IP Library Granted Patent US 9,175,345
Granted Patent B2
US 9,175,345 · App. 12/671,610 · Granted Nov 3, 2015

Use of genomic testing and ketogenic compounds for treatment of reduced cognitive function

Inventor: Samuel T. Henderson (Golden, CO)
Assignee: Accera, Inc.
C12Q1/6883C12Q2600/106C12Q2600/156
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Quick Facts
Patent No.
US 9,175,345
App. No.
12/671,610
Granted
Nov 3, 2015
Kind
B2
Abstract

This invention relates to methods of using genotyping to select patients for treatment with compounds capable of elevating ketone body concentrations in amounts effective to treat reduced neuronal metabolism associated with reduced neuronal metabolism, for example Alzheimer's disease.

Claims (12)

1. A method of treatment for Alzheimer's disease, comprising the steps of:

a. selecting a human patient having, or at risk of Alzheimer's disease;

b. determining in the patient the presence of at least one of the specific genotypes selected from the group consisting of:

i. heterozygosity for C/T for Insulin Degrading Enzyme (IDE) rs 2251101 at relevant portion shown by SEQ ID NO:3, and

ii. absence of homozygosity for C/C of IDE rs 2251101 at relevant portion shown by SEQ ID NO:3; and

administering to the patient having at least one of the specific genotypes in (b a composition comprising an effective amount of medium chain triglycerides (MCT) of the formula:

wherein the R1, R2, and R3 esterified to the glycerol backbone are each independently fatty acids having 5-12 carbon chains.

2. The method of claim 1 , wherein the method further comprises testing the patient for the absence of ApoE4 genotype.

3. The method of claim 1 , wherein the composition is an oral composition which further comprises glucose.

4. The method of claim 1 , wherein the composition is administered in an amount effective to raise the blood level of D-beta-hydroxybutyrate in the patient from about 0.1 mM to about 50 mM.

5. The method of claim 1 , wherein the composition is administered in an amount effective to raise the blood level of D-beta-hydroxybutyrate in the patient from about 0.2 mM to about 5 mM.

6. The method of claim 1 , wherein the composition is administered at a dose of about 0.05 g/kg/day to about 10 g/kg/day.

Assignments (4)
RELEASE OF SECURITY INTEREST Recorded Feb 10, 2025
From: NESTLÉ HEALTH SCIENCE US HOLDINGS, INC.
To: CERECIN INC.
Reel/Frame 070168/0946 →
CHANGE OF NAME Recorded Aug 26, 2020
From: ACCERA, INC.
To: CERECIN INC.
Reel/Frame 053605/0604 →
PATENT SECURITY AGREEMENT Recorded Jul 24, 2012
From: ACCERA, INC.
To: NESTLE HEALTH SCIENCE US HOLDINGS, INC., AS COLLATERAL AGENT
Reel/Frame 028624/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 10, 2010
From: HENDERSON, SAMUEL T.
To: ACCERA, INC.
Reel/Frame 024059/0381 →
Continuity (2)
Provisional Application 60953074 · Jul 31, 2007
Related Publication 20110243885A1 · Oct 6, 2011