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Published on: October 24, 2019
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The Basic Science of Dupuytren Disease
Andrew Y Zhang1, Jennifer S Kargel2
1Department of Plastic Surgery, University of Texas Southwestern Medical Center, 1801 Inwood Road, Dallas, TX 75390-1932, USA.
Hand Clinics
|July 18, 2018
Summary
Dupuytren disease, a hand condition, is linked to genetic factors and internal issues. Research highlights the Wnt signaling pathway
Area of Science:
- Hand surgery
- Genetics
- Fibroproliferative disorders
Background:
- Dupuytren disease is a widespread fibroproliferative hand condition.
- Its pathogenesis is hypothesized to involve both genetic and internal factors.
- Previous research suggested a genetic link, now supported by genome-wide association studies.
Purpose of the Study:
- To summarize the current understanding of Dupuytren disease pathogenesis.
- To highlight the role of genetic factors and internal influences.
- To emphasize the significance of the Wnt signaling pathway.
Main Methods:
- Review of recent genome-wide association studies.
- Analysis of evidence for genetic components in Dupuytren disease.
- Examination of internal factors like microvascular issues.
Main Results:
- Genome-wide association studies confirm a strong genetic component.
- Abnormal activation of the Wnt signaling pathway is implicated.
- Microvascular angiopathy and ischemia contribute via growth factor activation.
Conclusions:
- Genetic predisposition plays a key role in Dupuytren disease.
- The Wnt signaling pathway is a critical factor in its development.
- Internal factors such as ischemia exacerbate myofibroblast proliferation.
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