Published online Aug 14, 2025. doi: 10.3748/wjg.v31.i30.109585
Revised: June 8, 2025
Accepted: July 2, 2025
Published online: August 14, 2025
Processing time: 84 Days and 1.4 Hours
Celiac disease (CeD), an autoimmune disorder triggered by gluten ingestion, is characterized by non-specific clinical manifestations such as fatigue, abdominal pain, and nutritional deficiencies, often leading to substantial diagnostic delays. Prolonged delays (≥ 2 years from symptom onset) are associated with increased risks of complications like osteoporosis, small intestinal lymphoma, and reduced quality of life.
To estimate diagnostic delay prevalence and identify risk factors in Chinese CeD patients.
We reviewed clinical records of 166 patients diagnosed with CeD from 2017 onward. Patient-attributed delays were measured from symptom onset to first consultation, while physician-related delays were measured from initial visit to diagnosis/treatment. Data on demographics, symptoms, time from onset to diagnosis, and laboratory results were analyzed. Logistic regression models were used to identify associations, while restricted cubic splines explored nonlinearities. Mediation analysis assessed the roles of intermediate factors in delayed diagnosis.
Delayed diagnosis (over 2 years from symptom onset) was observed in 42.2% of patients. Patients with diagnostic delay exceeding 5 years accounted for 18.7%. The mean interval from symptom onset to the first medical visit was 12.32 months, with an average of 20.57 months from the first visit to diagnosis. The time from first consultation to diagnosis significantly increased with prolonged delay (P < 0.001). Multivariate analysis showed that blood urea nitrogen (BUN) was an independent risk factor (OR = 1.29, 95%CI: 1.01–1.65, P = 0.038). A nonlinear association was observed between BUN and delayed diagnosis, with a threshold of 4.3 mmol/L; the risk significantly increased above this threshold (OR = 1.39, P = 0.04). Subgroup analyses indicated that the risk effect of BUN was stronger in females, non-classical CeD patients, Kazak ethnic group members, individuals without vitamin D deficiency/anemia, and those with Marsh III pathology (all P < 0.05). Mediation analysis revealed that folic acid deficiency and anemia mediated 11.9% (P = 0.028) and 13.0% (P = 0.044) of the effect of BUN on diagnostic delay, respectively.
Elevated BUN levels are independent predictors of diagnostic delay in CeD, with heterogeneity observed across gender, disease subtype, ethnicity, and pathological type. Clinicians should prioritize high-risk populations with BUN ≥ 4.3 mmol/L, particularly female patients with non-classical CeD and Kazak individuals, to reduce diagno
Core Tip: This study presents the largest single-center cohort of Chinese celiac disease (CeD) patients (Marsh ≥ II histopathology) leveraging Xinjiang’s regional referral advantage. Among 166 CeD patients, 42.2% experienced diagnostic delay (> 2 years). Blood urea nitrogen (BUN) was identified as an independent risk factor (OR = 1.29), with risk significantly increasing at ≥ 4.3 mmol/L. Subgroup analyses showed stronger associations of BUN with diagnostic delay in females, patients with non-classical CeD phenotypes, Kazak individuals, and other subgroups. These findings highlight BUN as a novel predictor and provide evidence to prioritize high-risk subgroups for timely screening.