Genetic factors in blood pressure

US10697017B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10697017-B2
Application numberUS-201214367510-A
CountryUS
Kind codeB2
Filing dateDec 21, 2012
Priority dateDec 23, 2011
Publication dateJun 30, 2020
Grant dateJun 30, 2020

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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Abstract

Official abstract text for this publication.

The invention describes epistatic interactions between single nucleotide polymorphisms on genes associated with blood pressure and provides an application for their use in a method to determine an individual's susceptibility to hypertension and hence whether anti-hypertensive treatment will be beneficial for said individual. In addition gene expression levels are also linked to blood pressure and may also be used to determine susceptibility to hypertension.

First claim

Opening claim text (preview).

We claim: 1. A method of treating an individual predisposed to high blood pressure comprising: (a) obtaining a biological sample from the individual, wherein the individual has not been treated with antihypertensive drug therapy; (b) determining whether a rs5355C>T single nucleotide polymorphism in the SELE gene is present or absent in the biological sample by contacting the biological sample with a nucleic acid probe that hybridizes to the rs5355C>T single nucleotide polymorphism, wherein the rs5355C>T single nucleotide polymorphism is determined to be present; (c) determining whether a rs6046G>A single nucleotide polymorphism in the F7 gene is present or absent in the biological sample by contacting the biological sample with a nucleic acid probe that hybridizes to the rs6046G>A single nucleotide polymorphism, wherein the rs6046G>A single nucleotide polymorphism is determined to be present; (d) after said determining of (b) and (c), determining the individual is predisposed to high blood pressure; and (e) administering to the individual determined to have both the rs5355C>T and rs6046G>A single nucleotide polymorphism an anti-hypertensive therapy selected from the group consisting of a calcium channel blocker, renin-angiotensin system inhibitor, diuretic, adrenergic receptor antagonist, aldosterone antagonist, vasodilator, and alpha-2 agonist. 2. The method of claim 1 , wherein the biological sample of (a) is selected from the group consisting of whole blood, serum, plasma, urine, saliva, tissue sample, and hair. 3. The method of claim 1 , wherein said determining of (b) and (c) is conducted with an assay selected from among DNA microarray, polymerase chain reaction, and fluorescent in-situ hybridization.

Assignees

Inventors

Classifications

  • Polymorphic or mutational markers · CPC title

  • Pharmacogenomics, i.e. genetic variability in individual responses to drugs and drug metabolism · CPC title

  • C12Q1/6883Primary

    for diseases caused by alterations of genetic material · CPC title

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What does patent US10697017B2 cover?
The invention describes epistatic interactions between single nucleotide polymorphisms on genes associated with blood pressure and provides an application for their use in a method to determine an individual's susceptibility to hypertension and hence whether anti-hypertensive treatment will be beneficial for said individual. In addition gene expression levels are also linked to blood pressure a…
Who is the assignee on this patent?
Randox Laboratories Ltd
What technology area does this patent fall under?
Primary CPC classification C12Q1/6883. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jun 30 2020 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).