欧洲1型酪氨酸血症管理实践概述:迈向欧洲指南

IF 3.8 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Allysa M. Kuypers, Anibh M. Das, Arianna Maiorana, M. Rebecca Heiner-Fokkema, Francjan J. van Spronsen, The TT1 MetabERN Professional Collaboration Group
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引用次数: 0

摘要

尼替西酮(NTBC)的引入和1型酪氨酸血症(TT1)的新生儿筛查使患者能够进行先发制人的治疗,从而通过预防肝脏、肾脏和神经系统问题显著改善预后。治疗目标已从紧急治疗转向长期护理。为了评估因TT1本身或其治疗而发生衰老并发症的风险,长期随访是必要的。2014年,欧洲TT1管理实践概述发表。在代谢欧洲参考网络的氨基酸和有机酸尿子网络(MetabERN-AOA)中,我们认为有必要对欧洲目前的TT1管理实践进行更新。一项在线调查研究在MetabERN-AOA子网的成员和纽迪西亚欧洲代谢小组会议上关于TT1的研讨会的参与者中进行。研究结果与2014年上述出版物的现有数据和之前发表的建议进行了比较。32个中心(16个欧洲国家)完成了这项调查。TT1管理的一致性和不一致性都可以看到。在随访的频率和方法、NTBC的剂量和生化标志物的目标范围等方面观察到不一致。与2014年相比,主要差异包括新生儿筛查检测到的患者数量增加,NTBC剂量降低,以及主要关注肝脏转向肝脏和神经认知结果。这些结果与多年来TT1建议中看到的趋势一致。除了许多一致性之外,TT1管理的许多方面在欧洲仍然存在很大差异,这表明需要在现有建议之外制定统一的临床管理指南。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Overview of European Practices for Management of Tyrosinemia Type 1: Towards European Guidelines

Overview of European Practices for Management of Tyrosinemia Type 1: Towards European Guidelines

The introduction of nitisinone (NTBC) and newborn screening for Tyrosinemia type 1 (TT1) enabled preemptive treatment of patients, thereby significantly improving outcomes by preventing liver, kidney, and neurological issues. Treatment goals have shifted from emergency treatment to long-term care. To evaluate the risk of developing complications with aging, due to TT1 itself or its treatment, long-term follow-up is essential. In 2014, an overview of TT1 management practices in Europe was published. Within the Metabolic European Reference Network's subnetwork on amino-and-organic acidurias (MetabERN-AOA), we considered it important to give an update on current TT1 management practices in Europe. An online survey study was performed among members of the MetabERN-AOA subnetwork, and participants of a workshop on TT1 at the European Metabolic Group Meeting of Nutricia. Findings were compared to existing data from the aforementioned publication from 2014 and previously published recommendations. Thirty-two centers (16 European countries) completed the survey. Both consistencies and inconsistencies in TT1 management were seen. Inconsistencies were observed in the frequency and methods of follow-up, dosing of NTBC, and target ranges of biochemical markers. Compared to 2014, key differences included an increased number of patients detected by newborn screening, lower NTBC dosing, and a shift from interest in mainly hepatic to hepatic and neurocognitive outcomes. These results align with trends seen in TT1 recommendations over the years. In addition to numerous consistencies, many aspects in TT1 management still differ widely across Europe, suggesting the need for uniform guidance in clinical management beyond existing recommendations.

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来源期刊
Journal of Inherited Metabolic Disease
Journal of Inherited Metabolic Disease 医学-内分泌学与代谢
CiteScore
9.50
自引率
7.10%
发文量
117
审稿时长
4-8 weeks
期刊介绍: The Journal of Inherited Metabolic Disease (JIMD) is the official journal of the Society for the Study of Inborn Errors of Metabolism (SSIEM). By enhancing communication between workers in the field throughout the world, the JIMD aims to improve the management and understanding of inherited metabolic disorders. It publishes results of original research and new or important observations pertaining to any aspect of inherited metabolic disease in humans and higher animals. This includes clinical (medical, dental and veterinary), biochemical, genetic (including cytogenetic, molecular and population genetic), experimental (including cell biological), methodological, theoretical, epidemiological, ethical and counselling aspects. The JIMD also reviews important new developments or controversial issues relating to metabolic disorders and publishes reviews and short reports arising from the Society''s annual symposia. A distinction is made between peer-reviewed scientific material that is selected because of its significance for other professionals in the field and non-peer- reviewed material that aims to be important, controversial, interesting or entertaining (“Extras”).
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