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Reversal of cognitive decline in Alzheimer's disease
Alzheimer's disease is one of the most significant healthcare problems nationally and globally. Recently, the first description of the reversal of cognitive decline in patients with early Alzheimer's disease or its precursors, MCI (mild cognitive impairment) and SCI (subjective cognitive i...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4931830/ https://www.ncbi.nlm.nih.gov/pubmed/27294343 http://dx.doi.org/10.18632/aging.100981 |
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author | Bredesen, Dale E. Amos, Edwin C. Canick, Jonathan Ackerley, Mary Raji, Cyrus Fiala, Milan Ahdidan, Jamila |
author_facet | Bredesen, Dale E. Amos, Edwin C. Canick, Jonathan Ackerley, Mary Raji, Cyrus Fiala, Milan Ahdidan, Jamila |
author_sort | Bredesen, Dale E. |
collection | PubMed |
description | Alzheimer's disease is one of the most significant healthcare problems nationally and globally. Recently, the first description of the reversal of cognitive decline in patients with early Alzheimer's disease or its precursors, MCI (mild cognitive impairment) and SCI (subjective cognitive impairment), was published [1]. The therapeutic approach used was programmatic and personalized rather than monotherapeutic and invariant, and was dubbed metabolic enhancement for neurodegeneration (MEND). Patients who had had to discontinue work were able to return to work, and those struggling at work were able to improve their performance. The patients, their spouses, and their co-workers all reported clear improvements. Here we report the results from quantitative MRI and neuropsychological testing in ten patients with cognitive decline, nine ApoE4+ (five homozygous and four heterozygous) and one ApoE4−, who were treated with the MEND protocol for 5-24 months. The magnitude of the improvement is unprecedented, providing additional objective evidence that this programmatic approach to cognitive decline is highly effective. These results have far-reaching implications for the treatment of Alzheimer's disease, MCI, and SCI; for personalized programs that may enhance pharmaceutical efficacy; and for personal identification of ApoE genotype. |
format | Online Article Text |
id | pubmed-4931830 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-49318302016-07-18 Reversal of cognitive decline in Alzheimer's disease Bredesen, Dale E. Amos, Edwin C. Canick, Jonathan Ackerley, Mary Raji, Cyrus Fiala, Milan Ahdidan, Jamila Aging (Albany NY) Research Paper Alzheimer's disease is one of the most significant healthcare problems nationally and globally. Recently, the first description of the reversal of cognitive decline in patients with early Alzheimer's disease or its precursors, MCI (mild cognitive impairment) and SCI (subjective cognitive impairment), was published [1]. The therapeutic approach used was programmatic and personalized rather than monotherapeutic and invariant, and was dubbed metabolic enhancement for neurodegeneration (MEND). Patients who had had to discontinue work were able to return to work, and those struggling at work were able to improve their performance. The patients, their spouses, and their co-workers all reported clear improvements. Here we report the results from quantitative MRI and neuropsychological testing in ten patients with cognitive decline, nine ApoE4+ (five homozygous and four heterozygous) and one ApoE4−, who were treated with the MEND protocol for 5-24 months. The magnitude of the improvement is unprecedented, providing additional objective evidence that this programmatic approach to cognitive decline is highly effective. These results have far-reaching implications for the treatment of Alzheimer's disease, MCI, and SCI; for personalized programs that may enhance pharmaceutical efficacy; and for personal identification of ApoE genotype. Impact Journals LLC 2016-06-12 /pmc/articles/PMC4931830/ /pubmed/27294343 http://dx.doi.org/10.18632/aging.100981 Text en Copyright: © 2016 Bredesen et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Bredesen, Dale E. Amos, Edwin C. Canick, Jonathan Ackerley, Mary Raji, Cyrus Fiala, Milan Ahdidan, Jamila Reversal of cognitive decline in Alzheimer's disease |
title | Reversal of cognitive decline in Alzheimer's disease |
title_full | Reversal of cognitive decline in Alzheimer's disease |
title_fullStr | Reversal of cognitive decline in Alzheimer's disease |
title_full_unstemmed | Reversal of cognitive decline in Alzheimer's disease |
title_short | Reversal of cognitive decline in Alzheimer's disease |
title_sort | reversal of cognitive decline in alzheimer's disease |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4931830/ https://www.ncbi.nlm.nih.gov/pubmed/27294343 http://dx.doi.org/10.18632/aging.100981 |
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