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Overview of European Practices for Management of Tyrosinemia Type 1: Towards European Guidelines
Allysa M Kuypers1, Anibh M Das2,3, Arianna Maiorana3,4
1Section of Metabolic Diseases, Beatrix Children's Hospital, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
Insights
Newborn screening and nitisinone (NTBC) treatment have improved Tyrosinemia type 1 (TT1) outcomes. However, European management practices vary, highlighting the need for updated, uniform clinical guidance for long-term care.
Area of Science:
- Metabolic Disorders
- Genetics
- Pediatric Medicine
Background:
- Tyrosinemia type 1 (TT1) management has evolved with nitisinone (NTBC) and newborn screening, shifting focus to long-term care and complication prevention.
- Assessing aging-related risks in TT1 patients necessitates ongoing follow-up and evaluation of treatment impacts.
Purpose of the Study:
- To provide an updated overview of current Tyrosinemia type 1 management practices across Europe.
- To identify consistencies and inconsistencies in TT1 care compared to previous data and recommendations.
Main Methods:
- An online survey was distributed to members of the Metabolic European Reference Network's subnetwork on amino-and-organic acidurias (MetabERN-AOA).
- Participants from a TT1 workshop also contributed data, which was compared with 2014 findings and existing guidelines.
Main Results:
- Thirty-two centers across 16 European countries participated, revealing both uniform and varied management approaches.
- Key differences from 2014 include increased newborn screening detection, reduced NTBC dosage, and expanded focus on neurocognitive outcomes alongside hepatic health.
Conclusions:
- Despite advancements, significant variations persist in European TT1 management regarding follow-up, NTBC dosing, and biochemical targets.
- There is a clear need for standardized clinical management guidelines to ensure consistent, optimal long-term care for Tyrosinemia type 1 patients.
Abstract:
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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