Evidence map›Paper›PMID 18042721›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2007

Modulation of metabolic brain networks after subthalamic gene therapy for Parkinson's disease.

Andrew Feigin, Michael G Kaplitt, Chengke Tang, Tanya Lin, Paul Mattis, Vijay Dhawan, Matthew J During, David Eidelberg

2 registry-linked trialsOpen access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 88 papers.

0numbers the graph read from it
0cells of the map it votes in
88citing papers in PubMed
12.2field-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.

NCT00643890 phase2terminatednot on this mapstarted 2008, after this paper: background citation

Phase 2 Safety and Efficacy Study Evaluating Glutamic Acid Decarboxylase Gene Transfer to Subthalamic Nuclei in Subjects With Advanced Parkinson's Disease

TypeinterventionalSponsorNeurologix, Inc.Ran2008Enrolled44ConditionsParkinson's DiseaseArmsBilateral surgical infusion of AAV-GAD into the subthalamic nucleus
NCT04228172 active not recruitingnot on this mapstarted 2020, after this paper: background citation

Genotypic Influences on Network Progression in Parkinson's Disease

TypeobservationalSponsorNorthwell HealthRan2020 to 2026Enrolled32ConditionsParkinson's DiseaseArmsDNA/GeneticTesting, FDG PET scan, MRI scan, Clinical and neuropsychological assessments
3 · Its place in the literature

Who cites it

88 citing papers in PubMed, 178 citations in OpenAlex.

  1. Trial
  2. Review
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  8. Article
  9. Review
  10. Functional Brain Networks to Evaluate Treatment Responses in Parkinson's Disease.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2023
    Article
  11. Parkinson's Disease: A Tale of Many Players.Medical principles and practice : international journal of the Kuwait University, Health Science Centre · 2023
    Review
  12. Review
  13. Review
  14. Review
  15. Resting-State Functional Connectivity Predicts STN DBS Clinical Response.Movement disorders : official journal of the Movement Disorder Society · 2021
    Article
  16. Article
  17. Article
  18. Modulation of extrasynaptic GABANature communications · 2019
    Article
  19. Network Structure and Function in Parkinson's Disease.Cerebral cortex (New York, N.Y. : 1991) · 2018
    Article
  20. Review

28 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

8 authors at 5 institutions in 1 country.

Andrew FeiginCenter for Neurosciences, The Feinstein Institute for Medical Research, North Shore-Long Island Jewish Health System, 350 Community Drive, Manhasset, NY 11030, USA.
Michael G Kaplitt
Chengke Tang
Tanya Lin
Paul Mattis
Vijay Dhawan
Matthew J During
David Eidelberg
Feinstein Institute for Medical Research · USCenter for Neurosciences · USCornell University · USNew York University · USThe Ohio State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Parkinson's disease (PD) is characterized by elevated expression of an abnormal metabolic brain network that is reduced by clinically effective treatment. We used fluorodeoxyglucose (FDG) positron emission tomography (PET) to determine the basis for motor improvement in 12 PD patients receiving unilateral subthalamic nucleus (STN) infusion of an adenoassociated virus vector expressing glutamic acid decarboxylase (AAV-GAD). After gene therapy, we observed significant reductions in thalamic metabolism on the operated side as well as concurrent metabolic increases in ipsilateral motor and premotor cortical regions. Abnormal elevations in the activity of metabolic networks associated with motor and cognitive functioning in PD patients were evident at baseline. The activity of the motor-related network declined after surgery and persisted at 1 year. These network changes correlated with improved clinical disability ratings. By contrast, the activity of the cognition-related network did not change after gene transfer. This suggests that modulation of abnormal network activity underlies the clinical outcome observed after unilateral STN AAV-GAD gene therapy. Network biomarkers may be used as physiological assays in early-phase trials of experimental therapies for PD and other neurodegenerative disease.

Indexed as

Genetic TherapyAgedBrainDependovirusFemaleGlucoseGlutamate DecarboxylaseHumansMaleMetabolic Networks and PathwaysMiddle AgedParkinson DiseasePositron-Emission TomographySubthalamic NucleusGlucoseGlutamate Decarboxylase

Identifiers

PMID18042721
PMCPMC2148328
OpenAlexW2047000182

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.