| Title: | Coagulation factor XII haploinsufficiency is protective against venous thromboembolism in a population-scale multidimensional analysis |
| Journal: | Nature Communications |
| Published: | 1 Sep 2025 |
| Pubmed: | https://pubmed.ncbi.nlm.nih.gov/40890099/ |
| DOI: | https://doi.org/10.1038/s41467-025-62789-5 |
Publication 19603
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Abstract
Coagulation factor XII has been identified as a potential drug target that could prevent thrombosis without increasing the risk of bleeding. However, human data to support the development of factor XII-directed therapeutics are lacking. To assess the role of factor XII in venous thromboembolism, we examine genetic variation in the coding region of the F12 locus across 703,745 participants in the UK Biobank and NIH All of Us biorepositories. We find that heterozygous carriers of nonsense, frameshift, and essential splice site variants in F12 are protected against venous thromboembolism without an increased risk of bleeding or infection. We also show that F12 variant carriers generally experience a quantitative (type I) defect in circulating factor XII levels, though a subset of participants was also identified with possible qualitative (type II) deficiency. In vitro plasma-based thrombin generation is reduced at factor XII concentrations reflective of those seen in F12 variant carriers. We also show that F12 heterozygous mice are protected against venous thromboembolism and display an intermediate phenotype between wild-type and F12-null animals. We conclude that heterozygous loss of F12 represents a haploinsufficient state characterized by protection against venous thromboembolism and that therapeutically inhibiting factor XII is likely to be safe and effective.</p>
17 Keywords
- Adult
- Aged
- Animals
- Factor XII
- Factor XII Deficiency
- Female
- Haploinsufficiency
- Heterozygote
- Humans
- Male
- Mice
- Mice, Inbred C57BL
- Mice, Knockout
- Middle Aged
- Thrombin
- United Kingdom
- Venous Thromboembolism
21 Authors
- Amelia K. Haj
- David S. Paul
- Sean J. Jurgens
- Harish Eswaran
- Lu-Chen Weng
- Justine Ryu
- Alfonso Rodriguez Espada
- Sharjeel Chaudhry
- Louis M. Feingold
- Kristen Burke
- Satoshi Koyama
- Xin Wang
- Joyce Francis
- Seung Hoan Choi
- Nigel Mackman
- Wolfgang Bergmeier
- Alex Burgin
- Joel T. Rämö
- Patrick T. Ellinor
- Steven P. Grover
- Pavan K. Bendapudi
1 Application
| Application ID | Title |
|---|---|
| 17488 | Understanding the Genetic Basis of Cardiac Arrhythmias |
Enabling scientific discoveries that improve human health