Marenco-Flores Ana, Rojas Amaris Natalia, Kahan Tamara, Sierra Leandro, Barba Bernal Romelia, Medina-Morales Esli, Goyes Daniela, Patwardhan Vilas, Bonder Alan
Division of Gastroenterology, Hepatology, and Nutrition, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA.
Department of Internal Medicine, Texas Tech University System, Lubbock, TX 79430, USA.
J Clin Med. 2024 Aug 1;13(15):4497. doi: 10.3390/jcm13154497.
The cornerstone treatment for primary biliary cholangitis (PBC) is ursodeoxycholic acid (UDCA), but many patients exhibit an incomplete response, leading to disease progression. Risk prediction models like the GLOBE and UK-PBC scores hold promise for patient stratification and management. We aimed to independently assess the predictive accuracy of these risk scores for UDCA response in a prospective U.S. cohort. We conducted a prospective cohort study at a U.S. liver center, monitoring UDCA-treated PBC patients over a one-year follow-up. We evaluated the predictive efficacy of the GLOBE and UK-PBC scores for UDCA treatment response, comparing them to the Paris II criteria. Efficacy was assessed using univariate and multivariate analyses, followed by prognostic performance evaluation via receiver operating characteristic (ROC) curve analysis. We evaluated 136 PBC patients undergoing UDCA therapy. Based on the Paris II criteria, patients were categorized into UDCA full-response and non-response groups. The GLOBE score identified a non-responder rate of 18% ( = 0.205), compared to 20% ( = 0.014) with the Paris II criteria. Multivariate analysis, adjusted for age and biochemical markers, showed that both the GLOBE and UK-PBC scores were strongly associated with treatment response ( < 0.001). The area under the ROC curve was 0.87 (95% CI 0.83-0.95) for the GLOBE score and 0.94 (95% CI 0.86-0.99) for the UK-PBC risk score. Our study demonstrates that GLOBE and UK-PBC scores effectively predict UDCA treatment response in PBC patients. The early identification of patients at risk of an incomplete response could improve treatment strategies and identify patients who may need second-line therapies.
原发性胆汁性胆管炎(PBC)的基石治疗药物是熊去氧胆酸(UDCA),但许多患者对其反应不完全,导致疾病进展。像GLOBE和英国PBC评分这样的风险预测模型有望用于患者分层和管理。我们旨在在美国一个前瞻性队列中独立评估这些风险评分对UDCA反应的预测准确性。我们在美国一家肝脏中心进行了一项前瞻性队列研究,对接受UDCA治疗的PBC患者进行了为期一年的随访。我们评估了GLOBE和英国PBC评分对UDCA治疗反应的预测效力,并将它们与巴黎II标准进行比较。通过单因素和多因素分析评估效力,随后通过受试者工作特征(ROC)曲线分析进行预后性能评估。我们评估了136例接受UDCA治疗的PBC患者。根据巴黎II标准,患者被分为UDCA完全反应组和无反应组。GLOBE评分确定的无反应率为18%( = 0.205),而巴黎II标准确定的无反应率为20%( = 0.014)。在对年龄和生化标志物进行校正的多因素分析中,GLOBE和英国PBC评分均与治疗反应密切相关( < 0.