Efficacy and Safety of Ileal Bile Acid Transport Inhibitors in Inherited Cholestatic Liver Disorders: A Meta-analysis of Randomized Controlled Trials.

IF 3.3 Q2 GASTROENTEROLOGY & HEPATOLOGY
Muhammad Imran, Ahmed B Elsnhory, Ahmed A Ibrahim, Mohamed Elnaggar, Muhammad S Tariq, Areeba M Mehmood, Shujaat Ali, Saba Khalil, Sheharyar H Khan, Mansab Ali, Mohamed Abuelazm
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引用次数: 0

Abstract

Background: 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.

Methods: 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.

Results: 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], P < 0.01), serum bile acids (MD: -119.06, 95% CI [-152.37, -85.74], P < 0.01), total bilirubin (MD: -0.73, 95% CI [-1.32, -0.15], P = 0.01), and increased proportion of patients achieving ≥1 score reduction in Itch (ObsRo) score (RR: 2.54, 95% CI [3.83, 1.69], P < 0.01) and bile acid responders (RR: 8.76, 95% CI [2.46, 31.23], P < 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], P = 0.71), TEAs leading to drug discontinuation (1.03, 95% CI [5.56, 0.19], any serious TEAs, or liver-related TEAs.

Conclusion: IBATIs showed significant improvement in various cholestatic parameters with tolerable safety profile; however, future research on optimal dosage and long-term outcomes is needed.

回肠胆汁酸转运抑制剂治疗遗传性胆汁淤积性肝病的疗效和安全性:一项随机对照试验的荟萃分析。
背景:遗传性胆汁淤积性肝脏疾病,如进行性家族性肝内胆汁淤积症(PFIC)和Alagille综合征,可导致明显的瘙痒和血清胆汁酸升高,需要肝移植。本研究旨在评估回肠胆汁酸转运抑制剂(IBATIs)在PFIC和Alagille综合征患儿中的疗效和安全性。方法:我们在数据库中进行了全面检索,以确定相关的随机对照试验(RCTs),并使用covid筛选符合条件的文章。所有结局数据采用RevMan 5.4中95%可信区间的风险比(rr)或平均差异(MDs)进行综合。普洛斯彼罗:CRD42024564270。结果:纳入4项多中心随机对照试验,共215例患者。IBATIs与瘙痒观察者报告结果(瘙痒(ObsRo))评分显著降低相关(MD: -0.90, 95% CI [-1.17, -0.63], P P P = 0.01),瘙痒(ObsRo)评分降低≥1分的患者比例增加(RR: 2.54, 95% CI [3.83, 1.69], P P = 0.71), tea导致药物停药(1.03,95% CI[5.56, 0.19]),任何严重的tea或肝脏相关tea。结论:IBATIs可显著改善各种胆汁淤积参数,且具有可耐受的安全性;然而,需要对最佳剂量和长期疗效进行进一步研究。
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来源期刊
Journal of Clinical and Experimental Hepatology
Journal of Clinical and Experimental Hepatology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
4.90
自引率
16.70%
发文量
537
审稿时长
64 days
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