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June 3, 2026Connective Tissue Research0 citations

Investigating the genetic basis of fibrotic pathway dysregulation in Dupuytren’s contracture

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AVAlvita Vilkeviciute-PetraiteDBDovilė BasalykienėMBMigdolija Baltakyte

Key Points

  • Investigate the association between genetic variants in fibrotic pathways and susceptibility to Dupuytren’s contracture.
  • Analyzed genetic variants in fibrotic pathways in a Lithuanian population.
  • Focused on specific SNPs, including rs1668347.
  • Used statistical models to evaluate associations with Dupuytren's contracture.
  • Identified significant association of SNP rs1668347 with Dupuytren's contracture (P=0.010).
  • No significant associations were found for other SNPs investigated.

Abstract

PURPOSE: Dupuytren's contracture (DC) is a common fibroproliferative disorder with strong genetic predisposition. This study aimed to investigate the association between genetic variants in key fibrotic pathways and DC susceptibility in a Lithuanian population. MATERIALS AND METHODS: rs1668347. RESULTS: = 0.010) models. No significant associations were found for the other investigated SNPs. CONCLUSIONS: rs1668347 provide additional insights into the genetic basis of DC and may contribute to the development of predictive tools and targeted therapies for this debilitating condition.

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Cite This Study

Vilkeviciute-Petraite et al. (2026) studied this question.

synapsesocial.com/papers/6a1fc49adee9eb8c0dce6126https://doi.org/10.1080/03008207.2026.2680153
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