Imran Muhammad, Elsnhory Ahmed B, Ibrahim Ahmed A, Elnaggar Mohamed, Tariq Muhammad S, Mehmood Areeba M, Ali Shujaat, Khalil Saba, Khan Sheharyar H, Ali Mansab, Abuelazm Mohamed
University College of Medicine and Dentistry, The University of Lahore, Lahore, Pakistan.
Faculty of Medicine, Al-Azhar University, Cairo, Egypt.
J Clin Exp Hepatol. 2025 May-Jun;15(3):102462. doi: 10.1016/j.jceh.2024.102462. Epub 2024 Nov 21.
Inherited cholestatic liver disorders such as progressive familial intrahepatic cholestasis (PFIC) and Alagille syndrome result in significant pruritus and increased serum bile acids, necessitating liver transplantation. This study aims to evaluate the efficacy and safety of Ileal bile acid transport inhibitors (IBATIs) in children with PFIC and Alagille syndrome.
We conducted a comprehensive search across the databases to identify relevant randomized controlled trials (RCTs), and Covidence was used to screen eligible articles. All outcomes data were synthesized using risk ratios (RRs) or mean differences (MDs) with 95% confidence intervals (CIs) in RevMan 5.4. PROSPERO: CRD42024564270.
Four multicenter RCTs involving 215 patients were included. IBATIs were associated with a significant reduction in Itch Observer Reported Outcome (Itch (ObsRo)) score (MD: -0.90, 95% CI [-1.17, -0.63], < 0.01), serum bile acids (MD: -119.06, 95% CI [-152.37, -85.74], < 0.01), total bilirubin (MD: -0.73, 95% CI [-1.32, -0.15], = 0.01), and increased proportion of patients achieving ≥1 score reduction in Itch (ObsRo) score (RR: 2.54, 95% CI [3.83, 1.69], < 0.01) and bile acid responders (RR: 8.76, 95% CI [2.46, 31.23], < 0.01) compared with placebo. No differences were observed in any treatment-emergent adverse events (TEAs) (RR: 1.02, 95% CI [1.12, 0.93], = 0.71), TEAs leading to drug discontinuation (1.03, 95% CI [5.56, 0.19], any serious TEAs, or liver-related TEAs.
IBATIs showed significant improvement in various cholestatic parameters with tolerable safety profile; however, future research on optimal dosage and long-term outcomes is needed.
遗传性胆汁淤积性肝病,如进行性家族性肝内胆汁淤积症(PFIC)和阿拉吉列综合征,会导致严重瘙痒和血清胆汁酸升高,从而需要进行肝移植。本研究旨在评估回肠胆汁酸转运抑制剂(IBATIs)对PFIC和阿拉吉列综合征患儿的疗效和安全性。
我们对各数据库进行了全面检索,以识别相关的随机对照试验(RCT),并使用Covidence筛选符合条件的文章。所有结局数据均在RevMan 5.4中使用风险比(RRs)或均值差(MDs)及95%置信区间(CIs)进行合成。国际前瞻性注册系统(PROSPERO)注册号:CRD42024564270。
纳入了4项涉及215例患者的多中心RCT。与安慰剂相比,IBATIs与瘙痒观察者报告结局(Itch(ObsRo))评分显著降低(MD:-0.90,95%CI[-1.17,-0.63],P<0.01)、血清胆汁酸(MD:-119.06,95%CI[-152.3, -85.74],P<0.01)、总胆红素(MD:-0.73,95%CI[-1.32,-0.15],P = 0.01)相关,且瘙痒(ObsRo)评分降低≥1分的患者比例增加(RR:2.54,95%CI[1.69,3.83],P<0.01)以及胆汁酸反应者比例增加(RR:8.76,95%CI[2.46,31.23],P<0.01)。在任何治疗中出现的不良事件(TEAs)(RR:1.02,95%CI[0.93,1.12],P = 0.71)、导致停药的TEAs(RR:1.03,95%CI[0.19,5.56])、任何严重TEAs或与肝脏相关的TEAs方面均未观察到差异。
IBATIs在各种胆汁淤积参数方面显示出显著改善,且安全性可耐受;然而,需要对最佳剂量和长期结局进行进一步研究。