Granted Patent B2

US 12,576,102 · App. 18/120,189 · Granted Mar 17, 2026

Inventors: Gene Bowman (St-Sulpice, CH); Julie Hudry-Labbe (Epalinges, CH); Jeroen Antonius Johannes Schmitt (Moudon, CH); Corina Mudini (Lausanne, CH); Claus Rieker (Fribourg, CH)

Assignee: Societe des Produits Nestle S.A.

A61K31/714A61K31/14A61K31/198A61K31/202A61K31/592A61K31/593A61P25/28G01N33/6896G01N33/82G01N2800/2821

Abstract

Claims (18)

1 . A method for identifying pre-disposition to cognitive decline in a subject, the method comprising:

calculating a Nutritional Risk Index (NRI) of the subject, wherein the calculating the NRI of the subject comprises:

(a) obtaining an erythrocyte sample from the subject and determining a level of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) in the erythrocyte sample, wherein the level of EPA and DHA of less than or equal to about 4.82 weight percent of total fatty acids in the erythrocyte sample from the subject is assigned a score of n, and the level of EPA and DHA of more than about 4.82 weight percent of total fatty acids in the erythrocyte sample from the subject is assigned a score of zero;

(b) obtaining a serum sample from the subject and determining a level of 25-hydroxyvitamin D in the serum sample, wherein the level of 25-hydroxyvitamin D in the serum sample from the subject that is less than or equal to about 15 ng/ml is assigned a score of n, and the level of 25-hydroxyvitamin D in the serum sample from the subject that is more than about 15 ng/ml is assigned a score of zero; and

(c) obtaining a plasma sample from the subject and determining a level of homocysteine in the plasma sample, wherein the level of homocysteine in the plasma sample from the subject that greater than or equal to about 18.1 μmol/L is assigned a score of n, and the level of homocysteine in the plasma sample from the subject that is lower than about 18.1 μmol/L is assigned a score of zero,

wherein n is a positive integer,

wherein the NRI of the subject is calculated as the sum of scores obtained from steps (a), (b) and/or (c), and

an NRI score greater than zero is indicative of pre-disposition to cognitive decline of the subject.

2 . The method of claim 1 , wherein the 25-hydroxyvitamin D is selected from the group consisting of 25-hydroxyvitamin D3 and 25-hydroxyvitamin D2.

3 . The method of claim 1 , wherein the subject is selected from the group consisting of a human subject and companion animal subject.

4 . The method of claim 1 , wherein the determining the level of vitamin D in the serum sample comprises using electrochemiluminescence.

5 . The method of claim 1 , wherein the determining the level of homocysteine in the plasma sample comprises using an enzymatic cycling assay.

6 . The method of claim 1 , wherein the determining the level of EPA and DHA acids in the erythrocyte sample comprises using gas chromatography coupled with a flame ionization detector.

7 . The method of claim 1 , wherein the obtaining the erythrocyte sample comprises obtaining a plasma sample from the subject and separating erythrocytes from the plasma by centrifugation.

8 . The method of claim 1 , wherein the NRI score is calculated independent of age, gender, education, and APOE4 genotype.

9 . The method of claim 1 , wherein the EPA and DHA are both erythrocyte membrane EPA and erythrocyte membrane DHA.

10 . The method of claim 1 , wherein the subject does not have dementia.

11 . The method of claim 1 , wherein the subject has at least one risk factor selected from the group consisting of: a Clinical Dementia Rating (CDR) of 0.5, a risk score in Cardiovascular Risk Factors, Aging and Dementia (CAIDE) of 10 to 15, amyloid positive on amyloid PET scans, and a genotype indicating risk of dementia.

Assignments (1)

Priority Claims (3)

Continuity (4)

References Cited (65)