Maralixibat Reduces Serum Bile Acids and Improves Cholestatic Pruritus in Adolescents With Alagille Syndrome

被引:0
|
作者
Hirschfield, Gideon [1 ]
Vandriel, Shannon M. [2 ,3 ,4 ]
Mogul, Douglas B. [4 ]
Baek, Marshall [4 ]
Vig, Pamela [4 ]
Kamath, Binita M. [2 ,3 ,5 ,6 ]
机构
[1] Toronto Gen Hosp, Autoimmune & Rare Liver Dis Programme, Div Gastroenterol & Hepatol, Toronto, ON, Canada
[2] Hosp Sick Children, Div Gastroenterol Hepatol & Nutr, Toronto, ON, Canada
[3] Univ Toronto, Toronto, ON, Canada
[4] Mirum Pharmaceut Inc, Foster City, CA USA
[5] Childrens Hosp Philadelphia, Div Gastroenterol Hepatol & Nutr, Philadelphia, PA 19104 USA
[6] Univ Penn Perelman, Sch Med, Philadelphia, PA 19104 USA
关键词
Alagille syndrome; cholestatic pruritus; maralixibat; serum bile acids;
D O I
10.1111/liv.16201
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background Alagille syndrome (ALGS) is a multisystem cholestatic disorder. Maralixibat is approved for the treatment of cholestatic pruritus in ALGS with limited data in adults. Methods Participants were included if they received >= 2 doses of maralixibat at age >= 16 years in one of the three previously published maralixibat ALGS clinical trials. Results Eleven initiated treatment < 16 years old (median age, 13.0) with a median follow-up of 4.1 years. Three participants began maralixibat at >= 16 years old, with a median follow-up of 3.8 years. Participants starting maralixibat at age < 16 had minimal-to-no itch (change from baseline [CFB]: -1.8; p = 0.002) persisting throughout the study. Serum bile acids (sBA) decreased (CFB: 29 mu mol/L; p = 0.03), persisting throughout the study. Participants starting maralixibat >= 16 years old had pruritus improvements (CFB: -2.8, -0.6, -1.0). One had a large decrease in sBA (CFB: -112 mu mol/L), and two had small increases (CFB: 8, 11 mu mol/L). Maralixibat was well tolerated. Conclusion Participants receiving maralixibat in adolescence demonstrated improvements in pruritus and sBA, which persisted through young adulthood.
引用
收藏
页数:5
相关论文
共 50 条
  • [41] PRURITUS OF CHOLESTASIS - LACK OF CORRELATION WITH SERUM AND SKIN TISSUE LEVELS OF BILE-ACIDS
    GHENT, CN
    BLOOMER, JR
    KLATSKIN, G
    CLINICAL RESEARCH, 1977, 25 (03): : A311 - A311
  • [42] Pruritus in Chronic Hepatitis C (Association with High Serum Bile Acids, Advanced Pathology, and Bile Duct Abnormalities)
    Edward Lebovics
    Fayez Seif
    David Kim
    Abdelmonem Elhosseiny
    Brad M. Dworkin
    Ana Casellas
    Susan Clark
    William S. Rosenthal
    Digestive Diseases and Sciences, 1997, 42 : 1094 - 1099
  • [43] SERUM PRIMARY BILE-ACIDS IN GILBERTS SYNDROME
    SAMA, C
    RODA, E
    RODA, A
    MORSELLI, AM
    FESTI, D
    BARBARA, L
    GASTROENTEROLOGIE CLINIQUE ET BIOLOGIQUE, 1980, 4 (12): : 928 - 928
  • [44] MRGPRX4 is a G protein-coupled receptor activated by bile acids that may contribute to cholestatic pruritus
    Meixiong, James
    Vasavda, Chirag
    Snyder, Solomon H.
    Dong, Xinzhong
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2019, 116 (21) : 10525 - 10530
  • [45] SERUM PRIMARY BILE-ACIDS IN GILBERTS SYNDROME
    RODA, A
    RODA, E
    SAMA, C
    FESTI, D
    ALDINI, R
    MORSELLI, AM
    MAZZELLA, G
    BARBARA, L
    GASTROENTEROLOGY, 1982, 82 (01) : 77 - 83
  • [46] TOTAL SERUM BILE ACIDS IN PATIENTS WITH HEPATOPULMONARY SYNDROME
    Horvatits, T.
    Drolz, A.
    Mueller, C.
    Fauler, G.
    Schenk, P.
    Trauner, M.
    Fuhrmann, V.
    JOURNAL OF HEPATOLOGY, 2014, 60 (01) : S244 - S244
  • [47] EVOLUTION OF SERUM BILE-ACIDS IN CHOLESTASIS OF PREGNANCY (CP) - EVIDENCE FOR FLUCTUATION OF THE CHOLESTATIC PHENOMENON
    GLASINOVIC, JC
    MARINOVIC, I
    LOPEZ, J
    AHUMADA, E
    VALDIVIA, MT
    GOMEZ, X
    GASTROENTEROLOGY, 1980, 79 (05) : 1107 - 1107
  • [48] Sequential changes in serum levels of individual bile acids in patients with chronic cholestatic liver disease
    Azer, SA
    Coverdale, SA
    Byth, K
    Farrell, GC
    Stacey, NH
    JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 1996, 11 (03) : 208 - 215
  • [49] EVIDENCE FOR RENAL CONTROL OF URINARY-EXCRETION OF BILE-ACIDS AND BILE-ACID SULFATES IN CHOLESTATIC SYNDROME
    SUMMERFIELD, JA
    CULLEN, J
    BARNES, S
    BILLING, BH
    CLINICAL SCIENCE AND MOLECULAR MEDICINE, 1977, 52 (01): : 51 - 65
  • [50] Ileal Bile Acid Transporter Blockers for Cholestatic Liver Disease in Pediatric Patients with Alagille Syndrome: A Systematic Review and Meta-Analysis
    Muntaha, Hafiza Sidra Tul
    Munir, Mubashar
    Sajid, Syeda Haleema
    Sarfraz, Zouina
    Sarfraz, Azza
    Robles-Velasco, Karla
    Sarfraz, Muzna
    Felix, Miguel
    Cherrez-Ojeda, Ivan
    JOURNAL OF CLINICAL MEDICINE, 2022, 11 (24)