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Published on: June 28, 2019
Transient brain structure changes after high phenylalanine exposure in adults with phenylketonuria
Raphaela Muri1,2,3, Christian Rummel2, Richard McKinley2
1Department of Diabetes, Endocrinology, Nutritional Medicine and Metabolism, Inselspital, Bern University Hospital and University of Bern, 3010 Bern, Switzerland.
Insights
High phenylalanine exposure in adults with phenylketonuria temporarily reduces cortical thickness and increases white matter volume. These brain changes in phenylketonuria (PKU) patients were reversible after the exposure period.
Area of Science:
- Neuroscience
- Metabolic Disorders
- Medical Imaging
Background:
- Phenylketonuria (PKU) is a rare metabolic disorder caused by phenylalanine hydroxylase deficiency.
- Previous studies suggest altered brain structure in adults with PKU.
- The impact of high phenylalanine exposure on adult brain structure requires further investigation.
Purpose of the Study:
- To investigate the effects of a 4-week high phenylalanine exposure on brain structure in early-treated adult patients with PKU.
- To examine the relationship between phenylalanine exposure, brain structure, cognitive function, and metabolic parameters.
Main Methods:
- A double-blind, randomized, placebo-controlled crossover trial involving 28 adult PKU patients.
- Magnetic resonance imaging (MRI) was used to assess brain morphometry (cortical thickness, white matter, ventricular volumes) before and after phenylalanine and placebo interventions.
- Brain and blood phenylalanine levels, cognitive performance, and other metabolic parameters were measured.
Main Results:
- High phenylalanine exposure significantly increased blood phenylalanine levels and led to transient decreases in cortical thickness in 17 brain regions.
- Significant increases in white matter and ventricular volumes were observed during high phenylalanine exposure.
- Structural changes reversed to baseline after the washout and placebo period.
- Elevated phenylalanine levels correlated with increased white matter volume and decreased cortical thickness, which was linked to poorer cognitive performance.
Conclusions:
- A 4-week high phenylalanine exposure in adults with PKU causes temporary reductions in cortical grey matter and increases in white matter volume.
- These structural brain alterations are reversible, suggesting a transient impact.
- Further research is necessary to understand the long-term consequences of high phenylalanine levels on brain structure and function in adults with PKU.
Abstract:
Phenylketonuria is a rare metabolic disease resulting from a deficiency of the enzyme phenylalanine hydroxylase. Recent cross-sectional evidence suggests that early-treated adults with phenylketonuria exhibit alterations in cortical grey matter compared to healthy peers. However, the effects of high phenylalanine exposure on brain structure in adulthood need to be further elucidated. In this double-blind, randomized, placebo-controlled crossover trial, we investigated the impact of a 4-week high phenylalanine exposure on the brain structure and its relationship to cognitive performance and metabolic parameters in early-treated adults with phenylketonuria. Twenty-eight adult patients with early-treated classical phenylketonuria (19-48 years) underwent magnetic resonance imaging before and after the 4-week phenylalanine and placebo interventions (four time points). Structural T1-weighted images were preprocessed and evaluated using Direct Cortical Thickness Estimation using Deep Learning-based Anatomy Segmentation and Cortex Parcellation (DL+DiReCT), a deep-learning-based tool for brain morphometric analysis. Cortical thickness, white matter volume and ventricular volume were compared between the phenylalanine and placebo periods. Brain phenylalanine levels were measured using 1H spectroscopy. Blood levels of phenylalanine, tyrosine, and tryptophan were assessed at each of the four time points, along with performance in executive functions and attention. Blood phenylalanine levels were significantly higher after the phenylalanine period (1441 µmol/l) than after the placebo period (873 µmol/l, P < 0.001). Morphometric analyses revealed a statistically significant decrease in cortical thickness in 17 of 60 brain regions after the phenylalanine period compared to placebo. The largest decreases were observed in the right pars orbitalis (point estimate = -0.095 mm, P < 0.001) and the left lingual gyrus (point estimate = -0.070 mm, P < 0.001). Bilateral white matter and ventricular volumes were significantly increased after the phenylalanine period. However, the structural alterations in the phenylalanine-placebo group returned to baseline measures following the washout and placebo period. Additionally, elevated blood and brain phenylalanine levels were related to increased bilateral white matter volume (rs = 0.43 to 0.51, P ≤ 0.036) and decreased cortical thickness [rs = -0.62 to -0.39, not surviving false discovery rate (FDR) correction] after the phenylalanine and placebo periods. Moreover, decreased cortical thickness was correlated with worse cognitive performance after both periods (rs = -0.54 to -0.40, not surviving FDR correction). These findings provide evidence that a 4-week high phenylalanine exposure in adults with phenylketonuria results in transient reductions of the cortical grey matter and increases in white matter volume. Further research is needed to determine the potential long-term impact of high phenylalanine levels on brain structure and function in adults with phenylketonuria.
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