IP Library Patent Application 10519792
Patent Application
App. No. 10/519,792

Method of examining and diagnosing integration dysfunction syndrome

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Patent No.
US None
App. No.
10/519,792
Abstract

The present invention relates to a method of examining or diagnosing schizophrenia, which includes measuring concentrations of D-serine and L-serine in a biological sample. According to the method of the present invention, schizophrenia can be examined or diagnosed by measuring concentrations of D-serine and L-serine in a biological sample by analysis techniques such as high performance liquid chromatography and the like.

Claims (27)

1 . A method of examining schizophrenia, which comprises measuring concentration(s) of (a) D-serine, (b) L-serine or (c) D-serine and L-serine in a biological sample.

2 . The examination method of claim 1 , wherein an index is that the D-serine concentration in a biological sample is lower than an average of said concentration in a healthy individual or a group of healthy individuals.

3 . The examination method of claim 1 , wherein an index is that the D-serine concentration in a biological sample is lower than an average−standard deviation of the concentration in a healthy individual or a group of healthy individuals.

4 . The examination method of claim 1 , wherein an index is that the D-serine concentration in a biological sample is lower than the average+standard deviation of said concentration in an individual with schizophrenia or a group of individuals with schizophrenia.

5 . The examination method of claim 1 , wherein an index is that the L-serine concentration in a biological sample is higher than an average of said concentration in a healthy individual or a group of healthy individuals.

6 . The examination method of claim 1 , wherein an index is a ratio of the D-serine concentration to the total serine concentration in a biological sample.

7 . The examination method of claim 6 , wherein an index is that the ratio of the D-serine concentration to the total serine concentration in a biological sample is lower than an average of said ratio in a healthy individual or a group of healthy individuals.

8 . The examination method of claim 6 , wherein an index is that the ratio of the D-serine concentration to the total serine concentration in a biological sample is lower than an average−standard deviation of said ratio in a healthy individual or a group of healthy individuals.

9 . The examination method of claim 6 , wherein an index is that the ratio of the D-serine concentration to the total serine concentration in a biological sample is lower than an average+standard deviation of said ratio in an individual with schizophrenia or a group of individuals with schizophrenia.

10 . The examination method of claim 1 , further comprising selecting patients with schizophrenia for whom the D-serine therapy is effective.

11 . The examination method of claim 1 , which uses an amino acid labeling reagent.

12 . The examination method of claim 11 , further comprising steps of contacting an amino acid labeling reagent with a biological sample to label serine and separating or quantifying the labeled D-serine and the labeled L-serine.

13 . The examination method of claim 12 , further comprising a step of separating and quantifying the labeled serine before the step of separating or quantifying the labeled D-serine and the labeled L-serine.

14 - 15 . (canceled)

16 . The examination method of claim 13 , wherein the labeled serine is separated or quantified using chromatography.

17 . (canceled)

18 . The examination method of claim 16 , wherein the chromatography is high performance liquid chromatography.

19 . The examination method of claim 12 , wherein the labeled D-serine and the labeled L-serine are separated or quantified using a column or capillary.

20 . The examination method of claim 19 , wherein the column or capillary is a column or capillary for optical resolution.

21 . The examination method of claim 11 , wherein the amino acid labeling reagent is an amino acid fluorescence-labeling reagent.

22 . The examination method of claim 21 , wherein the amino acid fluorescence-labeling reagent is 4-fluoro-7-nitro-2,1,3-benzoxadiazole.

23 . A reagent for examining schizophrenia, which comprises an amino acid labeling reagent.

24 . The reagent of claim 23 , wherein the amino acid labeling reagent is an amino acid fluorescence-labeling reagent.

25 . The reagent of claim 24 , wherein the amino acid fluorescence-labeling reagent is 4-fluoro-7-nitro-2,1,3-benzoxadiazole.

26 . A method of examining or diagnosing schizophrenia, which comprises measuring concentrations of D-serine and L-serine in serum and using an increase or decrease in the concentration as an index.

27 . A method of examining or diagnosing schizophrenia, which comprises measuring a D-serine concentration in serum and using a decrease in the concentration as an index.

28 . A method of examining or diagnosing schizophrenia, which comprises measuring an L-serine concentration in serum and using an increase in the concentration as an index.

Assignments (2)
CHANGE OF NAME Recorded Apr 17, 2008
From: MITSUBISHI PHARMA CORPORATION
To: MITSUBISHI TANABE PHARMA CORPORATION
Reel/Frame 020838/0701 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 28, 2005
From: HASHIMOTO, KENJI; IYO, MASAOMI; FUKUSHIMA, TAKESHI; IMAI, KAZUHIRO
To: MITSUBISHI PHARMA CORPORATION
Reel/Frame 016402/0137 →