Evidence map›Paper›PMID 38942297›Full record

ArticleThe spine journal : official journal of the North American Spine Society2025

The association of lumbar intervertebral disc degeneration with low back pain is modified by underlying genetic propensity to pain.

Pradeep Suri, Maryam Kazemi Naeini, Patrick J Heagerty, Maxim B Freidin, Isabelle Granville Smith, Elizaveta E Elgaeva, Roger Compte, Yakov A Tsepilov, Frances M K Williams

Abstract readTwin Study
In one paragraph

Article in The spine journal : official journal of the North American Spine Society, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

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

  1. Pooled it
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  5. The Core Outcome Measures Index (COMI) comes of age: 18 years of efficient and effective patient-reported outcome measurement in the field of spinal disorders. Part 1. Development of the COMI, interpretation of scores, and use in research.European spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society · 2025
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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

9 authors.

Pradeep SuriDivision of Rehabilitation Care Services, VA Puget Sound Health Care System, Washington, USA; Seattle Epidemiologic Research and Information Center, VA Puget Sound Health Care System, Seattle, Washington, USA; Department of Rehabilitation Medicine, University of Washington, Seattle, Washington, USA; Clinical Learning, Evidence, and Research (CLEAR) Center, University of Washington, Seattle, Washington, USA. Electronic address: pradeep.suri@va.gov.
Maryam Kazemi NaeiniDepartment of Twin Research and Genetic Epidemiology, School of Life Course Sciences, King's College London, London, UK.
Patrick J HeagertyDepartment of Biostatistics, University of Washington, Seattle, Washington, USA.
Maxim B FreidinDepartment of Twin Research and Genetic Epidemiology, School of Life Course Sciences, King's College London, London, UK; Department of Biology, School of Biological and Behavioural Sciences, Queen Mary University of London, London, UK.
Isabelle Granville SmithDepartment of Twin Research and Genetic Epidemiology, School of Life Course Sciences, King's College London, London, UK.
Elizaveta E ElgaevaLaboratory of Recombination and Segregation Analysis, Institute of Cytology and Genetics, Novosibirsk, Russia; Department of Natural Sciences, Novosibirsk State University, Novosibirsk, Russia.
Roger CompteDepartment of Twin Research and Genetic Epidemiology, School of Life Course Sciences, King's College London, London, UK.
Yakov A TsepilovLaboratory of Recombination and Segregation Analysis, Institute of Cytology and Genetics, Novosibirsk, Russia; Wellcome Sanger Institute, Cambridge, UK.
Frances M K WilliamsDepartment of Twin Research and Genetic Epidemiology, School of Life Course Sciences, King's College London, London, UK.

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 AR072572
6 · The paper itself

Abstract

background contextAssociations between magnetic resonance imaging (MRI)-detected lumbar intervertebral disc degeneration (LDD) and LBP are often of modest magnitude. This association may be larger in specific patient subgroups. PURPOSE: To examine whether the association between LDD and LBP is modified by underlying genetic predispositions to pain. STUDY

designCross-sectional study in UK Biobank (UKB) and Twins UK. PATIENT SAMPLES: A genome-wide association study (GWAS) of the number of anatomical chronic pain locations was conducted in 347,538 UKB participants. The GWAS was used to develop a genome-wide polygenic risk score (PRS) in a holdout sample of 30,000 UKB participants. The PRS model was then used in analyses of 645 TwinsUK participants with standardized LDD MRI assessments. OUTCOME MEASURES: Ever having had LBP associated with disability lasting ≥1 month (LBP1).

methodsUsing the PRS as a proxy for "genetically-predicted propensity to pain", we stratified TwinsUK participants into PRS quartiles. A "basic" model examined the association between an LDD summary score (LSUM) and LBP1, adjusting for covariates. A "fully-adjusted" model also adjusted for PRS quartile and LSUM x PRS quartile interaction terms.

resultsIn the basic model, the odds ratio (OR) of LBP1 was 1.8 per standard deviation of LSUM (95% confidence interval [CI] 1.4-2.3). In the fully-adjusted model, there was a statistically significant LSUM-LBP1 association in quartile 4, the highest PRS quartile (OR=2.5 [95% CI 1.7-3.7], p=2.6×10

conclusionsGenetically-predicted propensity to pain modifies the LDD-LBP association, with the strongest association present in people with the highest genetic propensity to pain. Lumbar MRI findings may have stronger connections to LBP in specific subgroups of people.

Indexed as

Genetic Predisposition to DiseaseGenome-Wide Association StudyIntervertebral Disc DegenerationLow Back PainLumbar VertebraeAdultAgedCross-Sectional StudiesFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedUK BiobankEpidemiologyGeneticsIntervertebral discLow back painPatient stratificationPolygenic risk score

Identifiers

PMID38942297
PMCPMC11637947

What OpenQuestion holds

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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.