Abstract
Dupuytren’s disease is a connective tissue disorder of the hand causing excessive palmar fascial fibrosis with associated finger contracture and disability. The aetiology of the disease is heterogeneous, with both genetic and environmental components. The connective tissue is abnormally infiltrated by myofibroblasts that deposit collagen and other extracellular matrix proteins. We describe the clinical profile of Dupuytren’s disease along with current therapeutic schemes. Recent findings on molecular and cellular parameters that are dysregulated in Dupuytren’s disease, which may contribute to the onset of the disease, and the role of resident inflammation promoting fibrosis, are highlighted. We review recent literature focusing on non-myofibroblast cell types (stem cell-like cells), their pro-inflammatory and pro-fibrotic role that may account for abnormal wound healing response.
Original language | English |
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Pages (from-to) | 133–140 |
Number of pages | 8 |
Journal | Current Molecular Biology Reports |
Volume | 2 |
Issue number | 3 |
Early online date | 14 Jul 2016 |
DOIs | |
Publication status | Published - Sep 2016 |
Keywords
- Inflammation
- Dupuytren’s
- Fibrosis
- Regeneration
- Contracture
Profiles
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Ian Clark
- School of Biological Sciences - Professor of Musculoskeletal Biology
- Musculoskeletal Medicine - Member
- Nutrition and Preventive Medicine - Member
- HealthUEA - Academic Chair
Person: Research Group Member, Academic, Teaching & Research