Abstract

BackgroundA subset of patients with phenylketonuria benefit from treatment with tetrahydrobiopterin (BH4), although there is no consensus on the definition of BH4 responsiveness. The aim of this study therefore was to gain insight into the definitions of long-term BH4 responsiveness being used around the world. MethodsWe performed a web-based survey targeting healthcare professionals involved in the treatment of PKU patients. Data were analysed according to geographical region (Europe, USA/Canada, other). ResultsWe analysed 166 responses. Long-term BH4 responsiveness was commonly defined using natural protein tolerance (95.6%), improvement of metabolic control (73.5%) and increase in quality of life (48.2%). When a specific value for a reduction in phenylalanine concentrations was reported (n = 89), 30% and 20% were most frequently used as cut-off values (76% and 19% of respondents, respectively). When a specific relative increase in natural protein tolerance was used to define long-term BH4 responsiveness (n = 71), respondents most commonly reported cut-off values of 30% and 100% (28% of respondents in both cases). Respondents from USA/Canada (n = 50) generally used less strict cut-off values compared to Europe (n = 96). Furthermore, respondents working within the same center answered differently. ConclusionThe results of this study suggest a very heterogeneous situation on the topic of defining long-term BH4 responsiveness, not only at a worldwide level but also within centers. Developing a strong evidence- and consensus-based definition would improve the quality of BH4 treatment.

Highlights

  • A subset of patients with phenylketonuria benefit from treatment with tetrahydrobiopterin (BH4), there is no consensus on the definition of BH4 responsiveness

  • We performed a web-based survey targeting healthcare professionals involved in the treatment of PKU patients

  • Phenylketonuria (PKU, MIM 261600) is an inborn error of amino acid metabolism caused by a deficiency of the enzyme phenylalanine (Phe) hydroxylase (PAH) [1]

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Summary

Introduction

Phenylketonuria (PKU, MIM 261600) is an inborn error of amino acid metabolism caused by a deficiency of the enzyme phenylalanine (Phe) hydroxylase (PAH) [1]. Together with the intake of amino acid supplements, this life-long treatment is effective in preventing most complications associated with untreated PKU. A subset of patients with phenylketonuria benefit from treatment with tetrahydrobiopterin (BH4), there is no consensus on the definition of BH4 responsiveness. Long-term BH4 responsiveness was commonly defined using natural protein tolerance (95.6%), improvement of metabolic control (73.5%) and increase in quality of life (48.2%). When a specific relative increase in natural protein tolerance was used to define long-term BH4 responsiveness (n = 71), respondents most commonly reported cut-off values of 30% and 100% (28% of respondents in both cases). Conclusion: The results of this study suggest a very heterogeneous situation on the topic of defining long-term BH4 responsiveness, at a worldwide level and within centers. Developing a strong evidence- and consensus-based definition would improve the quality of BH4 treatment

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