Hospital Universitario Virgen del Rocío, Sevilla, Spain.
Instituto de Biomedicina de Sevilla, Spain.
Hepatology. 2024 Oct 1;80(4):791-806. doi: 10.1097/HEP.0000000000000826. Epub 2024 Mar 6.
The landscape in primary biliary cholangitis (PBC) has changed with the advent of second-line treatments. However, the use of obeticholic acid (OCA) and fibrates in PBC-related cirrhosis is challenging. We assessed the impact of receiving a second-line therapy as a risk factor for decompensated cirrhosis in a real-world population with cirrhosis and PBC, and identify the predictive factors for decompensated cirrhosis in these patients.
Multicenter study enrolling 388 patients with PBC-cirrhosis from the Spanish ColHai registry. Biopsy (20%), ultrasound (59%), or transient elastography (21%) defined cirrhosis, and the presence of varices and splenomegaly defined clinically significant portal hypertension (CSPH). Paris-II and PBC OCA international study of efficacy criteria determined the response to ursodeoxycholic acid (UDCA), fibrates (n=93), and OCA (n=104). The incidence of decompensated cirrhosis decreased for UDCA versus OCA or fibrates in the real-world population, but they were similar considering the propensity score-matched cohort (UDCA 3.77 vs. second-line therapy 4.5 100 persons-year, respectively), as patients on second-line therapy exhibited advanced liver disease. Consequently, GGT, albumin, platelets, clinically significant portal hypertension, and UDCA response were associated with a decompensating event. OCA response (achieved in 52% of patients) was associated with bilirubin (OR 0.21 [95% CI: 0.06-0.73]) and AST (OR 0.97 [95% CI: 0.95-0.99]), while fibrate response (achieved in 55% of patients) with AST [OR 0.96 (95% CI: 0.95-0.98]). In patients treated with OCA, drug response (sHR 0.23 [95% CI: 0.08-0.64]), diabetes (sHR 5.62 [95% CI: 2.02-15.68]), albumin (sHR 0.34 [95% CI: 0.13-0.89]), and platelets (sHR 0.99 [95% CI: 0.98-1.00]) were related to decompensation. In patients treated with fibrate, drug response (sHR 0.36 (95% CI: 0.14-0.95]), albumin (sHR 0.36 (95% CI: 0.16-0.81]), and clinically significant portal hypertension (sHR 3.70 (95% CI: 1.17-11.70]) were associated with decompensated cirrhosis.
Advanced PBC, rather than OCA and fibrates, was found to be associated with decompensating events. Therefore, biochemical and clinical variables should be considered when making decisions about the management of these drugs. Moreover, a positive response to OCA and fibrates reduced the risk of decompensation.
随着二线治疗的出现,原发性胆汁性胆管炎(PBC)的治疗格局发生了变化。然而,在 PBC 相关肝硬化患者中使用奥贝胆酸(OCA)和贝特类药物具有挑战性。我们评估了二线治疗作为肝硬化患者发生失代偿性肝硬化的风险因素,并确定了这些患者发生失代偿性肝硬化的预测因素。
这项多中心研究纳入了来自西班牙 ColHai 注册中心的 388 例 PBC 肝硬化患者。活检(20%)、超声(59%)或瞬时弹性成像(21%)定义为肝硬化,存在静脉曲张和脾肿大定义为临床显著门静脉高压(CSPH)。Paris-II 和 PBC OCA 国际疗效标准确定了熊去氧胆酸(UDCA)、贝特类(n=93)和 OCA(n=104)的反应。在真实世界人群中,与 UDCA 相比,OCA 或贝特类药物治疗的失代偿性肝硬化发生率降低,但在倾向评分匹配队列中,两者相似(UDCA 为 3.77,二线治疗为 4.5/100 人年),因为接受二线治疗的患者存在更严重的肝脏疾病。因此,GGT、白蛋白、血小板、临床显著门静脉高压和 UDCA 反应与失代偿事件相关。OCA 反应(在 52%的患者中实现)与胆红素(OR 0.21 [95%CI:0.06-0.73])和 AST(OR 0.97 [95%CI:0.95-0.99])相关,而贝特类药物反应(在 55%的患者中实现)与 AST [OR 0.96(95%CI:0.95-0.98])相关。在接受 OCA 治疗的患者中,药物反应(sHR 0.23 [95%CI:0.08-0.64])、糖尿病(sHR 5.62 [95%CI:2.02-15.68])、白蛋白(sHR 0.34 [95%CI:0.13-0.89])和血小板(sHR 0.99 [95%CI:0.98-1.00])与失代偿相关。在接受贝特类药物治疗的患者中,药物反应(sHR 0.36 [95%CI:0.14-0.95])、白蛋白(sHR 0.36 [95%CI:0.16-0.81])和临床显著门静脉高压(sHR 3.70 [95%CI:1.17-11.70])与失代偿性肝硬化相关。
晚期 PBC 而不是 OCA 和贝特类药物与失代偿事件相关。因此,在决定这些药物的管理时,应考虑生化和临床变量。此外,OCA 和贝特类药物的阳性反应降低了失代偿的风险。