Method for evaluating myocardial ischemic state using blood sample

Patent metadata

Field	Value
Publication number	US-9366680-B2
Application number	US-200813060552-A
Country	US
Kind code	B2
Filing date	Aug 28, 2008
Priority date	Aug 28, 2008
Publication date	Jun 14, 2016
Grant date	Jun 14, 2016

Abstract

The present invention provides a method and an index capable of less-invasively determining myocardial ischemia such as ischemic heart disease or restenosis after percutaneous coronary intervention. The present invention also provides an index that allows the cardiovascular disease other than heart failure to be determined even from a blood sample showing a BNP value from which the cardiovascular disease other than heart failure cannot be determined by a conventional method. A method for determining myocardial ischemia comprising subjecting a blood sample which is derived from a test subject and which contains a BNP molecular group containing at least two selected from the group consisting of BNP 1-32 molecule, BNP 3-32 molecule, BNP 4-32 molecule, BNP 5-32 molecule, and a molecule having a mass number larger than that of BNP 5-32 molecule by 16 Da to a detection process capable of distinguishing and quantifying the individual BNP molecules different in mass number to detect the BNP molecular group, wherein myocardial ischemia in the test subject is determined using, as an index, a ratio between a detected intensity of at least one molecule selected from the BNP molecular group and a detected intensity of at least one other molecule selected from the BNP molecular group.

First claim

The invention claimed is:

1. A method for assessing coronary restenosis in a test subject after percutaneous coronary intervention (PCI) based on a ratio between specific B-type natriuretic hormone (BNP) molecules, the method comprising:
immunologically enriching a B-type natriuretic hormone (BNP) molecular group containing BNP 1-32 molecule (SEQ ID No. 1), BNP 3-32 molecule (SEQ ID No. 2), and BNP 5-32 molecule (SEQ ID No. 4) from a blood sample obtained from the test subject at a time after PCI by contacting the blood sample with a solid phase-immobilized or -immobilizable antibody specific for the BNP molecular group to form an immobilized immune complex, wherein the antibody is KYBNPII anti-BNP monoclonal antibody,
isolating the immobilized immune complex from other components of the blood sample,
eluting the BNP molecular group from the isolated immune complex,
detecting levels of the BNP 1-32 molecule (SEQ ID No. 1), the BNP 3-32 molecule (SEQ ID No. 2), and the BNP-5-32 molecule (SEQ ID No. 4) in the eluate,
thereby distinguishing and quantifying the individual BNP molecules different in mass number in the blood sample,
calculating a ratio between a sum of the detected level of the BNP 1-32 molecule and the detected level of the BNP 3-32 molecule, to the detected level of the BNP 5-32 molecule, and
assessing coronary restenosis after PCI in the test subject based on the calculated ratio, wherein a ratio lower than that in control test subjects without restenosis is indicative of coronary restenosis after PCI in the test subject.

2. The method according to claim 1 , wherein the blood sample is a blood specimen itself of the test subject obtained at a time after PCI having a measured value of BNP of 18 pg/mL to 150 pg/mL, or is prepared from the blood specimen.

3. The method of claim 1 , wherein immunologically enriching is by immunoprecipitation or affinity column chromatography.

4. A method for assessing coronary restenosis in a test subject after percutaneous coronary intervention (PCI) based on a ratio between specific B-type natriuretic hormone (BNP) molecules, the method comprising:
immunologically enriching a B-type natriuretic hormone (BNP) molecular group containing BNP 5-32 molecule (SEQ ID No. 4) and a molecule having a mass number larger than that of BNP 5-32 molecule by 16 Da from a blood sample obtained from the test subject at a time after PCI by contacting the blood sample with a solid phase-immobilized or -immobilizable antibody specific for the BNP molecular group to form an immobilized immune complex, wherein the antibody is KYBNPII anti-BNP monoclonal antibody,
isolating the immobilized immune complex from other components of the blood sample,
eluting the BNP molecular group from the isolated immune complex,
detecting levels of the BNP 5-32 molecule (SEQ ID No. 4) and the molecule having a mass number larger than that of the BNP 5-32 molecule by 16 Da in the eluate, thereby distinguishing and quantifying the individual BNP molecules different in mass number in the blood sample,
calculating a ratio between the detected level of the molecule having a mass number larger than that of the BNP 5-32 molecule by 16D to the detected level of the BNP-5-32 molecule, and
assessing coronary restenosis after PCI in the test subject based on the calculated ratio, wherein a ratio higher than that in control test subjects without restenosis is indicative of coronary restenosis after PCI in the test subject.

5. The method according to claim 4 , wherein the blood sample is a blood specimen itself of the test subject obtained at a time after PCI having a measured value of BNP of 18 pg/mL to 150 pg/mL, or is prepared from the blood specimen.

6. The method of claim 4 , wherein immunologically enriching is by immunoprecipitation or affinity column chromatography.

Assignees

• Fujimoto Hirotaka
• Suzuki Toru
• Shimadzu Corp
• Univ Tokyo

Inventors

• Fujimoto Hirotaka
• Suzuki Toru

Classifications

• C07K2317/34

  Identification of a linear epitope shorter than 20 amino acid residues or of a conformational epitope defined by amino acid residues · CPC title

• C07K16/26

  against hormones {; against hormone releasing or inhibiting factors} · CPC title

• G01N33/6893 Primary

  related to diseases not provided for elsewhere · CPC title

• G01N2333/58

  Atrial natriuretic factor complex; Atriopeptin; Atrial natriuretic peptide [ANP]; Brain natriuretic peptide [BNP, proBNP]; Cardionatrin; Cardiodilatin · CPC title

• G01N2800/32

  Cardiovascular disorders · CPC title