Evidence map›Paper›PMID 38640169›Full record

ArticleJournal of Parkinson's disease2024

Prospective Role of PAK6 and 14-3-3γ as Biomarkers for Parkinson's Disease.

Elena Giusto, Lorenza Maistrello, Lucia Iannotta, Veronica Giusti, Ludovica Iovino, Rina Bandopadhyay, Angelo Antonini, Luigi Bubacco, Rita Barresi, Nicoletta Plotegher and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Journal of Parkinson's disease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
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

12 authors at 3 institutions in 2 countries.

Elena GiustoIRCCS San Camillo Hospital, Venice, Italy.
Lorenza MaistrelloIRCCS San Camillo Hospital, Venice, Italy.
Lucia IannottaDepartment of Biology, University of Padova, Padova, Italy.
Veronica GiustiIRCCS San Camillo Hospital, Venice, Italy.
Ludovica IovinoDepartment of Biology, University of Padova, Padova, Italy.
Rina BandopadhyayReta Lila Weston Institute of Neurological Studies, UCL Queen Square Institute of Neurology, London, UK.
Angelo AntoniniPadova Neuroscience Center, University of Padova, Padova, Italy.
Luigi BubaccoDepartment of Biology, University of Padova, Padova, Italy.
Rita BarresiIRCCS San Camillo Hospital, Venice, Italy.
Nicoletta PlotegherDepartment of Biology, University of Padova, Padova, Italy.
Elisa GreggioDepartment of Biology, University of Padova, Padova, Italy.
Laura CivieroIRCCS San Camillo Hospital, Venice, Italy.
University of Padua · ITIRCCS San Camillo Hospital · ITNational Hospital for Neurology and Neurosurgery · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Parkinson's disease is a progressive neurodegenerative disorder mainly distinguished by sporadic etiology, although a genetic component is also well established. Variants in the LRRK2 gene are associated with both familiar and sporadic disease. We have previously shown that PAK6 and 14-3-3γ protein interact with and regulate the activity of LRRK2. Objective: The aim of this study is to quantify PAK6 and 14-3-3γ in plasma as reliable biomarkers for the diagnosis of both sporadic and LRRK2-linked Parkinson's disease. Methods: After an initial quantification of PAK6 and 14-3-3γ expression by means of Western blot in post-mortem human brains, we verified the presence of the two proteins in plasma by using quantitative ELISA tests. We analyzed samples obtained from 39 healthy subjects, 40 patients with sporadic Parkinson's disease, 50 LRRK2-G2019S non-manifesting carriers and 31 patients with LRRK2-G2019S Parkinson's disease. Results: The amount of PAK6 and 14-3-3γ is significantly different in patients with Parkinson's disease compared to healthy subjects. Moreover, the amount of PAK6 also varies with the presence of the G2019S mutation in the LRRK2 gene. Although the generalized linear models show a low association between the presence of Parkinson's disease and PAK6, the kinase could be added in a broader panel of biomarkers for the diagnosis of Parkinson's disease. Conclusions: Changes of PAK6 and 14-3-3γ amount in plasma represent a shared readout for patients affected by sporadic and LRRK2-linked Parkinson's disease. Overall, they can contribute to the establishment of an extended panel of biomarkers for the diagnosis of Parkinson's disease.

Indexed as

14-3-3 ProteinsBiomarkersLeucine-Rich Repeat Serine-Threonine Protein Kinase-2p21-Activated KinasesParkinson DiseaseAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedMutationProspective Studies14-3-3 ProteinsBiomarkersLeucine-Rich Repeat Serine-Threonine Protein Kinase-2LRRK2 protein, humanp21-Activated KinasesPAK6 protein, human14-3-3γbiomarkersPAK6Parkinson’s disease

Identifiers

PMID38640169
PMCPMC11091598
OpenAlexW4394856013

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.