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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.
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.
Abstract:
The early introduction of a low phenylalanine (Phe) diet has been demonstrated to be the most successful treatment in subjects with phenylketonuria (PKU), especially for preventing severe cognitive and neurological damages. However, it still concerns that even if treated in the first months of life with supplements and following a diet, they can show slight scores below people without PKU in neuropsychological assignments. We investigated 20 adults with classical PKU aged 19-48 years (mean age 29 years) and 20 heathy controls matched by age, gender, and years of education. Patients and controls were assessed with an extended neuropsychological battery, as well as psychological aspects and quality of life, also the last Phe level result was obtained. Results showed that the most affected cognitive domains are processing speed, executive functioning, memory, and also theory of mind, but very well-preserved verbal fluency, language, and visuospatial functioning. In quality of life, some significant results were seen specially in anxiety of Phe levels, anxiety of Phe levels during pregnancy, guilt if poor adherence to supplements, and if dietary protein restriction not followed. No significant results were obtained for the psychological variables. In conclusion, it has been shown that a combination of a low Phe diet, supplement intake, and keeping Phe levels in a low range seems appropriate to have the most normal and alike cognitive performance to persons without PKU.
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