Pretreatment serum bile acid composition and predictability of subsequent response to odevixibat in patients with bile salt export pump (BSEP) deficiency

IF 12.9 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Mark Nomden, Folkert Kuipers, Willem S. Lexmond, Tao Gu, Velichka Valcheva, Erik Lindström, Henkjan J. Verkade
{"title":"Pretreatment serum bile acid composition and predictability of subsequent response to odevixibat in patients with bile salt export pump (BSEP) deficiency","authors":"Mark Nomden, Folkert Kuipers, Willem S. Lexmond, Tao Gu, Velichka Valcheva, Erik Lindström, Henkjan J. Verkade","doi":"10.1097/hep.0000000000001430","DOIUrl":null,"url":null,"abstract":"Background &amp; Aims: Bile salt export pump (BSEP) deficiency, or progressive familial intrahepatic cholestasis type 2, is a genetic liver disease characterized by defective biliary bile acid secretion. Odevixibat, an ileal bile acid transporter inhibitor (IBATi), impairs intestinal reabsorption of conjugated bile acids, reducing serum bile acid (sBA) concentration in some patients with BSEP deficiency. We evaluated association of pretreatment sBA levels and composition, and subsequent response to odevixibat in patients with BSEP deficiency to improve our understanding of the mechanism. Approach &amp; Results: In this blinded <jats:italic toggle=\"yes\">post hoc</jats:italic> analysis, pretreatment sBAs from 41 odevixibat-treated patients with BSEP deficiency who participated in PEDFIC were analyzed using liquid chromatography-tandem mass spectrometry. Patients were divided into sBA responders (Rs) and non-responders (NRs). Association of pretreatment individual sBAs with subsequent response was evaluated and receiver operating characteristic (ROC) curves were constructed to identify discriminating cutoff values. Rs had higher pretreatment percentages of unconjugated cholic acid (CA; area under the ROC curve [AUC]: 0.70 [95% CI: 0.52–0.87; <jats:italic toggle=\"yes\">P</jats:italic>=0.03]), unconjugated chenodeoxycholic acid (CDCA; AUC: 0.73 [0.56–0.90]; <jats:italic toggle=\"yes\">P</jats:italic>=0.01), and concentration of CA + CDCA (AUC: 0.76 [0.61–0.92]; <jats:italic toggle=\"yes\">P</jats:italic>=0.001). When ≥1 of 3 cutoffs were reached, 36/41 (87.8%) patients with BSEP deficiency were correctly classified as subsequent Rs (17/19; sensitivity: 89.5%) or NRs (19/22; specificity: 86.4%). Conclusions: Higher pretreatment serum levels of unconjugated CA and CDCA are associated with subsequent response to odevixibat in patients with BSEP deficiency. Response to odevixibat may be related to residual biliary bile acid secretion capacity in patients with BSEP deficiency.","PeriodicalId":177,"journal":{"name":"Hepatology","volume":"109 1","pages":""},"PeriodicalIF":12.9000,"publicationDate":"2025-07-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Hepatology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1097/hep.0000000000001430","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"GASTROENTEROLOGY & HEPATOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background & Aims: Bile salt export pump (BSEP) deficiency, or progressive familial intrahepatic cholestasis type 2, is a genetic liver disease characterized by defective biliary bile acid secretion. Odevixibat, an ileal bile acid transporter inhibitor (IBATi), impairs intestinal reabsorption of conjugated bile acids, reducing serum bile acid (sBA) concentration in some patients with BSEP deficiency. We evaluated association of pretreatment sBA levels and composition, and subsequent response to odevixibat in patients with BSEP deficiency to improve our understanding of the mechanism. Approach & Results: In this blinded post hoc analysis, pretreatment sBAs from 41 odevixibat-treated patients with BSEP deficiency who participated in PEDFIC were analyzed using liquid chromatography-tandem mass spectrometry. Patients were divided into sBA responders (Rs) and non-responders (NRs). Association of pretreatment individual sBAs with subsequent response was evaluated and receiver operating characteristic (ROC) curves were constructed to identify discriminating cutoff values. Rs had higher pretreatment percentages of unconjugated cholic acid (CA; area under the ROC curve [AUC]: 0.70 [95% CI: 0.52–0.87; P=0.03]), unconjugated chenodeoxycholic acid (CDCA; AUC: 0.73 [0.56–0.90]; P=0.01), and concentration of CA + CDCA (AUC: 0.76 [0.61–0.92]; P=0.001). When ≥1 of 3 cutoffs were reached, 36/41 (87.8%) patients with BSEP deficiency were correctly classified as subsequent Rs (17/19; sensitivity: 89.5%) or NRs (19/22; specificity: 86.4%). Conclusions: Higher pretreatment serum levels of unconjugated CA and CDCA are associated with subsequent response to odevixibat in patients with BSEP deficiency. Response to odevixibat may be related to residual biliary bile acid secretion capacity in patients with BSEP deficiency.
胆汁盐输出泵(BSEP)缺乏症患者预处理血清胆汁酸组成及对奥维西他后续反应的可预测性
背景,目的:胆汁盐输出泵(BSEP)缺乏症,或进行性家族性肝内胆汁淤积2型,是一种以胆汁酸分泌缺陷为特征的遗传性肝病。Odevixibat是一种回肠胆汁酸转运抑制剂(IBATi),可损害共轭胆汁酸的肠重吸收,降低一些BSEP缺乏患者的血清胆汁酸(sBA)浓度。我们评估了预处理sBA水平与BSEP缺乏症患者组成的关系,以及随后对奥维西坦的反应,以提高我们对其机制的理解。的方法,结果:在这项盲法事后分析中,使用液相色谱-串联质谱法分析了41名接受奥维昔巴治疗的参与PEDFIC的BSEP缺乏症患者的预处理sBAs。患者分为sBA应答者(Rs)和无应答者(nr)。评估预处理个体sBAs与后续反应的相关性,并构建受试者工作特征(ROC)曲线以确定判别临界值。非共轭胆酸(CA)预处理比例较高;ROC曲线下面积[AUC]: 0.70 [95% CI: 0.52-0.87;P=0.03]),非共轭鹅去氧胆酸(CDCA;Auc: 0.73 [0.56-0.90];P=0.01), CA + CDCA浓度(AUC: 0.76 [0.61 ~ 0.92];P = 0.001)。当达到3个临界值中的≥1个时,36/41 (87.8%)BSEP缺乏患者被正确归类为后续Rs (17/19;敏感性:89.5%)或NRs (19/22;特异性:86.4%)。结论:较高的预处理血清非共轭CA和CDCA水平与BSEP缺乏症患者随后对奥维西坦的反应相关。对奥维西坦的反应可能与BSEP缺乏患者的剩余胆汁酸分泌能力有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Hepatology
Hepatology 医学-胃肠肝病学
CiteScore
27.50
自引率
3.70%
发文量
609
审稿时长
1 months
期刊介绍: HEPATOLOGY is recognized as the leading publication in the field of liver disease. It features original, peer-reviewed articles covering various aspects of liver structure, function, and disease. The journal's distinguished Editorial Board carefully selects the best articles each month, focusing on topics including immunology, chronic hepatitis, viral hepatitis, cirrhosis, genetic and metabolic liver diseases, liver cancer, and drug metabolism.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信