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

Alzheimer’s disease amyloid-β dementia prevention diversity in science gender lifestyle factors lifestyle interventions pharmaceutical industry tau protein women in science

Journal

Journal of Alzheimer's disease reports
ISSN: 2542-4823
Titre abrégé: J Alzheimers Dis Rep
Pays: Netherlands
ID NLM: 101705500

Informations de publication

Date de publication:
2021
Historique:
accepted: 05 07 2021
entrez: 11 10 2021
pubmed: 12 10 2021
medline: 12 10 2021
Statut: epublish

Résumé

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. 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. 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. 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. 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.

Sections du résumé

BACKGROUND 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 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 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 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 CONCLUSIONS
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.

Identifiants

pubmed: 34632301
doi: 10.3233/ADR-210030
pii: ADR210030
pmc: PMC8461732
doi:

Types de publication

Journal Article

Langues

eng

Pagination

637-645

Informations de copyright

© 2021 – The authors. Published by IOS Press.

Déclaration de conflit d'intérêts

Timothy Daly, Marion Houot, Anouk Barberousse, and Amélie Petit declare no conflicts of interest. Stéphane Epelbaum has received consulting fees from Biogen, Roche, Eisai and GE Healthcare.

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Auteurs

Timothy Daly (T)

Sorbonne Université, Science Norms Democracy, Paris, France.

Marion Houot (M)

Sorbonne Université, Institut du Cerveau - Paris Brain Institute - ICM, Inserm, CNRS, APHP, Hôpital de la Pitié Salpêtrière, Paris, France.
AP-HP, Hôpital de la Pitié Salpêtrière, Institute of Memory and Alzheimer's Disease, Centre of Excellence of Neurodegenerative Disease (CoEN), National Reference Centre for Rare and Early Dementias, Department of Neurology, Paris, France.

Anouk Barberousse (A)

Sorbonne Université, Science Norms Democracy, Paris, France.

Amélie Petit (A)

Université Paris Saclay, Inserm, CESP, Paris, France.

Stéphane Epelbaum (S)

Sorbonne Université, Institut du Cerveau - Paris Brain Institute - ICM, Inserm, CNRS, APHP, Hôpital de la Pitié Salpêtrière, Paris, France.
AP-HP, Hôpital de la Pitié Salpêtrière, Institute of Memory and Alzheimer's Disease, Centre of Excellence of Neurodegenerative Disease (CoEN), National Reference Centre for Rare and Early Dementias, Department of Neurology, Paris, France.

Classifications MeSH