Kuypers Allysa M, Das Anibh M, Maiorana Arianna, Heiner-Fokkema M Rebecca, van Spronsen Francjan J
Section of Metabolic Diseases, Beatrix Children's Hospital, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
Clinic for Pediatric Kidney-, Liver- and Metabolic Diseases and Neuropaediatrics, Hannover Medical School, Hannover, Germany.
J Inherit Metab Dis. 2025 Sep;48(5):e70089. doi: 10.1002/jimd.70089.
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.
尼替西农(NTBC)的引入以及对1型酪氨酸血症(TT1)的新生儿筛查使患者能够得到预防性治疗,从而通过预防肝脏、肾脏和神经问题显著改善了治疗效果。治疗目标已从紧急治疗转向长期护理。为了评估因TT1本身或其治疗而随着年龄增长出现并发症的风险,长期随访至关重要。2014年,欧洲发表了一篇关于TT1管理实践的综述。在欧洲代谢参考网络的氨基酸和有机酸尿症子网(MetabERN - AOA)内,我们认为有必要更新欧洲目前的TT1管理实践。在MetabERN - AOA子网成员以及纽迪希亚欧洲代谢组会议上TT1研讨会的参与者中进行了一项在线调查研究。将研究结果与2014年上述出版物中的现有数据以及先前发表的建议进行了比较。32个中心(来自16个欧洲国家)完成了调查。在TT1管理中既发现了一致性,也发现了不一致性。在随访频率和方法、NTBC剂量以及生化标志物的目标范围方面观察到了不一致性。与2014年相比,主要差异包括通过新生儿筛查检测出的患者数量增加、NTBC剂量降低,以及从主要关注肝脏结果转向关注肝脏和神经认知结果。这些结果与多年来TT1建议中所呈现的趋势一致。除了众多的一致性之外,TT1管理的许多方面在欧洲各地仍存在很大差异,这表明除了现有建议之外,临床管理还需要统一的指导。