Prognostic Markers for Phenylketonuria

  • Research type

    Research Study

  • Full title

    Evaluation of current and novel circulating prognostic biomarkers for phenylketonuria

  • IRAS ID

    164331

  • Contact name

    Radha Ramachandran

  • Contact email

    radha.ramachandran@gstt.nhs.uk

  • Sponsor organisation

    Guys and St Thomas NHS foundation Trust

  • Duration of Study in the UK

    3 years, 8 months, 1 days

  • Research summary

    Phenylalainine is an amino acid precursor for tyrosine, which in turn is a precursor synthesis of neurotransmitters like catecholamines and serotonin. Circulating phenylalanine and tyrosine are transported to the brain for synthesis of neurotransmitters. An autosomal recessive defect in the gene encoding the phenylalanine hydroxylase enzyme, results in Phenylketonuria. With an incidence of approximately 1: 10, 000, Phenylketonuria is the most common genetically inherited metabolic disorder in the UK. Patients with phenylketonuria are unable to metabolise phenylalanine. Symptoms are secondary to both accumulation of phenylalanine and its toxic metabolites and due to poor availability of tyrosine leading to suboptimal neurotransmitter synthesis. Untreated, patients develop severe intellectual, behavioural and speech difficulties and almost always need institutionalised care. Treatment, if started in the neonatal period, is successful. It involves lowering circulating phenylalanine levels, using a combination of a very strict low protein diet and supplementation with synthetic phenylalanine free proteins. Good compliance results in excellent outcome, with patients able to lead independent lives in the community. However, it is now increasingly recognised that adult patients often present with varying degrees of problems in mood, executive function and memory despite being on treatment. These symptoms, although more common in patients who have discontinued the diet, do not seem to be related to circulating phenylalanine levels. A significant number of patients with phenylalanine levels in the therapeutic range also experience these problems. This suggests that phenylalanine levels alone are not reflective of the brain function.
    Our preliminary study (13 NW 1601)has enabled us to identify a number of potential novel biomarkers. This current study aims to further evaluate these prognostic biomarkers markers for phenylketonuria by correlating levels of targeted metabolites and proteins in the blood with the clinical features of neuropsychiatric disturbance and brain imaging.

  • REC name

    East Midlands - Derby Research Ethics Committee

  • REC reference

    14/EM/1293

  • Date of REC Opinion

    9 Feb 2015

  • REC opinion

    Further Information Favourable Opinion