# A propensity score-matched study including 250,000 patients with Factor V Leiden shows significantly increased mortality in comparison with individuals without thrombophilia

**Authors:** Moritz Hertel, Max Heiland, Susanne Nahles, Saskia Preissner, Robert Preissner

PMC · DOI: 10.1016/j.puhip.2026.100751 · Public Health in Practice · 2026-02-16

## TL;DR

A large study found that people with Factor V Leiden, a blood clotting disorder, have higher mortality rates, especially young women.

## Contribution

This is the first large-scale real-world study to show a significant link between Factor V Leiden and increased all-cause mortality.

## Key findings

- Factor V Leiden is strongly associated with venous thromboembolism and all-cause mortality.
- Young females with Factor V Leiden face a significantly higher mortality risk compared to older females.
- Survival probabilities were consistently lower in Factor V Leiden-positive patients across all age and sex subgroups.

## Abstract

Factor V Leiden (FVL) is a common inherited thrombophilia that increases the risk of venous thromboembolism (VTE). However, its effect on all-cause mortality remains uncertain, and previous studies yielded conflicting results.

To assess the association between FVL and all-cause mortality using a large international database, including age- and sex-stratified analyses.

Retrospective propensity score-matched cohort study using real-world electronic health records.

We analyzed electronic health records from the TriNetX Global Health Research Network, comparing 241,572 patients with FVL to 20,779,115 patients without thrombophilia. One-to-one propensity score matching for age was applied. Incidences of VTE and all-cause mortality were compared over a 19-year follow-up. Subgroup analyses were performed for female patients and three age categories: <20, 20–50, and >50 years.

FVL was significantly associated with both VTE (OR: 9.325; 95% CI: 9.109–9.546) and all-cause mortality (OR: 1.423; 95% CI: 1.396–1.451). The mortality risk was particularly elevated in young females (<20 years: OR: 9.681; 20–50 years: OR: 2.345) and attenuated in older females (>50 years: OR: 1.432). Kaplan-Meier analyses showed significantly reduced survival probabilities in FVL-positive patients across all subgroups.

This large-scale real-world study indicates that FVL is not only a major risk factor for thrombosis but also associated with increased all-cause mortality—particularly among young women. These findings may have implications for screening and risk stratification in selected populations.

## Linked entities

- **Diseases:** venous thromboembolism (MONDO:0005399)

## Full-text entities

- **Genes:** PROC (protein C, inactivator of coagulation factors Va and VIIIa) [NCBI Gene 5624] {aka APC, PC, PROC1, THPH3, THPH4}, F5 (coagulation factor V) [NCBI Gene 2153] {aka FVL, PCCF, RPRGL1, THPH2, fV}, LYPD4 (LY6/PLAUR domain containing 4) [NCBI Gene 147719] {aka SMR}
- **Diseases:** pulmonary embolism (MESH:D011655), inherited thrombophilia (MESH:C540694), thrombophilia (MESH:D019851), Venous thrombosis (MESH:D020246), Thrombosis (MESH:D013927), VTE (MESH:D054556), death (MESH:D003643)
- **Chemicals:** estrogen-containing contraceptives (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** Arg506Gln

## Full text

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## References

9 references — full list in the complete paper: https://tomesphere.com/paper/PMC12926590/full.md

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Source: https://tomesphere.com/paper/PMC12926590