Evidence map›Paper›PMID 32652692›Full record

ArticleMovement disorders : official journal of the Movement Disorder Society2020

Elevated In Vitro Kinase Activity in Peripheral Blood Mononuclear Cells of Leucine-Rich Repeat Kinase 2 G2019S Carriers: A Novel Enzyme-Linked Immunosorbent Assay-Based Method.

Katerina Melachroinou, Min Suk Kang, Christopher Liong, Sushma Narayan, Najah Levers, Neal Joshi, Katie Kopil, Samantha J Hutten, Marco A S Baptista, Shalini Padmanabhan and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Movement disorders : official journal of the Movement Disorder Society, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.2field-weighted citation impact, top 9% 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

19 citing papers in PubMed, 32 citations in OpenAlex.

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  13. Differential Phospho-Signatures in Blood Cells Identify LRRK2 G2019S Carriers in Parkinson's Disease.Movement disorders : official journal of the Movement Disorder Society · 2022
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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

14 authors at 5 institutions in 2 countries.

Katerina MelachroinouDivision of Basic Neurosciences, Biomedical Research Foundation of the Academy of Athens, Athens, Greece.
Min Suk KangDepartment of Neurology, Columbia University, New York, New York, USA.
Christopher LiongDepartment of Neurology, Columbia University, New York, New York, USA.
Sushma NarayanDepartment of Neurology, Columbia University, New York, New York, USA.
Najah LeversDepartment of Neurology, Columbia University, New York, New York, USA.
Neal JoshiDepartment of Neurology, Columbia University, New York, New York, USA.
Katie KopilThe Michael J. Fox Foundation for Parkinson's Research, New York, New York, USA.
Samantha J HuttenThe Michael J. Fox Foundation for Parkinson's Research, New York, New York, USA.
Marco A S BaptistaThe Michael J. Fox Foundation for Parkinson's Research, New York, New York, USA.
Shalini PadmanabhanThe Michael J. Fox Foundation for Parkinson's Research, New York, New York, USA.
Un Jung KangDepartment of Neurology, NYU Langone Health, New York, New York, USA.ORCID 0000-0002-5970-6839
Leonidas StefanisDivision of Basic Neurosciences, Biomedical Research Foundation of the Academy of Athens, Athens, Greece.
Roy N AlcalayDepartment of Neurology, Columbia University, New York, New York, USA.
Hardy J RideoutDivision of Basic Neurosciences, Biomedical Research Foundation of the Academy of Athens, Athens, Greece.
Columbia University · USMichael J. Fox Foundation · USBiomedical Research Foundation of the Academy of Athens · GRNational and Kapodistrian University of Athens · GRNYU Langone Health · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLeucine-rich repeat kinase 2 kinase inhibitors are being vigorously pursued as potential therapeutic options; however, there is a critical need for sensitive and quantitative assays of leucine-rich repeat kinase 2 function and target engagement.

objectivesOur objective was to compare collection and storage protocols for peripheral blood mononuclear cells, and to determine the optimal conditions for downstream analyses of leucine-rich repeat kinase 2 in PD cohorts.

methodsHere, we describe enzyme-linked immunosorbent assay-based assays capable of detecting multiple aspects of leucine-rich repeat kinase 2 function at endogenous levels in human tissues.

resultsIn peripheral blood mononuclear cells from both healthy and affected carriers of the G2019S mutation in leucine-rich repeat kinase 2, we report, for the first time, significantly elevated in vitro kinase activity, while detecting a significant increase in pS935/leucine-rich repeat kinase 2 in idiopathic PD patients.

conclusionsQuantitative assays such as these described here could potentially uncover specific markers of leucine-rich repeat kinase 2 function that are predictive of disease progression, aid in patient stratification, and be a critical component of upcoming clinical trials. © 2020 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Indexed as

Leukocytes, MononuclearParkinson DiseaseEnzyme-Linked Immunosorbent AssayHumansLeucineLeucine-Rich Repeat Serine-Threonine Protein Kinase-2MutationLeucineLeucine-Rich Repeat Serine-Threonine Protein Kinase-2ELISAkinaseLRRK2Parkinson's diseasePBMC

Identifiers

PMID32652692
PMCPMC7754308
OpenAlexW3041462171

What OpenQuestion holds

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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.