Goel Akshat, Tucker Bethany, Casale Lorena Soler, Grammatikopoulos Tassos
Paediatric Liver, GI and Nutrition Centre and MowatLabs King's College Hospital London UK.
Gibraltar Health Authority Gibraltar.
JPGN Rep. 2024 Apr 4;5(3):296-302. doi: 10.1002/jpr3.12069. eCollection 2024 Aug.
Odevixibat, a reversible ileal bile acid transport inhibitor, has been shown to reduce serum bile acids (sBA) and pruritus mostly in children with progressive familial intrahepatic cholestasis (PFIC) 1 and 2 in clinical trials and case reports. There are currently no published case reports or series describing its use in rare variants of cholestatic liver disease.
We describe three children with progressive cholestatic liver disease who developed refractory pruritus, who had a genotypic diagnosis of , variant, and and variants; all being variants of unknown significance as per the American College of Medical Genetics and Genomics guidelines.
On Odevixibat there was a significant improvement in sBA (absolute change from baseline: -196 and -393 μmol/L) and pruritus in two children with heterozygous and mutations. The child with variants was found to have features of sclerosing cholangitis along with a diagnosis of Crohn's disease, which represents the first reported usage of Odevixibat in such a case with good response. There was some reported improvement in the third child with and variants; however, we hypothesize that no sustained improvement could be due to severe and progressive nature of the disease. There were no side effects reported and it was well tolerated in all.
We suggest that Odevixibat may be used as an adjunctive drug in refractory pruritus and could be started early in the course of disease if clinically and phenotypically indicated.
奥地维西巴特是一种可逆性回肠胆汁酸转运抑制剂,在临床试验和病例报告中已显示,它主要可降低进行性家族性肝内胆汁淤积症(PFIC)1型和2型患儿的血清胆汁酸(sBA)并减轻瘙痒症状。目前尚无已发表的病例报告或系列研究描述其在胆汁淤积性肝病罕见变异型中的应用。
我们描述了3例患有进行性胆汁淤积性肝病且出现难治性瘙痒的儿童,他们经基因诊断分别为 、 变异型以及 与 变异型;根据美国医学遗传学与基因组学学会的指南,所有这些变异型的意义均不明确。
在使用奥地维西巴特治疗后,两名携带杂合 与 突变的儿童的sBA(相对于基线的绝对变化:-196和-393 μmol/L)及瘙痒症状有显著改善。发现携带 变异型的儿童除诊断为克罗恩病外,还具有硬化性胆管炎的特征,这是奥地维西巴特在该病例中的首次报道应用,且反应良好。据报道,第三名携带 与 变异型的儿童也有一定改善;然而,我们推测未能持续改善可能是由于该疾病严重且呈进行性发展。未报告有副作用,所有患儿对药物耐受性良好。
我们建议,奥地维西巴特可作为难治性瘙痒的辅助药物使用,若临床和表型提示有必要,可在疾病早期开始用药。