Evidence map›Paper›PMID 39556446›Full record

ReviewJournal of neurochemistry2025

Modulating the cholinergic system-Novel targets for deep brain stimulation in Parkinson's disease.

V Witzig, R Pjontek, S K H Tan, J B Schulz, F Holtbernd

Abstract readReview
In one paragraph

Review in Journal of neurochemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
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

5 authors.

V WitzigDepartment of Neurology, RWTH Aachen University, Aachen, Germany.ORCID 0000-0002-1141-6736
R PjontekDepartment of Neurosurgery, RWTH Aachen University, Aachen, Germany.
S K H TanDepartment of Neurosurgery, Antwerp University Hospital, Edegem, Belgium.
J B SchulzDepartment of Neurology, RWTH Aachen University, Aachen, Germany.ORCID 0000-0002-8903-0593
F HoltberndDepartment of Neurology, RWTH Aachen University, Aachen, Germany.

Funding

Medizinische Fakultät, RWTH Aachen University
6 · The paper itself

Abstract

Parkinson's disease (PD) is the second-fastest growing neurodegenerative disease in the world. The major clinical symptoms rigor, tremor, and bradykinesia derive from the degeneration of the nigrostriatal pathway. However, PD is a multi-system disease, and neurodegeneration extends beyond the degradation of the dopaminergic pathway. Symptoms such as postural instability, freezing of gait, falls, and cognitive decline are predominantly caused by alterations of transmitter systems outside the classical dopaminergic axis. While levodopa and deep brain stimulation (DBS) of the subthalamic nucleus or globus pallidus internus effectively address PD primary motor symptoms, they often fall short in mitigating axial symptoms and cognitive impairment. Along these lines, the cholinergic system is increasingly recognized to play a crucial role in governing locomotion, postural stability, and cognitive function. Thus, there is a growing interest in bolstering the cholinergic tone by DBS of cholinergic targets such as the pedunculopontine nucleus (PPN) and nucleus basalis of Meynert (NBM), aiming to alleviate these debilitating symptoms resistant to traditional treatment strategies targeting the dopaminergic network. This review offers a comprehensive overview of the role of cholinergic dysfunction in PD. We discuss the impact of PPN and NBM DBS on the management of symptoms not readily accessible to established DBS targets and pharmacotherapy in PD and seek to provide guidance on patient selection, surgical approach, and stimulation paradigms.

Indexed as

Cholinergic NeuronsDeep Brain StimulationParkinson DiseaseAnimalsBasal Nucleus of MeynertHumansPedunculopontine Tegmental Nucleusacetylcholinedeep brain stimulationneuromodulationnucleus basalis of MeynertParkinson's diseasepedunculopontine nucleus

Identifiers

PMID39556446
PMCPMC11808463

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Registered trials

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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.