Evidence map›Paper›PMID 32472577›Full record

ArticleAnnals of the New York Academy of Sciences2020

Alternatives to amyloid for Alzheimer's disease therapies-a symposium report.

Jennifer Cable, David M Holtzman, Bradley T Hyman, Malú Gámez Tansey, Marco Colonna, Manolis Kellis, Roberta D Brinton, Marilyn Albert, Cheryl L Wellington, Sangram S Sisodia and 1 more

Abstract readConference Proceedings
In one paragraph

Article in Annals of the New York Academy of Sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Review
  2. Article
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  8. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Jennifer CablePhD Science Writer, New York, New York.
David M HoltzmanDepartment of Neurology, Washington University in St. Louis, St. Louis, Missouri.
Bradley T HymanMassachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
Malú Gámez TanseyDepartment of Neuroscience, Center for Translational Research in Neurodegenerative Disease, University of Florida College of Medicine, McKnight Brain Institute, Gainesville, Florida.
Marco ColonnaDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri.
Manolis KellisMIT Computer Science and Artificial Intelligence Laboratory, Cambridge, Massachusetts.
Roberta D BrintonDepartments of Pharmacology and Neurology, College of Medicine, the University of Arizona, Tucson, Arizona.
Marilyn AlbertDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Cheryl L WellingtonDepartment of Pathology and Laboratory Medicine, Djavad Mowafaghian Centre for Brain Health, International Collaboration on Repair Discoveries, School of Biomedical Engineering, University of British Columbia, Vancouver, British Columbia, Canada.
Sangram S SisodiaDepartment of Neurobiology, the University of Chicago, Chicago, Illinois.
Rudolph E TanziDepartment of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.

Funding

Timing of Menopausal Hormone Therapy across Perimenopause to Menopause Transition: Neuroimmune System in BrainP01AG026572 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Schantel Williams · 2006 to 2026
$53.7M
NIA NIH HHS P01 AG026572
6 · The paper itself

Abstract

For decades, Alzheimer's disease research has focused on amyloid as the primary pathogenic agent. This focus has driven the development of numerous amyloid-targeting therapies; however, with one possible exception, none of these therapies have been effective in preventing or delaying cognitive decline in patients, and there are no approved disease-modifying agents. It is becoming more apparent that alternative drug targets are needed to address this complex disease. An increased understanding of Alzheimer's disease pathology has highlighted the need to target the appropriate disease pathology at the appropriate time in the disease course. Preclinical and early clinical studies have focused on targets, including inflammation, tau, vascular health, and the microbiome. This report summarizes the presentations from a New York Academy of Sciences' one-day symposium entitled "Alzheimer's Disease Therapeutics: Alternatives to Amyloid," held on November 20, 2019.

Indexed as

Molecular Targeted TherapyAlzheimer DiseaseAmyloidEpigenesis, GeneticHumansMicrobiotaMicrogliaNerve Regenerationtau ProteinsAmyloidtau ProteinsallopregnanoloneAlzheimer's diseaseamyloidAPOEcognitive impairmentdementiaHDLmicrobiomemicroglianeuroinflammationtauTREM2

Identifiers

PMID32472577
PMCPMC9621603

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.