Evidence map›Paper›PMID 37373966›Full record

ArticleJournal of personalized medicine2023

Development and Replication of a Genome-Wide Polygenic Risk Score for Chronic Back Pain.

Yakov A Tsepilov, Elizaveta E Elgaeva, Arina V Nostaeva, Roger Compte, Ivan A Kuznetsov, Lennart C Karssen, Maxim B Freidin, Pradeep Suri, Frances M K Williams, Yurii S Aulchenko

Abstract read
In one paragraph

Article in Journal of personalized medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

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

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. 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

10 authors.

Yakov A TsepilovLaboratory of Recombination and Segregation Analysis, Institute of Cytology and Genetics, Novosibirsk 630090, Russia.ORCID 0000-0002-4931-6052
Elizaveta E ElgaevaLaboratory of Recombination and Segregation Analysis, Institute of Cytology and Genetics, Novosibirsk 630090, Russia.ORCID 0000-0002-2484-553X
Arina V NostaevaDepartment of Natural Sciences, Novosibirsk State University, Novosibirsk 630090, Russia.
Roger CompteDepartment of Twin Research and Genetic Epidemiology, School of Life Course Sciences, King's College London, London SE1 7EH, UK.
Ivan A KuznetsovCenter of Life Sciences, Skolkovo Institute of Science and Technology, Moscow 121205, Russia.ORCID 0000-0002-4873-0729
Lennart C KarssenPolyOmica, 5237 PA s-Hertogenbosch, The Netherlands.ORCID 0000-0002-1959-342X
Maxim B FreidinDepartment of Biology, School of Biological and Behavioural Sciences, Queen Mary University of London, London E1 4NS, UK.ORCID 0000-0002-1439-6259
Pradeep SuriDivision of Rehabilitation Care Services, VA Puget Sound Health Care System, Seattle, WA 98208, USA.
Frances M K WilliamsDepartment of Twin Research and Genetic Epidemiology, School of Life Course Sciences, King's College London, London SE1 7EH, UK.ORCID 0000-0002-2998-2744
Yurii S AulchenkoLaboratory of Recombination and Segregation Analysis, Institute of Cytology and Genetics, Novosibirsk 630090, Russia.

Funding

UW Core Center for Clinical Research of Musculoskeletal ConditionsP30AR072572 · NIAMS · UNIVERSITY OF WASHINGTON · PI JEFFREY G JARVIK, Pradeep Suri · 2017 to 2026
$8.3M
NIAMS NIH HHS P30 AR072572NIAMS NIH HHS P30AR072572
6 · The paper itself

Abstract

Chronic back pain (CBP) is a complex heritable trait and a major cause of disability worldwide. We developed and validated a genome-wide polygenic risk score (PRS) for CBP using a large-scale GWAS based on UK Biobank participants of European ancestry (N = 265,000). The PRS showed poor overall predictive ability (AUC = 0.56 and OR = 1.24 per SD, 95% CI: 1.22-1.26), but individuals from the 99th percentile of PRS distribution had a nearly two-fold increased risk of CBP (OR = 1.82, 95% CI: 1.60-2.06). We validated the PRS on an independent TwinsUK sample, obtaining a similar magnitude of effect. The PRS was significantly associated with various ICD-10 and OPCS-4 diagnostic codes, including chronic ischemic heart disease (OR = 1.1,

Indexed as

chronic back painGWASlow back painpolygenic risk score

Identifiers

PMID37373966
PMCPMC10304922

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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.