Evidence map›Paper›PMID 29955650›Full record

ArticleAlzheimer's & dementia (New York, N. Y.)2018

Translational inhibition of APP by Posiphen: Efficacy, pharmacodynamics, and pharmacokinetics in the APP/PS1 mouse.

Andrew F Teich, Ekta Sharma, Eliza Barnwell, Hong Zhang, Agnieszka Staniszewski, Tadanobu Utsuki, Vasudevaraju Padmaraju, Cheryl Mazell, Apostolia Tzekou, Kumar Sambamurti and 2 more

Open access · goldAbstract read
In one paragraph

Article in Alzheimer's & dementia (New York, N. Y.), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.4field-weighted citation impact, top 12% of its field
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

31 citing papers in PubMed, 42 citations in OpenAlex.

  1. Trial
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  4. Article
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  6. Neuroprotection in Parkinson Disease.Neurology and therapy · 2025
    Review
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  9. Article
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  15. ACS pharmacology & translational science · 2022
    Article
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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

12 authors at 3 institutions in 1 country.

Andrew F TeichDepartment of Pathology and Cell Biology, Taub Institute, Columbia University, New York City, NY, USA.
Ekta SharmaDepartment of Neurosciences and Ophthalmology, Medical University of South Carolina, Charleston, SC, USA.
Eliza BarnwellDepartment of Neurosciences and Ophthalmology, Medical University of South Carolina, Charleston, SC, USA.
Hong ZhangDepartment of Pathology and Cell Biology, Taub Institute, Columbia University, New York City, NY, USA.
Agnieszka StaniszewskiDepartment of Pathology and Cell Biology, Taub Institute, Columbia University, New York City, NY, USA.
Tadanobu UtsukiDepartment of Neurosciences and Ophthalmology, Medical University of South Carolina, Charleston, SC, USA.
Vasudevaraju PadmarajuDepartment of Neurosciences and Ophthalmology, Medical University of South Carolina, Charleston, SC, USA.
Cheryl MazellDepartment of Neurosciences and Ophthalmology, Medical University of South Carolina, Charleston, SC, USA.
Apostolia TzekouQR Pharma Inc., Berwyn, PA, USA.
Kumar SambamurtiDepartment of Neurosciences and Ophthalmology, Medical University of South Carolina, Charleston, SC, USA.
Ottavio ArancioDepartment of Pathology and Cell Biology, Taub Institute, Columbia University, New York City, NY, USA.
Maria L MaccecchiniQR Pharma Inc., Berwyn, PA, USA.
Medical University of South Carolina · USColumbia University · USQR Pharma (United States) · US

Funding

Understanding the Neuroprotective Activities of PosiphenR21AG046200 · NIA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI SAMBAMURTI, KUMAR · 2013 to 2014
$411k
Small molecule inhibitor of amyloid precursor protein synthesisR43AG037247 · NIA · ANNOVIS BIO, INC. · PI MACCECCHINI, MARIA · 2010 to 2010
$214k
NIA NIH HHS R21 AG046200NIA NIH HHS R43 AG037247
6 · The paper itself

Abstract

introductionTranslational inhibition of amyloid precursor protein (APP) by Posiphen has been shown to reduce APP and its fragments in cell culture, animal models, and mildly cognitively impaired patients, making it a promising drug candidate for the treatment of Alzheimer's disease.

methodsWe used a mouse model of Alzheimer's disease (APP/presenilin-1) to examine Posiphen's efficacy, pharmacodynamics, and pharmacokinetics.

resultsPosiphen treatment normalized impairments in spatial working memory, contextual fear learning, and synaptic function in APP/presenilin-1 mice, without affecting their visual acuity, motor skills, or motivation and without affecting wild-type mice. Posiphen had a prolonged effect in reducing APP and all related peptides for at least 9 hours after the last dose. Its concentration was higher in the brain than in plasma, and the most abundant metabolite was N DISCUSSION: This is the first study demonstrating the therapeutic efficacy of inhibiting the translation of APP and its fragments in an Alzheimer's disease model.

Indexed as

Alzheimer's diseaseAPPAPP/PS1Aβ42CognitionCTFαCTFβLong-term potentiationPosiphen

Identifiers

PMID29955650
PMCPMC6021259
OpenAlexW2789361163

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.