IP Library Granted Patent US 11,788,144
Granted Patent B2
US 11,788,144 · App. 17/403,024 · Granted Oct 17, 2023

Methods of identifying and treating a person having a predisposition to or afflicted with a cardiometabolic disease

Inventors: Benjamin Levine Ebert (Brookline, MA); Siddhartha Jaiswal (Cambridge, MA); Sekar Kathiresan (Newton, MA)
Assignees: The Brigham and Women's Hospital, Inc.; The General Hospital Corporation
C12Q1/6883C12Q1/6886C12Q2600/156C12Q2600/158G01N33/68G01N2800/32
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Quick Facts
Patent No.
US 11,788,144
App. No.
17/403,024
Granted
Oct 17, 2023
Kind
B2
Abstract

The invention relates to method for identifying and selecting a subject with increased risk of developing a cardiometabolic disease and optionally, providing a personalized medicine method, which may involve sequencing at least part of a genome of one or more cells in a blood sample of the subject and identifying from the sequencing one or more mutations in one or more somatic mutations.

Claims (15)

1. A method of treating or preventing coronary heart disease (CHD) in a human subject, comprising the steps of:

(a) sequencing at least part of a genome of one or more cells from a blood sample of the subject, wherein the at least part of said genome comprises a TET2 gene,

(b) detecting a loss-of-function mutation in the TET2 gene selected from a frameshift mutation and a nonsense mutation; and

(c) administering a lipid modifying medicine to the subject.

2. The method according to claim 1 , wherein the one more cells in the blood sample are hematopoietic stem cells (HSCs), committed myeloid progenitor cells having long term self-renewal capacity or mature lymphoid cells having long term self-renewal capacity.

3. The method according to claim 1 , wherein the sequencing is whole exome sequencing (WES).

4. The method according to claim 1 , wherein the subject also exhibits one or more risk factors of being a smoker, having a high level of total cholesterol or having high level of high-density lipoprotein (HDL).

5. The method of claim 1 , wherein the lipid-modifying medicine is a statin.

6. The method of claim 1 , wherein the lipid-modifying medicine is a PCSK9 inhibitor.

7. The method of claim 6 , wherein the PCSK9 inhibitor is a monoclonal antibody.

8. A method of treating or preventing CHD in a human subject, wherein the genome of a blood cell in said subject comprises a loss of function mutation in a TET2 gene selected from a frame shift mutation or a nonsense mutation, the method comprising administering a lipid-modifying medicine to the subject.

9. The method according to claim 8 , wherein the subject also exhibits one or more risk factors of being a smoker, having a high level of total cholesterol or having high level of high-density lipoprotein (HDL).

10. The method of claim 8 , wherein the lipid-modifying medicine is a statin.

11. The method of claim 8 , wherein the lipid-modifying medicine is a PCSK9 inhibitor.

12. The method of claim 11 , wherein the PCSK9 inhibitor is a monoclonal antibody.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 22, 2022
From: KATHIRESAN, SEKAR
To: THE GENERAL HOSPITAL CORPORATION
Reel/Frame 062186/0010 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 22, 2022
From: EBERT, BENJAMIN LEVINE; JAISWAL, SIDDHARTHA
To: THE BRIGHAM AND WOMEN'S HOSPITAL, INC.
Reel/Frame 062186/0022 →
Continuity (3)
Continuation 15529010
Provisional Application 62084127 · Nov 25, 2014
Related Publication 20220170100A1 · Jun 2, 2022
Cited By (1)
US 12,503,733