Thrombosis in inflammatory bowel diseases: what’s the link?
© Giannotta et al.; licensee BioMed Central. 2015
Received: 24 October 2014
Accepted: 26 February 2015
Published: 2 April 2015
Inflammatory bowel disease affects more than 2 million people in Europe, with almost 20% of patients being diagnosed in pediatric age. Patients with inflammatory bowel disease are at increased risk of thromboembolic complications which may affect patients’ morbidity and mortality. The risk of the most common thromboembolic events, such as deep venous thrombosis and pulmonary embolism, are estimated to be three-fold increased compared to controls, but many other districts can be affected. Moreover, patients with ulcerative colitis and Crohn’s disease experience thromboembolic events at a younger age compared to general population. Many factors have been investigated as determinants of the pro-thrombotic tendency such as acquired risk factors or genetic and immune abnormalities, but a unique cause has not been found. Many efforts have been focused on the study of abnormalities in the coagulation cascade, its natural inhibitors and the fibrinolytic system components and both quantitative and qualitative alterations have been demonstrated. Recently the role of platelets and microvascular endothelium has been reviewed, as the possible link between the inflammatory and hemostatic process.
Inflammatory bowel disease (IBD), whose major forms are ulcerative colitis (UC) and Crohn’s disease (CD), is a chronic inflammatory condition characterized by local and systemic inflammation predominantly affecting the gastrointestinal tract but that may be associated to numerous extra-intestinal manifestations including thrombosis. IBD affects more than 2 million people in Europe, with almost 20% of patients being diagnosed in pediatric age; in Italy over 200 thousands patients are estimated to suffer from such diseases.
The association between IBD and venous thromboembolism (VTE) was first described in 1936 by Bargen et al., who observed 18 patients with VTE among over 1000 IBD patients followed at the Mayo Clinic . Since then, several publications reported an increased risk of thromboembolic events (TE) affecting both the venous and arterial district in UC and CD patients. This condition seems to be a characteristic of IBD, not simply of inflammatory or intestinal chronic disease, because it has not been demonstrated in other conditions such as rheumatoid arthritis or coeliac disease [2,3]. The overall incidence of VTE in IBD patients is estimated to be 1%-8% [2-4] although necroscopy studies report higher rates, approximately 40% [5-8]. No significant difference was found in the risk of VTE between UC and CD patients. The risk of VTE in lower extremities and pulmonary embolism in IBD patients is reported to be 3-fold increased compared to the general population [3,9,10] even after correction for known pro-thrombotic factors [6,7]. Other venous districts may occasionally be involved as the cerebral , hepatic and portal , retinal  and mesenteric veins . Arterial thrombosis occur less frequently but has been described especially in cerebral, retinal and limbs arteries [15-17]. Some authors also reported an increased incidence of coronary  and aortic  thrombotic involvement in young IBD patients. IBD patients experiencing a VTE episode were generally younger compared to the general population , with the young age of first VTE being associated with a higher risk of recurrence . The overall mortality rate per episode is estimated to be as high as 25% . The risk of TE is estimated to be almost three times higher in males than in females . Some authors reported an increased risk of TE in pregnant IBD women when compared with the non-IBD obstetric population [22,23], but others did not . Generally most of TE occur during active disease, even if a high rate of thrombosis (almost one third) is reported during remission and well controlled disease, supporting the hypothesis of a greater pro-thrombotic tendency in IBD independent of disease activity [25,26]. The incidence of TE also correlates with the extent of the disease, i.e. especially pancolonic involvement in UC or colonic involvement in CD [27,28], and with the presence of complications such as fistulas, abscesses or strictures .
The pathogenesis of thrombosis in IBD is complex and not fully explained. It is thought to be multifactorial as no consistent unifying etiology has been found yet. Numerous investigations have been conducted on major pro-thrombotic genetic predispositions and IBD, but no significant association has been found to explain the increased VTE risk both in UC and CD patients [29-31]. Many reports tried to explain the increased risk of TE in IBD focusing on the different components of the coagulation cascade demonstrating both qualitative and quantitative abnormalities in procoagulant, anticoagulant and fibrinolytic factors, although others could not find any identifiable reason in approximately half IBD patients which developed TE . Finally, interesting results have been found observing that in patients with inherited bleeding disorders (hemophilia A and B, von Willebrand disease) UC and CD occurred less frequently than in general population, giving indirect evidence that vascular thrombosis may be involved in IBD pathogenesis and in the inflammatory process .
Acquired risks factors for thrombosis in IBD
Acquired risks factors for thrombosis in IBD
Central venous catheters
Oral contractive/hormone replacement theraphy
Genetic risks factors for thrombosis in IBD
The most frequent causes of inherited thrombophilia in the general population are the prothrombin G20210A polymorphismfactor and V Leiden, a genetic polymorphism that makes activated factor V relatively resistant to degradation by activated protein C. Less relevant is the C677T polymorphism of methylenetetrahydrofolate reductase (MTHFR) gene that favors hyperhomocysteinemia. These genetic mutations have been studied in IBD population but no significant difference has been found in their incidence in IBD patients when compared to health controls, nor in IBD patients that experienced or not TE [38,39]. An inherited polymorphism (Val34Leu) of factor XIII which protects against thrombosis has been evaluated in IBD patients and no difference has been found versus the general population [40,41]. Finally protein C, protein S and antithrombin deficiencies have also been investigated and they seem to have no increased prevalence among IBD patients independently of previous history of TE .
In conclusion, in spite of the big effort in terms of numerous genetic studies performed, no significant association has been demonstrated to date between genetic factors cause of hyper-coagulability and IBD. Thus, genetics of thrombophilia does not explain the increased TE risk in CD and UC patients, suggesting a most relevant role of acquired factors.
Abnormalities of the coagulation cascade in IBD
Abnormalities in coagulation, anticoagulation and fibrinolytic system in IBD
Plasma coagulation inhibotors
↓ AT III
↑ Factors: Va, VIIa, VIIIa, Xa,XIa, XIIa
Conflicting data about PS and PC
↑ Prothrombin factors 1+2
↑ Thrombin-antithrombin III complex (TAT)
↑ Fibrinopeptide A and B
↓ Factor XIII
Abnormalities of the natural coagulation inhibitors in IBD
A pro-thrombotic condition may result from a decrease in natural anticoagulant factors. The system of natural coagulation inhibitors is composed by antithrombin (AT), protein C (PC) pathway and TF pathway inhibitor (TFPI). AT is a physiological inhibitor of thrombin and FIXa, FXa, FXIa and FXIIa and its activation is triggered by heparin secreted by mast cells or exogenously administered. TFPI is a protein produced by the vascular endothelium and by megakaryocytes, and is an inhibitor of the TF-depending coagulation cascade and a raker of endothelial damage [54,55]. The PC pathway is a complex system which also involves protein S (PS) and several membrane receptors such as TM and endothelial protein C receptor (EPCR). PC is activated, especially if bounded to the EPRC, by the complex thrombin-TM. Once activated, in the presence of the cofactor PS, PC is able to inactivate FVIIIa and FVa and also has pro-fibrinolytic properties by binding PAI-1 [54,56]. See Figure 1 for schematic representation of coagulation cascade and natural anticoagulant system.
Data about the plasma concentration of natural coagulation inhibitors in IBD patients are conflicting: some authors reported no differences in PS [3,57,58] and AT [49,59] levels between IBD patients and controls, whereas others described a decrease in AT, TFPI, PC and PS in active vs inactive disease or vs controls [43,56,57,60]; finally some others found higher levels of PC and PS in IBD patients vs controls . Some studies reported higher concentrations of TM in active CD and UC . It is possible that changes in systemic levels of these factors do not necessarily reflect the local loss of inhibition of coagulation occurring within the enteric mucosa, where a loss of function of natural anticoagulants may occur .
Which seems important to remark is that there is a growing body of evidence that AT and TM are implicated in the inflammatory process. AT, when present at high concentrations , has been demonstrated to reduce the inflammatory response by decreasing leukocyte adhesion (by reducing expression of CD11b/CD18 cell surface receptors), TF and IL6 expression in monocytes and endothelium . Furthermore AT seems to increase endothelial prostacyclin formation and inhibits endothelial pro-inflammatory mediators production by decreasing nuclear factor (NFkB) activation [54,62-64]. TM also seems to affect the course of inflammatory process, apoptosis and endothelial barrier integrity [54,55] and it has been suggested that increased TM levels may be associated with anti-inflammatory properties . Abnormalities of coagulation inhibitors in IBD are summarized in Table 2.
Abnormalities of the fibrinolytic system in IBD
The circulating concentration of the fibrinolytic system’s factors is impaired in UC and CD patients and favors the pro-thrombotic mechanisms. In IBD patients a reduction in fibrinolysis activators (such as tPA) and an increase in inhibitors (such as PAI-1 and TAFI) has been described, inducing a reduced activity of the system [49,70,71]. Recently the activated form of TAFI (TAFIa) has been investigated because of its potential anti-inflammatory properties with recognition of its ability to inactivate anaphylotoxines, C3a, C5a and other pro-inflammatory mediators [72,73]. Moreover a significant correlation has been found in IBD patients between TAFIa, disease activity and inflammatory markers such as CRP, fibrinogen and platelets . Abnormalities of the fibrinolytic system in IBD are summarized in Table 2.
Abnormalities of the endothelium in IBD
Endothelium plays a central role in contributing to the inflammatory process by regulating leukocytes adhesion and transmigration and by the production of cytokines and chemokines. Furthermore it is responsible for the regulation of platelet adhesion and activation, and for the regulation of blood coagulation . Endothelial disfunction has been demonstrated in IBD and markers of its damage such as von Willebrand factor (vWF), EPCR and TM are increased in IBD patients serum and seem to correlate with disease activity [74-77]. The knot seems to be an imbalance between nitric oxide (NO), a vasodilator and anti-aggregant agent, and reactive oxygen species (ROS) formation in the inflamed endothelium . In fact NO production seems to be impaired in chronic inflamed IBD endothelium both from NO synthase 2 (NOS2) deficient transcription  and from induction of NOS competitor arginase by inflammatory citokynes such as IL2 and TNF-alpha . On the other hand, an increased production of ROS has been demonstrated within the inflamed endothelium and it contributes to oxidative stress in vWF molecules leading to the accumulation of ultra-large vWF multimers - because of a reduced sensitivity to ADAMTS-13 proteolytic activity - which are most hemostatically active and favor platelet adhesion and aggregation [36,80].
Endothelium plays a key role in inflammation due to its ability to control the amount and type of leukocytes that transmigrate to the interstitial space and to regulate vascular tone and platelet adhesion and aggregation, thus it directly affects the hemostatic system potentially favoring thrombosis . Which still remains unclear is if the vascular involvement in IBD is a pathogenetic factor or a consequence, inducing amplification of local and systemic inflammation [81,82].
Abnormalities of platelets in IBD
In IBD patients there are quantitative, morphological and qualitative alterations in platelet characteristic. Thrombocytosis and IBD have been first correlated in 1968  and it is now well established that trombocytosis is related to disease activity and severity . Thrombocytosis is considered a non specific response to inflammation which may occur in chronic inflammatory conditions other than IBD , but it has also been proposed that thrombocytosis in UC and CD may reflect an aberration in thrombopoiesis induced by greater plasma levels of thrombopoietin and IL6, which are involved in megakaryocytes maturation process . On the other hand, platelets in IBD patients have smaller mean corpuscular volume (MCV) than in controls , and platelet MCV seems to be smaller during active phases of the disease as compared to remission . MCV has also been demonstrated to be inversely proportional to some inflammation markers levels such as C-reactive protein (CRP) and erythrocyte sedimentation rate (ESR) so that this has been proposed as a marker of disease activity . It has been hypothesized that during active disease platelet agglomerates (platelet-platelet, platelet-leukocyte, platelet-endothelium) - that are found to be elevated in IBD patients  - mainly involve younger platelets with a higher MCV and consequently that would relatively increase the circulating amount of older and smaller platelets . Moreover, platelets in IBD seem to circulate in a chronic activated status and to be more reactive and more sensitive to activation induced by pro-aggregating agents. First of all, platelets have been demonstrated to aggregate in vitro in over 30% of IBD patients, independently of disease severity, compared to none of the healthy controls . This was thought to be a consequence of the inflammatory condition but it has subsequently been demonstrated that platelet aggregates are found in IBD patients but not in other inflammatory diseases, thus being a specific characteristic of IBD . The same author found an increase in surface and serum platelet activation markers such as P-selectin, GP53 and beta-thromboglobulin (beta-TG), whose increase was independent from disease activity so suggesting that once stimulated, platelets may remain chronically activated even during remission phases of the disease [25,91]. In the recent years another piece has come to partially complete the picture. In fact, in CD and UC patients high values - up to 4 times greater than healthy controls - of the surface CD40 ligand (CD40L), an activation markers that allows platelets to interact with a broad of immune and non immune cells with pro inflammatory consequences [25,92], and that acts as an inducer of the TF mediated coagulation cascade  have been detected. Together with its increase on the platelet surface, even the soluble form of CD40L (sCD40L) in IBD patients serum is increased - almost 15 fold compared to controls - as released by such platelets . High levels of sCD40L have been associated with an increased risk of TE . Others reported that in vitro activated platelets may directly increase CD40L expression in intestinal endothelial cells favoring their interaction with numerous immune cells and sustaining chronic inflammation . Recent data reported an increased expression of CD40/CD40L in the intestinal epithelial cells, in particular in samples from inflamed ileal and colonic mucosa from CD and UC patients, whereas that increase was not found in uninvolved intestinal segments . This finding provide, for the first time, a piece of evidence of the interaction between activated platelets and IBD affected intestinal mucosa via the CD40/CD40L pathway . That leads to a key point: platelets could themselves act as inflammatory cells and enhance the inflammatory process in IBD mucosa. One of the first suggestion of the platelet role in intestinal inflammation came from the finding of capillary microthrombi in the mucosa of IBD patients, independently of the severity of inflammation. Those findings were consistently absent in healthy subjects . It has then been suggested that platelet activation occurs in the intestinal mucosa because of the finding of greater platelet aggregates in the mesenteric blood of CD patients . This process has recently been reproduced in vitro using human intestinal microvascular endothelial cells (HIMEC) exposed to IL-1beta to mimic IBD endothelial changes [25,93]. Activated CD40L positive platelets are then thought to enhance themselves intestinal inflammation by the interaction with CD40 positive microvascular endothelium in the intestinal mucosa. That is thought to be the trigger to up-regulation of endothelial IL8 production and adhesion molecule expression (as ICAM-1 and VCAM-1) on the endothelium surface, leading to inflammatory cell, specifically T-cell, recruitment and inflammatory response amplification .
The role of inflammation
Inflammation and coagulation are two crucial systems that are in balance and constantly influence each other . The impact of inflammation on coagulation has been confirmed by several experimental studies showing that inflammatory mechanism shift the hemostatic balance to favor the activation of coagulation [36,54] which, in turn, can also sustain inflammation promoting a vicious circle between chronic inflammation and thrombosis . We have seen above how platelets, endothelium and many components of the coagulation cascade, fibrinolytic system and natural anticoagulant inhibitors are directly involved in the inflammatory process but other considerations need to be done. Many studies reported that tumor necrosis factor alpha (TNF-alpha), CD40L and CRP are able to induce the expression of TF on the leucocytes cell surface, so promoting activation of the intrinsic coagulation pathway [98-100]. On the other hand, natural anticoagulant pathways as the PC pathway and the heparin-AT pathway have been demonstrated to be down-regulated by inflammatory citokynes as TNF-alpha and IL1beta [101,102]. Furthermore, CRP has been shown to inhibit TFPI  and tPA  and to increase the expression of PAI-1  leading to a more procoagulant tendency. Another inflammatory citokyne, IL6, has been shown to have a pro-thrombotic activity by increasing platelet production and enhancing thrombin formation in concert with TNF-alpha [106,107]. Another trigger to the procoagulant profile by TNF-alpha is the down regulation of the expression of anticoagulant TM and EPCR . Recently, homocysteine has been shown to participate to microvascular inflammation by triggering, together with TNF-alpha, the expression of VCAM-1 and MCP-1 on endothelial surface thus leading to an enhanced capacity to recruit T cells and monocytes .
Abnormalities of the immune system in IBD
Anti-phospholipid antibodies (APLA) are a group of pro-thrombotic antibodies including lupus anticoagulant (LAC), anti-cardiolipin antibodies (aCL) and anti-beta-2-glicoprotein-I (anti-beta-2-GPI). APLA may be associated with both venous and arterial thrombosis. IBD patients seem to have higher rates of aCL and anti-beta-2-GPI positivity - with an incidence of 20%-30% for the first and 9% for the latter - compared to general population, but the real association with thrombosis in IBD is still unclear [110,111]. In fact, LAC, aCL and anti-beta-2-GPI levels were similar in IBD patients with or without history of VTE [36,110].
In IBD patients anti-PS antibodies have also been detected, which may cause a reduction in the natural anticoagulant potential but there is still not enough evidence that they play any role in thrombotic risk .
Thrombotic mechanism in IBD patients is complex, multifactorial and not completely understood. Acquired risk factors for thrombosis, often present in IBD patients, only partially explain the increased thrombotic risk in this particular population. No relevant association has been found regarding genetic pro-thrombotic risk factors in UC and CD patients. Moreover, many quantitative and qualitative alterations in single components of cascade factors, fibrinolytic system and natural anticoagulants has been found, but none of them was sufficient per se to explain the increased thromboembolic risk. What seems to be the case is that maintaining the pro-thrombotic tendency in this context is multifactorial, thus coagulation components and their inhibitors, as well as hemostatic relevant cells as platelets and endothelial cells, interact in a context of inflamed mucosa that is chronically activated and contributes to maintain chronic inflammation as well. In turn, inflammatory molecules and cytokines have been demonstrated to imbalance the haemostatic system towards hyper-coagulability. The two complex mechanisms of inflammation and coagulation deeply interact in IBD mucosa amplifying and potentiating each other.
- Bargen J, Barker NW. Extensive arterial and venous thrombosis complicating chronic ulcerative colitis. Arch Intern Med. 1936;58:17–31.Google Scholar
- Miehsler W, Reinisch W, Valic E, Osterode W, Tillinger W, Feichtenschlager T, et al. Is inflammatory bowel disease an indepen- dent and disease specific risk factor for thromboembolism? Gut. 2004;53:542–8.PubMed CentralPubMedGoogle Scholar
- Kume K, Yamasaki M, Tashiro M, Yoshikawa I, Otsuki M. Activations of coagulation and fibrinolysis secondary to bowel inflammation in patients with ulcerative colitis. Intern Med. 2007;46:1323–9.PubMedGoogle Scholar
- Talbot RW, Heppell J, Dozois RR, Beart Jr RW. Vascular complications of inflammatory bowel disease. Mayo Clin Proc. 1986;61:140–5.PubMedGoogle Scholar
- Murthy SK, Nguyen GC. Venous thromboembolism in inflammatory bowel disease: an epidemiological review. Am J Gastroenterol. 2011;106:713–8.PubMedGoogle Scholar
- Yuhara H, Steinmaus C, Corley D, Koike J, Igarashi M, Suzuki T, et al. Meta-analysis: the risk of venous thromboembolism in patients with inflammatory bowel disease. Aliment Pharmacol Ther. 2013;37:953–62.PubMedGoogle Scholar
- Tan VP, Chung A, Yan BP, Gibson PR. Venous and arterial disease in inflammatory bowel disease. J Gastroenterol Hepatol. 2013;28:1095–113.PubMedGoogle Scholar
- Tichelaar YI, Kluin-Nelemans HJ, Meijer K. Infections and inflammatory diseases as risk factors for venous thrombosis. A systematic review. Thromb Haemost. 2012;107:827–37.PubMedGoogle Scholar
- Bernstein CN, Blanchard JF, Houston DS, Wajda A. The incidence of deep venous thrombosis and pulmonary embolism among patients with inflammatory bowel disease: a population-based cohort study. Thromb Haemost. 2001;85:430–4.PubMedGoogle Scholar
- Bernstein CN, Wajda A, Blanchard JF. The incidence of arterial thromboembolic diseases in inflammatory bowel disease: a population-based study. Clin Gastroenterol Hepatol. 2008;6:41–5.PubMedGoogle Scholar
- Umit H, Asil T, Celik Y, Tezel A, Dokmeci G, Tuncbilek N, et al. Cerebral sinus thrombosis in patients with inflammatory bowel disease: A case report. World J Gastroenterol. 2005;11:5404–7.PubMedGoogle Scholar
- Dacha S, Devidi M, Osdmunson E. Budd-Chiari syndrome in a patient with ulcerative colitis and no inherited coagulopathy. World J Hepatol. 2011;3:164–9.PubMed CentralPubMedGoogle Scholar
- Keyser BJ, Hass AN. Retinal vascular disease in ulcerative colitis. Am J Ophthalmol. 1994;118:395–6.PubMedGoogle Scholar
- Hatoum OA, Spinelli KS, Abu-Hajir M, Attila T, Franco J, Otterson MF, et al. Mesenteric venous thrombosis in inflammatory bowel disease. J Clin Gastroenterol. 2005;39:27–31.PubMedGoogle Scholar
- Novotny DA, Rubin RJ, Slezak FA, Porter JA. Arterial thromboembolic complications of inflammatory bowel disease. Report of three cases. Dis Colon Rectum. 1992;35:193–6.PubMedGoogle Scholar
- Levy PJ, Tabares AH, Olin JW. Lower extremity arterial occlusions in young patients with Crohn’s colitis and pre- mature atherosclerosis: Report of six cases. Am J Gastroenterol. 1997;92:494–7.PubMedGoogle Scholar
- Di Fabio F, Obrand D, Satin R, Gordon PH. Intra-abdominal venous and arterial thromboembolism in inflammatory bowel disease. Dis Colon Rectum. 2009;52:336–42.PubMedGoogle Scholar
- Mutlu B, Ermeydan CM, Enç F, Fotbolcu H, Demirkol O, Bayrak F, et al. Acute myocardial infarction in a young woman with severe ulcerative colitis. Int J Cardiol. 2002;83:183–5.PubMedGoogle Scholar
- Novacek G, Haumer M, Schima W, Müller C, Miehsler W, Polterauer P, et al. Aortic mural thrombi in patients with inflammatory bowel disease: re- port of two cases and review of the literature. Inflamm Bowel Dis. 2004;10:430–5.PubMedGoogle Scholar
- Grip O, Svensson PJ, Lindgren S. Inflammatory bowel disease promotes venous thrombosis earlier in life. Scand J Gastroenterol. 2000;35:619–23.PubMedGoogle Scholar
- Novacek G, Weltermann A, Sobala A, Tilg H, Petritsch W, Reinisch W, et al. Inflammatory bowel disease is a risk factor for recurrent venous thromboembolism. Gastroenterology. 2010;139:779–87.PubMedGoogle Scholar
- Nguyen GC, Boudreau H, Harris ML, Maxwell CV. Out- comes of obstetric hospitalizations among women with inflammatory bowel disease in the United States. Clin Gastroenterol Hepatol. 2009;7:329–34.PubMedGoogle Scholar
- Bröms G, Granath F, Linder M, Stephansson O, Elmberg M, Kieler H. Complications from inflammatory bowel disease during pregnancy and delivery. Clin Gastroenterol Hepatol. 2012;10:1246–52.PubMedGoogle Scholar
- Suarez Ferrer C, Veramendoza MI. Amo San Roman L, Gonzalez Lama Y, Calvo Moya M, Garcia Casas M, Abreu Garcia L. Risk of thromboembolic phenomena in patients with inflammatory bowel disease. Gastroenterol Hepatol. 2012;35:634–9.PubMedGoogle Scholar
- Danese S, Papa A, Saibeni S, Repici A, Malesci A, Vecchi M. Inflammation and coagulation in inflammatory bowel disease: The clot thickens. Am J Gastroenterol. 2007;102:174–86.PubMedGoogle Scholar
- Grainge J, West J, Card TR. Venous thromboembolism during active disease and remission in inflammatory bowel disease: a cohort study. Lancet. 2010;375:657–63.PubMedGoogle Scholar
- Solem CA, Loftus EV, Tremaine WJ, Sandborn WJ. Venous thromboembolism in inflammatory bowel disease. Am J Gastroenterol. 2004;99:97–101.PubMedGoogle Scholar
- Nguyen GC, Sam J. Rising prevalence of venous thromboembolism and its impact on mortality among hospitalized inflammatory bowel disease patients. Am J Gastroenterol. 2008;103:2272–80.PubMedGoogle Scholar
- Tsiolakidou G, Koutroubakis IE. Thrombosis and inflammatory bowel disease - the role of genetic risk factors. World J Gastroenterol. 2008;14:4440–4.PubMed CentralPubMedGoogle Scholar
- Bernstein CN, Sargent M, Vos HL, Rosendaal FR. Mutations in clotting factors and inflammatory bowel disease. Am J Gastroenterol. 2007;102:338–43.PubMedGoogle Scholar
- Guédon C, Le Cam-Duchez V, Lalaude O, Ménard JF. Le- rebours E, Borg JY. Prothrombotic inherited abnormalities other than factor V Leiden mutation do not play a role in venous thrombosis in inflammatory bowel disease. Am J Gastroenterol. 2001;96:1448–54.PubMedGoogle Scholar
- Jackson LM, O’Gorman PJ, O’Connell J, Cronin CC, Cotter KP, Shanahan F. Thrombosis in inflammatory bowel disease: Clinical setting, procoagulant profile and factor V Leiden. Q J Med. 1997;90:183–8.Google Scholar
- Thompson NP, Wakefield AJ, Pounder RE. Inherited disorders of coagulation appear to protect against inflammatory bowel disease. Gastroenterology. 1995;108:1011–5.PubMedGoogle Scholar
- Danese S, Sans M, Fiocchi C. Inflammatory bowel disease: The role of environmental factors. Autoimmun Rev. 2004;3:394–400.PubMedGoogle Scholar
- Koutroubakis IE. Therapy insight: Vascular complications in patients with inflammatory bowel disease. Nat Clin Pract Gastroenterol Hepatol. 2005;2:266–72.PubMedGoogle Scholar
- Magro F, Soares JB, Fernandes D. Venous thrombosis and prothrombotic factors in inflammatory bowel disease. World J Gastroenterol. 2014;20(17):4857–72.PubMed CentralPubMedGoogle Scholar
- Oussalah A, Guéant JL, Peyrin-Biroulet L. Meta-analysis: hyperhomocysteinaemia in inflammatory bowel diseases. Aliment Pharmacol Ther. 2011;34:1173–84.PubMedGoogle Scholar
- Vecchi M, Sacchi E, Saibeni S, Meucci G, Tagliabue L, Duca F, et al. Inflammatory bowel diseases are not associated with major hereditary conditions predisposing to thrombosis. Dig Dis Sci. 2000;45:1465–9.PubMedGoogle Scholar
- Mahmood A, Needham J, Prosser J, Mainwaring J, Trebble T, Mahy G, et al. Prevalence of hyperhomocysteinaemia, activated protein C resistance and prothrombin gene mutation in inflammatory bowel disease. Eur J Gastroenterol Hepatol. 2005;17:739–44.PubMedGoogle Scholar
- Saibeni S, Vecchi M, Faioni EM, Franchi F, Rondonotti E, Borsi G, et al. Val34Leu factor XIII polymorphism in Italian patients with inflammatory bowel disease. Dig Liver Dis. 2003;35:32–6.PubMedGoogle Scholar
- Heliö T, Wartiovaara U, Halme L, Turunen UM, Mikkola H, Palotie A, et al. Arg506Gln factor V mutation and Val34Leu factor XIII polymorphism in Finnish patients with inflammatory bowel disease. Scand J Gastroenterol. 1999;34:170–4.PubMedGoogle Scholar
- Chamouard P, Grunebaum L, Wiesel ML, Frey PL, Wittersheim C, Sapin R, et al. Prothrombin fragment 1 + 2 and thrombin-antithrombin III complex as markers of activation of blood coagulation in inflammatory bowel diseases. Eur J Gastroenterol Hepatol. 1995;7:1183–8.PubMedGoogle Scholar
- Chiarantini E, Valanzano R, Liotta AA, Cellai AP, Fedi S, Ilari I, et al. Hemostatic abnormalities in inflammatory bowel disease. Thromb Res. 1996;82:137–46.PubMedGoogle Scholar
- Hudson M, Chitolie A, Hutton RA, Smith MS, Pounder RE, Wakefield AJ. Thrombotic vascular risk factors in inflammatory bowel disease. Gut. 1996;38:733–7.PubMed CentralPubMedGoogle Scholar
- Smith CJ, Haire WD, Kaufman SS, Mack DR. Determination of prothrombin activation fragments in young patients with inflammatory bowel disease. Am J Gastroenterol. 1996;91:1221–5.PubMedGoogle Scholar
- Zezos P, Papaioannou G, Nikolaidis N, Vasiliadis T, Giouleme O, Evgenidis N. Elevated plasma von Willebrand factor levels in patients with active ulcerative colitis reflect endothelial perturbation due to systemic inflammation. World J Gastroenterol. 2005;11:7639–45.PubMedGoogle Scholar
- Lake AM, Stauffer JQ, Stuart MJ. Hemostatic alterations in inflammatory bowel disease: response to therapy. Am J Dig Dis. 1978;23:897–902.PubMedGoogle Scholar
- Chamouard P, Grunebaum L, Wiesel ML, Sibilia J, Coumaros G, Wittersheim C, et al. Significance of diminished factor XIII in Crohn’s disease. Am J Gastroenterol. 1998;93:610–4.PubMedGoogle Scholar
- van Bodegraven AA. Haemostasis in inflammatory bowel diseases: Clinical relevance. Scand J Gastroenterol. 2003;239(suppl):51–62.Google Scholar
- Soendergaard C, Kvist PH, Seidelin JB, Nielsen OH. Tissue-regenerating functions of coagulation factor XIII. J Thromb Haemost. 2013;11:806–16.PubMedGoogle Scholar
- Hayat M, Ariëns RA, Moayyedi P, Grant PJ, O’Mahony S. Coagulation factor XIII and markers of thrombin generation and fibrinolysis in patients with inflammatory bowel disease. Eur J Gastroenterol Hepatol. 2002;14:249–56.PubMedGoogle Scholar
- Diamant M, Tushuizen ME, Sturk A, Nieuwland R. Cellular microparticles: New players in the field of vascular disease? Eur J Clin Invest. 2004;34:392–401.PubMedGoogle Scholar
- Andoh A, Tsujikawa T, Hata K, Araki Y, Kitoh K, Sasaki M, et al. Elevated circulating platelet-derived microparticles in patients with active inflammatory bowel disease. Am J Gastroenterol. 2005;100:2042–8.PubMedGoogle Scholar
- Esmon CT. The interactions between inflammation and coagulation. Br J Haematol. 2005;131:417–30.PubMedGoogle Scholar
- Owczarek D, Cibor D, Glowacki MK, Rodacki T, Mach T. Inflammatory bowel disease: Epidemiology, pathology and risk factors for hyper coagulability. World J Gastroenterol. 2014;20:53–63.PubMed CentralPubMedGoogle Scholar
- Scaldaferri F, Lancellotti S, Pizzoferrato M, De Cristofaro R. Haemostatic system in inflammatory bowel disease: new players in gut inflammation. World J Gastroenterol. 2011;17:594–608.PubMed CentralPubMedGoogle Scholar
- Ghosh S, Mackie MJ, McVerry BA, Galloway M, Ellis A, McKay J. Chronic inflammatory bowel disease, deep-venous thrombosis and antithrombin activity. Acta Haematol. 1983;70:50–3.PubMedGoogle Scholar
- Heneghan MA, Cleary B, Murray M, O’Gorman TA, McCarthy CF. Activated protein C resistance, thrombophilia, and inflammatory bowel disease. Dig Dis Sci. 1998;43:1356–61.PubMedGoogle Scholar
- Yurekli BP, Aksoy DY, Aybar M, Egesel T, Gurgey A, Has- celik G, et al. The search for a common thrombophilic state during the active state of inflammatory bowel disease. J Clin Gastroenterol. 2006;40:809–13.PubMedGoogle Scholar
- Aadland E, Odegaard OR, Røseth A, Try K. Free protein S deficiency in patients with chronic inflammatory bowel disease. Scand J Gastroenterol. 1992;27:957–60.PubMedGoogle Scholar
- Owczarek D, Cibor D, Salapa K, Ciesla A, Glowacki MK, Pocztar H, et al. Anti-inflammatory and anticoagulants properties of the protein C system in inflammatory bowel disease. Pol Arch Med Wewn. 2012;122:209–16.PubMedGoogle Scholar
- Uchiba M, Okajima K, Murakami K. Effects of various doses of antithrombin III on endotoxin-induced endothelial cell in- jury and coagulation abnormalities in rats. Thromb Res. 1998;89:233–41.PubMedGoogle Scholar
- Oelschläger C, Römisch J, Staubitz A, Stauss H, Leithäuser B, Tillmanns H, et al. Antithrombin III inhibits nuclear factor kappaB activation in human monocytes and vascular endothelial cells. Blood. 2002;99:4015–20.PubMedGoogle Scholar
- Uchiba M, Okajima K, Kaun C, Wojta J, Binder BR. Inhibi- tion of the endothelial cell activation by antithrombin in vitro. Thromb Haemost. 2004;92:1420–7.PubMedGoogle Scholar
- Hoylaerts M, Rijken DC, Lijnen HR, Collen D. Kinetics of the activation of plasminogen by human tissue plasminogen activator. Role of fibrin. J Biol Chem. 1982;257:2912–9.PubMedGoogle Scholar
- Lijnen HR. Plasmin and matrix metalloproteinases in vascular remodeling. Thromb Haemost. 2001;86:324–33.PubMedGoogle Scholar
- Chmielewska J, Rånby M, Wiman B. Kinetics of the inhibi- tion of plasminogen activators by the plasminogen-activator inhibitor. Evidence for “second-site” interactions. Biochem J. 1988;251:327–32.PubMed CentralPubMedGoogle Scholar
- Collen D. Identification and some properties of a new fast-reacting plasmin inhibitor in human plasma. Eur J Biochem. 1976;69:209–16.PubMedGoogle Scholar
- Mosnier LO, Bouma BN. Regulation of fibrinolysis by thrombin activatable fibrinolysis inhibitor, an unstable carboxypeptidase B that unites the pathways of coagulation and fibrinolysis. Arterioscler Thromb Vasc Biol. 2006;26:2445–53.PubMedGoogle Scholar
- Gris JC, Schved JF, Raffanel C, Dubois A, Aguilar-Martinez P, Arnaud A, et al. Impaired fibrinolytic capacity in patients with inflammatory bowel disease. Thromb Haemost. 1990;63:472–5.PubMedGoogle Scholar
- Saibeni S, Bottasso B, Spina L, Bajetta M, Danese S, Gasbarrini A, et al. Assessment of thrombin-activatable fibrinolysis inhibitor (TAFI) plasma levels in inflammatory bowel diseases. Am J Gastroenterol. 2004;99:1966–70.PubMedGoogle Scholar
- Koutroubakis IE, Sfiridaki A, Tsioulakidou G, Coucouctsi C, Theodoropoulou A, Kouroumalis EA. Plasma thrombin-activatable fibrinolysis inhibitor and plasminogen activator inhibitor-1 levels in inflammatory bowel disease. Eur J Gastroenterol Hepatol. 2008;20:912–6.PubMedGoogle Scholar
- Owczarek D, Undas A, Foley JH, Nesheim ME, Jablonski K, Mach T. Activated thrombin activatable fibrinolysis inhibitor (TAFIa) is associated with inflammatory markers in inflammatory bowel disease TAFIa levels in patients with IBD. J Crohns Colitis. 2012;6:13–20.PubMedGoogle Scholar
- Stevens TR, James JP, Simmonds NJ, McCarthy DA, Laurenson IF, Maddison PJ, et al. Circulating von Willebrand factor in inflammatory bowel disease. Gut. 1992;33:502–6.PubMed CentralPubMedGoogle Scholar
- Boehme MW, Autschbach F, Zuna I, Scherbaum WA, Stange E, Raeth U, et al. Elevated serum levels and reduced immunohistochemical expression of thrombomodulin in active ulcerative colitis. Gastroenterology. 1997;113:107–17.PubMedGoogle Scholar
- Meucci G, Pareti F, Vecchi M, Saibeni S, Bressi C, de Franchis R. Serum von Willebrand factor levels in patients with inflammatory bowel disease are related to systemic inflammation. Scand J Gastroenterol. 1999;34:287–90.PubMedGoogle Scholar
- Papa A, Scaldaferri F, Danese S, Guglielmo S, Roberto I, Bonizzi M, et al. Vascular involvement in inflammatory bowel disease: pathogenesis and clinical aspects. Dig Dis. 2008;26:149–55.PubMedGoogle Scholar
- Hatoum OA, Binion DG, Otterson MF, Gutterman DD. Acquired microvascular dysfunction in inflammatory bowel disease: Loss of nitric oxide-mediated vasodilation. Gastroenterology. 2003;125:58–69.PubMedGoogle Scholar
- Horowitz S, Binion DG, Nelson VM, Kanaa Y, Javadi P, Lazarova Z, et al. Increased arginase activity and endothelial dysfunction in human inflammatory bowel disease. Am J Physiol Gastrointest Liver Physiol. 2007;292:G1323–36.PubMedGoogle Scholar
- Lancellotti S, De Filippis V, Pozzi N, Peyvandi F, Palla R, Rocca B, et al. Formation of methionine sulfoxide by peroxynitrite at position 1606 of von Willebrand factor inhibits its cleavage by ADAMTS-13: A new prothrombotic mechanism in diseases associated with oxidative stress. Free Radic Biol Med. 2010;48:446–56.PubMedGoogle Scholar
- Wakefield AJ, Sawyerr AM, Dhillon AP, Pittilo RM, Rowles PM, Lewis AA, et al. Pathogenesis of Crohn’s disease: Multifocal gastrointestinal infarction. Lancet. 1989;2:1057–62.PubMedGoogle Scholar
- Binion DG, West GA, Volk EE, Drazba JA, Ziats NP, Petras RE, et al. Acquired increase in leucocyte binding by intestinal microvascular endothelium in inflammatory bowel disease. Lancet. 1998;352:1742–6.PubMedGoogle Scholar
- Morowitz DA, Allen LW, Kirsner JB. Thrombocytosis in chronic inflammatory bowel disease. Ann Intern Med. 1968;68:1013–21.PubMedGoogle Scholar
- Talstad I, Rootwelt K, Gjone E. Thrombocytosis in ulcerative colitis and Crohn’s disease. Scand J Gastroenterol. 1973;8:135–8.PubMedGoogle Scholar
- Heits F, Stahl M, Ludwig D, Stange EF, Jelkmann W. Elevated serum thrombopoietin and interleukin-6 concentrations in thrombocytosis associated with inflammatory bowel disease. J Interferon Cytokine Res. 1999;19:757–60.PubMedGoogle Scholar
- Jaremo P, Sandberg-Gertzen H. Platelet density and size in inflammatory bowel disease. Thromb Haemost. 1996;75:560–1.PubMedGoogle Scholar
- Kapsoritakis AN, Koukourakis MI, Sfiridaki A, Potamianos SP, Kosmadaki MG, Koutroubakis IE, et al. Mean platelet volume: A useful marker of inflammatory bowel disease activity. Am J Gastroenterol. 2001;96:776–81.PubMedGoogle Scholar
- Irving PM, Macey MG, Shah U, Webb L, Langmead L, Rampton DS. Formation of platelet-leukocyte aggregates in inflammatory bowel disease. Inflamm Bowel Dis. 2004;10:361–72.PubMedGoogle Scholar
- Vizioli L, Muscari S, Muscari A. The relationship of mean platelet volume with the risk and prognosis of cardiovascular diseases. Int J Clin Pract. 2009;63:1509–15.PubMedGoogle Scholar
- Webberley MJ, Hart MT, Melikian V. Thromboembolism in inflammatory bowel disease: Role of platelets. Gut. 1993;34:247–51.PubMed CentralPubMedGoogle Scholar
- Collins CE, Cahill MR, Newland AC, Rampton DS. Platelets circulate in an activated state in inflammatory bowel disease. Gastroenterology. 1994;106:840–5.PubMedGoogle Scholar
- Danese S, Fiocchi C. Platelet activation and the CD40/CD40L pathway: mechanisms and implications for human disease. Crit Rev Immunol. 2005;25:103–22.PubMedGoogle Scholar
- Danese S, Katz J, Saibeni S, Papa A, Gasbarrini A, Vecchi M, et al. Activated platelets are the source of elevated levels of soluble CD40 ligand in the circulation of inflammatory bowel disease patients. Gut. 2003;52:1435–41.PubMed CentralPubMedGoogle Scholar
- Danese S, Scaldaferri F, Papa A, Pola R, Gasbarrini A, Sgambato A, et al. CD40L-positive platelets induce CD40L expression de novo in endothelial cells: adding a loop to microvascular inflammation. Arterioscler Thromb Vasc Biol. 2004;24:e162.PubMedGoogle Scholar
- Borcherding F, Nitschke M, Hundorfean G, Rupp J, von Smolinski D, Bieber K, et al. The CD40-CD40L pathway contributes to the proinflammatory function of intestinal epithelial cells in inflammatory bowel disease. Am J Pathol. 2010;176:1816–27.PubMed CentralPubMedGoogle Scholar
- Dhillon AP, Anthony A, Sim R, Wakefield AJ, Sankey EA, Hudson M, et al. Mucosal capillary thrombi in rectal biopsies. Histopathology. 1992;21:127–33.PubMedGoogle Scholar
- Collins CE, Rampton DS, Rogers J, Williams NS. Platelet aggregation and neutrophil sequestration in the mesenteric circulation in inflammatory bowel disease. Eur J Gastroenterol Hepatol. 1997;9:1213–7.PubMedGoogle Scholar
- Cermak J, Key NS, Bach RR, Balla J, Jacob HS, Vercellotti GM. C-reactive protein induces human peripheral blood monocytes to synthesize tissue factor. Blood. 1993;82:513–20.PubMedGoogle Scholar
- Parry GC, Mackman N. NF-κB Mediated Transcription in Human Monocytic Cells and Endothelial Cells. Trends Cardiovasc Med. 1998;8:138–42.PubMedGoogle Scholar
- Lindmark E, Tenno T, Siegbahn A. Role of platelet P-selectin and CD40 ligand in the induction of monocytic tissue factor expression. Arterioscler Thromb Vasc Biol. 2000;20:2322–8.PubMedGoogle Scholar
- Klein NJ, Shennan GI, Heyderman RS, Levin M. Alteration in glycosaminoglycan metabolism and surface charge on hu- man umbilical vein endothelial cells induced by cytokines, endotoxin and neutrophils. J Cell Sci. 1992;102(Pt 4):821–32.PubMedGoogle Scholar
- Fukudome K, Esmon CT. Identification, cloning, and regulation of a novel endothelial cell protein C/activated protein C receptor. J Biol Chem. 1994;269:26486–91.PubMedGoogle Scholar
- Chen Y, Wang J, Yao Y, Yuan W, Kong M, Lin Y, et al. CRP regulates the expression and activity of tissue factor as well as tissue factor pathway inhibitor via NF-kappaB and ERK 1/2 MAPK pathway. FEBS Lett. 2009;583:2811–8.PubMedGoogle Scholar
- Singh U, Devaraj S, Jialal I. C-reactive protein decreases tissue plasminogen activator activity in human aortic endothelial cells: evidence that C-reactive protein is a procoagulant. Arterioscler Thromb Vasc Biol. 2005;25:2216–21.PubMedGoogle Scholar
- Chen C, Nan B, Lin P, Yao Q. C-reactive protein increases plasminogen activator inhibitor-1 expression in human endothelial cells. Thromb Res. 2008;122:125–33.PubMed CentralPubMedGoogle Scholar
- van der Poll T, Büller HR, ten Cate H, Wortel CH, Bauer KA, van Deventer SJ, et al. Activation of coagulation after administration of tumor necrosis factor to normal subjects. N Engl J Med. 1990;322:1622–7.PubMedGoogle Scholar
- Stouthard JM, Levi M, Hack CE, Veenhof CH, Romijn HA, Sauerwein HP, et al. Interleukin-6 stimulates coagulation, not fibrinolysis, in humans. Thromb Haemost. 1996;76:738–42.PubMedGoogle Scholar
- Van de Wouwer M, Collen D, Conway EM. Thrombomodulin-protein C-EPCR system: integrated to regulate coagulation and inflammation. Arterioscler Thromb Vasc Biol. 2004;24:1374–83.PubMedGoogle Scholar
- Danese S, Sgambato A, Papa A, Scaldaferri F, Pola R, Sans M, et al. Homocysteine triggers mucosal microvascular activation in inflammatory bowel disease. Am J Gastroenterol. 2005;100:886–95.PubMedGoogle Scholar
- Koutroubakis IE, Petinaki E, Anagnostopoulou E, Kritikos H, Mouzas IA, Kouroumalis EA, et al. Anti-cardiolipin and anti-beta2-glycoprotein I antibodies in patients with inflammatory bowel disease. Dig Dis Sci. 1998;43:2507–12.PubMedGoogle Scholar
- Koutroubakis IE. Role of thrombotic vascular risk factors in inflammatory bowel disease. Dig Dis. 2000;18:161–7.PubMedGoogle Scholar
- Saibeni S, Vecchi M, Valsecchi C, Faioni EM, Razzari C, de Franchis R. Reduced free pro- tein S levels in patients with inflammatory bowel disease: Prevalence, clinical relevance, and role of anti-protein S antibodies. Dig Dis Sci. 2001;46:637–43.PubMedGoogle Scholar
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