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A Proposal to Make Biomedical Research into Alzheimer’s Disease More Democratic Following an International Survey with Researchers

BACKGROUND: Therapeutic research into Alzheimer’s disease (AD) has been dominated by the amyloid cascade hypothesis (ACH) since the 1990s. However, targeting amyloid in AD patients has not yet resulted in highly significant disease-modifying effects. Furthermore, other promising theories of AD etiol...

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Autores principales: Daly, Timothy, Houot, Marion, Barberousse, Anouk, Petit, Amélie, Epelbaum, Stéphane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8461732/
https://www.ncbi.nlm.nih.gov/pubmed/34632301
http://dx.doi.org/10.3233/ADR-210030
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author Daly, Timothy
Houot, Marion
Barberousse, Anouk
Petit, Amélie
Epelbaum, Stéphane
author_facet Daly, Timothy
Houot, Marion
Barberousse, Anouk
Petit, Amélie
Epelbaum, Stéphane
author_sort Daly, Timothy
collection PubMed
description BACKGROUND: Therapeutic research into Alzheimer’s disease (AD) has been dominated by the amyloid cascade hypothesis (ACH) since the 1990s. However, targeting amyloid in AD patients has not yet resulted in highly significant disease-modifying effects. Furthermore, other promising theories of AD etiology exist. OBJECTIVE: We sought to directly investigate whether the ACH still dominates the opinions of researchers working on AD and explore the implications of this question for future directions of research. METHODS: During 2019, we undertook an international survey promoted with the help of the Alzheimer’s Association with questions on theories and treatments of AD. Further efforts to promote a similar study in 2021 did not recruit a significant number of participants. RESULTS: 173 researchers took part in the 2019 survey, 22% of which held “pro-ACH” opinions, tended to have more publications, were more likely to be male, and over 60. Thus, pro-ACH may now be a minority opinion in the field but is nevertheless the hypothesis on which the most clinical trials are based, suggestive of a representation bias. Popular vote of all 173 participants suggested that lifestyle treatments and anti-tau drugs were a source of more therapeutic optimism than anti-amyloid treatments. CONCLUSION: We propose a more democratic research structure which increases the likelihood that promising theories are published and funded fairly, promotes a broader scientific view of AD, and reduces the larger community’s dependence on a fragile economic model.
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spelling pubmed-84617322021-10-07 A Proposal to Make Biomedical Research into Alzheimer’s Disease More Democratic Following an International Survey with Researchers Daly, Timothy Houot, Marion Barberousse, Anouk Petit, Amélie Epelbaum, Stéphane J Alzheimers Dis Rep Research Report BACKGROUND: Therapeutic research into Alzheimer’s disease (AD) has been dominated by the amyloid cascade hypothesis (ACH) since the 1990s. However, targeting amyloid in AD patients has not yet resulted in highly significant disease-modifying effects. Furthermore, other promising theories of AD etiology exist. OBJECTIVE: We sought to directly investigate whether the ACH still dominates the opinions of researchers working on AD and explore the implications of this question for future directions of research. METHODS: During 2019, we undertook an international survey promoted with the help of the Alzheimer’s Association with questions on theories and treatments of AD. Further efforts to promote a similar study in 2021 did not recruit a significant number of participants. RESULTS: 173 researchers took part in the 2019 survey, 22% of which held “pro-ACH” opinions, tended to have more publications, were more likely to be male, and over 60. Thus, pro-ACH may now be a minority opinion in the field but is nevertheless the hypothesis on which the most clinical trials are based, suggestive of a representation bias. Popular vote of all 173 participants suggested that lifestyle treatments and anti-tau drugs were a source of more therapeutic optimism than anti-amyloid treatments. CONCLUSION: We propose a more democratic research structure which increases the likelihood that promising theories are published and funded fairly, promotes a broader scientific view of AD, and reduces the larger community’s dependence on a fragile economic model. IOS Press 2021-08-06 /pmc/articles/PMC8461732/ /pubmed/34632301 http://dx.doi.org/10.3233/ADR-210030 Text en © 2021 – The authors. Published by IOS Press https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC 4.0) License (https://creativecommons.org/licenses/by-nc/4.0/) , which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Report
Daly, Timothy
Houot, Marion
Barberousse, Anouk
Petit, Amélie
Epelbaum, Stéphane
A Proposal to Make Biomedical Research into Alzheimer’s Disease More Democratic Following an International Survey with Researchers
title A Proposal to Make Biomedical Research into Alzheimer’s Disease More Democratic Following an International Survey with Researchers
title_full A Proposal to Make Biomedical Research into Alzheimer’s Disease More Democratic Following an International Survey with Researchers
title_fullStr A Proposal to Make Biomedical Research into Alzheimer’s Disease More Democratic Following an International Survey with Researchers
title_full_unstemmed A Proposal to Make Biomedical Research into Alzheimer’s Disease More Democratic Following an International Survey with Researchers
title_short A Proposal to Make Biomedical Research into Alzheimer’s Disease More Democratic Following an International Survey with Researchers
title_sort proposal to make biomedical research into alzheimer’s disease more democratic following an international survey with researchers
topic Research Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8461732/
https://www.ncbi.nlm.nih.gov/pubmed/34632301
http://dx.doi.org/10.3233/ADR-210030
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