<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kim JM</submitter><funding>Seoul National University</funding><pagination>204-211</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10943302</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>100(2)</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>This study aimed to evaluate the diagnostic utility, disease activity, and phenotypic association of serum anti-Saccharomyces cerevisiae antibody (ASCA), perinuclear anti-neutrophil cytoplasmic antibody (pANCA), PR3-ANCA, and MPO-ANCA in pediatric patients with inflammatory bowel disease (IBD).&lt;h4>Methods&lt;/h4>Pediatric patients diagnosed with IBD were recruited and classified as Crohn's disease (CD), ulcerative colitis (UC), and IBD-unclassified (IBD-U) through full investigation. The Paris classification was used to evaluate disease phenotypes of pediatric CD and UC.&lt;h4>Results&lt;/h4>In all, 229 pediatric patients with IBD (CD 147, UC 53, IBD-U 29) were included. The ASCA IgG seropositivity significantly differed among the three groups (CD 75.4%, UC 17.5%, and IBD-U 60.0%; p &lt; 0.001). PR3-ANCA positive rates were the highest in UC (24.0%), followed by IBD-U (17.6%), and none in CD (p = 0.002); pANCA-positive rates were higher in IBD-U (33.6%), followed by UC (28.0%) than in CD (1.4%) (p &lt; 0.001). Regarding disease phenotype, perianal disease revealed higher serum ASCA IgG titers (median 36.7 U/mL in P1 vs. 25.2 U/mL in P0, p = 0.019). Serum ASCA IgG and IgA cutoff values to distinguish CD were 32.7 (U/mL) and 11.9 (U/mL), respectively, with a specificity of 80.0%.&lt;h4>Conclusion&lt;/h4>Serological biomarkers of ASCA IgG and IgA were effective for differentiating CD in pediatric IBD patients, and serum pANCA and PR3-ANCA, but not MPO-ANCA, were effective in distinguishing UC and IBD-U. Furthermore, measuring serological titers of ASCA IgG and IgA may help differentiate CD and evaluate the disease activity and phenotype of pediatric IBD in practice.</pubmed_abstract><journal>Jornal de pediatria</journal><pubmed_title>Diagnostic utility, disease activity, and disease phenotype correlation of serum ASCA, pANCA, and PR3-ANCA in pediatric inflammatory bowel disease.</pubmed_title><pmcid>PMC10943302</pmcid><funding_grant_id>800-20210277</funding_grant_id><pubmed_authors>Choi YM</pubmed_authors><pubmed_authors>Kim JM</pubmed_authors><pubmed_authors>Yang HR</pubmed_authors><pubmed_authors>Jung SA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Diagnostic utility, disease activity, and disease phenotype correlation of serum ASCA, pANCA, and PR3-ANCA in pediatric inflammatory bowel disease.</name><description>&lt;h4>Objective&lt;/h4>This study aimed to evaluate the diagnostic utility, disease activity, and phenotypic association of serum anti-Saccharomyces cerevisiae antibody (ASCA), perinuclear anti-neutrophil cytoplasmic antibody (pANCA), PR3-ANCA, and MPO-ANCA in pediatric patients with inflammatory bowel disease (IBD).&lt;h4>Methods&lt;/h4>Pediatric patients diagnosed with IBD were recruited and classified as Crohn's disease (CD), ulcerative colitis (UC), and IBD-unclassified (IBD-U) through full investigation. The Paris classification was used to evaluate disease phenotypes of pediatric CD and UC.&lt;h4>Results&lt;/h4>In all, 229 pediatric patients with IBD (CD 147, UC 53, IBD-U 29) were included. The ASCA IgG seropositivity significantly differed among the three groups (CD 75.4%, UC 17.5%, and IBD-U 60.0%; p &lt; 0.001). PR3-ANCA positive rates were the highest in UC (24.0%), followed by IBD-U (17.6%), and none in CD (p = 0.002); pANCA-positive rates were higher in IBD-U (33.6%), followed by UC (28.0%) than in CD (1.4%) (p &lt; 0.001). Regarding disease phenotype, perianal disease revealed higher serum ASCA IgG titers (median 36.7 U/mL in P1 vs. 25.2 U/mL in P0, p = 0.019). Serum ASCA IgG and IgA cutoff values to distinguish CD were 32.7 (U/mL) and 11.9 (U/mL), respectively, with a specificity of 80.0%.&lt;h4>Conclusion&lt;/h4>Serological biomarkers of ASCA IgG and IgA were effective for differentiating CD in pediatric IBD patients, and serum pANCA and PR3-ANCA, but not MPO-ANCA, were effective in distinguishing UC and IBD-U. Furthermore, measuring serological titers of ASCA IgG and IgA may help differentiate CD and evaluate the disease activity and phenotype of pediatric IBD in practice.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar-Apr</publication><modification>2026-06-27T03:15:50.375Z</modification><creation>2025-04-06T17:25:22.322Z</creation></dates><accession>S-EPMC10943302</accession><cross_references><pubmed>38012956</pubmed><doi>10.1016/j.jped.2023.10.005</doi></cross_references></HashMap>