and Plasminogen activator inhibitor-1 (PAI-1), which are important for hemostasis in CCHF cases.

3. Patients and Methods

The patients who were diagnosed by positive polymerase chain reaction (PCR) and IgM results at the reference laboratory were included in the study. The demographic data, initial biochemical values and hematologic counts were recorded. The patients who lacked laboratory results for the first five days of the disease were excluded. Tissue Plasminogen activator and PAI-1 levels were studied by a commercial enzyme linked immunosorbent assay (ELISA) kit (human t-PA ELISA and human PAL-1 ELISA; BioVendor research and diagnostic products, BioVendor-Laboratorni medicina a.s., Brno, Czech Republic). The study protocol was reviewed and approved by the ethics committee for clinical researches of Diskapi Yildirim Beyazit training and research hospital (clinical trial registry number 22/11). The SPSS 15.0 program and Mann-Whitney U test was used for statistical analysis. For correlation analysis, the Pearson’s test was preferred and P level was accepted as < 0.05.

4. Results

Forty-six patients enrolled in this study; twenty-four (%52.2) were male and 22 were (%47.8) female. The mean age was 48.8 (SD: 17.4; 15 - 85) years. Eight patients (17.4%) died, while 38 (82.6%) cases recovered. The levels of Aspartate Aminotransferase (AST), Alanine Aminotransferase (ALT), Creatine Phosphokinase (CPK) and Lactate Dehydrogenase (LDH) were found to be higher in fatal cases when compared to the recovered patients. Also aPTT and PT were significantly prolonged in non-survivors. Thrombocyte counts and fibrinogen levels were significantly lower in fatal cases. The differences regarding AST, LDH, CPK, PT, aPTT, thrombocyte and fibrinogen levels were statistically significant amongst the two groups (Table 1).

Table 1. Comparison of the Laboratory Results of Patients Who Recovered and Those Who Dieda,b
Recovered Patients (n = 38)Those Who Died (n = 8)P Value
AST, U/L215.9 ± 144.81888.1 ± 3722.90.013
ALT, U/L113.7 ± 90.4475.8 ± 782.70.062
LDH, U/L834.0 ± 392.52051.8 ± 1583.30.002
CPK, U/L501.1 ± 482.51184.5 ± 1128.80.028
WBC × 109/L2.579 ± 1.4944.870 ± 5.1830.524
PT, s13.3 ± 2.418.5 ± 7.00.009
aPTT, s44.8 ± 8.884.5 ± 26.20.001
Platelets × 109/L35.973 ± 24.78311.750 ± 4.7730.001
Fibrinogen, mg/dL393.3 ± 177.0286.1 ± 192.10.031
PAI, pg/ml1913.8 ± 1015.15054.3 ± 2562.60.008
tPA, pg/ml791.4 ± 366.31083.4 ± 227.20.046

aAbbreviations: ALT, alanine aminotransferase; aPTT, activated partial thromboplastin time; AST, aspartate aminotransferase; CPK, creatine phosphokinase; LDH, lactate dehydrogenase; PAI, plasminogen activator inhibitor; PT, prothrombin time; tPA, tissue plasminogen activator; WBC, white blood cell.

bData are presented as mean ± SD.

The tPA and PAI-1 levels were significantly higher in fatal cases than patients who recovered (Table 1). The PAI-1 levels exhibited a positive correlation with PT and aPTT values (PT: r = 500, P < 0.001, aPTT: r = 724, P < 0.001) (Figure 1).

The Correlation Between Plasminogen Activator Inhibitor-1 Levels and Bleeding Scores (PT And Aptt) in Crimean-Congo Hemorrhagic Fever Patients
Figure 1. The Correlation Between Plasminogen Activator Inhibitor-1 Levels and Bleeding Scores (PT And Aptt) in Crimean-Congo Hemorrhagic Fever Patients

5. Discussion

Crimean-Congo hemorrhagic fever is a severe tick-borne viral disease with high mortality and has been endemic in Turkey for more than ten years. The reason why some patients have a negative outcome while others recover is not fully understood. The pathogenesis is still unclear. Vascular endothelial injury may be the major disorder in the background (6). Thus, new studies on the pathogenesis of CCHF may contribute to existing treatment modalities. The incidence of mortality in our country is nearly 5% for CCHF cases (15). In our study, mortality was found to be higher than the reported level (17.4%). This may be related to the fact that our hospital is a tertiary hospital with level three intensive care units. Therefore, the patients who were least expected to recover were sent to and followed up in our hospital. Overall, 52.2% of the patients were male with a mean age of 48.8. Most of our cases were rural workers, which was coherent with previous data. However, it is possible for CCHF to be found amongst all age groups in Turkey.

The CCHF patients may exhibit rapid deteriorations in biochemical and hematologic parameters during their follow-up. The most prominent alterations include: a rise in liver enzymes and bleeding times and a decrease of thrombocyte counts and fibrinogen levels. Many studies were performed that analyzed these parameters to determine prognostic prediction rules (16-21). In accordance with the literature, our study found statistically significant differences in AST, LDH, CPK, PT, aPTT, and thrombocyte and fibrinogen levels between fatal cases and recovered patients.

Hemostasis is mostly impaired in severe viral hemorrhagic fever cases. In a normal body, hemostasis is balanced between clotting and bleeding poles and controlled by two main mechanisms. Primary hemostasis involves vascular contraction, thrombocyte activation and aggregation steps. Secondary hemostasis is mainly maintained by activation of clotting cascade, and formation of clot and lysis (12). The fibrinolytic process is controlled by tPA and PAI-1 levels (22). Tissue Plasminogen activator activates production of plasmin from plasminogen and leads to destruction of fibrin and accumulation of end products. However, PAI-1 acts as an inhibitor of fibrinolysis; it inhibits regeneration of plasmin (12). Increased production of tPA in endothelial cells was reported in Dengue hemorrhagic fever (DHF) patients (14, 23).

Serine protease inhibitor of PAI-1 was further shown to effect fibrinolysis, sepsis and fever events (24). Vascular endothelial injury was reported to be an important step in many studies for the pathogenesis of viral hemorrhagic diseases (6, 8). A study of Dengue fever patients pointed out that acute cytokine release was the main factor for endothelial damage instead of a physical injury (12). These cytokines trigger coagulation and in fact contribute to tPA production. Also, a subsequent rise of tPA leads to hyperfibrinolysis in the next step. Fibrin deposits and plugs are the end products of this process. These interactions lead to the final result of hipoperfusion of tissues and multi-organ failure (12-14). Moreover, there are many studies linking hyperfibrinolysis and bleedings to the pathogenesis of hemorrhagic fevers (14, 22, 25-27).

The literature review revealed that the effects of tPA and PAI-1 levels have only been studied in DHF and Argentine hemorrhagic fever (AHF) patients. These diseases are also viral hemorrhagic fevers, which may eventually lead to DIC and organ failures (12-14). A study from Thailand by Sosothikul et al. reported that high PAI-1 levels were correlated with poor prognosis in DHF patients. In addition, they found a significant positive correlation between bleeding scores and aPTT, PT and plasma tPA, and a significant negative correlation between bleeding scores and platelet counts (25). A similar study in DHF patients from Taiwan reported that a rise of tPA and IL6 levels was a prominent feature in patients with septic shock after observation for 48 hours (28). Another study of DHF patients demonstrated a correlation between disease severity and the fibrinolysis process. It was shown that there was an acute rise in tPA and a subsequent PAI-1 increase in these patients (23). A study of AHF patients found elevated levels of tPA in all cases while more severe cases tended to have higher PAI-1 levels (27).

Several previous studies demonstrated an acute rise of cytokines and adhesion molecules such as IL-6, IL-8, TNF-α, ICAM-1 and VCAM-1 in CCHF patients (7-11). To the best of our knowledge, this is the first report regarding tPA and PAI-1 levels in CCHF patients. The results of this study demonstrated that tPA and PAI-1 levels were significantly higher in fatal cases than in recovered patients. Plasminogen Activator Inhibitor-1 levels exhibited a positive correlation with PT and aPTT values. We think that these results may, in fact, contribute to the understanding of CCHF pathogenesis. Supportive therapy is essential in CCHF patients (6) and any antiviral drug therapy or vaccine is not yet available. Jiang et al. suggested that prophylactic treatment against blood coagulation and the imbalance in fibrinolysis system is critically important to prevent pathogenesis and development of severe symptoms such as hemorrhage for patients at the acute stage of DHF (22). Huang et al. suggested that therapeutic intervention to prevent plasmin activation in the acute stage might be beneficial to prevent complications in DHF (23). The suggested treatment options for DHF by the authors may also be considered in CCHF.

The major limitation of our study was the small sample size making it difficult to generalize the results to a larger population. However, this study provides initial evidence that tPA and PAI-1 may contribute to the pathogenesis of CCHF.

In conclusion, higher levels of tPa and PAI-1 were correlated with higher mortality rate in CCHF. The imbalance of the fibrinolytic system in fatal cases shown in this study may contribute to the understanding of pathogenesis. Moreover, these results may further contribute to the development of new therapeutic options other than supportive treatment in the future.

Footnote

References

  • 1.

    Ergonul O, Celikbas A, Dokuzoguz B, Eren S, Baykam N, Esener H. Characteristics of patients with Crimean-Congo hemorrhagic fever in a recent outbreak in Turkey and impact of oral ribavirin therapy. Clin Infect Dis. 2004; 39(2) : 284 -7 [DOI][PubMed]

  • 2.

    Leblebicioglu H. Crimean-Congo haemorrhagic fever in Eurasia. Int J Antimicrob Agents. 2010; 36 Suppl 1 -6 [DOI][PubMed]

  • 3.

    Whitehouse C. Crimean?Congo hemorrhagic fever. Antiviral Res. 2004; 64(3) : 145 -60 [DOI]

  • 4.

    Gunes T, Poyraz O, Vatansever Z. Crimean-Congo hemorrhagic fever virus in ticks collected from humans, livestock, and picnic sites in the hyperendemic region of Turkey. Vector Borne Zoonotic Dis. 2011; 11(10) : 1411 -6 [DOI][PubMed]

  • 5.

    Bakir M, Ugurlu M, Dokuzoguz B, Bodur H, Tasyaran MA, Vahaboglu H, et al. Crimean-Congo haemorrhagic fever outbreak in Middle Anatolia: a multicentre study of clinical features and outcome measures. J Med Microbiol. 2005; 54 : 385 -9 [DOI][PubMed]

  • 6.

    Ergönül Ö. Crimean-Congo haemorrhagic fever. Lancet Infect Dis. 2006; 6(4) : 203 -14 [DOI]

  • 7.

    Akinci E, Bodur H, Leblebicioglu H. Pathogenesis of Crimean-Congo hemorrhagic fever. Vector Borne Zoonotic Dis. 2013; 13(7) : 429 -37 [DOI][PubMed]

  • 8.

    Weber F, Mirazimi A. Interferon and cytokine responses to Crimean Congo hemorrhagic fever virus; an emerging and neglected viral zonoosis. Cytokine Growth Factor Rev. 2008; 19(5-6) : 395 -404 [DOI][PubMed]

  • 9.

    Ergonul O, Tuncbilek S, Baykam N, Celikbas A, Dokuzoguz B. Evaluation of serum levels of interleukin (IL)-6, IL-10, and tumor necrosis factor-alpha in patients with Crimean-Congo hemorrhagic fever. J Infect Dis. 2006; 193(7) : 941 -4 [DOI][PubMed]

  • 10.

    Papa A, Bino S, Velo E, Harxhi A, Kota M, Antoniadis A. Cytokine levels in Crimean-Congo hemorrhagic fever. J Clin Virol. 2006; 36(4) : 272 -6 [DOI][PubMed]

  • 11.

    Ozturk B, Kuscu F, Tutuncu E, Sencan I, Gurbuz Y, Tuzun H. Evaluation of the association of serum levels of hyaluronic acid, sICAM-1, sVCAM-1, and VEGF-A with mortality and prognosis in patients with Crimean-Congo hemorrhagic fever. J Clin Virol. 2010; 47(2) : 115 -9 [DOI][PubMed]

  • 12.

    Chuang YC, Lin YS, Liu CC, Liu HS, Liao SH, Shi MD, et al. Factors contributing to the disturbance of coagulation and fibrinolysis in dengue virus infection. J Formos Med Assoc. 2013; 112(1) : 12 -7 [DOI][PubMed]

  • 13.

    Djamiatun K, Faradz SM, Setiati TE, Netea MG, van der Ven AJ, Dolmans WM. Increase of plasminogen activator inhibitor-1 and decrease of transforming growth factor-b1 in children with dengue haemorrhagic fever in Indonesia. J Trop Pediatr. 2011; 57(6) : 424 -32 [DOI][PubMed]

  • 14.

    Rachman A, Rinaldi I. Coagulopathy in dengue infection and the role of interleukin-6. Acta Med Indones. 2006; 38(2) : 105 -8 [PubMed]

  • 15.

    Yilmaz GR, Buzgan T, Irmak H, Safran A, Uzun R, Cevik MA, et al. The epidemiology of Crimean-Congo hemorrhagic fever in Turkey, 2002-2007. Int J Infect Dis. 2009; 13(3) : 380 -6 [DOI][PubMed]

  • 16.

    Swanepoel R, Gill DE, Shepherd AJ, Leman PA, Mynhardt JH, Harvey S. The clinical pathology of Crimean-Congo hemorrhagic fever. Rev Infect Dis. 1989; 11 Suppl 4 -800 [PubMed]

  • 17.

    Bakir M, Gozel MG, Koksal I, Asik Z, Gunal O, Yilmaz H, et al. Validation of a severity grading score (SGS) system for predicting the course of disease and mortality in patients with Crimean-Congo hemorrhagic fever (CCHF). Eur J Clin Microbiol Infect Dis. 2015; 34(2) : 325 -30 [DOI][PubMed]

  • 18.

    Ergonul O, Celikbas A, Baykam N, Eren S, Dokuzoguz B. Analysis of risk-factors among patients with Crimean-Congo haemorrhagic fever virus infection: severity criteria revisited. Clin Microbiol Infect. 2006; 12(6) : 551 -4 [DOI][PubMed]

  • 19.

    Cevik MA, Erbay A, Bodur H, Gulderen E, Bastug A, Kubar A, et al. Clinical and laboratory features of Crimean-Congo hemorrhagic fever: predictors of fatality. Int J Infect Dis. 2008; 12(4) : 374 -9 [DOI][PubMed]

  • 20.

    Tasdelen Fisgin N, Tanyel E, Doganci L, Tulek N. Risk factors for fatality in patients with Crimean-Congo haemorrhagic fever. Trop Doct. 2009; 39(3) : 158 -60 [DOI][PubMed]

  • 21.

    Ozturk B, Tutuncu E, Kuscu F, Gurbuz Y, Sencan I, Tuzun H. Evaluation of factors predictive of the prognosis in Crimean-Congo hemorrhagic fever: new suggestions. Int J Infect Dis. 2012; 16(2) -93 [DOI][PubMed]

  • 22.

    Jiang Z, Tang X, Xiao R, Jiang L, Chen X. Dengue virus regulates the expression of hemostasis-related molecules in human vein endothelial cells. J Infect. 2007; 55(2) -8 [DOI][PubMed]

  • 23.

    Huang Y, Liu C, Wang S, Lei H, Liu H, Lin Y, et al. Activation of coagulation and fibrinolysis during dengue virus infection. J Med Virol. 2001; 63(3) : 247 -51 [DOI]

  • 24.

    Shyu HW, Lin YY, Chen LC, Wang YF, Yeh TM, Su SJ, et al. The dengue virus envelope protein induced PAI-1 gene expression via MEK/ERK pathways. Thromb Haemost. 2010; 104(6) : 1219 -27 [DOI][PubMed]

  • 25.

    Sosothikul D, Seksarn P, Pongsewalak S, Thisyakorn U, Lusher J. Activation of endothelial cells, coagulation and fibrinolysis in children with Dengue virus infection. Thromb Haemost. 2007; [DOI]

  • 26.

    Wills BA, Oragui EE, Stephens AC, Daramola OA, Dung NM, Loan HT, et al. Coagulation abnormalities in dengue hemorrhagic Fever: serial investigations in 167 Vietnamese children with Dengue shock syndrome. Clin Infect Dis. 2002; 35(3) : 277 -85 [DOI][PubMed]

  • 27.

    Heller MV, Marta RF, Sturk A, Maiztegui JI, Hack CE, Cate JW, et al. Early markers of blood coagulation and fibrinolysis activation in Argentine hemorrhagic fever. Thromb Haemost. 1995; 73(3) : 368 -73 [PubMed]

  • 28.

    Huang YH, Lei HY, Liu HS, Lin YS, Chen SH, Liu CC, et al. Tissue plasminogen activator induced by dengue virus infection of human endothelial cells. J Med Virol. 2003; 70(4) : 610 -6 [DOI][PubMed]

  • COMMENTS

    LEAVE A COMMENT HERE: