Fatty acid composition for treatment of alzheimer's disease and cognitive dysfunction
This invention relates to the use of a fatty acid composition comprising at least (all-Z omega-3)-4,7,10,13,16,19-docosahexaenoic acid (DHA), or derivatives thereof, and (all-Z omega-3)-5,8,11,14,17-eicosapentaenoic acid (EPA), or derivatives thereof for manufacturing of a medicinal product or a food stuff for the treatment and/or prevention of amyloidos-related diseases, such as Alzheimer's disease, as well as treatment/prevention of cognitive dysfunction.
1. A method for alleviating an amyloidosis related disease in a subject in need thereof, wherein said disease is Alzheimer's disease, comprising administering to the subject a therapeutically effective amount of a fatty acid composition comprising (all-Z omega-3)-4,7,10,13,16,19-docosahexaenoic acid (DHA) and (all-Z omega-3)-5,8,11,14,17-eicosapentaenoic acid (EPA), with a daily dosage of the composition ranging from 2 g to 10 g, wherein said composition is chosen from a medicinal product and a food supplement,
wherein the composition comprises at least 70% unsaturated omega-3 fatty acids.
2. A method for alleviating cognitive dysfunction in a subject in need thereof comprising administering to the subject a therapeutically effective amount of a fatty acid composition comprising (all-Z omega-3)-4,7,10,13,16,19-docosahexaenoic acid (DHA), and (all-Z omega-3)-5,8,11,14,17-eicosapentaenoic acid (EPA), with a daily dosage of the composition ranging from 2 g to 10 g, wherein said composition is chosen from a medicinal product and a food supplement,
wherein the composition comprises at least 70% unsaturated omega-3 fatty acids.
3. The method according to claim 1 , wherein EPA and DHA are present in the composition in an EPA:DHA ratio ranging from about 1:2 to 2:1.55.
4. The method according to claim 1 , wherein the weight ratio of EPA:DHA in the fatty acid composition is 1:X, where X is equal or greater than 1.
5. The method according to claim 4 , wherein EPA and DHA are present in the composition in an EPA:DHA ratio ranging from 1:1 to 1:8.
6. The method according to claim 1 , wherein the fatty acids in the composition are present in at least one form chosen from esterified form, ethyl ester form, salt form, free acid form, and phospholipid form, or any combinations thereof.
7. The method according to claim 1 , wherein DHA is obtained from at least one of vegetable, microbial, and animal origins, or combinations thereof.
8. The method according to claim 1 , wherein the DHA, EPA, or both are obtained from at least one of vegetable, microbial, and animal origins, or combinations thereof.
9. The method according to claim 1 , wherein the EPA, DHA, or both are produced from a marine oil.
10. The method according to claim 1 , wherein the fatty acid composition is produced from a marine oil.
11. The method according to claim 1 , wherein the fatty acid composition comprises a combination of EPA and DHA in triglyceride form.
12. The method according to claim 1 , wherein the fatty acid composition is administered orally to a human or an animal.
13. The method according to claim 1 , wherein the fatty acid composition is chosen from an amyloid-preventing agent and an amyloid-decreasing agent.
14. The method according to claim 2 , wherein said cognitive dysfunction is a mild cognitive dysfunction.
15. The method according to claim 1 , wherein said fatty acid composition is in an oral dosage form chosen from a capsule and a sachet.
16. The method according to claim 15 , wherein said oral dosage form is flavoured.
17. The method according to claim 5 , wherein the combination of EPA and DHA is present in the composition in an EPA:DHA ratio ranging from 1:1 to 1:6.
18. The method according to claim 9 , wherein at least a part of the EPA, DHA, or both is produced from a fish oil.
19. The method according to claim 1 , wherein said fatty acid composition is administered in an amount providing a daily dosage ranging from 2 to 6 g in a human.
20. A method for delaying cognitive decline in a subject in need thereof comprising administering to the subject a therapeutically effective amount of a fatty acid composition comprising (all-Z omega-3)-4,7,10,13,16,19-docosahexaenoic acid (DHA), and (all-Z omega-3)-5,8,11,14,17-eicosapentaenoic acid (EPA), wherein said fatty acid composition is chosen from a medicinal product and a food supplement,
wherein the composition comprises at least 70% unsaturated omega-3 fatty acids.
21. The method according to claim 20 , wherein the fatty acids in the composition are present in at least one form chosen from esterified form, ethyl ester form, salt form, free acid form, and phospholipid form, or any combinations thereof.
22. The method according to claim 20 , wherein at least one of DHA and EPA is obtained from a marine oil.
23. The method according to claim 20 , wherein EPA and DHA are present in the composition in an EPA:DMA ratio ranging from 1:1 to 1:8.
24. The method according to claim 20 , wherein the fatty acid composition comprises a combination of EPA and DHA in triglyceride form.
25. The method according to claim 20 , wherein said fatty acid composition is a food supplement.
26. The method according to claim 20 , wherein said fatty acid composition is administered in an amount providing a daily dosage ranging from 1 to 15 g in a human.