Different HLA class II associations in ulcerative colitis patients with and without primary sclerosing cholangitis

被引:42
作者
Karlsen, T. H. [1 ]
Boberg, K. M.
Vatn, M.
Bergquist, A.
Hampe, J.
Schrumpf, E.
Thorsby, E.
Schreiber, S.
Lie, B. A.
机构
[1] Natl Hosp Norway, Raduimhosp, Med Ctr, Inst Immunol, N-0027 Oslo, Norway
[2] Natl Hosp Norway, Raduimhosp, Med Ctr, Dept Med, N-0027 Oslo, Norway
[3] Univ Oslo, N-0316 Oslo, Norway
[4] Karolinska Univ Hosp, Dept Gastroenterol & Hepatol, Stockholm, Sweden
[5] Univ Kiel, Dept Med 1, D-24098 Kiel, Germany
[6] Univ Kiel, Inst Clin Mol Biol, D-24098 Kiel, Germany
关键词
primary sclerosing cholangitis; inflammatory bowel disease; ulcerative colitis; genetic susceptibility; human leukocyte antigen;
D O I
10.1038/sj.gene.6364377
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Approximately 80% of patients with primary sclerosing cholangitis (PSC) of Northern European origin have inflammatory bowel disease (IBD), the majority ulcerative colitis (UC). An inherent problem in interpreting positive findings in genetic association studies of PSC is thus to distinguish between factors associated with hepatobiliary versus intestinal pathology. We aimed to clarify to what extent human leukocyte antigen (HLA) class II associations in UC patients with and without PSC differ. High-resolution DRB1 and DQB1 typing was performed in 365 Scandinavian PSC patients, an independent cohort of 330 Norwegian UC patients and 368 healthy controls. HLA associations found in PSC were mostly distinct from those seen in UC, and no significant differences were noted between PSC patients with concurrent UC and PSC patients without IBD. This suggests different HLA associated genetic susceptibility to PSC and UC, and supports notions that UC in PSC may represent a distinct UC phenotype.
引用
收藏
页码:275 / 278
页数:4
相关论文
共 21 条
[1]   The contribution of human leucocyte antigen complex genes to disease phenotype in ulcerative colitis [J].
Ahmad, T ;
Armuzzi, A ;
Neville, M ;
Bunce, M ;
Ling, KL ;
Welsh, KI ;
Marshall, SE ;
Jewell, DP .
TISSUE ANTIGENS, 2003, 62 (06) :527-535
[2]   Genetics of inflammatory bowel disease: The role of the HLA complex [J].
Ahmad, Tariq ;
Marshall, Sara E. ;
Jewell, Derek .
WORLD JOURNAL OF GASTROENTEROLOGY, 2006, 12 (23) :3628-3635
[3]   Increased prevalence of primary sclerosing cholangitis among first-degree relatives [J].
Bergquist, A ;
Lindberg, G ;
Saarinen, S ;
Broomé, U .
JOURNAL OF HEPATOLOGY, 2005, 42 (02) :252-256
[4]   The immunological and genetic basis of inflammatory bowel disease [J].
Bouma, G ;
Strober, W .
NATURE REVIEWS IMMUNOLOGY, 2003, 3 (07) :521-533
[5]   Outcome following liver transplantation for primary sclerosing cholangitis in the Nordic countries [J].
Brandsæter, B ;
Friman, S ;
Broomé, U ;
Isoniemi, H ;
Olausson, M ;
Bäckman, L ;
Hansen, B ;
Schrumpf, E ;
Oksanen, A ;
Ericzon, BG ;
Höckerstedt, K ;
Mäkisalo, H ;
Kirkegaard, P ;
Bjoro, K .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 2003, 38 (11) :1176-1183
[6]   PRIMARY SCLEROSING CHOLANGITIS - A REVIEW OF ITS CLINICAL-FEATURES, CHOLANGIOGRAPHY, AND HEPATIC HISTOLOGY [J].
CHAPMAN, RWG ;
ARBORGH, BAM ;
RHODES, JM ;
SUMMERFIELD, JA ;
DICK, R ;
SCHEUER, PJ ;
SHERLOCK, S .
GUT, 1980, 21 (10) :870-877
[7]   Review article: current management of primary sclerosing cholangitis [J].
Cullen, SN ;
Chapman, RW .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2005, 21 (08) :933-948
[8]   Evaluation of the role of MHC class II alleles, haplotypes and selected amino acid sequences in primary sclerosing cholangitis [J].
Donaldson, PT ;
Norris, S .
AUTOIMMUNITY, 2002, 35 (08) :555-564
[9]   Immunogenetics in PSC [J].
Donaldson, PT ;
Norris, S .
BEST PRACTICE & RESEARCH CLINICAL GASTROENTEROLOGY, 2001, 15 (04) :611-627
[10]   RELATIONSHIP OF INFLAMMATORY BOWEL-DISEASE AND PRIMARY SCLEROSING CHOLANGITIS [J].
FAUSA, O ;
SCHRUMPF, E ;
ELGJO, K .
SEMINARS IN LIVER DISEASE, 1991, 11 (01) :31-39