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PA01.42. New alternative therapies in mild cognitive impairment
PURPOSE: Mild cognitive impairment (MCI) is a frequent clinical entity, considered today to be a prodromal stage of Alzheimer's dementia, but not having until now a standardized pharmacological treatment. The aim of this study is to follow the outcome of the patients diagnosed with MCI non trea...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3800975/ |
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author | Podea, Delia Marina Mila, Camelia Blaj, Maria Magdalena |
author_facet | Podea, Delia Marina Mila, Camelia Blaj, Maria Magdalena |
author_sort | Podea, Delia Marina |
collection | PubMed |
description | PURPOSE: Mild cognitive impairment (MCI) is a frequent clinical entity, considered today to be a prodromal stage of Alzheimer's dementia, but not having until now a standardized pharmacological treatment. The aim of this study is to follow the outcome of the patients diagnosed with MCI non treated and treated with nootropics, alternative herbal agents, and cholinesterase inhibitors. METHOD: The study comprises a number of 200 patients (over 60 years) diagnosed with MCI. The patients were evaluated using MMSE (Mini Mental State Evaluation) at the inclusion into the study and after 1 year of treatment. The patients were divided in four different groups: Group A - 50 patients diagnosed with MCI treated with Piracetamum 1600mg/day, Group B - 50 patients diagnosed with MCI treated with Rhodiola rosea, 2 capsules/day, Group C - 50 patients diagnosed with MCI treated with Galantamine (16mg/day), Group D - 50 patients diagnosed with MCI non treated RESULT: The average of MMSE scores at screening was 23.96 points for group A, 24.16 points for group B, 23.96 for group C and 24.5 points for group D. After 1 year of treatment, cognitive performance improves with 2.12 points for Group A, 1.97 points for Group B, 2.04 points for Group C and without any improvement for Group D. CONCLUSION: Comparing the outcome of treated and non-treated groups, we observed that the early treatment of mild cognitive impairment delay the transition to dementia. The outcome of the treated groups after 1 year of pharmacological treatment was approximately the same. This study proves the necessity of early treatment and of the enlargement of therapies in mild cognitive impairment. The acceptance of nonconventional therapies can change the relationships between physicians and well educated patients who more frequently advocate for a broad range of treatment choices. |
format | Online Article Text |
id | pubmed-3800975 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-38009752013-10-25 PA01.42. New alternative therapies in mild cognitive impairment Podea, Delia Marina Mila, Camelia Blaj, Maria Magdalena Anc Sci Life Poster Presentation PURPOSE: Mild cognitive impairment (MCI) is a frequent clinical entity, considered today to be a prodromal stage of Alzheimer's dementia, but not having until now a standardized pharmacological treatment. The aim of this study is to follow the outcome of the patients diagnosed with MCI non treated and treated with nootropics, alternative herbal agents, and cholinesterase inhibitors. METHOD: The study comprises a number of 200 patients (over 60 years) diagnosed with MCI. The patients were evaluated using MMSE (Mini Mental State Evaluation) at the inclusion into the study and after 1 year of treatment. The patients were divided in four different groups: Group A - 50 patients diagnosed with MCI treated with Piracetamum 1600mg/day, Group B - 50 patients diagnosed with MCI treated with Rhodiola rosea, 2 capsules/day, Group C - 50 patients diagnosed with MCI treated with Galantamine (16mg/day), Group D - 50 patients diagnosed with MCI non treated RESULT: The average of MMSE scores at screening was 23.96 points for group A, 24.16 points for group B, 23.96 for group C and 24.5 points for group D. After 1 year of treatment, cognitive performance improves with 2.12 points for Group A, 1.97 points for Group B, 2.04 points for Group C and without any improvement for Group D. CONCLUSION: Comparing the outcome of treated and non-treated groups, we observed that the early treatment of mild cognitive impairment delay the transition to dementia. The outcome of the treated groups after 1 year of pharmacological treatment was approximately the same. This study proves the necessity of early treatment and of the enlargement of therapies in mild cognitive impairment. The acceptance of nonconventional therapies can change the relationships between physicians and well educated patients who more frequently advocate for a broad range of treatment choices. Medknow Publications & Media Pvt Ltd 2012-12 /pmc/articles/PMC3800975/ Text en Copyright: © 2012 Delia Marina Podea; licensee Ancient Science of Life. http://creativecommons.org/licenses/by-nc-sa/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Poster Presentation Podea, Delia Marina Mila, Camelia Blaj, Maria Magdalena PA01.42. New alternative therapies in mild cognitive impairment |
title | PA01.42. New alternative therapies in mild cognitive impairment |
title_full | PA01.42. New alternative therapies in mild cognitive impairment |
title_fullStr | PA01.42. New alternative therapies in mild cognitive impairment |
title_full_unstemmed | PA01.42. New alternative therapies in mild cognitive impairment |
title_short | PA01.42. New alternative therapies in mild cognitive impairment |
title_sort | pa01.42. new alternative therapies in mild cognitive impairment |
topic | Poster Presentation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3800975/ |
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