ArticleJournal of inherited metabolic disease2010
Tyrosine monitoring in children with early and continuously treated phenylketonuria: results of an international practice survey.
Article in Journal of inherited metabolic disease, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed, 1 citations in OpenAlex.
- Melatonin and dopamine as biomarkers to optimize treatment in phenylketonuria: effects of tryptophan and tyrosine supplementation.The Journal of pediatrics · 2014Trial
- Large neutral amino acid supplementation increases melatonin synthesis in phenylketonuria: a new biomarker.The Journal of pediatrics · 2013Trial
- Comparison of Tandem Mass Spectrometry and the Fluorometric Method-Parallel Phenylalanine Measurement on a Large Fresh Sample Series and Implications for Newborn Screening for Phenylketonuria.International journal of molecular sciences · 2023Article
- Attention Deficit Disorder with Hyperactivity Symptoms in Early-Treated Phenylketonuria Patients.Iranian journal of child neurology · 2020Article
- The complete European guidelines on phenylketonuria: diagnosis and treatment.Orphanet journal of rare diseases · 2017Review
- Article
- Inherited Metabolic Disorders: Aspects of Chronic Nutrition Management.Nutrition in clinical practice : official publication of the American Society for Parenteral and Enteral Nutrition · 2015Review
- Recommendations for the nutrition management of phenylalanine hydroxylase deficiency.Genetics in medicine : official journal of the American College of Medical Genetics · 2014Review
- Neuroradiological findings of an adolescent with early treated phenylketonuria: is phenylalanine restriction enough?Clinics and practice · 2011Article
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Authors and funding
4 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Investigations into the biochemical markers associated with executive function (EF) impairment in children with early and continuously treated phenylketonuria (ECT-PKU) remain largely phenylalanine-only focused, despite experimental data showing that a high phenylalanine:tyrosine (phe:tyr) ratio is more strongly associated with EF deficit than phe alone. A high phe:tyr ratio is hypothesized to lead to a reduction in dopamine synthesis within the brain, which in turn results in the development of EF impairment. This paper provides a snapshot of current practice in the monitoring and/or treatment of tyrosine levels in children with PKU, across 12 countries from Australasia, North America and Europe. Tyrosine monitoring in this population has increased over the last 5 years, with over 80% of clinics surveyed reporting routine monitoring of tyrosine levels in infancy alongside phe levels. Twenty-five percent of clinics surveyed reported actively treating/managing tyrosine levels (with supplemental tyrosine above that contained in PKU formulas) to ensure tyrosine levels remain within normal ranges. Anecdotally, supplemental tyrosine has been reported to ameliorate symptoms of both attention deficit hyperactivity disorder and depression in this population. EF assessment of children with ECT-PKU was likewise highly variable, with 50% of clinics surveyed reporting routine assessments of intellectual function. However when function was assessed, test instruments chosen tended towards global measures of IQ prior to school entry, rather than specific assessment of EF development. Further investigation of the role of tyrosine and its relationship with phe and EF development is needed to establish whether routine tyrosine monitoring and increased supplementation is recommended.
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