Use of a lactate salt for the treatment and prophylaxis of atherosclerosis
View Patent ↗The use of a lactate metal salt, in particular an L-lactate, for the treatment of atheroscloerosis and/or for the prophylaxis or treatment of diseases caused by atherosclerosis is disclosed.
1. A method for the treatment of atherosclerosis or diseases caused by atherosclerosis in a subject, comprising administering to the subject a pharmaceutical composition comprising calcium lactate, wherein calcium lactate is present as the only effective anti-atherosclerosis agent and the only effective agent against diseases caused by atherosclerosis.
2. A method for the treatment of atherosclerosis in a subject, comprising administering to the subject a pharmaceutical composition comprising calcium lactate, wherein calcium lactate is present as the only effective anti-atherosclerosis agent.
3. A method for the treatment of diseases caused by atherosclerosis in a subject comprising administering to the subject a pharmaceutical composition comprising calcium lactate, wherein calcium lactate is present as the only effective agent against diseases caused by atherosclerosis.
4. The method according to any one of claims 1 or 2 - 3 , wherein the lactate is L-lactate.
5. The method according to any one of claims 1 or 2 - 3 , wherein the composition is micro-encapsulated.
6. The method according to any one of claims 1 or 2 - 3 , wherein the composition is for oral administration.
7. The method according to any one of claims 1 or 2 - 3 , wherein the composition is administered at a daily dose of between 2.0 g and 6.0 g of lactate.
8. The method according to claim 1 or claim 3 , wherein the diseases caused by atherosclerosis are coronary heart diseases.
9. The method according to any one of claims 1 or 2 - 3 , wherein the composition further contains additives suitable for preparing food, especially dietetic food or food supplements.
10. The method according to any one of claims 1 or 2 - 3 , wherein the composition further comprises pharmaceutically acceptable additives and/or corners.
11. The method according to any one of claims 1 or 2 - 3 , wherein the composition is present in solid farm as a lozenge, powder or granulate or in liquid form as a syrup or juice.
12. The method according to any one of claims 1 or 2 - 3 , wherein the daily dose is between 3.0 g and 5.0 g of lactate.
13. The method according to any one of claims 1 or 2 - 3 , wherein the daily dose is 4.0 of lactate.