Evidence map›Paper›PMID 39907297›Full record

ArticleActa medica academica2024

Translational Research on Polygenic Risk Scores in Common Neurodegenerative Diseases - A Scoping Review Protocol.

Mojca Čižek Sajko, Jana Suklan, Džanan Osmanović, Borut Peterlin

Abstract read
In one paragraph

Article in Acta medica academica, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Mojca Čižek SajkoClinical Institute for Genomic Medicine, University Medical Centre Ljubljana, Slovenia. mojca.cizek.sajko@kclj.si.
Jana SuklanNational Institute for Health and Care Research (NIHR) HealthTech Research Centre (HRC) in Diagnostic and Technology Evaluation, Newcastle, United Kingdom; Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, United Kingdom.
Džanan OsmanovićFaculty of Science and Mathematics, University of Tuzla, Bosnia and Herzegovina.
Borut PeterlinClinical Institute for Genomic Medicine, University Medical Centre Ljubljana, Slovenia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe purpose of this protocol is to clearly describe the process for the scoping review we plan to conduct on the topic of polygenic risk scores (PRS) in common neurodegenerative diseases. We will present the review's objective, the strategy for evidence search, the data extraction and analysis procedure, and how the results will be presented.

methodsThe inclusion criteria for the planned scoping review will focus on evidence sources that involve PRS applied to neurogenerative diseases such as Multiple sclerosis, Parkinson's disease, Alzheimer's disease, and Amyotrophic lateral sclerosis in any phase of translational research, from early development to clinical implementation. This includes its use in risk prediction, early diagnosis, prognosis, and treatment decision-making. The research questions were created based on the population, context, and concept framework. We will consider both peer-reviewed papers and grey literature published in English or German for inclusion. Two independent reviewers will search for information. CONCLUISON: The findings from the scoping review will be presented descriptively and summarized according to the research questions to illustrate the current status of translational research on PRS in common neurodegenerative diseases.

Indexed as

Genetic Risk ScoreMultifactorial InheritanceNeurodegenerative DiseasesTranslational Research, BiomedicalAlzheimer DiseaseAmyotrophic Lateral SclerosisGenetic Predisposition to DiseaseHumansMultiple SclerosisParkinson DiseaseResearch DesignRisk AssessmentRisk FactorsScoping Reviews as TopicEvidence GapsGenetic Risk ScoreNervous System Diseases

Identifiers

PMID39907297
PMCPMC11831539

What OpenQuestion holds

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LicenceCC BY-NC
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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.