Show simple item record

Placebo‐Controlled Randomized Trial of an Intestinal Bile Salt Transport Inhibitor for Pruritus in Alagille Syndrome

dc.contributor.authorShneider, Benjamin L.
dc.contributor.authorSpino, Cathie
dc.contributor.authorKamath, Binita M.
dc.contributor.authorMagee, John C.
dc.contributor.authorBass, Lee M.
dc.contributor.authorSetchell, Kenneth D.
dc.contributor.authorMiethke, Alexander
dc.contributor.authorMolleston, Jean P.
dc.contributor.authorMack, Cara L.
dc.contributor.authorSquires, Robert H.
dc.contributor.authorMurray, Karen F.
dc.contributor.authorLoomes, Kathleen M.
dc.contributor.authorRosenthal, Philip
dc.contributor.authorKarpen, Saul J.
dc.contributor.authorLeung, Daniel H.
dc.contributor.authorGuthery, Stephen L.
dc.contributor.authorThomas, Danny
dc.contributor.authorSherker, Averell H.
dc.contributor.authorSokol, Ronald J.
dc.date.accessioned2018-11-20T15:33:19Z
dc.date.available2019-12-02T14:55:09Zen
dc.date.issued2018-10
dc.identifier.citationShneider, Benjamin L.; Spino, Cathie; Kamath, Binita M.; Magee, John C.; Bass, Lee M.; Setchell, Kenneth D.; Miethke, Alexander; Molleston, Jean P.; Mack, Cara L.; Squires, Robert H.; Murray, Karen F.; Loomes, Kathleen M.; Rosenthal, Philip; Karpen, Saul J.; Leung, Daniel H.; Guthery, Stephen L.; Thomas, Danny; Sherker, Averell H.; Sokol, Ronald J. (2018). "Placebo‐Controlled Randomized Trial of an Intestinal Bile Salt Transport Inhibitor for Pruritus in Alagille Syndrome." Hepatology Communications 2(10): 1184-1198.
dc.identifier.issn2471-254X
dc.identifier.issn2471-254X
dc.identifier.urihttps://hdl.handle.net/2027.42/146363
dc.description.abstractMedically refractory, severe, cholestasis‐induced pruritus in Alagille syndrome may be improved by surgical interruption of the enterohepatic circulation. This multicenter trial (NCT02057692) tested the hypothesis that the intestinal bile acid transport inhibitor maralixibat would similarly reduce pruritus in Alagille syndrome. Thirty‐seven children with Alagille syndrome were randomly assigned to double‐blinded administration of placebo, 70, 140, or 280 µg/kg/day of maralixibat for 13 weeks. Pruritus was assessed by caregiver (itch‐reported outcome instrument [ItchRO]) and clinician report (range, 0‐4 [severe]). Liver chemistries and serum bile acids were measured. The primary outcome was the change from baseline to week 13 in ItchRO relative to placebo. In the a priori first analysis of the primary efficacy endpoint, the mean adjusted difference between participants receiving 140 or 280 µg/kg/day and placebo was –0.47 (95% confidence interval [CI], –1.14, 0.20; P = 0.16). Statistically significant decreases were observed with doses of 70 and 140 µg/kg/day (mean adjusted difference, –0.89; 95% CI, –1.70, –0.08; P = 0.032; and mean adjusted difference, –0.91; 95% CI, –1.62, –0.19; P = 0.014) but not 280 µg/kg/day (mean adjusted difference, –0.04; 95% CI, –0.94, 0.86; P = 0.44) or all doses combined (mean adjusted difference, –0.61; 95% CI, –1.24, 0.20; P = 0.055). A 1‐point reduction in pruritus was more common in maralixibat‐treated versus placebo‐treated participants (caregiver ItchRO, 65% versus 25%; P = 0.06; clinician score, 76% versus 25%; P = 0.01). There were no significant changes in liver chemistries or bile acids relative to placebo. Adverse and serious adverse events were similar between maralixibat and placebo. Conclusion: Although the prespecified primary analyses of ItchRO were not all statistically significant, the data suggest that maralixibat is safe and may reduce pruritus in Alagille syndrome.
dc.publisherWiley Periodicals, Inc.
dc.titlePlacebo‐Controlled Randomized Trial of an Intestinal Bile Salt Transport Inhibitor for Pruritus in Alagille Syndrome
dc.typeArticleen_US
dc.rights.robotsIndexNoFollow
dc.subject.hlbsecondlevelInternal Medicine
dc.subject.hlbtoplevelHealth Sciences
dc.description.peerreviewedPeer Reviewed
dc.description.bitstreamurlhttps://deepblue.lib.umich.edu/bitstream/2027.42/146363/1/hep41244.pdf
dc.description.bitstreamurlhttps://deepblue.lib.umich.edu/bitstream/2027.42/146363/2/hep41244_am.pdf
dc.identifier.doi10.1002/hep4.1244
dc.identifier.sourceHepatology Communications
dc.identifier.citedreferenceEmerick KM, Whitington PF. Partial external biliary diversion for intractable pruritus and xanthomas in Alagille syndrome. Hepatology 2002; 35: 1501 ‐ 1506.
dc.identifier.citedreferenceEmerick K, Rand E, Goldmuntz E, Krantz I, Spinner N, Piccoli D. Features of Alagille syndrome in 92 patients: frequency and relation to prognosis. Hepatology 1999; 29: 822 ‐ 829.
dc.identifier.citedreferenceWhitington PF, Whitington GL. Partial external diversion of bile for the treatment of intractable pruritus associated with intrahepatic cholestasis. Gastroenterology 1988; 95: 130 ‐ 136.
dc.identifier.citedreferenceNeimark E, Shneider B. Novel surgical and pharmacological approaches to chronic cholestasis in children: partial external biliary diversion for intractable pruritus and xanthomas in Alagille syndrome. J Pediatr Gastroenterol Nutr 2003; 36: 296 ‐ 297.
dc.identifier.citedreferenceHofmann AF. Inappropriate ileal conservation of bile acids in cholestatic liver disease: homeostasis gone awry. Gut 2003; 52: 1239 ‐ 1241.
dc.identifier.citedreferenceNeimark E, Chen F, Li X, Shneider BL. Bile acid‐induced negative feedback regulation of the human ileal bile acid transporter. Hepatology 2004; 40: 149 ‐ 156.
dc.identifier.citedreferenceWang KS, Tiao G, Bass LM, Hertel PM, Mogul D, Kerkar N, et al. Childhood Liver Disease Research Network (ChiLDReN). Analysis of surgical interruption of the enterohepatic circulation as a treatment for pediatric cholestasis. Hepatology 2017; 65: 1645 ‐ 1654.
dc.identifier.citedreferenceChalasani N, Regev A. Drug‐induced liver injury in patients with preexisting chronic liver disease in drug development: how to identify and manage? Gastroenterology 2016; 151: 1046 ‐ 1051.
dc.identifier.citedreferenceBuchwald H, Varco RL, Matts JP, Long JM, Fitch LL, Campbell GS, et al. Effect of partial ileal bypass surgery on mortality and morbidity from coronary heart disease in patients with hypercholesterolemia. Report of the program on the surgical control of the hyperlipidemias (POSCH). New Engl J Med 1990; 323: 946 ‐ 955.
dc.identifier.citedreferenceBaumann U, Lacaille F, Sturm E, Gonzales E, Arnell H, Jorgensen MH, et al. The ileal bile acid transport inhibitor A4250 decreases pruritus and serum bile acids in cholestatic liver diseases‐an ongoing multiple dose, open‐label, multicentre study. J Hepatol 2017; 66 ( Suppl.): S91.
dc.identifier.citedreferenceSlijepcevic D, van de Graaf SF. Bile acid uptake transporters as targets for therapy. Dig Dis 2017; 35: 251 ‐ 258.
dc.identifier.citedreferenceHegade VS, Kendrick SF, Dobbins RL, Miller SR, Thompson D, Richards D, et al. Effect of ileal bile acid transporter inhibitor GSK2330672 on pruritus in primary biliary cholangitis: a double‐blind, randomised, placebo‐controlled, crossover, phase 2a study. Lancet 2017; 389: 1114 ‐ 1123.
dc.identifier.citedreferenceKamath BM, Shneider BL, Spino C, Magee JC, Whitingon PF, Setchell KD, et al. Unraveling the relationship between itching, scratch scales, and biomarkers in children with Alagille syndrome. Hepatology 2017; 66: 653A.
dc.identifier.citedreferenceShneider BL, Magee JC, Bezerra JA, Haber B, Karpen SJ, Raghunathan T, et al. Childhood Liver Disease Research Education Network (ChiLDREN). Efficacy of fat‐soluble vitamin supplementation in infants with biliary atresia. Pediatrics 2012; 130: e607 ‐ e614.
dc.identifier.citedreferenceZhang W, Jha P, Wolfe B, Gioiello A, Pellicciari R, Wang J, et al. Tandem mass spectrometric determination of atypical 3beta‐hydroxy‐delta5‐bile acids in patients with 3beta‐hydroxy‐delta5‐C27‐steroid oxidoreductase deficiency: application to diagnosis and monitoring of bile acid therapeutic response. Clin Chem 2015; 61: 955 ‐ 963.
dc.identifier.citedreferenceYerushalmi B, Sokol RJ, Narkewicz MR, Smith D, Karrer FM. Use of rifampin for severe pruritus in children with chronic cholestasis. J Pediatr Gastroenterol Nutr 1999; 29: 442 ‐ 447.
dc.identifier.citedreferenceKamath BM, Abetz‐Webb L, Kennedy C, Hepburn B, Gauthier M, Johnson N, et al. Development of a novel tool to assess the impact of itching in pediatric cholestasis. Patient 2018; 11: 69 ‐ 82.
dc.owningcollnameInterdisciplinary and Peer-Reviewed


Files in this item

Show simple item record

Remediation of Harmful Language

The University of Michigan Library aims to describe library materials in a way that respects the people and communities who create, use, and are represented in our collections. Report harmful or offensive language in catalog records, finding aids, or elsewhere in our collections anonymously through our metadata feedback form. More information at Remediation of Harmful Language.

Accessibility

If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.