Fungal colonization and ASCA/p-ANCA positivity in inflammatory bowel disease: a cross-sectional study from Turkey
DOI:
https://doi.org/10.3855/jidc.21755Keywords:
Inflammatory bowel disease, ulcerative colitis, Crohn's disease, ASCA, p-ANCA, fungal colonizationAbstract
Introduction: Recent research indicates that individuals with inflammatory bowel disease (IBD) exhibit distinct intestinal fungal communities compared with healthy individuals. This study examined the relationship among anti-Saccharomyces cerevisiae antibodies (ASCA), perinuclear anti-neutrophil cytoplasmic antibodies (p-ANCA), and Candida spp. colonization to assess their utility in diagnosing IBD, differentiating subtypes, and predicting disease localization.
Methodology: Serum samples from 240 patients with IBD and 61 healthy controls were tested for ASCA and p-ANCA using indirect immunofluorescence assay (IIFA). Fecal samples were cultured to identify Candida species.
Results: ASCA positivity was significantly higher in Crohn’s disease (CD) (61.7%), whereas p-ANCA positivity was more frequent in ulcerative colitis (UC) (51.6%) (p = 0.005 and p = 0.002, respectively). Fluorescence intensity showed stronger ASCA reactivity in CD and higher p-ANCA intensity in UC. Candida colonization (≥ 5 CFU) was detected in 64.2% of IBD patients, with Candida albicans the most common species. Saccharomyces cerevisiae was detected exclusively in IBD patients (3.7%, p = 0.038). Higher colonization rates were observed in UC with pancolitis (78.9%) and in CD with colonic involvement (80%). ASCA intensity inversely correlated with Candida load in CD (p = 0.021), whereas p-ANCA intensity positively correlated with Candida load in UC (p = 0.038). No significant differences in Candida species diversity were observed between subtypes.
Conclusions: These findings support the diagnostic value of ASCA and p-ANCA in distinguishing IBD subtypes and highlight their association with Candida colonization. Further studies are warranted to elucidate fungal antigen–antibody interactions and to refine subtype-specific diagnostic and therapeutic strategies.
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Copyright (c) 2026 Zulal Asci Toraman, PINAR ÖNER, MERYEM ERDOĞAN, BERÇEM AFŞAR KARATEPE, ABDURRAHMAN SAHIN, YASEMİN ÜSTÜNDAĞ, HANDAN AKBULUT

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