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通过产物替代治疗先天性代谢缺陷:以胆汁酸合成先天性代谢缺陷为例

Treatment of Inborn Errors by Product Replacement: The Example of Inborn Errors of Bile Acid Synthesis.

作者信息

Clayton Peter T, Hirachan Rohit, Murphy Elaine

机构信息

Inborn Errors of Metabolism, Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, London, UK.

Chemical Pathology, Great Ormond Street Hospital for Children NHS Trust, London, UK.

出版信息

J Inherit Metab Dis. 2025 Sep;48(5):e70081. doi: 10.1002/jimd.70081.

Abstract

Many inborn errors of metabolism affect pathways involved in the synthesis of a metabolite that has an important biochemical or physiological function, and adverse effects of the disorder can be attributed to the lack of this metabolite. Thus, there is the opportunity for treatment by 'product replacement'. One of the disorders in the pathways for the synthesis of bile acids from cholesterol, 3β-hydroxy-Δ5-C27-steroid dehydrogenase deficiency, causes cholestatic liver disease in infancy that can be treated very effectively with chenodeoxycholic acid (CDCA) and/or cholic acid (CA). There are several other enzyme deficiencies that can cause liver disease in infancy that improve with CDCA or CA or both (alongside a reduction of abnormal bile acids or alcohols); however, individuals with the same gene variant(s) may remain asymptomatic or have transient liver dysfunction that resolves spontaneously. In some disorders, the more usual presentation is with neurological disease later in childhood or in adolescence or adult life, for example, cerebrotendinous xanthomatosis (CTX), α-methylacyl-CoA racemase deficiency, and oxysterol 7α-hydroxylase deficiency. Treatment with CDCA has been dramatically effective in the neurological disease of CTX. In the disorders of peroxisome biogenesis, liver disease is a part of the clinical picture although neurological symptoms tend to be predominant. Treatment with CDCA and CA (or CA alone) leads to a reduction in the levels of C27 bile acids. Some trials suggest this treatment leads to significant improvement in clinical status and liver function tests; others do not. Defects in individual peroxisomal enzymes and transporters vary in their clinical presentations. Treatment of acyl-CoA oxidase 2 deficiency with ursodeoxycholic acid is discussed.

摘要

许多先天性代谢缺陷会影响参与合成具有重要生化或生理功能的代谢物的途径,而该疾病的不良反应可归因于这种代谢物的缺乏。因此,存在通过“产物替代”进行治疗的机会。从胆固醇合成胆汁酸的途径中的一种疾病,即3β-羟基-Δ5-C27-类固醇脱氢酶缺乏症,会导致婴儿期胆汁淤积性肝病,可用鹅去氧胆酸(CDCA)和/或胆酸(CA)进行有效治疗。还有其他几种酶缺乏症也可导致婴儿期肝病,使用CDCA或CA或两者(同时减少异常胆汁酸或醇类)可使其改善;然而,具有相同基因变异的个体可能无症状或仅有短暂的肝功能障碍,且可自发缓解。在某些疾病中,更常见的表现是在儿童后期、青少年期或成年期出现神经疾病,例如,脑腱黄瘤病(CTX)、α-甲基酰基辅酶A消旋酶缺乏症和氧甾醇7α-羟化酶缺乏症。用CDCA治疗对CTX的神经疾病非常有效。在过氧化物酶体生物发生障碍中,肝病是临床表现的一部分,尽管神经症状往往占主导地位。用CDCA和CA(或仅用CA)治疗可降低C27胆汁酸的水平。一些试验表明这种治疗可使临床状况和肝功能检查有显著改善;其他试验则不然。个体过氧化物酶体酶和转运蛋白的缺陷在临床表现上各不相同。本文讨论了用熊去氧胆酸治疗酰基辅酶A氧化酶2缺乏症。

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