Sibling recurrence risk in Dupuytren's disease.

Dupuytren's disease is a complex condition, with both genetic and environmental factors contributing to its aetiology. We aimed to quantify the extent to which genetic factors predispose to the disease, through the calculation of sibling recurrence risk (ls), and to calculate the proportion of...

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Main Authors: Capstick, R, Bragg, T, Giele, H, Furniss, D
Format: Journal article
Language:English
Published: 2013
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author Capstick, R
Bragg, T
Giele, H
Furniss, D
author_facet Capstick, R
Bragg, T
Giele, H
Furniss, D
author_sort Capstick, R
collection OXFORD
description Dupuytren's disease is a complex condition, with both genetic and environmental factors contributing to its aetiology. We aimed to quantify the extent to which genetic factors predispose to the disease, through the calculation of sibling recurrence risk (ls), and to calculate the proportion of heritability accounted for by currently known genetic loci. From 174 siblings of patients with surgically confirmed disease, 100 were randomly selected. Controls were recruited from patients attending an ophthalmology outpatient clinic for eye conditions unrelated to diabetes. There were no statistically significant differences in baseline characteristics between the case and control groups. In siblings, 47% had Dupuytren's disease, compared with 10% of controls, giving a ls of 4.5. Currently known loci that predispose to Dupuytren's disease account for 12.1% of the total heritability of the disease. Dupuytren's disease was significantly more common in siblings than in controls. These results accurately quantify the magnitude of the genetic predisposition to Dupuytren's disease.
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spelling oxford-uuid:7dba2c58-2c9c-4216-af82-c621924422642022-03-26T21:05:30ZSibling recurrence risk in Dupuytren's disease.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:7dba2c58-2c9c-4216-af82-c62192442264EnglishSymplectic Elements at Oxford2013Capstick, RBragg, TGiele, HFurniss, DDupuytren's disease is a complex condition, with both genetic and environmental factors contributing to its aetiology. We aimed to quantify the extent to which genetic factors predispose to the disease, through the calculation of sibling recurrence risk (ls), and to calculate the proportion of heritability accounted for by currently known genetic loci. From 174 siblings of patients with surgically confirmed disease, 100 were randomly selected. Controls were recruited from patients attending an ophthalmology outpatient clinic for eye conditions unrelated to diabetes. There were no statistically significant differences in baseline characteristics between the case and control groups. In siblings, 47% had Dupuytren's disease, compared with 10% of controls, giving a ls of 4.5. Currently known loci that predispose to Dupuytren's disease account for 12.1% of the total heritability of the disease. Dupuytren's disease was significantly more common in siblings than in controls. These results accurately quantify the magnitude of the genetic predisposition to Dupuytren's disease.
spellingShingle Capstick, R
Bragg, T
Giele, H
Furniss, D
Sibling recurrence risk in Dupuytren's disease.
title Sibling recurrence risk in Dupuytren's disease.
title_full Sibling recurrence risk in Dupuytren's disease.
title_fullStr Sibling recurrence risk in Dupuytren's disease.
title_full_unstemmed Sibling recurrence risk in Dupuytren's disease.
title_short Sibling recurrence risk in Dupuytren's disease.
title_sort sibling recurrence risk in dupuytren s disease
work_keys_str_mv AT capstickr siblingrecurrenceriskindupuytrensdisease
AT braggt siblingrecurrenceriskindupuytrensdisease
AT gieleh siblingrecurrenceriskindupuytrensdisease
AT furnissd siblingrecurrenceriskindupuytrensdisease