CANDIDATE GENES AND BLOOD BIOMARKERS FOR BIPOLAR MOOD DISORDER, ALCOHOLISM AND STRESS DISORDER

• US 20110045998A1
• Filed: 09/25/2008
• Published: 02/24/2011
• Est. Priority Date: 10/08/2007
• Status: Abandoned Application

• Current Assignee: Indiana University Research & Technology Corporation (Indiana University)
• Original Assignee: Indiana University Research & Technology Corporation (Indiana University)
• Inventors: Le-Niculescu, Helen, Niculescu, Alexander B.
• Application Number:
  US12/681,154
• Publication Number:
  US 20110045998A1
• Time in Patent Office: Days
• US Class Current: 506/9
• CPC Class Codes: A01K 2217/075 inducing loss of function, i.e. knock out
• CPC Class Codes: A01K 2227/105 Murine
• CPC Class Codes: A01K 2267/035 Animal model for multifactorial diseases
• CPC Class Codes: A01K 67/0276 Knock-out vertebrates
• CPC Class Codes: C12N 15/8509 for producing genetically modified animals, e.g. transgenic
• CPC Class Codes: C12Q 1/6883 for diseases caused by alterations of genetic material
• CPC Class Codes: C12Q 2600/136 Screening for pharmacological compounds
• CPC Class Codes: C12Q 2600/158 Expression markers

Abstract

Analysis of the gene expression changes identified a series of novel candidate genes and blood biomarkers for bipolar disorder, alcoholism and stress disorder. These are used for diagnosing the disorders, predicting and monitoring response to treatment. A novel treatment for these co-morbid disorders, DHA (Docosahexaenoic acid—an omega-3 fatty acid) was identified, using these genes and biomarkers, as well as the transgenic animal model.

Claims

1. A method of diagnosing bipolar disorder, alcoholism and/or stress disorder in an individual, the method comprising:

determining the level of a plurality of biomarkers for the disorders in a sample from the individual, the plurality of biomarkers selected from the group consisting of biomarkers listed in Table 4 and/or Table 5 and/or 6.

2. The method of claim 1, wherein the plurality of biomarkers comprise a subset of about 17 biomarkers designated as Drd2 (dopamine receptor 2), Clk1 (CDC-like kinase 1), Itgav (integrin alpha V), Gls (glutaminase), Cnp (cyclic nucleotide phosphodiesterase 1), Hnrpdl (heterogeneous nuclear ribonucleoprotein D-like), Kcnj4 (potassium inwardly-rectifying channel, subfamily J, member 4), Gnb1 (guanine nucleotide binding protein, beta 1), Clic4 (chloride intracellular channel 4), Ywhaz (tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide), Sgk (serum/glucocorticoid regulated kinase), Slc38a2 (solute carrier family 38, member 2), Gpm6b (Glycoprotein M6B), Abhd14a (abhydrolase domain containing 14A), Ap1s2 (adaptor-related protein complex 1, sigma 2 subunit), B230337E12Rik (RIKEN cDNA B230337E12 gene), and Snca (synuclein, alpha).

3. The method of claim 1, wherein the plurality of biomarkers comprise a subset of blood biomarkers selected from the group consisting of Cnp (cyclic nucleotide phosphodiesterase 1), Hnrpdl (heterogeneous nuclear ribonucleoprotein D-like), Ywhaz tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide), Sgk (serum/glucocorticoid regulated kinase), Slc38a2 (solute carrier family 38, member 2), Abhd14a (abhydrolase domain containing 14A), Ap1s2 (adaptor-related protein complex 1, sigma 2 subunit), B230337E12Rik (RIKEN cDNA B230337E12 gene), and Snca (synuclein alpha).

4. The method of claim 1, wherein the sample is a bodily fluid.

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

6. The method of claim 1, wherein the level of the biomarker is determined in a tissue biopsy sample of the individual.

7. The method of claim 1, wherein the level of the biomarker is determined by analyzing the expression level of RNA transcripts.

8. The method of claim 1, wherein the expression level of the biomarker is determined by analyzing the level of protein or peptides or fragments thereof.

9. The method of claim 1, wherein the expression level is determined by an analytical technique selected from the group consisting of microarray gene expression analysis, polymerase chain reaction (PCR), real-time PCR, quantitative PCR, immunohistochemistry, enzyme-linked immunosorbent assays (ELISA), and antibody arrays.

10. The method of claim 1, wherein the determination of the level of the plurality of biomarkers is performed by an analysis of the presence or absence of the biomarkers.

15. The method of claim 1 further comprising

selecting a treatment for bipolar disorder, alcoholism and/or stress disorder based on the determination whether the patient suffers from delusion or hallucination.

16. The method of claim 15, wherein the treatment plan is a personalized plan for the patient.

11. A method of predicting the probable course and outcome (prognosis) of bipolar disorder, alcoholism and/or stress disorder in a subject, the method comprising:

analyzing a test sample from a subject, wherein the subject is suspected of having bipolar disorder, alcoholism and/or stress disorder for the presence or level of a plurality of biomarkers, wherein the markers are selected from the group consisting of biomarkers listed in Tables 4-6 and

thereby determining the prognosis of the subject based on the presence or level of the biomarkers and one or more clinicopathological data to implement a particular treatment plan for the subject.

12. The method of claim 11, wherein the clinicopathological data is selected from the group consisting of patient age, previous personal and/or familial history of psychiatric illness, previous personal and/or familial history of response to medications, and any genetic or biochemical predisposition to psychiatric illness.

13. The method of claim 11, wherein the test sample from the subject is of a test sample selected from the group consisting of fresh blood, stored blood, fixed, paraffin-embedded tissue, tissue biopsy, tissue microarray, fine needle aspirates, peritoneal fluid, ductal lavage and pleural fluid or a derivative thereof.

14. (canceled)

17. A method for clinical screening of agents capable of affecting bipolar disorder, alcoholism and/or stress disorder, the method comprising:

(a) administering a candidate agent to a population of individuals suspected of suffering from bipolar disorder, alcoholism and/or stress disorder;

(b) monitoring the expression profile of one or more of the biomarkers listed in Tables 4-5 in blood samples obtained from the individuals receiving the candidate agent compared to a control group; and

(c) determining that the candidate agent is capable of affecting bipolar disorder, alcoholism and/or stress disorder based on the expression profile of one or more of the biomarkers in the blood samples obtained from the individuals receiving the candidate drug compared to the control.

18. The method of claim 17, wherein the individuals are mice.

19. The method of claim 17, wherein the candidate agent is a pharmaceutical composition.

20. A diagnostic microarray for bipolar disorder, alcoholism and/or stress disorder comprising a plurality of nucleic acid molecules representing genes selected from the group of genes listed in Tables 4-6.

22. The diagnostic microarray of claim 20 comprising a panel of biomarkers that are predictive of bipolar disorder, alcoholism and/or stress disorder, wherein the microarray comprises nucleic acid fragments representing biomarkers designated as Cnp (cyclic nucleotide phosphodiesterase 1), Hnrpdl (heterogeneous nuclear ribonucleoprotein D-like), Ywhaz tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide), Sgk (serum/glucocorticoid regulated kinase), Slc38a2 (solute carrier family 38, member 2), Abhd14a (abhydrolase domain containing 14A), Ap1s2 (adaptor-related protein complex 1, sigma 2 subunit), B230337E12Rik (RIKEN cDNA B230337E12 gene), and Snca (synuclein alpha).

21. (canceled)

23. (canceled)

24. (canceled)

25. (canceled)

26. (canceled)