Document Detail

Dupuytren diathesis and genetic risk.
MedLine Citation:
PMID:  23021175     Owner:  NLM     Status:  In-Data-Review    
PURPOSE: Dupuytren disease (DD) is a benign fibrosing disorder of the hand and fingers. Recently, we identified 9 single nucleotide polymorphisms (SNPs) associated with DD in a genome-wide association study. These SNPs can be used to calculate a genetic risk score for DD. The aim of this study was to test whether certain clinical characteristics (including the DD diathesis features) of patients with DD are associated with a high genetic risk score.
METHODS: Between 2007 and 2010, we prospectively invited all DD patients (1,120 in total) to participate. Clinical characteristics were noted using patient- and doctor-completed questionnaires, and blood was obtained for DNA analysis. We analyzed a total of 933 subjects with genetic and clinical data. The 9 previously identified DD SNPs were used to calculate a weighted genetic risk score. Patients were categorized into high and low genetic risk score groups, according to their weighted genetic risk score. Logistic regression was performed to study the association of clinical characteristics with a high genetic risk score.
RESULTS: In a univariate regression model, patients with an age of onset of DD younger than 50 years, a family history positive for DD, knuckle pads, and Ledderhose disease were statistically significantly associated with a high genetic risk score. In an additional analysis using high and low genetic risk groups that deviate further from the median, Ledderhose disease was no longer significantly associated with DD.
CONCLUSIONS: Patients with DD who present with these diathesis features, and predominantly patients with knuckle pads, are more likely to carry more risk alleles for the discovered DD SNPs than patients without these diathesis features.
CLINICAL RELEVANCE: These markers may prove useful in predicting disease progression or recurrence.
Guido H Dolmans; Geertruida H de Bock; Paul M Werker
Related Documents :
24381495 - Screening of genetic polymorphisms of cyp3a4 and cyp3a5 genes.
23882135 - Genetic heterogeneity and consanguinity lead to a "double hit": homozygous mutations of...
23244545 - Genetic architecture of complex agronomic traits examined in two testcross populations ...
24487965 - Association of the polymorphisms of mmp-9 and timp-3 genes with thoracic aortic dissect...
24381495 - Screening of genetic polymorphisms of cyp3a4 and cyp3a5 genes.
25396745 - Characterization of a spontaneous novel mutation in the npc2 gene in a cat affected by ...
Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  The Journal of hand surgery     Volume:  37     ISSN:  1531-6564     ISO Abbreviation:  J Hand Surg Am     Publication Date:  2012 Oct 
Date Detail:
Created Date:  2012-10-01     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  7609631     Medline TA:  J Hand Surg Am     Country:  United States    
Other Details:
Languages:  eng     Pagination:  2106-11     Citation Subset:  IM    
Copyright Information:
Copyright © 2012 American Society for Surgery of the Hand. Published by Elsevier Inc. All rights reserved.
Departments of Plastic Surgery and Epidemiology, University Medical Center Groningen and University of Groningen, Groningen, the Netherlands. Electronic address:
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  Recurrence of radial bowing after soft tissue distraction and subsequent radialization for radial lo...
Next Document:  Stress shielding around radial head prostheses.