Document Detail

Increased risk of primary sclerosing cholangitis and ulcerative colitis in first-degree relatives of patients with primary sclerosing cholangitis.
MedLine Citation:
PMID:  18674735     Owner:  NLM     Status:  MEDLINE    
BACKGROUND & AIMS: The importance of genetic factors for the development of primary sclerosing cholangitis (PSC) is incompletely understood. This study assessed the risk of PSC and inflammatory bowel disease (IBD) among first-degree relatives of patients with PSC, compared with the first-degree relatives of a cohort without PSC. METHODS: Subjects from the national Swedish cohort of PSC patients (n = 678) were matched for date of birth, sex, and region to up to 10 subjects without a diagnosis of PSC (n = 6347). Linkage through general population registers identified first-degree relatives of subjects in both the PSC and comparison cohorts (n = 34,092). Diagnoses among first-degree relatives were identified by using the Inpatient Register. RESULTS: The risk of cholangitis was statistically significantly increased in offspring, siblings, and parents of the PSC patient cohort, compared with relatives of the comparison cohort, with the hazard ratios and 95% confidence intervals, 11.5 (1.6-84.4), 11.1 (3.3-37.8), and 2.3 (0.9-6.1), respectively. The hazard ratios for ulcerative colitis (UC) among first-degree relatives of all PSC patients was 3.3 (2.3-4.9) and for Crohn's disease 1.4 (0.8-2.5). The risk of UC for relatives of PSC patients without IBD was also increased, 7.4 (2.9-18.9). CONCLUSIONS: First-degree relatives of patients with PSC run an increased risk of PSC, indicating the importance of genetic factors in the etiology of PSC. First-degree relatives of PSC patients without IBD are also at an increased risk of UC, which might indicate shared genetic susceptibility factors for PSC and UC.
Annika Bergquist; Scott M Montgomery; Shahram Bahmanyar; Rolf Olsson; Ake Danielsson; Stefan Lindgren; Hanne Prytz; Rolf Hultcrantz; L A R S Lööf; Hanna Sandberg-Gertzén; Sven Almer; Johan Askling; Anna Ehlin; Anders Ekbom
Related Documents :
16984505 - The +1059g/c polymorphism in the c-reactive protein (crp) gene is associated with invol...
19714485 - Mutations of mc4r gene and its association with economic traits in qinchuan cattle.
15637755 - Nod2/card15 gene polymorphism in patients with inflammatory bowel disease: is hungary d...
19850125 - Common cyp7a1 promoter polymorphism associated with risk of neuromyelitis optica.
16571085 - Lack of a genetic association between the ctla-4 gene and graves' disease in koreans.
23161105 - A new insight into structural and functional impact of single-nucleotide polymorphisms ...
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association     Volume:  6     ISSN:  1542-7714     ISO Abbreviation:  Clin. Gastroenterol. Hepatol.     Publication Date:  2008 Aug 
Date Detail:
Created Date:  2008-08-04     Completed Date:  2008-10-23     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  101160775     Medline TA:  Clin Gastroenterol Hepatol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  939-43     Citation Subset:  IM    
Department of Gastroenterology and Hepatology, Karolinska University Hospital, Karolinska Institute, Huddinge and Solna, Stockholm, Sweden.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Case-Control Studies
Child of Impaired Parents
Cholangitis, Sclerosing / epidemiology*
Colitis, Ulcerative / epidemiology*
Genetic Predisposition to Disease*
Middle Aged

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

Previous Document:  Regression of hepatic fibrosis after intestinal transplantation in total parenteral nutrition liver ...
Next Document:  Effect of common KCNE1 and SCN5A ion channel gene variants on T-wave alternans, a marker of cardiac ...