Evidence map›Paper›PMID 30541602›Full record

ReviewMolecular neurodegeneration2018

Advances in developing novel therapeutic strategies for Alzheimer's disease.

Jiqing Cao, Jianwei Hou, Jing Ping, Dongming Cai

Abstract readReview
In one paragraph

Review in Molecular neurodegeneration, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 126 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
126citing papers in PubMed, 3 pooled it
–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

126 citing papers in PubMed, 3 syntheses or guidelines pooled it.

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  15. Gaultheria leucocarpa inhibits Aβ fibrillization and enhances mitophagy-mediated degradation of pathogenic proteins.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2025
    Article
  16. Article
  17. Wine-ProcessedFood science & nutrition · 2025
    Article
  18. Review
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66 more citing papers are in PubMed but not listed here.

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

4 authors.

Jiqing CaoJames J Peters VA Medical Center, Research & Development, Bronx, NY, 10468, USA.
Jianwei HouJames J Peters VA Medical Center, Research & Development, Bronx, NY, 10468, USA.
Jing PingThe Central Hospital of The Hua Zhong University of Science and Technology, Wuhan, China.
Dongming CaiJames J Peters VA Medical Center, Research & Development, Bronx, NY, 10468, USA. dongming.cai@mssm.edu.ORCID 0000-0002-0601-6826

Funding

Molecular Characterization and Validation of Gender Differences in Alzheimers Disease PathogenesisRF1AG054014 · NIA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CAI, DONGMING, ZHANG, BIN · 2016 to 2016
$4.2M
Characterization of ApoE4 Induced Phospholipid Dysregulation in AD PathogenesisR01AG048923 · NIA · UNIVERSITY OF MINNESOTA · PI CAI, DONGMING · 2015 to 2025
$3.1M
MicroRNA Regulation of Phospholipid Homeostasis in Alzheimer's Disease PathogenesisI01BX003380 · VA · MINNEAPOLIS VA MEDICAL CENTER · PI CAI, DONGMING · 2017 to 2025
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Novel small molecules targeting brain phospholipid dysregulation in ADI01RX002290 · VA · JAMES J PETERS VA MEDICAL CENTER · PI CAI, DONGMING · 2018 to 2022
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BLRD VA I01 BX003380NIA NIH HHS R01 AG048923NIA NIH HHS RF1 AG054014RRD VA I01 RX002290
6 · The paper itself

Abstract

Alzheimer's Disease (AD), the most prevalent neurodegenerative disease of aging, affects one in eight older Americans. Nearly all drug treatments tested for AD today have failed to show any efficacy. There is a great need for therapies to prevent and/or slow the progression of AD. The major challenge in AD drug development is lack of clarity about the mechanisms underlying AD pathogenesis and pathophysiology. Several studies support the notion that AD is a multifactorial disease. While there is abundant evidence that amyloid plays a role in AD pathogenesis, other mechanisms have been implicated in AD such as tangle formation and spread, dysregulated protein degradation pathways, neuroinflammation, and loss of support by neurotrophic factors. Therefore, current paradigms of AD drug design have been shifted from single target approach (primarily amyloid-centric) to developing drugs targeted at multiple disease aspects, and from treating AD at later stages of disease progression to focusing on preventive strategies at early stages of disease development. Here, we summarize current strategies and new trends of AD drug development, including pre-clinical and clinical trials that target different aspects of disease (mechanism-based versus non-mechanism based, e.g. symptomatic treatments, lifestyle modifications and risk factor management).

Indexed as

Clinical Trials as TopicDisease ProgressionDrug DevelopmentAlzheimer DiseaseAnimalsDisease Models, AnimalHumansRisk FactorsAlzheimer’s diseaseDrug developmentNovel therapiesPre-clinical and clinical trials

Identifiers

PMID30541602
PMCPMC6291983

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.