Methods and compositions for preventing and treating osteoporosis
Methods and compositions for treating and preventing osteoporosis are disclosed. Osteoporosis is prevented and treated by administering an effective amount of a composition to a patient. The composition may be prepared from New Zealand green-lipped mussel ( Perna canaliculus ) and may comprise one or more proteins, amino acids, minerals, sterol esters, sterols, polar lipids, triglycerides, fats, lipids, fatty acids, and polyunsaturated fatty acids (PUFAs) derived from the mussel. The active ingredients in the composition include one or more of an octadecatetraenoic acid (SDA), an eicosatetraenoic acid (ETA), an eicosapentaenoic acid (EPA), and a docosahexaenoic acid (DHA).
1. A method for treating osteoporosis comprising:
administering an effective amount of a green-lipped mussel (GLM) composition to a patient suffering from osteoporosis.
2. The method of claim 1 , wherein the GLM composition is prepared from a New Zealand green-lipped mussel, Perna canaliculus.
3. The method of claim 1 , wherein the GLM composition comprises one or more proteins, amino acids, minerals, sterol esters, sterols, polar lipids, triglycerides, fats, lipids, fatty acids, or polyunsaturated fatty acids (PUFAs) derived from a New Zealand green-lipped mussel ( Perna canaliculus ).
4. The method of claim 1 , wherein the GLM composition comprises one or more of an octadecatetraenoic acid, an eicosatetraenoic acid, an eicosapentaenoic acid, and a docosahexaenoic acid.
5. The method of claim 1 , wherein the patient has a bone mineral density of less than 2.5 standard deviations from an average bone mineral density.
6. The method of claim 1 , wherein the patient has experienced an osteoporosis-related fracture.
7. The method of claim 1 , wherein the effective amount of a GLM composition comprises a daily dosage of 50 mg of lipid extract prepared from rapid cold-dried GLM powder.
8. A method for reducing a patient's risk for developing osteoporosis comprising:
identifying a patient at risk for developing osteoporosis; and
administering to the patient an effective amount of a composition consisting essentially of a lipid extract of New Zealand green-lipped mussel.
9. The method of claim 8 , wherein identifying that the patient has a risk for developing osteoporosis comprises determining that the patient has a bone mineral density of less than 1 standard deviation and not less than 2.5 standard deviations from an average bone mineral density.
10. The method of claim 8 , wherein identifying that the patient has a risk for developing osteoporosis comprises determining that the patient has one or more risk factors associated with osteoporosis.
11. The method of claim 10 , wherein the risk factors associated with osteoporosis comprise one or more of age, gender, race, lifestyle, diet, level of activity, family history of osteoporosis, tobacco use, alcohol use, body frame size, menopause, hormone levels, medication use, and history of eating disorders.
12. The method of claim 8 , wherein the effective amount of the composition comprises a daily dosage of 50 mg of lipid extract prepared from rapid cold-dried New Zealand green-lipped mussel powder.
13. The method of claim 8 , wherein the composition comprises one or more of an octadecatetraenoic acid, an eicosatetraenoic acid, an eicosapentaenoic acid, and a docosahexaenoic acid.
14. A method for increasing bone mineral density in a patient, the method comprising:
identifying a patient having a less than average bone mineral density; and
administering to the patient an effective amount of an active ingredient from a lipid extract of New Zealand green-lipped mussel.
15. The method of claim 14 , wherein the active ingredient comprises one or more of proteins, amino acids, minerals, sterol esters, sterols, polar lipids, triglycerides, fats, lipids, fatty acids, and polyunsaturated fatty acids (PUFAs) derived from GLM.
16. The method of claim 14 , wherein the active ingredient comprises lipid extract prepared from rapid cold-dried New Zealand green-lipped mussel powder.
17. The method of claim 16 , wherein the effective amount comprises a daily dosage of 50 mg of lipid extract prepared from rapid cold-dried New Zealand green-lipped mussel powder.
18. The method of claim 14 , wherein the active ingredient comprises one or more of an octadecatetraenoic acid, an eicosatetraenoic acid, an eicosapentaenoic acid, and a docosahexaenoic acid.
19. The method of claim 14 , wherein the patient has an initial bone mineral density of less than 1 standard deviation from an average bone mineral density.
20. The method of claim 14 , wherein the patient has an initial bone mineral density of less than 2.5 standard deviations from an average bone mineral density.