Ethnic Variation in Disease Progression and Treatment

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Mandal P.
Elsaadany S.
Kallis, Y.

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2025

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Abstract

Introduction Evidence suggests ethnic variation in primary biliary cholangitis (PBC) disease progression, but existing literature focuses on North American populations, with limited data from the UK.1 2 We aimed to compare PBC disease progression and treatment response across ethnic groups at a UK tertiary hepatology centre, which serves an ethnically diverse London borough3. Methods We conducted a single-centre cross-sectional study of PBC outpatients at The Royal London Hospital hub centre. Data were collected from clinical records, including demographics, markers of disease progression, and treatment response rates. Comparative subgroup analysis was undertaken across ethnic groups. Results 116 patients were identified, of which 20 were excluded due to unavailability of ethnicity data. 96 patients were included. Findings are summarised in table 1. Results are reported as mean +/- standard deviation, or percentage of patients. Statistical significance was not reached in subgroup analysis due to limited sample sizes. 73% of included patients were Caucasian, 20% Asian, and 7% Black. All groups showed comparable age at diagnosis. ALP at diagnosis was noted to be higher in Caucasian patients (334 +/- 277 U/L) than Asian (263 +/- 204 U/L) and Black (250 +/- 183 U/L) patients. Recent LSM readings appeared comparable among Caucasian (9.9 +/- 10.6 kPa) and Asian (10.2 +/- 11.8 kPa ) patients; there was insufficient LSM data among Black patients for analysis (n=3). First-line treatment rates with ursodeoxycholic acid (UDCA) were comparable across groups. Progression to SLT was more commonly seen in Black (43%) and Caucasian (39%) patients than in Asian patients (26%). Obeticholic acid was more widely prescribed than bezafibrate in all groups. Asian patients were observed to have a higher response rate to SLT (80%) than Caucasian (63%) and Black (67%) patients. Discussion We observed variability in PBC disease progression and treatment among ethnic groups. In particular, Caucasian patients tended to present with higher ALP at diagnosis, and Asian patients were observed to have lower SLT initiation rates and higher response rates. In contrast to existing literature, Asian patients represented the largest ethnic minority group in our cohort, reflecting UK demographic data; disease characteristics in this group are not well studied4. If validated in multi-centre cohorts on a national scale, these trends could inform tailored treatment approaches in an increasingly diverse UK PBC population. (Table presented).

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