CMPF as a biomarker for diabetes and associated methods

Patent metadata

Field	Value
Publication number	US-9726659-B2
Application number	US-201314429977-A
Country	US
Kind code	B2
Filing date	Sep 20, 2013
Priority date	Sep 21, 2012
Publication date	Aug 8, 2017
Grant date	Aug 8, 2017

Abstract

Provided are methods for identifying or monitoring a subject having, or at risk of developing, impaired glucose homeostasis. Carboxy-4-methyl-5-propyl-2-furanpropanoic acid (CMPF) is shown to be a biomarker for impaired glucose homeostasis and/or conditions characterized by β-cell dysfunction. Comparing a test level of CMPF in a subject to a control level identifies subjects having, or at risk of developing, impaired glucose homeostasis. Also provided are methods of causing impaired glucose homeostasis or β-cell dysfunction and methods of screening for compounds that affect the activity of β-cells. Also provided are methods for the treatment of β-cell dysfunction by reducing the physiological levels of CMPF in a subject as well as the use of a OAT modulator for the treatment of β-cell dysfunction.

First claim

The invention claimed is:

1. A method of treating impaired glucose homeostasis comprising:
(a) detecting a test level of 3-carboxy-4-methyl-5-propyl-2-furanpropanoic acid (CMPF) in a sample from a subject; and
(b) comparing the test level of CMPF to a control level wherein:
i) the control level is representative of a level of CMPF in subjects without impaired glucose homeostasis and a subject having an increase in the level of CMPF relative to the control level is identified as having, or at risk of developing, impaired glucose homeostasis; or
ii) the control level is representative of a level of CMPF in subjects with impaired glucose homeostasis and a subject having a similarity in the level of CMPF relative to the control level is identified as having, or at risk of developing, impaired glucose homeostasis; and

(c) administering to the subject identified as having, or at risk of developing, impaired glucose homeostasis in part b) an agent suitable for the treatment of impaired glucose homeostasis selected from the group consisting of a CMPF inhibitor, insulin, metformin, GLP-1 receptor agonist, GLP-1 analog, sulfonylureas, or insulin sensitizer.

2. The method of claim 1 , wherein the impaired glucose homeostasis is gestational diabetes mellitus, type 2 diabetes, impaired glucose tolerance, pre-diabetes, or insulin resistance.

3. The method of claim 2 , wherein the control level is:
i) representative of a level of CMPF in subjects without gestational diabetes mellitus, type 2 diabetes, impaired glucose tolerance, pre-diabetes, or insulin resistance and an increased test level of CMPF relative to the control is indicative of the subject having, or at risk of developing gestational diabetes mellitus, type 2 diabetes, impaired glucose tolerance pre-diabetes, or insulin resistance; or
ii) representative of a level of CMPF in subjects with gestational diabetes mellitus, type 2 diabetes, impaired glucose tolerance, pre-diabetes, or insulin resistance and a similar or greater test level of CMPF relative to the control is indicative of the subject having, or at risk of developing gestational diabetes mellitus, type 2 diabetes, impaired glucose tolerance, pre-diabetes, or insulin resistance.

4. The method of claim 1 , wherein the control level is representative of a level of CMPF in subjects with normal glucose tolerance.

5. The method of claim 1 , wherein the control level is a pre-determined standardized control level.

6. The method of claim 1 , wherein the control level is a level of CMPF in plasma greater than 50 μM.

7. The method of claim 1 , wherein detecting CMPF in the sample comprises using mass spectrometry (MS), gas chromatography/mass spectrometry (GC-MS) or liquid chromatography mass spectrometry (LC-MS).

8. The method of claim 1 , wherein detecting CMPF in the sample comprises using High Performance Liquid Chromatography (HPLC) or Nuclear Magnetic Resonance (NMR) spectroscopy.

9. The method of claim 1 , wherein detecting CMPF in the sample comprises using antibodies that specifically bind CMPF.

10. The method of claim 9 , wherein detecting CMPF in the sample comprises using an Enzyme-Linked Immunosorbent Assay (ELISA).

11. The method of claim 1 , wherein the sample is a blood sample.

12. The method of claim 1 , wherein the sample is sweat or urine.

13. The method of claim 1 , wherein the subject is human.

14. The method of claim 1 wherein the control level is a level of CMPF from the subject at an earlier time point, and an increase in the level of CMPF is indicative of more severe impaired glucose homeostasis in the subject or a decrease in the level of CMPF is indicative of improved glucose homeostasis in the subject.

Assignees

• Governing Council Univ Toronto

Inventors

• Wheeler Michael
• Prentice Kacey
• Dai Feihan
• Retnakaran Ravi

Classifications

• G01N2800/52

  Predicting or monitoring the response to treatment, e.g. for selection of therapy based on assay results in personalised medicine; Prognosis · CPC title

• G01N2800/042

  Disorders of carbohydrate metabolism, e.g. diabetes, glucose metabolism · CPC title

• G01N2800/50

  Determining the risk of developing a disease · CPC title

• Y10T436/142222

  Hetero-O [e.g., ascorbic acid, etc.] · CPC title

• G01N33/507

  Pancreatic cells · CPC title