Evidence map›Paper›PMID 31524631›Full record

ArticleThe Journal of clinical investigation2019

Enhancing glycolysis attenuates Parkinson's disease progression in models and clinical databases.

Rong Cai, Yu Zhang, Jacob E Simmering, Jordan L Schultz, Yuhong Li, Irene Fernandez-Carasa, Antonella Consiglio, Angel Raya, Philip M Polgreen, Nandakumar S Narayanan and 9 more

4 registry-linked trialsOpen access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 4 registered trials, which are not on this map. Cited by 155 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
155citing papers in PubMed, 1 pooled it
16.8field-weighted citation impact, top 1% 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.

NCT04551040 phase1active not recruitingnot on this mapstarted 2021, after this paper: background citation

Assessing Target Engagement of Terazosin in Healthy Adults

TypeinterventionalSponsorUniversity of IowaRan2021 to 2025Enrolled18ConditionsHealthyArmsTerazosin
NCT04760860 phase1 / phase2not yet recruitingnot on this mapstarted 2027, after this paper: background citation

a Randomized, Double Blind, Placebo Controlled Clinical Trial Exploring the Target Engagement and Tolerability of Terazosin Hydrochloride in Patients With Dementia With Lewy Bodies

TypeinterventionalSponsorQiang ZhangRan2027 to 2030Enrolled40ConditionsDementia With Lewy BodiesArmsTerazosin Hydrochloride, Placebo
NCT05109364 phase2active not recruitingnot on this mapstarted 2022, after this paper: background citation

The Effect of alpha1- Adrenergic Receptor Antagonist Therapy on Cardiac and Striatal Transporter Uptake in Pre-Motor and Symptomatic Parkinson's Disease: A Follow up Study

TypeinterventionalSponsorCedars-Sinai Medical CenterRan2022 to 2026Enrolled15ConditionsSymptomatic Parkinson Disease, REM Sleep Behavior Disorder, Pre-motor Parkinson's DiseaseArmsTerazosin therapy
NCT07464028 phase2not yet recruitingnot on this mapstarted 2026, after this paper: background citation

Assessing Target Engagement for Terazosin in Parkinson's Disease (TZPD2)

TypeinterventionalSponsorNandakumar NarayananRan2026 to 2031Enrolled120ConditionsParkinson's Disease (PD)ArmsTerazosin 5 MG, Placebo
3 · Its place in the literature

Who cites it

155 citing papers in PubMed, 1 synthesis or guideline pooled it, 276 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Glycolysis-enhancing αAlzheimer's research & therapy · 2026
    Article
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  8. Review
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  16. Catecholaminergic storm and extreme blood pressure lability induced by combined levodopa/benserazide, selegiline, and piribedil in Parkinson's disease: a case report.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
    Article
  17. Article
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  20. Article

95 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 7 institutions in 4 countries.

Rong CaiInstitute of Hypoxia Medicine, Xuanwu Hospital and Key Laboratory for Neurodegenerative Diseases of the Ministry of Education, and.
Yu ZhangState Key Laboratory of Membrane Biology, School of Life Sciences, Peking University, Beijing, China.
Jacob E SimmeringDepartment of Internal Medicine and.
Jordan L SchultzDepartments of Pharmaceutical Care and Neurology, Carver College of Medicine, University of Iowa, Iowa City, Iowa, USA.
Yuhong LiCenter of Stroke, Beijing Institute for Brain Disorders, Capital Medical University, Beijing, China.
Irene Fernandez-CarasaDepartment of Pathology and Experimental Therapeutics, Bellvitge University Hospital-IDIBELL, Hospitalet de Llobregat and Institute of Biomedicine of the University of Barcelona (IBUB), Barcelona, Spain.
Antonella ConsiglioDepartment of Pathology and Experimental Therapeutics, Bellvitge University Hospital-IDIBELL, Hospitalet de Llobregat and Institute of Biomedicine of the University of Barcelona (IBUB), Barcelona, Spain.
Angel RayaCenter of Regenerative Medicine in Barcelona (CMRB) and Networking Biomedical Research Center in Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN), Hospital Duran i Reynals, Hospitalet de Llobregat, Barcelona, Spain.
Philip M PolgreenDepartments of Internal Medicine and Epidemiology and.
Nandakumar S NarayananDepartment of Neurology, Carver College of Medicine, University of Iowa, Iowa City, Iowa, USA.
Yanpeng YuanInstitute of Hypoxia Medicine, Xuanwu Hospital and Key Laboratory for Neurodegenerative Diseases of the Ministry of Education, and.
Zhiguo ChenInstitute of Hypoxia Medicine, Xuanwu Hospital and Key Laboratory for Neurodegenerative Diseases of the Ministry of Education, and.
Wenting SuCenter of Stroke, Beijing Institute for Brain Disorders, Capital Medical University, Beijing, China.
Yanping HanInstitute of Hypoxia Medicine, Xuanwu Hospital and Key Laboratory for Neurodegenerative Diseases of the Ministry of Education, and.
Chunyue ZhaoBeijing Advanced Innovation Center for Big Data-Based Precision Medicine, Beihang University, Beijing, China.
Lifang GaoCenter of Stroke, Beijing Institute for Brain Disorders, Capital Medical University, Beijing, China.
Xunming JiInstitute of Hypoxia Medicine, Xuanwu Hospital and Key Laboratory for Neurodegenerative Diseases of the Ministry of Education, and.
Michael J WelshHoward Hughes Medical Institute, Departments of Internal Medicine, Neurology, and Molecular Physiology and Biophysics, Carver College of Medicine, University of Iowa, Iowa City, Iowa, USA.
Lei LiuCenter of Stroke, Beijing Institute for Brain Disorders, Capital Medical University, Beijing, China.
Capital Medical University · CNBellvitge University Hospital · ESUniversity of Iowa · USBeihang University · CNHoward Hughes Medical Institute · USInstitució Catalana de Recerca i Estudis Avançats · ESPeking University · CN

Funding

Respiratory virus infection in early cystic fibrosis lung diseaseP01HL091842 · NHLBI · UNIVERSITY OF IOWA · PI ZABNER, JOSEPH · 2008 to 2022
$34.2M
The University of Iowa Clinical and Translational Science AwardUL1TR002537 · NCATS · UNIVERSITY OF IOWA · PI HANSEN, MARLAN R, WINOKUR, PATRICIA · 2018 to 2022
$20.0M
The University of Iowa Clinical and Translational Science AwardKL2TR002536 · NCATS · UNIVERSITY OF IOWA · PI BASSUK, ALEXANDER G · 2018 to 2022
$3.3M
NCATS NIH HHS KL2 TR002536NCATS NIH HHS UL1 TR002537NHLBI NIH HHS P01 HL091842
6 · The paper itself

Abstract

Parkinson's disease (PD) is a common neurodegenerative disease that lacks therapies to prevent progressive neurodegeneration. Impaired energy metabolism and reduced ATP levels are common features of PD. Previous studies revealed that terazosin (TZ) enhances the activity of phosphoglycerate kinase 1 (PGK1), thereby stimulating glycolysis and increasing cellular ATP levels. Therefore, we asked whether enhancement of PGK1 activity would change the course of PD. In toxin-induced and genetic PD models in mice, rats, flies, and induced pluripotent stem cells, TZ increased brain ATP levels and slowed or prevented neuron loss. The drug increased dopamine levels and partially restored motor function. Because TZ is prescribed clinically, we also interrogated 2 distinct human databases. We found slower disease progression, decreased PD-related complications, and a reduced frequency of PD diagnoses in individuals taking TZ and related drugs. These findings suggest that enhancing PGK1 activity and increasing glycolysis may slow neurodegeneration in PD.

Indexed as

Adenosine TriphosphateAgedAged, 80 and overAnimalsBrainDisease ProgressionDopamineDrosophila melanogasterFemaleGlycolysisHumansInduced Pluripotent Stem CellsMaleMiceMice, Inbred C57BLNerve DegenerationAdenosine TriphosphateDopaminePGK1 protein, humanPhosphoglycerate KinasePrazosinTerazosinNeuroscienceParkinson’s disease

Identifiers

PMID31524631
PMCPMC6763248
OpenAlexW2973064436

What OpenQuestion holds

Textmetadata
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.