Evidence map›Paper›PMID 29614701›Full record

ReviewJournal of Parkinson's disease2018

Targeting AMPK Signaling as a Neuroprotective Strategy in Parkinson's Disease.

Daniel W Curry, Bernardo Stutz, Zane B Andrews, John D Elsworth

Open access · bronzeAbstract readReview
In one paragraph

Review in Journal of Parkinson's disease, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed, 2 pooled it
6.5field-weighted citation impact, top 2% 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

74 citing papers in PubMed, 2 syntheses or guidelines pooled it, 153 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Can maternal metformin protect the developing fetal brain?American journal of obstetrics and gynecology · 2026
    Trial
  4. Exploring the impacts of type 2 diabetes and metformin use on Parkinson's disease: Mendelian randomization analysis and a national cohort study.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
    Article
  5. Review
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  7. Autophagy-lysosomal pathway in neurodegeneration.Molecular neurodegeneration advances · 2026
    Review
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14 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 at 2 institutions in 2 countries.

Daniel W CurryDepartment of Psychiatry, Yale University School of Medicine, New Haven, Connecticut, USA.
Bernardo StutzDepartment of Psychiatry, Yale University School of Medicine, New Haven, Connecticut, USA.
Zane B AndrewsDepartment of Physiology, Monash University, Melbourne, VIC, Australia.
John D ElsworthDepartment of Psychiatry, Yale University School of Medicine, New Haven, Connecticut, USA.
Yale University · USAustralian Regenerative Medicine Institute · AU

Funding

Developmental Factors for Reducing Dopamine Loss in Primate Models of PD & AgingR01AG048918 · NIA · YALE UNIVERSITY · PI ELSWORTH, JOHN D · 2016 to 2020
$2.4M
NIA NIH HHS R01 AG048918
6 · The paper itself

Abstract

Parkinson's disease (PD) is the second most common neurodegenerative disorder. It is characterized by the accumulation of intracellular α-synuclein aggregates and the degeneration of nigrostriatal dopaminergic neurons. While no treatment strategy has been proven to slow or halt the progression of the disease, there is mounting evidence from preclinical PD models that activation of 5'-AMP-activated protein kinase (AMPK) may have broad neuroprotective effects. Numerous dietary supplements and pharmaceuticals (e.g., metformin) that increase AMPK activity are available for use in humans, but clinical studies of their effects in PD patients are limited. AMPK is an evolutionarily conserved serine/threonine kinase that is activated by falling energy levels and functions to restore cellular energy balance. However, in response to certain cellular stressors, AMPK activation may exacerbate neuronal atrophy and cell death. This review describes the regulation and functions of AMPK, evaluates the controversies in the field, and assesses the potential of targeting AMPK signaling as a neuroprotective treatment for PD.

Indexed as

alpha-SynucleinAMP-Activated Protein KinasesAnimalsAutophagyBrainDopaminergic NeuronsHumansNeuroprotective AgentsParkinson DiseaseSignal Transductionalpha-SynucleinAMP-Activated Protein KinasesNeuroprotective Agents5′-AMP-activated protein kinasealpha-synucleinautophagymetforminmitochondriaParkinson’s diseaseresveratrol

Identifiers

PMID29614701
PMCPMC6004921
OpenAlexW2794932818

What OpenQuestion holds

Textmetadata
LicenceTDM
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.