The clinical and biochemical effectiveness and safety of cholic acid treatment for bile acid synthesis defects: a systematic review

被引:0
作者
Polak, Yasmin [1 ,8 ]
van Dussen, Laura [8 ]
Kemper, E. Marleen [1 ,8 ]
Vaz, Frederic M. [4 ,5 ,6 ,7 ]
Klouwer, Femke C. C. [3 ]
Engelen, Marc [3 ]
Hollak, Carla E. M. [2 ,8 ]
机构
[1] Univ Amsterdam, Dept Pharm & Clin Pharmacol, Amsterdam UMC, Amsterdam, Netherlands
[2] Univ Amsterdam, Dept Endocrinol & Metab, Amsterdam UMC, Meibergdreef 9, NL-1105 AZ Amsterdam, Netherlands
[3] Univ Amsterdam, Dept Pediat Neurol, Amsterdam UMC, Amsterdam, Netherlands
[4] Univ Amsterdam, Amsterdam UMC, Emma Childrens Hosp, Lab Genet Metab Dis,Dept Lab Med & Pediat, Amsterdam, Netherlands
[5] Amsterdam Gastroenterol Endocrinol Metab, Inborn Errors Metab, Amsterdam, Netherlands
[6] Amsterdam UMC Locat Univ Amsterdam, Core Facil Metabol, Amsterdam, Netherlands
[7] United Metab Dis, Amsterdam, Netherlands
[8] Univ Amsterdam, Med Soc, Platform Amsterdam UMC, Amsterdam, Netherlands
关键词
Bile acid synthesis defects; Cholic acid; Toxic bile acid intermediates; Single enzyme defects; Zellweger spectrum disorders; INBORN-ERRORS; LIVER-DISEASE; METABOLISM; DISORDERS;
D O I
10.1186/s13023-024-03449-7
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
BackgroundBile acid synthesis defects (BASDs) can be severely disabling involving the liver and nervous system, potentially due to elevated levels of toxic C27-bile acid intermediates. Cholic acid (CA) supplementation is hypothesized to decrease bile acid production, stimulate bile secretion and -flow, and slowing down disease progression. This systematic review assesses the clinical and biochemical effectiveness, and safety of CA in BASDs patients.MethodsA systematic review of MEDLINE, Embase and clinical trial registries (ClinicalTrials.gov, ICTRP registry) using controlled MeSH- and Emtree terms.ResultsFrom 526 articles 70 publications were deemed eligible for inclusion based on title and abstract. 14 publications were included after full-text assessment comprising case reports and -series with 1-35 patients (162 patients in total) receiving 1 week to 16,5 years of CA treatment. All presented data on effectiveness, 8 studies also presented data on safety. The included population concerned patients with Zellweger spectrum disorders (n = 73), 3 beta-Hydroxy-Delta 5-C27-steroid oxidoreductase deficiency (n = 62), cerebrotendinous xanthomatosis (n = 22), Delta 4-3-oxosteroid 5 beta-reductase deficiency (n = 13), and alpha-methylacyl-CoA racemase deficiency (n = 3). Main outcomes concerned liver disease (12 studies), general physical examinations, biochemical outcomes, and safety (9 studies), and fat-soluble vitamin absorption (7 studies). The overall risk of bias score was considered to be critical (1 study), serious (4 studies), and moderate (9 studies). Major issues were missing data (10 studies), generalized data (8 studies), and no wash-out between treatments (4 studies).ConclusionMore controlled studies are required as the available data is insufficient to draw definite conclusions on the effectiveness and safety of CA treatment in BASD patients. Establishing an independent international disease registry could better utilize existing real-world data.
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页数:16
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