IP Library Granted Patent US 8,697,361
Granted Patent B2
US 8,697,361 · App. 12/919,905 · Granted Apr 15, 2014

Serotonin transporter gene and treatment of alcoholism

Inventor: Bankole A. Johnson (Charlottesville, VA)
Assignee: University of Virginia Patent Foundation
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,697,361
App. No.
12/919,905
Granted
Apr 15, 2014
Kind
B2
Abstract

The gene responsible for encoding SERT has a functional polymorphism at the 5′-regulatory promoter region, which results in two forms, long (L) and short (S). The LL-genotype is hypothesized to play a key role in the early onset of alcohol use. The present invention discloses the differences in treatment and diagnosis based on the L or short genotypes as well as on a single nucleotide polymorphism of the SERT gene, the 3′ UTR SNP rs 1042173. The present invention demonstrates the efficacy of using the drug ondansetron and similar drugs for treatment based on variations in the polymorphisms of the SERT gene as well as methods for diagnosing susceptibility to abuse of alcohol and other addiction-related diseases and disorders.

Claims (24)

1. A method of treating an alcohol-related disease, comprising: administering an antagonist of the serotonin receptor 5-HT3 to a patient known to have the LL genotype of functional polymorphism serotonin transporter-linked polymorphic region 5-HTTLPR of the serotonin transporter gene SLC6A4 and known to have the TT genotype of the single nucleotide polymorphism rs1042173 of the serotonin transporter gene SLC6A4.

2. The method of claim 1 , wherein the 5-HT3 antagonist is ondansetron.

3. The method of claim 1 , wherein the alcohol-related disease is alcohol dependence.

4. The method of claim 1 , wherein the patient suffers from early onset alcoholism.

5. The method of claim 1 , wherein the patient suffers from late onset alcoholism.

6. The method of claim 2 , wherein the ondansetron is administered at a dosage ranging from about 1.0 μg/kg per application to about 5.0 μg/kg per application.

7. The method of claim 2 , wherein ondansetron is administered at a dosage of about 3.0 μg/kg per application or about 4.0 μg/kg per application.

8. The method of claim 2 , wherein ondansetron is administered at least twice a day.

9. The method of claim 2 , wherein the alcohol-related disease is alcohol dependence.

10. The method of claim 9 , wherein the ondansetron is administered at a dosage ranging from about 1.0 μg/kg per application to about 5.0 μg/kg per application.

11. The method of claim 9 , wherein ondansetron is administered at a dosage of about 3.0 μg/kg per application or about 4.0 μg/kg per application.

12. The method of claim 9 , wherein ondansetron is administered at least twice a day.

13. A method of treating an alcohol-related disease, comprising: (a) determining whether serotonin transporter gene SLC6A4 of a patient has an LL genotype of functional polymorphism serotonin transporter-linked polymorphic region 5-HTTLPR; (b) determining whether a patient has the G allele or is homozygous for the T allele of the single nucleotide polymorphism rs1042173 of the serotonin transporter gene SLC6A4; and (c) administering an antagonist of the serotonin receptor 5-HT3 to the patient if the patient is found to have the LL genotype and the TT genotype so as to treat an alcohol-related disease.

14. The method of claim 13 , wherein the 5-HT3 antagonist is ondansetron.

15. The method of claim 13 , wherein the alcohol-related disease is alcohol dependence.

16. The method of claim 13 , wherein the patient suffers from early onset alcoholism.

17. The method of claim 13 , wherein the patient suffers from late onset alcoholism.

18. The method of claim 14 , wherein the ondansetron is administered at a dosage ranging from about 1.0 μg/kg per application to about 5.0 μg/kg per application.

19. The method of claim 14 , wherein ondansetron is administered at a dosage of about 3.0 μg/kg per application or about 4.0 μg/kg per application.

20. The method of claim 14 , wherein ondansetron is administered at least twice a day.

21. The method of claim 14 , wherein the alcohol-related disease is alcohol dependence.

22. The method of claim 14 , wherein the ondansetron is administered at a dosage ranging from about 1.0 μg/kg per application to about 5.0 μg/kg per application.

23. The method of claim 21 , wherein ondansetron is administered at a dosage of about 3.0 μg/kg per application or about 4.0 μg/kg per application.

24. The method of claim 21 , wherein ondansetron is administered at least twice a day.

Assignments (3)
CONFIRMATORY LICENSE Recorded Sep 17, 2010
From: UNIVERSITY OF VIRGINIA PATENT FOUNDATION
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 025003/0130 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 3, 2010
From: JOHNSON, BANKOLE A.
To: UNIVERSITY OF VIRGINIA
Reel/Frame 024939/0784 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 3, 2010
From: UNIVERSITY OF VIRGINIA
To: UNIVERSITY OF VIRGINIA PATENT FOUNDATION
Reel/Frame 024939/0828 →
Continuity (4)
Provisional Application 61032263 · Feb 28, 2008
Provisional Application 61059301 · Jun 6, 2008
Provisional Application 61146440 · Jan 22, 2009
Related Publication 20110112159A1 · May 12, 2011