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Endoscopic activity, tissue factor and Crohn's disease: findings in clinical remission patients
Adriana Ribas Andrade1, Tania Rubia Flores da Rocha1, Carmen Lucia Ortiz-Agostinho1
1Gastroenterology, Laboratório de Gastroenterologia Clínica e Experimental (LIM 07), University of Sao Paulo School of Medicine, Sao Paulo, Brazil.
Insights
Crohn's disease patients with endoscopic activity show higher tissue factor levels, indicating coagulation activation. Further research is needed to validate thromboprophylaxis for these patients.
Area of Science:
- Gastroenterology
- Hematology
- Immunology
Background:
- Crohn's disease (CD) is linked to increased risk of thromboembolic events (TE).
- Subclinical inflammation in CD patients may contribute to TE risk.
- Endoscopic activity (EA) in clinically remissed CD patients warrants investigation for its impact on coagulation.
Purpose of the Study:
- To evaluate the correlation between endoscopic activity (EA) and coagulation profiles in Crohn's disease (CD) patients.
- To assess if EA in clinically remissed CD patients influences markers of coagulation activation.
- To identify potential prothrombotic states in CD patients with varying degrees of endoscopic inflammation.
Main Methods:
- 164 consecutive CD patients in clinical remission (CDAI < 150) were divided into EA (SES-CD ≥ 7) and endoscopic remission (ER) (SES-CD ≤ 2) groups.
- 75 patients were in the EA group, 89 in the ER group, and 50 healthy individuals served as controls.
- Coagulation markers including tissue factor (TF), factor VIII (FVIII), thrombomodulin (TM), ADAMTS-13, von Willebrand factor (VWF), and endogenous thrombin potential (ETP) were analyzed.
Main Results:
- Mean plasma TF activity was significantly higher in the EA group (127 pM) compared to ER (103 pM) and controls (84 pM).
- VWF:Ag, VWF/ADAMTS-13, FVIII, and TM levels were elevated in CD patients (both EA and ER groups) compared to controls, but not significantly different between EA and ER groups.
- Endogenous thrombin potential (ETP) remained consistent across all three groups.
Conclusions:
- Endoscopic activity in clinically remissed CD patients is associated with endothelial lesions and increased tissue factor exposure.
- This leads to activation of the coagulation cascade in CD patients with EA.
- Further investigation is recommended to validate thromboprophylaxis strategies for CD patients with endoscopic activity.
Background:
As Crohn's disease (CD) is associated with a high risk of thromboembolic events (TE), including patients with subclinical inflammation, we aim to evaluate the correlation between the impact of endoscopic activity (EA) in the coagulation profiling of CD patients while in clinical remission.
Methods:
From 164 consecutive CD patients included in clinical remission [Crohn's disease activity index (CDAI) < 150], 75 were in the EA group [Simplified Endoscopic Score for CD (SES-CD) ⩾ 7], 89 were in the endoscopic remission (ER) group (SES-CD ⩽ 2), and 50 were included as healthy controls in the study. Blood samples were analyzed for tissue factor (TF), factor VIII (FVIII), thrombomodulin (TM), ADAMTS-13, von Willebrand factor (VWF), and endogenous thrombin potential (ETP), as well as collecting data regarding risk factors for TE and CD profile.
Results:
Mean plasma TF activity showed significantly higher levels in the EA group when compared with the ER and control groups (127 pM versus 103 pM versus 84 pM; p = 0.001), although the VWF:Ag (160% versus 168% versus 110%; p = 0.001), VWF/ADAMTS-13 (191 versus 219 versus 138; p = 0.003), FVIII (150% versus 144% versus 90%; p = 0.001) and TM (5.13 ng/ml versus 4.91 ng/mL versus 3.81 ng/ml; p < 0.001) were only increased in CD regardless of EA status when compared with controls. Lastly, ETP with and without TM remained the same in all three groups.
Conclusions:
CD patients in clinical remission with EA present endothelial lesion inducing TF exposure and subsequent coagulation cascade activation. Recommended thromboprophylaxis for EA outpatient subgroups will require additional investigation in order to be validated.
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