CA2393004A1 - Method of diagnosing neurodegenerative disease - Google Patents
Method of diagnosing neurodegenerative disease Download PDFInfo
- Publication number
- CA2393004A1 CA2393004A1 CA002393004A CA2393004A CA2393004A1 CA 2393004 A1 CA2393004 A1 CA 2393004A1 CA 002393004 A CA002393004 A CA 002393004A CA 2393004 A CA2393004 A CA 2393004A CA 2393004 A1 CA2393004 A1 CA 2393004A1
- Authority
- CA
- Canada
- Prior art keywords
- alpha
- test sample
- acetylcholine receptor
- nicotinic acetylcholine
- receptor protein
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/94—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving narcotics or drugs or pharmaceuticals, neurotransmitters or associated receptors
- G01N33/9406—Neurotransmitters
- G01N33/944—Acetylcholine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
- C07K14/47—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
- C07K14/4701—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals not used
- C07K14/4711—Alzheimer's disease; Amyloid plaque core protein
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
- C07K16/286—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against neuromediator receptors, e.g. serotonin receptor, dopamine receptor
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/68—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
- G01N33/6893—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids related to diseases not provided for elsewhere
- G01N33/6896—Neurological disorders, e.g. Alzheimer's disease
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2333/00—Assays involving biological materials from specific organisms or of a specific nature
- G01N2333/435—Assays involving biological materials from specific organisms or of a specific nature from animals; from humans
- G01N2333/46—Assays involving biological materials from specific organisms or of a specific nature from animals; from humans from vertebrates
- G01N2333/47—Assays involving proteins of known structure or function as defined in the subgroups
- G01N2333/4701—Details
- G01N2333/4709—Amyloid plaque core protein
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2333/00—Assays involving biological materials from specific organisms or of a specific nature
- G01N2333/435—Assays involving biological materials from specific organisms or of a specific nature from animals; from humans
- G01N2333/705—Assays involving receptors, cell surface antigens or cell surface determinants
- G01N2333/70571—Assays involving receptors, cell surface antigens or cell surface determinants for neuromediators, e.g. serotonin receptor, dopamine receptor
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2800/00—Detection or diagnosis of diseases
- G01N2800/28—Neurological disorders
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2800/00—Detection or diagnosis of diseases
- G01N2800/28—Neurological disorders
- G01N2800/2814—Dementia; Cognitive disorders
- G01N2800/2821—Alzheimer
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2800/00—Detection or diagnosis of diseases
- G01N2800/52—Predicting or monitoring the response to treatment, e.g. for selection of therapy based on assay results in personalised medicine; Prognosis
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Molecular Biology (AREA)
- Biomedical Technology (AREA)
- Immunology (AREA)
- Biochemistry (AREA)
- Medicinal Chemistry (AREA)
- Hematology (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Urology & Nephrology (AREA)
- Neurology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Microbiology (AREA)
- Food Science & Technology (AREA)
- Biotechnology (AREA)
- Genetics & Genomics (AREA)
- Biophysics (AREA)
- General Physics & Mathematics (AREA)
- Pathology (AREA)
- Cell Biology (AREA)
- Physics & Mathematics (AREA)
- Analytical Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Neurosurgery (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Zoology (AREA)
- Gastroenterology & Hepatology (AREA)
- Toxicology (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Investigating Or Analysing Biological Materials (AREA)
- Peptides Or Proteins (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
Abstract
The present invention provides methods for diagnosing neurodegenerative disease such as Alzheimer's disease, monitoring the progression and prognosis of the disease and/or monitoring the therapeutic efficacy of any intervention or treatment of the disease comprising measuring the level of .alpha.7 nicotinic acetylcholine receptor protein.
Description
METHOD
Claims (11)
1. A method of diagnosis, determining prognosis, progression, or monitoring therapeutic efficacy of any intervention or treatment of neurodegenerative disease comprising:
(a) obtaining a test sample from a subject wherein the test sample comprises a cell, said cell expressing .alpha.7 nicotinic acetylcholine receptor protein;
(b) contacting the test sample with a compound capable of specific interaction with the .alpha.7 nicotinic acetylcholine receptor protein; and (c) measuring the binding of the compound to .alpha.7 nicotinic acetylcholine receptor protein as an indication of .alpha.7 nicotinic acetylcholine receptor protein in the test sample.
(a) obtaining a test sample from a subject wherein the test sample comprises a cell, said cell expressing .alpha.7 nicotinic acetylcholine receptor protein;
(b) contacting the test sample with a compound capable of specific interaction with the .alpha.7 nicotinic acetylcholine receptor protein; and (c) measuring the binding of the compound to .alpha.7 nicotinic acetylcholine receptor protein as an indication of .alpha.7 nicotinic acetylcholine receptor protein in the test sample.
2. The method of claim 1 wherein the neurodegenerative disease is Alzheimer's disease.
3. The method of claim 1 wherein the compound is a labeled compound.
4. The method of claim 1, 2 or 3 further comprising adding a step (d) of comparing changes in the level of .alpha.7 nicotinic acetylcholine receptor protein in the test sample with a normal sample from a subject known to lack neurodegenerative disease.
5. The method of claim 1, 2 or 3 wherein the test sample comprises a cell selected from the group consisting of circulating lymphocytes, olfactory neuroepithelial neuronal cell bodies or their neuronal processes, and hippocampal cells.
6. The method of claim 1 or 2 wherein the compound is selected from the group consisting of A.beta.1-40 peptide, A.beta.1-42 peptide, A.beta.1-43 peptide, a monoclonal antibody, and a polyclonal antibody.
7. The method of claim 1, 2, or 3 wherein the change is a decrease in the level of the .alpha.7 nicotinic acetylcholine receptor protein.
8. A method of diagnosis, determining prognosis, progression, or monitoring the therapeutic efficacy of any intervention or treatment of Alzheimer's disease comprising:
(a) obtaining a test sample from a subject wherein the test sample comprises a cell selected from the group consisting of circulating lymphocytes, olfactory neuroepithelial neuronal cell bodies or their neuronal processes, or hippocampal cells, said cell expressing .alpha.7 nicotinic acetylcholine receptor protein in healthy individuals;
(b) contacting the test sample with an antibody capable of specific interaction with the .alpha.7 nicotinic acetylcholine receptor protein; and (c) measuring the binding of the antibody to the .alpha.7 nicotinic acetylcholine receptor protein as an indication of decreases in the level of .alpha.7 nicotinic acetylcholine receptor protein in the test sample.
(a) obtaining a test sample from a subject wherein the test sample comprises a cell selected from the group consisting of circulating lymphocytes, olfactory neuroepithelial neuronal cell bodies or their neuronal processes, or hippocampal cells, said cell expressing .alpha.7 nicotinic acetylcholine receptor protein in healthy individuals;
(b) contacting the test sample with an antibody capable of specific interaction with the .alpha.7 nicotinic acetylcholine receptor protein; and (c) measuring the binding of the antibody to the .alpha.7 nicotinic acetylcholine receptor protein as an indication of decreases in the level of .alpha.7 nicotinic acetylcholine receptor protein in the test sample.
9. The method of claim 8 further comprises adding a step (d) of comparing changes in the level of .alpha.7 acetylcholine receptor protein in the test sample with a normal sample, from a subject known to lack neurodegenerative and neurological diseases.
10. A method to detect intracellular .alpha.7 nicotinic acetylcholine receptor protein in an Alzheimer's Disease subject which comprises the steps:
(a) obtaining a test sample from a subject wherein the test sample comprises a cell, said cell expressing .alpha.7 nicotinic acetylcholine receptor protein in healthy individuals;
(b) contacting the test sample with a membrane perforating agent;
(c) contacting the test sample with a labeled compound capable of specific interaction with the .alpha.7 nicotinic acetylcholine receptor; and (d) measuring the binding of the compound to .alpha.7 nicotinic acetylcholine receptor protein as an indication of .alpha.7 nicotinic acetylcholine receptor protein in the test sample.
(a) obtaining a test sample from a subject wherein the test sample comprises a cell, said cell expressing .alpha.7 nicotinic acetylcholine receptor protein in healthy individuals;
(b) contacting the test sample with a membrane perforating agent;
(c) contacting the test sample with a labeled compound capable of specific interaction with the .alpha.7 nicotinic acetylcholine receptor; and (d) measuring the binding of the compound to .alpha.7 nicotinic acetylcholine receptor protein as an indication of .alpha.7 nicotinic acetylcholine receptor protein in the test sample.
11. An immunoassay method to detect .alpha.7 nicotinic acetylcholine receptor protein in an Alzheimer's Disease subject which comprises the steps:
(a) obtaining a test sample from a subject wherein the test sample comprises a cell, said cell expressing .alpha.7 nicotinic acetylcholine receptor protein in healthy individuals;
(b) contacting the test sample with a labeled antibody capable of specific interaction with the .alpha.7 nicotinic acetylcholine receptor, wherein the antibody becomes a bound antibody or an unbound antibody;
(c) removing the unbound antibody from the test sample; and (d) measuring the quantity of bound or unbound antibody to indicate changes in the level of .alpha.7 nicotinic acetylcholine receptor protein in the test sample.
(a) obtaining a test sample from a subject wherein the test sample comprises a cell, said cell expressing .alpha.7 nicotinic acetylcholine receptor protein in healthy individuals;
(b) contacting the test sample with a labeled antibody capable of specific interaction with the .alpha.7 nicotinic acetylcholine receptor, wherein the antibody becomes a bound antibody or an unbound antibody;
(c) removing the unbound antibody from the test sample; and (d) measuring the quantity of bound or unbound antibody to indicate changes in the level of .alpha.7 nicotinic acetylcholine receptor protein in the test sample.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US16823899P | 1999-12-01 | 1999-12-01 | |
US60/168,238 | 1999-12-01 | ||
PCT/US2000/031467 WO2001040261A1 (en) | 1999-12-01 | 2000-11-16 | Method of diagnosing neurodegenerative disease |
Publications (1)
Publication Number | Publication Date |
---|---|
CA2393004A1 true CA2393004A1 (en) | 2001-06-07 |
Family
ID=22610681
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002393004A Abandoned CA2393004A1 (en) | 1999-12-01 | 2000-11-16 | Method of diagnosing neurodegenerative disease |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP1233979A1 (en) |
JP (1) | JP2003530542A (en) |
AU (1) | AU1920401A (en) |
CA (1) | CA2393004A1 (en) |
WO (1) | WO2001040261A1 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8569354B2 (en) | 2008-11-19 | 2013-10-29 | Envivo Pharmaceuticals, Inc. | Treatment of cognitive disorders with (R)-7-chloro-N-(quinuclidin-3-yl)benzo[b]thiophene-2-carboxamide and pharmaceutically acceptable salts thereof |
US8710227B2 (en) | 2010-05-17 | 2014-04-29 | Envivo Pharmaceuticals, Inc. | Crystalline form of (R)-7-chloro-N-(quinuclidin-3-yl)benzo[b]thiophene-2-carboxamide hydrochloride monohydrate |
US8884017B2 (en) | 2001-12-27 | 2014-11-11 | Bayer Intellectual Property Gmbh | 2-heteroarylcarboxylic acid amides |
US9585877B2 (en) | 2012-05-08 | 2017-03-07 | Forum Pharmaceuticals, Inc. | Methods of maintaining, treating or improving cognitive function |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2004095031A1 (en) * | 2003-04-24 | 2004-11-04 | Universität Zürich | Method of monitoring immunotherapy |
US8314119B2 (en) | 2006-11-06 | 2012-11-20 | Abbvie Inc. | Azaadamantane derivatives and methods of use |
US8436145B2 (en) | 2008-12-04 | 2013-05-07 | Yeda Research And Development Co. Ltd. | Compositions and methods for diagnosing and treating cancer and neurodegenerative diseases related to Beclin-1 |
EP2385071A1 (en) | 2008-12-04 | 2011-11-09 | Yeda Research And Development Co. Ltd. | Compositions and methods for diagnosing and treating cancer and neurodegenerative diseases related to beclin-1 |
KR20130108586A (en) | 2010-09-23 | 2013-10-04 | 애브비 인코포레이티드 | Monohydrate of an azaadamantane derivative |
EP2872899B1 (en) * | 2012-07-13 | 2018-07-11 | Pain Therapeutics, Inc. | Alzheimer's disease assay in a living patient |
US10282875B2 (en) | 2015-12-11 | 2019-05-07 | International Business Machines Corporation | Graph-based analysis for bio-signal event sensing |
WO2020188051A1 (en) | 2019-03-19 | 2020-09-24 | Cambridge Cognition Limited | Method and uses of diagnosing and recommending treatment for a psychotic disorder |
KR102246021B1 (en) * | 2019-10-10 | 2021-04-29 | 연세대학교 산학협력단 | A composition for diagnosing of fibrosis and using thereof |
-
2000
- 2000-11-16 WO PCT/US2000/031467 patent/WO2001040261A1/en not_active Application Discontinuation
- 2000-11-16 CA CA002393004A patent/CA2393004A1/en not_active Abandoned
- 2000-11-16 AU AU19204/01A patent/AU1920401A/en not_active Abandoned
- 2000-11-16 JP JP2001541016A patent/JP2003530542A/en active Pending
- 2000-11-16 EP EP00982134A patent/EP1233979A1/en not_active Withdrawn
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8884017B2 (en) | 2001-12-27 | 2014-11-11 | Bayer Intellectual Property Gmbh | 2-heteroarylcarboxylic acid amides |
US8569354B2 (en) | 2008-11-19 | 2013-10-29 | Envivo Pharmaceuticals, Inc. | Treatment of cognitive disorders with (R)-7-chloro-N-(quinuclidin-3-yl)benzo[b]thiophene-2-carboxamide and pharmaceutically acceptable salts thereof |
US8642638B2 (en) | 2008-11-19 | 2014-02-04 | Envivo Pharmaceuticals, Inc. | Treatment of cognitive disorders with (R)-7-chloro-N-(quinuclidin-3-yl)benzo[b]thiophene-2-carboxamide and pharmaceutically acceptable salts thereof |
US8815933B2 (en) | 2008-11-19 | 2014-08-26 | Forum Pharmaceuticals, Inc. | Treatment of cognitive disorders with (R)-7-chloro-N-(quinuclidin-3-yl)benzo[b]thiophene-2-carboxamide and pharmaceutically acceptable salts thereof |
US8710227B2 (en) | 2010-05-17 | 2014-04-29 | Envivo Pharmaceuticals, Inc. | Crystalline form of (R)-7-chloro-N-(quinuclidin-3-yl)benzo[b]thiophene-2-carboxamide hydrochloride monohydrate |
US9108961B2 (en) | 2010-05-17 | 2015-08-18 | Forum Pharmaceuticals, Inc. | Crystalline form of (R)-7-chloro-N-(quinuclidin-3-yl)benzo[b]thiophene-2-carboxamide hydrochloride |
US9273044B2 (en) | 2010-05-17 | 2016-03-01 | Forum Pharmaceuticals, Inc. | Crystalline form of (R)-7-chloro-N-(quinuclidin-3-yl)benzo[b]thiophene-2-carboxamide hydrochloride monohydrate |
US9550767B2 (en) | 2010-05-17 | 2017-01-24 | Forum Pharmaceuticals, Inc. | Crystalline form of (R)-7-chloro-N-(quinuclidin-3-yl)benzo[b]thiophene-2-carboxamide hydrochloride monohydrate |
US9585877B2 (en) | 2012-05-08 | 2017-03-07 | Forum Pharmaceuticals, Inc. | Methods of maintaining, treating or improving cognitive function |
Also Published As
Publication number | Publication date |
---|---|
WO2001040261A1 (en) | 2001-06-07 |
EP1233979A1 (en) | 2002-08-28 |
JP2003530542A (en) | 2003-10-14 |
AU1920401A (en) | 2001-06-12 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FZDE | Discontinued |