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Increased thrombin generation is linked to first hepatic decompensation in patients with compensated cirrhosis
Alberto Zanetto1,2, Kymentie Ferdinande1,2, Elisa Pinto1,2
1Department of Surgery, Oncology and Gastroenterology, University of Padova, Padova, Italy.
Insights
Increased thrombomodulin-modified thrombin generation (TM-TG) is linked to the first hepatic decompensation event in patients with compensated cirrhosis. This finding suggests TM-TG may be a valuable biomarker for predicting disease progression in cirrhosis patients.
Area of Science:
- Hepatology
- Coagulation Science
- Internal Medicine
Background:
- Coagulation alterations are implicated in the progression of cirrhosis.
- Understanding predictors of hepatic decompensation is crucial for patient management.
Purpose of the Study:
- To investigate the association between increased thrombomodulin-modified thrombin generation (TM-TG) and the first occurrence of hepatic decompensation in patients with compensated cirrhosis.
Main Methods:
- Retrospective analysis of 171 patients with compensated cirrhosis.
- Measurement of TM-TG at enrollment.
- Time-to-event analyses using Cox and Fine-Gray models to assess the primary endpoint: first hepatic decompensation.
Main Results:
- Higher TM-TG levels (ETP-TM and ETP ratio >0.80) were independently associated with an increased risk of first hepatic decompensation.
- Patients who decompensated had lower platelet counts, higher MELD scores, and more frequent large varices.
- Multivariable analyses confirmed TM-TG as an independent predictor, even after adjusting for MELD score, varices, and platelet count.
Conclusions:
- Increased TM-TG is associated with the first hepatic decompensation in compensated cirrhosis.
- TM-TG may serve as a potential biomarker for predicting cirrhosis progression.
- Further validation in prospective studies is recommended.
Background:
Coagulation alterations may contribute to cirrhosis progression. We explored whether increased thrombomodulin-modified thrombin generation (TM-TG) was associated with first hepatic decompensation in compensated cirrhosis.
Methods:
We retrospectively analyzed a prospectively collected cohort of 171 patients with compensated cirrhosis. TM-TG was measured at enrolment. The primary endpoint was the first hepatic decompensation. Time-to-event analyses were performed using cause-specific Cox models, with Fine-Gray models as a complementary competing risk approach.
Results:
Median age was 66 years, 66.7% were male, and 90.1% were Child-Pugh A; 70 (40.9%) patients had large varices. During a median follow-up of 3.3 years, 37 patients (21.6%) developed first hepatic decompensation. The 1-year, 2-year, 3-year, and 5-year cumulative incidences were 4.7%, 11.5%, 17.8%, and 31.5%, respectively. Compared with patients who remained compensated, those who developed first hepatic decompensation had lower platelet count (56 vs. 111 × 109/L), higher MELD score (9.97 vs. 8.93), more frequent large varices (73% vs. 36%), higher ETP-TM (822 vs. 752 nM min), and more often an ETP ratio >0.80 (70.3% vs. 44.0%) (all p<0.05). In multivariable analyses, higher ETP-TM remained independently associated with first hepatic decompensation in models including MELD (HR 1.27; sHR 1.30), large varices (HR 1.24; sHR 1.30), and platelet count (HR 1.29; sHR 1.31) (all p<0.05). Similarly, an ETP ratio >0.80 was independently associated with first hepatic decompensation in models including MELD (HR 2.81; sHR 2.9), large varices (HR 2.96; sHR 2.7), and platelet count (HR 3.41; sHR 3.32) (all p<0.05).
Conclusion:
In compensated cirrhosis, increased TM-TG is associated with the first hepatic decompensation, although confirmation in prospective studies is warranted.
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