HLA-DR and HLA-DQ are not markers for rapid disease progression in primary sclerosing cholangitis☆
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Primary Sclerosing Cholangitis as a Premalignant Biliary Tract Disease: Surveillance and Management
2015, Clinical Gastroenterology and HepatologyCitation Excerpt :PSC has robust associations within the HLA complex, which provides further credence to the notion that immunity plays a role in its pathogenesis.22 Haplotypes with well-established associations with PSC include HLA-DRB1*1301-DQB1*0603, HLA-A1-B8-DRB1*0301-DQB1*0201, and HLA-DRB1*1501-DQB1*0602.23,24 Overall, there are 16 known genome-wide significant loci in PSC, including the HLA complex on chromosome 6.25–27
Diagnosis and classification of primary sclerosing cholangitis
2014, Autoimmunity ReviewsPrimary Sclerosing Cholangitis
2013, The Autoimmune Diseases: Fifth EditionPathogenesis of primary sclerosing cholangitis and advances in diagnosis and management
2013, GastroenterologyCitation Excerpt :Patients who have a first-degree relative with PSC have a 9- to 39-fold increased risk of development of the disease.14 In the past 2 decades, candidate gene studies associated specific HLAs with PSC, including the haplotypes HLA-DRB1*1501-DQB1*0602, HLA-DRB1*1301-DQB1* 0603, and HLA-A1-B8-DRB1*0301-DQB1*0201.58–61 Recent genome-wide association studies have also reported that the strongest genetic risk to PSC lies within the major histocompatibility complex, where the heritability represented by these loci is twice that of all other risk loci combined.62
Primary sclerosing cholangitis
2012, Blumgart's Surgery of the Liver, Biliary Tract and Pancreas
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Supported by grants from the Swedish Medical Research Council (projects 10137 and 10393), the Swedish Society of Medicine, and the Foundation of Professor Nanna Svartz.