• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

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.

DOI:10.1002/jimd.70081
PMID:40847535
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。

相似文献

1
Treatment of Inborn Errors by Product Replacement: The Example of Inborn Errors of Bile Acid Synthesis.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
J Inherit Metab Dis. 2025 Sep;48(5):e70081. doi: 10.1002/jimd.70081.
2
Prescription of Controlled Substances: Benefits and Risks管制药品的处方:益处与风险
3
Cholic acid as a treatment for cerebrotendinous xanthomatosis: a comprehensive review of safety and efficacy.胆酸治疗脑腱黄瘤病:安全性和有效性的全面综述
Orphanet J Rare Dis. 2025 Jul 29;20(1):387. doi: 10.1186/s13023-025-03889-9.
4
The Black Book of Psychotropic Dosing and Monitoring.《精神药物剂量与监测黑皮书》
Psychopharmacol Bull. 2024 Jul 8;54(3):8-59.
5
Effectiveness and Safety of Personalized Cholic Acid Treatment in Patients With Bile Acid Synthesis Defects.个性化胆酸治疗对胆汁酸合成缺陷患者的有效性和安全性
J Inherit Metab Dis. 2025 Jul;48(4):e70062. doi: 10.1002/jimd.70062.
6
Ornithine Transcarbamylase Deficiency鸟氨酸转氨甲酰酶缺乏症
7
Isolated Methylmalonic Acidemia孤立性甲基丙二酸血症
8
-Related Tetrahydrobiopterin Deficiency (PTPSD)- 相关四氢生物蝶呤缺乏症(PTPSD)
9
Zellweger Spectrum Disorder泽尔韦格谱线障碍症
10
The clinical and biochemical effectiveness and safety of cholic acid treatment for bile acid synthesis defects: a systematic review.胆酸治疗胆汁酸合成缺陷的临床及生化有效性与安全性:一项系统评价
Orphanet J Rare Dis. 2024 Dec 19;19(1):466. doi: 10.1186/s13023-024-03449-7.

本文引用的文献

1
Variable clinical phenotypes of alpha-methylacyl-CoA racemase deficiency: Report of four cases and review of the literature.α-甲基酰基辅酶A消旋酶缺乏症的可变临床表型:4例报告及文献复习
JIMD Rep. 2024 Jul 11;65(5):305-312. doi: 10.1002/jmd2.12437. eCollection 2024 Sep.
2
[Congenital bile acid synthetic disorder type 3 caused by CYP7B1 gene variation in 2 cases and literature review].2例由CYP7B1基因变异引起的先天性胆汁酸合成障碍3型及文献复习
Zhonghua Er Ke Za Zhi. 2024 Sep 2;62(9):877-882. doi: 10.3760/cma.j.cn112140-20240415-00269.
3
Chenodeoxycholic acid (CDCA) treatment during pregnancy in women with cerebrotendinous xanthomatosis (CTX): Lessons learned from 19 pregnancies.
妊娠期间对脑腱黄瘤病(CTX)女性使用鹅去氧胆酸(CDCA)治疗:19 例妊娠的经验教训。
Genet Med. 2024 May;26(5):101086. doi: 10.1016/j.gim.2024.101086. Epub 2024 Jan 27.
4
∆-3-oxo-5β-reductase deficiency: favorable outcome in 16 patients treated with cholic acid.∆-3-氧代-5β-还原酶缺乏症:16 例患者用胆酸治疗的良好结局。
Orphanet J Rare Dis. 2023 Dec 7;18(1):383. doi: 10.1186/s13023-023-02984-z.
5
Healthy Patients With Mutation Not Requiring Primary Bile Acid Therapy: A Case Series.无需原发性胆汁酸治疗的突变健康患者:病例系列
JPGN Rep. 2023 Oct 9;4(4):e372. doi: 10.1097/PG9.0000000000000372. eCollection 2023 Nov.
6
Chenodeoxycholic acid rescues axonal degeneration in induced pluripotent stem cell-derived neurons from spastic paraplegia type 5 and cerebrotendinous xanthomatosis patients.鹅去氧胆酸可挽救 5 型痉挛性截瘫和脑腱黄瘤病诱导多能干细胞源性神经元的轴突变性。
Orphanet J Rare Dis. 2023 Apr 6;18(1):72. doi: 10.1186/s13023-023-02666-w.
7
Cerebrotendinous Xanthomatosis: A practice review of pathophysiology, diagnosis, and treatment.脑腱黄瘤病:病理生理学、诊断及治疗的实践综述
Front Neurol. 2022 Dec 23;13:1049850. doi: 10.3389/fneur.2022.1049850. eCollection 2022.
8
Beneficial effect of ursodeoxycholic acid in patients with acyl-CoA oxidase 2 (ACOX2) deficiency-associated hypertransaminasemia.熊去氧胆酸对酰基辅酶A氧化酶2(ACOX2)缺乏相关高转氨酶血症患者的有益作用。
Hepatology. 2022 Nov;76(5):1259-1274. doi: 10.1002/hep.32517. Epub 2022 Jul 1.
9
Successful treatment of an infant with congenital bile acid synthesis disorder type 3 by ursodeoxycholic acid: a case report.熊去氧胆酸成功治疗婴儿先天性胆汁酸合成障碍 3 型:1 例报告。
J Med Case Rep. 2022 Apr 7;16(1):139. doi: 10.1186/s13256-022-03365-z.
10
Prognosis and clinical characteristics of patients with 3β-hydroxy-Δ5-C27-steroid dehydrogenase deficiency diagnosed in childhood: A systematic review of the literature.儿童期诊断的 3β-羟基-Δ5-C27-甾体脱氢酶缺乏症患者的预后和临床特征:文献系统评价。
Medicine (Baltimore). 2022 Feb 18;101(7):e28834. doi: 10.1097/MD.0000000000028834.