Methods and compositions for improving cognitive function
This invention relates to treating age-related cognitive impairment. This invention in particular relates to the use of inhibitors of synaptic vesicle protein 2A (SV2A), such as levetiracetam, seletracetam, and brivaracetam, in improving cognitive function in subjects that exhibit age-related cognitive impairment or are at risk thereof, including, without limitation, subjects having or at risk for Mild Cognitive Impairment (MCI), Age-related Cognitive Decline (ARCD) or Age-Associated Memory Impairment (AAMI).
1. A method for treating age-related cognitive impairment in a human subject in need thereof, the method comprising the step of administering to said human subject levetiracetam or a pharmaceutically acceptable salt thereof at a daily dose of 125-250 mg.
2. The method of claim 1 , wherein the age-related cognitive impairment is selected from the group consisting of mild cognitive impairment, age-associated memory impairment, and age-related cognitive decline.
3. The method of claim 1 , wherein the levetiracetam or the pharmaceutically acceptable salt thereof is administered once or twice daily.
4. The method of claim 1 , wherein the effect of the treatment is measured by the Clinical Dementia Rating Scale.
5. The method of claim 1 , wherein the daily dose is 125 mg.
6. The method of claim 1 , wherein the daily dose is 250 mg.
7. A method for delaying or slowing the progression of cognitive impairment in a human subject suffering from age-related cognitive impairment, the method comprising the step of administering to said human subject levetiracetam or a pharmaceutically acceptable salt thereof at a daily dose of 125-250 mg.
8. The method of claim 7 , wherein the age-related cognitive impairment is selected from the group consisting of mild cognitive impairment, age-associated memory impairment, and age-related cognitive decline.
9. The method of claim 7 , wherein the progression of cognitive impairment is measured by the Clinical Dementia Rating Scale.
10. The method of claim 7 , wherein the levetiracetam or the pharmaceutically acceptable salt thereof is administered once or twice daily.
11. The method of claim 7 , wherein the daily dose is 125 mg.
12. The method of claim 7 , wherein the daily dose is 250 mg.
13. A method for reducing the rate of decline of cognitive function in a human subject suffering from age-related cognitive impairment, the method comprising the step of administering to said human subject levetiracetam or a pharmaceutically acceptable salt thereof at a daily dose of 125-250 mg.
14. The method of claim 13 , wherein the age-related cognitive impairment is selected from the group consisting of mild cognitive impairment, age-associated memory impairment, and age-related cognitive decline.
15. The method of claim 13 , wherein the levetiracetam or the pharmaceutically acceptable salt thereof is administered once or twice daily.
16. The method of claim 13 , wherein the rate of decline of cognitive function is measured by the Clinical Dementia Rating Scale.
17. The method of claim 13 , wherein the daily dose is 125 mg.
18. The method of claim 13 , wherein the daily dose is 250 mg.