Anti-Proteinase 3 Antibodies as a Biomarker for Ulcerative Colitis and Primary Sclerosing Cholangitis in Children

被引:15
|
作者
Laass, Martin Walter [1 ,2 ]
Ziesmann, Josefine [1 ,2 ,3 ,4 ]
de laffolie, Jan [5 ]
Roeber, Nadja [3 ]
Conrad, Karsten [3 ,6 ]
机构
[1] Tech Univ Dresden, Univ Hosp, Dept Paediat, Fetscherstr 74, D-01307 Dresden, Germany
[2] Tech Univ Dresden, Med Fac Carl Gustav Carus, Fetscherstr 74, D-01307 Dresden, Germany
[3] Tech Univ Dresden, Inst Immunol, Dresden, Germany
[4] Univ Coll Hosp, Dept Obstet, London WC1E 6DB, England
[5] Justus Liebig Univ Giessen, Univ Childrens Hosp, Dept Gen Paediat & Neonatol, Giessen, Germany
[6] Assoc Adv Immune Diagnost, D-01219 Dresden, Germany
关键词
anti-neutrophil cytoplasmic antibodies; backwash ileitis; granulomatosis with polyangiitis; inflammatory bowel disease; proteinase; 3; INFLAMMATORY-BOWEL-DISEASE; ANTINEUTROPHIL CYTOPLASMIC AUTOANTIBODIES; WEGENER GRANULOMATOSIS; CONSENSUS STATEMENTS; PREDICTING OUTCOMES; SEROLOGIC MARKERS; DISTINCTIVE FORM; DIAGNOSIS; MANAGEMENT; POLYANGIITIS;
D O I
10.1097/MPG.0000000000003359
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Objectives: Anti-neutrophil cytoplasmic antibody (ANCA) directed against proteinase 3 (PR3) is a marker for granulomatosis with polyangiitis, but is also found in patients with inflammatory bowel disease (IBD), mainly ulcerative colitis (UC). The aim of our study was to investigate ANCA and PR3-ANCA in paediatric IBD. Methods: We tested 326 paediatric IBD patients and 164 controls for anti-Saccharomyces cerevisiae antibodies (ASCA), ANCA (indirect immunofluorescence, IIF) and PR3-ANCA (chemiluminescence immunoassay). We applied the Paris classification for paediatric IBD and documented liver manifestations such as primary sclerosing cholangitis (PSC) and autoimmune hepatitis (AIH). Results: We found PR3-ANCA in 49/121 (40%) of UC, 20/187 (11%) of Crohn disease (CD) and 2/18 (11%) of IBD-unclassified (IBD-U) patients but in none of the controls. 54% UC and 12% CD patients were positive for ANCA (IIF). PR3-ANCA positive UC patients were characterised by more extensive disease (P = .070). Fourteen of 21 (67%) of UC patients with backwash ileitis were anti-PR3 ANCA-positive (P = .011). We diagnosed PSC or PSC/AIH in 19 UC and 3 IBD-U patients. Fifteen of 22 (68%) patients with PSC or PSC/AIH were anti-PR3-ANCA positive in contrast to 36 of 117 (32%) patients without PSC (P = .001). PR3-ANCA positive patients showed higher levels of gamma-glutamyl transferase, alanine transaminase and aspartate transferase (P< 0.001, 0.001, 0.006, respectively). Forty-seven percent of CD and 6% of UC patients were ASCA-IgA positive. PR3-ANCA-positive and -negative patients showed no significant differences concerning age at diagnosis, disease activity, need for drugs, and number of hospitalisations. Conclusions: Our study provides data for PR3-ANCA as a potential serological marker for paediatric UC and PSC.
引用
收藏
页码:463 / 470
页数:8
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