Claims for Patent: 6,165,716
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Summary for Patent: 6,165,716
Title: | Screening for disorders of serotonergic dysfunction |
Abstract: | Three novel alleles of the serotonin transporter gene are disclosed and shown to be effective markers for screening and diagnosis of migraine and psychiatric disorders. The sequences of the alleles are given. Methods for in vitro screening of individuals using DNA taken from blood samples are taught. |
Inventor(s): | Battersby; Sharon (Edinburgh, GB), Fink; George (Edinburgh, GB), Goodwin; Guy Manning (Edinburgh, GB), Harmar; Anthony John (Edinburgh, GB), Ogilvie; Alan David (Edinburgh, GB), Smith; Christopher Albert Dale (Edinburgh, GB) |
Assignee: | Medical Research Council (London, GB) |
Application Number: | 09/043,507 |
Patent Claims: | 1. A method of diagnosis of migraine or bipolar disorder or unipolar depression, or of susceptibility thereof in a human patient, said method comprising obtaining a sample of
genetic material from said patient, analysing the number of copies of one or more alleles selected from the group consisting of STin2.9 (SEQ ID No. 1), Stin2.10 (SEQ ID No. 2) and Stin2.12 (SEQ ID No. 3) of the VNTR region in the second intron of the
serotonin transporter gene present in said genetic material, wherein said number of copies indicates the likelihood of the patient suffering from migraine or bipolar disorder or unipolar depression.
2. A method as claimed in claim 1, wherein said method analyses the number of copies of one or more alleles selected from the group consisting of STin2.9 (SEQ ID NO 1), STin2.10 (SEQ ID NO 2) and STin2.12 (SEQ ID NO 3), and wherein the presence of STin2.9 (SEQ ID NO 1) indicates that the patient is at risk of or suffering from bipolar disorder or unipolar depression or MA migraine and wherein the presence of STin2.12 (SEQ ID NO 3) indicates that the patient is at risk of or suffering from MO migraine. 3. A method as claimed in claim 1 or claim 2 wherein the number of VNTR repeats or said alleles occurring in intron 2 of the serotonin transporter gene is determined in vitro. 4. A method as claimed in claims 1 or 2, wherein the number of VNTR repeats or the presence of said alleles is determined using one or more techniques selected from the group consisting of polymerase chain reaction, heteroduplex analysis, comparative genome hybridisation, single stand conformational polymorphism analysis, ligase chain reaction and Southern blotting. 5. A method as claimed in claim 1 or 2 wherein the sample comprises body tissue or body fluids containing DNA. 6. A method of diagnosis of migraine or bipolar disorder or unipolar depression or of susceptibility thereof by analysing the number of human VNTR repeats in the second intron of the serotonin transporter gene. |
Details for Patent 6,165,716
Applicant | Tradename | Biologic Ingredient | Dosage Form | BLA | Approval Date | Patent No. | Expiredate |
---|---|---|---|---|---|---|---|
Merck Sharp & Dohme Corp. | INTRON A | interferon alfa-2b | For Injection | 103132 | 06/04/1986 | ⤷ Try a Trial | 2015-09-23 |
Merck Sharp & Dohme Corp. | INTRON A | interferon alfa-2b | For Injection | 103132 | ⤷ Try a Trial | 2015-09-23 | |
Merck Sharp & Dohme Corp. | INTRON A | interferon alfa-2b | Injection | 103132 | ⤷ Try a Trial | 2015-09-23 | |
>Applicant | >Tradename | >Biologic Ingredient | >Dosage Form | >BLA | >Approval Date | >Patent No. | >Expiredate |
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