Evidence map›Paper›PMID 29316249›Full record

ArticleAging cell2018

The mitochondrial ATP synthase is a shared drug target for aging and dementia.

Joshua Goldberg, Antonio Currais, Marguerite Prior, Wolfgang Fischer, Chandramouli Chiruta, Eric Ratliff, Daniel Daugherty, Richard Dargusch, Kim Finley, Pau B Esparza-Moltó and 4 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Aging cell, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03838185 (A Phase I, Randomized, Double-Blind, Placebo-Controlled Study to Assess the Safety, Tolerability and Pharmacokinetics of Single Ascending Oral Doses of J147 in Healthy Young Volunteers and Healthy Elderly Volunteers), which is not on this map. Cited by 72 papers.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed
6.2field-weighted citation impact, top 3% 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.

NCT03838185 phase1completednot on this mapstarted 2019, after this paper: background citation

A Phase I, Randomized, Double-Blind, Placebo-Controlled Study to Assess the Safety, Tolerability and Pharmacokinetics of Single Ascending Oral Doses of J147 in Healthy Young Volunteers and Healthy Elderly Volunteers

TypeinterventionalSponsorAbrexa Pharmaceuticals, Inc.Ran2019 to 2020Enrolled64ConditionsAlzheimer's DiseaseArmsJ147, Placebo
3 · Its place in the literature

Who cites it

72 citing papers in PubMed, 122 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Period3 modulates the NADJournal of advanced research · 2025
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  9. Review
  10. Transcriptional drift in aging cells: A global decontroller.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  11. The Influence of Cannabinoids onCannabis and cannabinoid research · 2024
    Article
  12. Mitochondrial Targeted Interventions for Aging.Cold Spring Harbor perspectives in medicine · 2024
    Review
  13. Content of stress granules reveals a sex difference at the early phase of cold exposure in mice.American journal of physiology. Endocrinology and metabolism · 2024
    Article
  14. Article
  15. Article
  16. Article
  17. Transcriptional drift in aging cells: A global de-controller.bioRxiv : the preprint server for biology · 2023
    Article
  18. Review
  19. Article
  20. Article

12 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

14 authors at 4 institutions in 2 countries.

Joshua GoldbergCellular Neurobiology, The Salk Institute for Biological Studies, La Jolla, CA, USA.
Antonio CurraisCellular Neurobiology, The Salk Institute for Biological Studies, La Jolla, CA, USA.
Marguerite PriorCellular Neurobiology, The Salk Institute for Biological Studies, La Jolla, CA, USA.
Wolfgang FischerCellular Neurobiology, The Salk Institute for Biological Studies, La Jolla, CA, USA.
Chandramouli ChirutaCellular Neurobiology, The Salk Institute for Biological Studies, La Jolla, CA, USA.
Eric RatliffDonald P. Shiley BioScience Center, San Diego State University, San Diego, CA, USA.
Daniel DaughertyCellular Neurobiology, The Salk Institute for Biological Studies, La Jolla, CA, USA.
Richard DarguschCellular Neurobiology, The Salk Institute for Biological Studies, La Jolla, CA, USA.
Kim FinleyDonald P. Shiley BioScience Center, San Diego State University, San Diego, CA, USA.
Pau B Esparza-MoltóCentro de Biología Molecular, CIBERER, Universidad Autónoma de Madrid, Madrid, Spain.
José M CuezvaCentro de Biología Molecular, CIBERER, Universidad Autónoma de Madrid, Madrid, Spain.
Pamela MaherCellular Neurobiology, The Salk Institute for Biological Studies, La Jolla, CA, USA.
Michael PetrascheckChemical Physiology, The Scripps Research Institute, La Jolla, CA, USA.
David SchubertCellular Neurobiology, The Salk Institute for Biological Studies, La Jolla, CA, USA.
Salk Institute for Biological Studies · USCentro de Biología Molecular Severo Ochoa · ESSan Diego State University · USScripps Research Institute · US

Funding

Salk Institute for Biological Studies NINDS Center Core GrantP30NS072031 · NINDS · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI O'LEARY, DENNIS D · 2011 to 2015
$4.2M
Identification of Old-Age-Associated Alzheimer's Disease Drug TargetsR01AG046153 · NIA · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI MAHER, PAMELA ANNE, SCHUBERT, DAVID R · 2014 to 2018
$2.9M
Modulation of the Innate Immune Response by Fisetin Derivatives for the Treatment of ADR44AI104034 · NIAID · VIROGENICS, INC. · PI RASCHKE, WILLIAM C · 2018 to 2020
$2.9M
Modulation of the Innate Immune Response by Fisetin Derivatives for the Treatment of ADR42AI104034 · NIAID · VIROGENICS, INC. · PI MAHER, PAMELA ANNE · 2016 to 2017
$1.5M
Identifying Drugs to Treat Age-Dependent NeurodegenerationR44AG033427 · NIA · EXPRESSION DRUG DESIGNS, LLC · PI FINLEY, KIM D. · 2011 to 2012
$1.3M
Modulation of the Innate Immune System by Fisetin for the Treatment of ADR41AI104034 · NIAID · VIROGENICS, INC. · PI MAHER, PAMELA ANNE · 2013 to 2014
$600k
NIAID NIH HHS R41 AI104034NIAID NIH HHS R42 AI104034NIAID NIH HHS R44 AI104034NIA NIH HHS R01 AG046153NIA NIH HHS R44 AG033427NINDS NIH HHS P30 NS072031
6 · The paper itself

Abstract

Aging is a major driving force underlying dementia, such as that caused by Alzheimer's disease (AD). While the idea of targeting aging as a therapeutic strategy is not new, it remains unclear how closely aging and age-associated diseases are coupled at the molecular level. Here, we discover a novel molecular link between aging and dementia through the identification of the molecular target for the AD drug candidate J147. J147 was developed using a series of phenotypic screening assays mimicking disease toxicities associated with the aging brain. We have previously demonstrated the therapeutic efficacy of J147 in several mouse models of AD. Here, we identify the mitochondrial α-F

Indexed as

AgingDementiaHumansMitochondriaMitochondrial Proton-Translocating ATPasesMitochondrial Proton-Translocating ATPasesagingAlzheimer's diseaseATP synthasedementiametabolismmitochondrianeurodegeneration

Identifiers

PMID29316249
PMCPMC5847861
OpenAlexW2783029224

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.