Department of Rheumatology and Clinical Immunology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.
Hepatology. 2013 Jul;58(1):264-72. doi: 10.1002/hep.26322. Epub 2013 May 27.
The biochemical response to ursodeoxycholic acid (UDCA) in primary biliary cirrhosis is a strong predictor of long-term outcome and thus facilitates the rapid identification of patients needing new therapeutic approaches. Numerous criteria for predicting outcome of treatment have been studied based on biochemical response to UDCA at 1 year. We sought to determine whether an earlier biochemical response at 3 or 6 months could as efficiently identify patients at risk of poor outcome, as defined by liver-related death, liver transplantation, and complications of cirrhosis. We analyzed the prospectively collected data of 187 patients with a median follow-up of 5.8 years (range, 1.3-14 years). The survival rates without adverse outcome at 5 years and 10 years were 86% and 63%. Under UDCA therapy, laboratory liver parameters experienced the most prominent improvement in the first 3 months (P < 0.0001) and then stayed relatively stable for the following months. The Paris, Barcelona, Toronto, and Ehime definitions, but not the Rotterdam definition, applied at 3, 6, and 12 months significantly discriminated the patients in terms of long-term outcome. Compared with biochemical responses evaluated after 1 year of UDCA therapy, biochemical responses at the third month demonstrated higher positive predictive value (PPV) but lower negative predictive value (NPV) and increased negative likelihood ratio (NLR) by all definitions; biochemical responses at the sixth month showed higher or the same PPV and NPV and lower NLR by all definitions.
For the previously published criteria, biochemical responses at the sixth month can be used in place of those evaluated after 1 year of UDCA therapy. Our findings justify a more rapid identification of patients who need new therapeutic approaches.
熊去氧胆酸(UDCA)在原发性胆汁性肝硬化中的生化反应是长期预后的强有力预测指标,因此有助于快速识别需要新治疗方法的患者。已经基于 UDCA 在 1 年时的生化反应研究了许多用于预测治疗结果的标准。我们试图确定在 3 或 6 个月时更早的生化反应是否可以同样有效地识别出有不良预后风险的患者,定义为与肝脏相关的死亡、肝移植和肝硬化并发症。我们分析了 187 例患者的前瞻性收集数据,中位随访时间为 5.8 年(范围,1.3-14 年)。5 年和 10 年无不良结局的生存率分别为 86%和 63%。在 UDCA 治疗下,实验室肝功能参数在头 3 个月改善最明显(P < 0.0001),随后几个月相对稳定。巴黎、巴塞罗那、多伦多和 Ehime 定义,但不是鹿特丹定义,在 3、6 和 12 个月时显著区分了长期预后的患者。与 UDCA 治疗 1 年后评估的生化反应相比,第 3 个月的生化反应具有更高的阳性预测值(PPV)但较低的阴性预测值(NPV)和更高的负似然比(NLR);第 6 个月的生化反应具有更高或相同的 PPV 和 NPV 和更低的 NLR。
对于之前发表的标准,6 个月时的生化反应可以替代 UDCA 治疗 1 年后评估的标准。我们的发现证明了更快地识别需要新治疗方法的患者是合理的。