Evidence map›Paper›PMID 31958098›Full record

ReviewJournal of Parkinson's disease2020

Does Developmental Variability in the Number of Midbrain Dopamine Neurons Affect Individual Risk for Sporadic Parkinson's Disease?

Christian U von Linstow, Merritt DeLano-Taylor, Jeffrey H Kordower, Patrik Brundin

Abstract readReview
In one paragraph

Review in Journal of Parkinson's disease, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
–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

18 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Impact of aging on animal models of Parkinson's disease.Frontiers in aging neuroscience · 2022
    Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Genetic Elements at the Alpha-Synuclein Locus.Frontiers in neuroscience · 2022
    Review
  12. Review
  13. Review
  14. Review
  15. Review
  16. Review
  17. Review
  18. 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

4 authors.

Christian U von LinstowCenter for Neurodegenerative Science, Van Andel Institute, Grand Rapids, MI, USA.
Merritt DeLano-TaylorCenter for Neurodegenerative Science, Van Andel Institute, Grand Rapids, MI, USA.
Jeffrey H KordowerDepartment of Neurological Sciences, Rush University Medical Center, Chicago, IL, USA.
Patrik BrundinCenter for Neurodegenerative Science, Van Andel Institute, Grand Rapids, MI, USA.

Funding

Linking Synucleinopathy and Dysfunction of Olfactory PathwaysR01DC016519 · NIDCD · VAN ANDEL RESEARCH INSTITUTE · PI MOORE, DARREN JOHN, WESSON, DANIEL W · 2017 to 2021
$2.8M
Combining synucleinopathy and mitochondrial deficits in a novel mouse model of Parkinsons diseaseR21NS106078 · NINDS · VAN ANDEL RESEARCH INSTITUTE · PI BRUNDIN, PATRIK, KORDOWER, JEFFREY H · 2019 to 2020
$921k
Does Microglial Activation Influence Propagation of Alpha-synuclein PathologyR21NS093993 · NINDS · VAN ANDEL RESEARCH INSTITUTE · PI BRUNDIN, PATRIK · 2016 to 2017
$523k
Promoting survival of dopamine neurons in models of Parkinsons disease using a novel transcriptional regulatorR21NS105436 · NINDS · VAN ANDEL RESEARCH INSTITUTE · PI BRUNDIN, PATRIK, TAYLOR, MERRITT KEARNY · 2018 to 2019
$508k
NIDCD NIH HHS R01 DC016519NINDS NIH HHS R21 NS093993NINDS NIH HHS R21 NS105436NINDS NIH HHS R21 NS106078
6 · The paper itself

Abstract

Parkinson's disease (PD) is a slowly progressing neurodegenerative disorder that is coupled to both widespread protein aggregation and to loss of substantia nigra dopamine (DA) neurons, resulting in a wide variety of motor and non-motor signs and symptoms. Recent findings suggest that the PD process is triggered several years before there is sufficient degeneration of DA neurons to cause onset of overt motor symptoms. According to this concept, the number of DA neurons present in the substantia nigra at birth could influence the time from the molecular triggering event until the clinical diagnosis with lower number of neurons at birth increasing the risk to develop the disease. Conversely, the risk for diagnosis would be reduced if the number of DA neurons is high at birth. In this commentary, we discuss the genetic and epigenetic factors that might influence the number of nigral DA neurons that each individual is born with and how these may be linked to PD risk.

Indexed as

Epigenesis, GeneticParkinson DiseaseAnimalsDopaminergic NeuronsHumansSubstantia Nigracis-regulationdopamine neuron numbermotor dysfunctionneural developmentParkinson’s disease risksubstantia nigra

Identifiers

PMID31958098
PMCPMC7242832

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.