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US 11,535,894 B2Granted
Method and kit for predicting the risk of deep vein thrombosis and pulmonary embolism
AssigneeGene Gender S.R.L.
InventorsGoranka Tanackovic Abbas-Terki, Joëlle Michaud Schutz, Thierry Daniel Pache
Life of this patent
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Abstract
Specific single nucleotide polymorphisms (SNPs) in the human genome, and their association with deep vein thrombosis (DVT) and related pathologies, such as pulmonary embolism (PE).
Claims6
A method for identifying if a woman subject undergoing a change in hormone levels is at risk of developing a blood clotting disease, the method comprising:
- determining, in a sample from said woman subject, genotyping data including the single nucleotide polymorphisms of rs1799853 (SEQ ID NO:
- 1) and rs4379368 (SEQ ID NO:
- 2), wherein the presence of allele T in rs1799853 (SEQ ID NO:
- 1) and allele T in rs4379368 (SEQ ID NO:
- 2) in heterozygous or homozygous form indicates that said woman subject has an increased risk of developing a blood clotting disease;
- and
- administering an effective amount of a compound adapted to the prevention of the blood clotting disease to the woman subject based on the risk for developing a blood clotting disease,
- wherein the blood clotting disease is selected from the group consisting of deep vein thrombosis, pulmonary embolism, vein thrombosis, and arterial thrombosis.
5 more elements
Dependencies are inferred from the claim text.