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可治疗的先天性代谢疾病的临床治疗方法:引言

Clinical approach to treatable inborn metabolic diseases: an introduction.

作者信息

Saudubray J-M, Sedel F, Walter J H

机构信息

Centre de Référence des Maladies Héréditaires du Métabolisme, Hôpital Necker Enfants-Malades, Université René Descartes, 149 rue de Sèvres, 75743, Paris Cedex 15, France.

出版信息

J Inherit Metab Dis. 2006 Apr-Jun;29(2-3):261-74. doi: 10.1007/s10545-006-0358-0.

DOI:10.1007/s10545-006-0358-0
PMID:16763886
Abstract

In view of the major improvements in treatment, it has become increasingly important that in order for first-line physicians not to miss a treatable disorder they should be able initiate a simple method of clinical screening, particularly in the emergency room. We present a simplified classification of treatable inborn errors of metabolism in three groups. Group 1 includes inborn errors of intermediary metabolism that give rise to an acute or chronic intoxication. It encompasses aminoacidopathies, organic acidurias, urea cycle disorders, sugar intolerances, metal disorders and porphyrias. Clinical expression can be acute or systemic or can involve a specific organ, and can strike in the neonatal period or later and intermittently from infancy to late adulthood. Most of these disorders are treatable and require the emergency removal of the toxin by special diets, extracorporeal procedures, cleansing drugs or vitamins. Group 2 includes inborn errors of intermediary metabolism that affect the cytoplasmic and mitochondrial energetic processes. Cytoplasmic defects encompass those affecting glycolysis, glycogenosis, gluconeogenesis, hyperinsulinisms, and creatine and pentose phosphate pathways; the latter are untreatable. Mitochondrial defects include respiratory chain disorders, and Krebs cycle and pyruvate oxidation defects, mostly untreatable, and disorders of fatty acid oxidation and ketone bodies that are treatable. Group 3 involves cellular organelles and includes lysosomal, peroxisomal, glycosylation, and cholesterol synthesis defects. Among these, some lysosomal disorders can be efficiently treated by enzyme replacement or substrate reduction therapies. Physicians can be faced with the possibility of a treatable inborn error in an emergency, either in the neonatal period or late in infancy to adulthood, or as chronic and progressive symptoms--general (failure to thrive), neurological, or specific for various organs or systems. These symptoms are summarized in four tables. In addition, an extensive list of medications used in the treatment of inborn errors is presented.

摘要

鉴于治疗方面的重大进展,一线医生为了不遗漏可治疗的疾病,应能够启动一种简单的临床筛查方法,这一点变得越来越重要,尤其是在急诊室。我们提出了一种将可治疗的先天性代谢缺陷简化为三组的分类方法。第一组包括导致急性或慢性中毒的中间代谢先天性缺陷。它包括氨基酸病、有机酸尿症、尿素循环障碍、糖不耐受、金属紊乱和卟啉病。临床表现可以是急性的或全身性的,也可以涉及特定器官,可以在新生儿期或以后发病,从婴儿期到成年后期呈间歇性发作。这些疾病大多是可治疗的,需要通过特殊饮食、体外程序、解毒药物或维生素紧急清除毒素。第二组包括影响细胞质和线粒体能量过程的中间代谢先天性缺陷。细胞质缺陷包括影响糖酵解、糖原病、糖异生、高胰岛素血症以及肌酸和磷酸戊糖途径的缺陷;后者是不可治疗的。线粒体缺陷包括呼吸链障碍、三羧酸循环和丙酮酸氧化缺陷,大多不可治疗,以及可治疗的脂肪酸氧化和酮体紊乱。第三组涉及细胞器,包括溶酶体、过氧化物酶体、糖基化和胆固醇合成缺陷。其中,一些溶酶体疾病可以通过酶替代或底物减少疗法得到有效治疗。医生在急诊时可能会面对可治疗的先天性代谢缺陷的可能性,无论是在新生儿期,还是在婴儿后期到成年期,或者是作为慢性和进行性症状——一般症状(发育不良)、神经症状,或针对各种器官或系统的特定症状。这些症状总结在四张表格中。此外,还列出了用于治疗先天性代谢缺陷的大量药物清单。

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1
Transaldolase deficiency: a new cause of hydrops fetalis and neonatal multi-organ disease.转醛醇酶缺乏症:胎儿水肿和新生儿多器官疾病的新病因。
J Pediatr. 2006 Nov;149(5):713-7. doi: 10.1016/j.jpeds.2006.08.016.
2
Impact of diets and nutrients/drugs on early epigenetic programming.饮食及营养素/药物对早期表观遗传编程的影响。
J Inherit Metab Dis. 2006 Apr-Jun;29(2-3):359-65. doi: 10.1007/s10545-006-0299-7.
3
Treatment with amino acids in serine deficiency disorders.丝氨酸缺乏症的氨基酸治疗。
成人遗传性代谢病患者的智力障碍和神经认知障碍:英国单中心经验。
Genes (Basel). 2024 Jul 15;15(7):923. doi: 10.3390/genes15070923.
4
Splice-Modulating Antisense Oligonucleotides as Therapeutics for Inherited Metabolic Diseases.剪接调节反义寡核苷酸作为遗传性代谢疾病的治疗方法。
BioDrugs. 2024 Mar;38(2):177-203. doi: 10.1007/s40259-024-00644-7. Epub 2024 Jan 22.
5
A one-year pilot study comparing direct-infusion high resolution mass spectrometry based untargeted metabolomics to targeted diagnostic screening for inherited metabolic diseases.一项为期一年的试点研究,比较基于直接进样高分辨率质谱的非靶向代谢组学与遗传性代谢疾病的靶向诊断筛查。
Front Mol Biosci. 2023 Nov 2;10:1283083. doi: 10.3389/fmolb.2023.1283083. eCollection 2023.
6
The Reciprocal Interplay between Infections and Inherited Metabolic Disorders.感染与遗传性代谢紊乱之间的相互作用
Microorganisms. 2023 Oct 12;11(10):2545. doi: 10.3390/microorganisms11102545.
7
Effect of Special Low-Protein Foods Consumption in the Dietary Pattern and Biochemical Profile of Patients with Inborn Errors of Protein Metabolism: Application of a Database of Special Low-Protein Foods.特殊低蛋白食品摄入对蛋白质代谢先天缺陷患者饮食模式和生化特征的影响:特殊低蛋白食品数据库的应用。
Nutrients. 2023 Aug 6;15(15):3475. doi: 10.3390/nu15153475.
8
Neuroimaging findings of inborn errors of metabolism: urea cycle disorders, aminoacidopathies, and organic acidopathies.神经影像学在先天性代谢缺陷疾病中的应用:尿素循环障碍、氨基酸代谢病和有机酸血症。
Jpn J Radiol. 2023 Jul;41(7):683-702. doi: 10.1007/s11604-023-01396-0. Epub 2023 Feb 2.
9
Intronic variants in inborn errors of metabolism: Beyond the exome.先天性代谢缺陷中的内含子变异:外显子之外
Front Genet. 2022 Dec 6;13:1031495. doi: 10.3389/fgene.2022.1031495. eCollection 2022.
10
Diagnostic reasoning in neurogenetics: a general approach.神经遗传学中的诊断推理:一种通用方法。
Arq Neuropsiquiatr. 2022 Sep;80(9):944-952. doi: 10.1055/s-0042-1755275. Epub 2022 Nov 9.
J Inherit Metab Dis. 2006 Apr-Jun;29(2-3):347-51. doi: 10.1007/s10545-006-0269-0.
4
Anaplerotic diet therapy in inherited metabolic disease: therapeutic potential.遗传性代谢疾病中的回补饮食疗法:治疗潜力
J Inherit Metab Dis. 2006 Apr-Jun;29(2-3):332-40. doi: 10.1007/s10545-006-0290-3.
5
A mutation in para-hydroxybenzoate-polyprenyl transferase (COQ2) causes primary coenzyme Q10 deficiency.对羟基苯甲酸聚异戊二烯基转移酶(COQ2)的突变会导致原发性辅酶Q10缺乏症。
Am J Hum Genet. 2006 Feb;78(2):345-9. doi: 10.1086/500092. Epub 2005 Dec 22.
6
Biotin-responsive basal ganglia disease maps to 2q36.3 and is due to mutations in SLC19A3.生物素反应性基底节疾病定位于2q36.3,由SLC19A3基因突变所致。
Am J Hum Genet. 2005 Jul;77(1):16-26. doi: 10.1086/431216. Epub 2005 May 3.
7
L-arginine improves the symptoms of strokelike episodes in MELAS.L-精氨酸可改善线粒体脑肌病伴乳酸血症和卒中样发作(MELAS)的卒中样发作症状。
Neurology. 2005 Feb 22;64(4):710-2. doi: 10.1212/01.WNL.0000151976.60624.01.
8
Inherited metabolic diseases and pregnancy.
BJOG. 2005 Jan;112(1):2-11. doi: 10.1111/j.1471-0528.2004.00297.x.
9
Failure of short-term mannose therapy of patients with carbohydrate-deficient glycoprotein syndrome type 1A.1A型糖蛋白缺乏综合征患者短期甘露糖治疗失败。
Acta Paediatr. 1998 Aug;87(8):884-8. doi: 10.1080/080352598750013680.
10
Continuous mannose infusion in carbohydrate-deficient glycoprotein syndrome type I.I型糖基化缺陷糖蛋白综合征中的持续甘露糖输注。
Acta Paediatr. 1997 Oct;86(10):1138-40. doi: 10.1111/j.1651-2227.1997.tb14825.x.