Evidence map›Paper›PMID 40018183›Full record

ArticleBMJ public health2024

Is joint hypermobility linked to self-reported non-recovery from COVID-19? Case-control evidence from the British COVID Symptom Study Biobank.

Jessica A Eccles, Dorina Cadar, Lisa Quadt, Alan J Hakim, Nicholas Gall, Covid Symptom Survey Biobank Consortium, Vicky Bowyer, Nathan Cheetham, Claire J Steves, Hugo D Critchley and 1 more

Abstract read
In one paragraph

Article in BMJ public health, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

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

7 citing papers in PubMed.

  1. Article
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  4. ADHD: overdiagnosis or opportunity?The British journal of general practice : the journal of the Royal College of General Practitioners · 2025
    Article
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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

11 authors.

Jessica A EcclesDepartment of Clinical Neuroscience, Brighton and Sussex Medical School, Brighton, UK.
Dorina CadarDepartment of Clinical Neuroscience, Brighton and Sussex Medical School, Brighton, UK.
Lisa QuadtDepartment of Clinical Neuroscience, Brighton and Sussex Medical School, Brighton, UK.ORCID 0000-0002-5896-916X
Alan J HakimDivision of Medicine, School of Medicine, Penn State University, University Park, Pennsylvania, USA.
Nicholas GallDepartment of Neurocardiology, King's College Hospital NHS Foundation Trust, London, UK.
Covid Symptom Survey Biobank Consortium
Vicky BowyerDepartment of Twin Research and Genetic Epidemiology, King's College London, London, UK.
Nathan CheethamDepartment of Twin Research and Genetic Epidemiology, King's College London, London, UK.
Claire J StevesDepartment of Twin Research and Genetic Epidemiology, King's College London, London, UK.
Hugo D CritchleyDepartment of Clinical Neuroscience, Brighton and Sussex Medical School, Brighton, UK.
Kevin A DaviesDepartment of Clinical and Experimental Medicine, Brighton and Sussex Medical School, Brighton, UK.

Funding

Wellcome Trust
6 · The paper itself

Abstract

Objectives: This study sought to explore whether generalised joint hypermobility (GJH, a common marker of variant connective tissue) was a risk factor for self-reported non-recovery from COVID-19 infection. Design: Prospective observational study. Setting: COVID Symptom Study Biobank (https://cssbiobank.com/) UK. Participants: Participants were surveyed in August 2022. 3064 (81.4%) reported at least one infection with COVID-19. These individuals self-reported on recovery and completed a self-report questionnaire to detect GJH (Hakim and Grahame 5-part questionnaire, 5PQ). Main outcome measures: The primary outcome was the presence of self-reported non-recovery from COVID-19 infection at the time of the survey. Additional outcomes included scores on 5PQ and self-reported fatigue level (Chalder Fatigue Scale). Results: The presence of GJH was not specifically associated with reported COVID-19 infection risk per se. However, it was significantly associated with non-recovery from COVID-19 (OR 1.43 (95% CI 1.20 to 1.70)). This association remained after sequential models adjusting for age, sex, ethnic group, education level and index of multiple deprivation (OR 1.33 (95% CI 1.10 to 1.61)) and further adjustment for vaccination status and number of vaccinations (OR 1.33 (95% CI 1.10 to 1.60)). Additionally, including in a model adjusting for all covariates, hypermobility significantly predicted higher fatigue levels (B=0.95, SE=0.25, t=3.77, SE, p=0.002). Fatigue levels mediated the link between GJH and non-recovery from COVID-19 (estimate of indirect effect=0.18, 95% bootstrapped CI 0.08 to 0.29). Conclusions: Individuals with GJH were approximately 30% more likely not to have recovered fully from COVID-19 infection at the time of the questionnaire, and this predicted the fatigue level. This observation is clinically important through its potential impact for understanding and identifying sub-phenotypes of long COVID for screening and personalised targeted interventions. More generally, greater awareness of GJH and its extra-articular associations is needed for effective patient stratification and implementation of personalised medicine.

Indexed as

COVID-19mass screeningPost-Acute COVID-19 SyndromeSARS-CoV-2translational science, biomedical

Identifiers

PMID40018183
PMCPMC11812800

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.