Identifying non-genetic factors associated with trigger finger.

J Plast Reconstr Aesthet Surg

Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Botnar Research Centre, Windmill Road, Oxford OX3 7LD, UK; Department of Plastic and Reconstructive Surgery, Oxford University Hospitals NHS Foundation Trust, John Radcliffe Hospital, Oxford OX3 9DU, UK.

Published: July 2024

AI Article Synopsis

  • A study was conducted using UK Biobank data to explore non-genetic factors associated with trigger finger (TF), focusing on a large population sample for more comprehensive insights.
  • The analysis identified 2250 individuals with TF and revealed significant associations with factors such as age, female sex, body mass index, carpal tunnel syndrome, Dupuytren's disease, and diabetes, among others.
  • The findings confirm known risk factors and introduce new associations, particularly emphasizing a strong link between TF and Dupuytren's disease, suggesting a shared underlying cause.

Article Abstract

Background: The non-genetic factors predisposing to trigger finger (TF) have mostly been characterised in small studies from individual institutions. Here, we aimed to provide a more complete picture of TF and its associations.

Methodology: This case-control study used cross-sectional data from the UK Biobank population-based cohort to identify and determine the strength of associations of phenotypic variables with TF. We performed multivariable logistic regression of a multitude of phenotypic factors associated with TF.

Results: We identified 2250 individuals with medical and surgical diagnostic codes for TF, and 398,495 controls. TF was found to be significantly associated with age (OR 1.04, 95% CI 1.03-1.04, P < 2.23×10), female sex (OR 1.22, 95% CI 1.08-1.39, P = 2.35×10), body mass index (OR 1.10, 95% CI 1.04-1.16, P = 5.52×10), carpal tunnel syndrome (OR 9.59, 95% CI 8.68-10.59, P < 2.23×10), Dupuytren's disease (OR 4.89, 95% CI 4.06-5.89, P < 2.23×10), diabetes mellitus without complications (OR 1.35, 95% CI 1.15-1.58, P = 2.03×10) and with complications (OR 2.46, 95% CI 1.90-3.17, P = 4.98×10), HbA1c (OR 1.01, 95% CI 1.01-1.02, P = 8.99×10), hypothyroidism (OR 1.24, 95% CI 1.07-1.43, P = 4.75×10) and rheumatoid arthritis (OR 1.33, 95% CI 1.06-1.68, P = 0.014).

Conclusion: Our results provide evidence supporting the well-known risk factors such as diabetes mellitus, carpal tunnel syndrome, age and female sex. Furthermore, we can confirm putative associations such as hypothyroidism, obesity and rheumatoid arthritis, while providing evidence against others such as hypertension and hyperlipidaemia. A novel finding arising from this study is the strong association with Dupuytren's disease. Our study design allowed us to identify these associations as being independent from carpal tunnel syndrome, thereby indicating a shared pathophysiology between this disease and TF.

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Source
http://dx.doi.org/10.1016/j.bjps.2024.04.066DOI Listing

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