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Updated: Jan 2, 2026

An In Vitro Batch-culture Model to Estimate the Effects of Interventional Regimens on Human Fecal Microbiota
Published on: July 31, 2019
The intestinal microbiome potentially affects thrombin generation in human subjects
Yassene Mohammed1,2,3, Ruud S Kootte4, Wil F Kopatz4
1Center for Proteomics and Metabolomics, Leiden University Medical Center, Leiden, the Netherlands.
Fecal microbiota transplant (FMT) from healthy donors modestly suppressed thrombin generation in metabolic syndrome patients. This suggests the gut microbiome composition may influence human coagulation, warranting further research into its clinical implications.
Area of Science:
- Gastroenterology
- Hematology
- Microbiology
Background:
- The intestinal microbiome's role in arterial thrombosis is known, but its involvement in venous thrombosis, primarily driven by plasma coagulation, remains unestablished.
- This study investigates the potential impact of intestinal microbiome composition on human coagulation.
Purpose of the Study:
- To determine if altering the intestinal microbiome composition affects coagulation in patients with metabolic syndrome.
- To explore the relationship between gut microbiota and thrombin generation.
Main Methods:
- Healthy donor fecal microbiota transplant (FMT) was administered to 35 metabolic syndrome patients in a blinded, randomized controlled trial.
- Thrombin generation was measured using calibrated thrombinography, and plasma coagulation proteins were quantified via targeted mass spectrometry.
Main Results:
- Healthy donor FMT significantly prolonged the thrombinography lag time (P = .039).
- Unsupervised analysis indicated a general downregulation of coagulation-related proteins in patients responding metabolically to healthy donor FMT.
Conclusions:
- A single healthy donor FMT demonstrated a modest suppression of thrombin generation onset in metabolic syndrome patients.
- These findings provide initial proof-of-principle for the gut microbiota's influence on human coagulation and suggest potential clinical implications.
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