Cognitive Functioning in Adults with Phenylketonuria in a Cohort of Spanish Patients

P M Luna1, J F López-Paz1, M García1

  • 1University of Deusto, Department of Psychology, Av. de las Universidades 24, Bilbao 48007, Spain.

Behavioural Neurology
|February 23, 2023
PubMed

Insights

Early low phenylalanine (Phe) diet is crucial for phenylketonuria (PKU) treatment. Even with treatment, adults with PKU show subtle cognitive differences, highlighting the need for ongoing management.

Area of Science:

  • Neuroscience
  • Metabolic Disorders
  • Genetics

Background:

  • Phenylketonuria (PKU) is a genetic disorder requiring early dietary intervention.
  • Despite treatment, individuals with PKU may experience subtle cognitive deficits.
  • Neuropsychological outcomes in adults with PKU require further investigation.

Purpose of the Study:

  • To assess cognitive functioning and quality of life in adults with PKU compared to healthy controls.
  • To identify specific cognitive domains affected by PKU and its management.
  • To explore the impact of phenylalanine (Phe) levels and treatment adherence on outcomes.

Main Methods:

  • A cohort of 20 adults with classical PKU and 20 matched healthy controls were evaluated.
  • Participants underwent an extensive neuropsychological assessment.
  • Psychological aspects, quality of life, and recent Phe levels were recorded.

Main Results:

  • Adults with PKU exhibited deficits in processing speed, executive functions, memory, and theory of mind.
  • Verbal fluency, language, and visuospatial skills were well-preserved.
  • Quality of life was impacted by anxiety regarding Phe levels and guilt over dietary non-adherence.

Conclusions:

  • While early intervention is vital, adults with PKU may still face cognitive challenges.
  • Maintaining low Phe levels through diet and supplements is essential for optimal cognitive performance.
  • Comprehensive management strategies are needed to improve quality of life for individuals with PKU.

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