Literature DB >> 27677920

Improved Measurement of Brain Phenylalanine and Tyrosine Related to Neuropsychological Functioning in Phenylketonuria.

Susan E Waisbren1,2, Sanjay P Prabhu3, Patricia Greenstein4,5, Carter Petty3, Donald Schomer4,5, Vera Anastasoaie3, Kalin Charette3, Daniel Rodriguez6, Sai Merugumala6, Alexander P Lin4,6.   

Abstract

INTRODUCTION: Researchers hypothesized that in phenylketonuria (PKU) high brain phenylalanine (Phe) levels and low brain tyrosine (Tyr) levels affect neuropsychological functioning. However, traditional magnetic resonance spectroscopy (MRS) yielded uncertain results of brain Phe and could not adequately measure brain Tyr. This pilot study examined the potential of correlated spectroscopy (COSY) to quantify these biomarkers and explain variability in neuropsychological functioning.
METHODS: Nine adults with early treated classic PKU received magnetic resonance imaging (MRI) with COSY and a battery of neuropsychological tests. Brain Phe and Tyr in parietal white matter (PWM) were compared to results in gray matter of the posterior cingulate gyrus (PCG).
RESULTS: Brain Phe ranged from 101 to 182 (mean = 136.76 ± 23.77) μmol/L in PCG and 76 to 185 (mean = 130.11 ± 37.88) μmol/L in PWM. Brain Tyr ranged from 4.0 to 7.4 (mean = 5.44 ± 1.01) μmol/L in PCG and 4.1 to 8.4 (mean = 5.90 ± 1.48) μmol/L in PWM. Correlation coefficients were largest for brain Phe PWM and measures of auditory memory (rho = -0.79), anxiety (rho = 0.79), and executive functioning (rho = 0.69). Associations were in the expected direction, with higher brain Phe and lower brain Tyr related to poorer functioning. The two participants with severe structural MRI abnormalities had low brain Tyr levels in PCG and 3/5 of the participants with moderate to severe MRI abnormalities had higher than average brain Phe levels.
CONCLUSION: COSY has the potential to quantify brain Phe and Tyr at low concentrations and in specific brain regions. In this pilot study, these biomarkers were associated with indices of neuropsychological functioning. Additional studies are needed to validate the COSY results.

Entities:  

Keywords:  Correlated spectroscopy (COSY); MRI spectroscopy; Neuropsychological outcome; Phenylketonuria (PKU)

Year:  2016        PMID: 27677920      PMCID: PMC5509554          DOI: 10.1007/8904_2016_11

Source DB:  PubMed          Journal:  JIMD Rep        ISSN: 2192-8304


  26 in total

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2.  Localized two-dimensional shift correlated MR spectroscopy of human brain.

Authors:  M A Thomas; K Yue; N Binesh; P Davanzo; A Kumar; B Siegel; M Frye; J Curran; R Lufkin; P Martin; B Guze
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3.  Use of in vivo two-dimensional MR spectroscopy to compare the biochemistry of the human brain to that of glioblastoma.

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4.  Prefrontal cortex cognitive deficits in children treated early and continuously for PKU.

Authors:  A Diamond; M B Prevor; G Callender; D P Druin
Journal:  Monogr Soc Res Child Dev       Date:  1997

5.  Individual blood-brain barrier phenylalanine transport determines clinical outcome in phenylketonuria.

Authors:  J Weglage; D Wiedermann; J Denecke; R Feldmann; H G Koch; K Ullrich; E Harms; H E Möller
Journal:  Ann Neurol       Date:  2001-10       Impact factor: 10.422

Review 6.  Fluctuations in phenylalanine concentrations in phenylketonuria: a review of possible relationships with outcomes.

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7.  Reproducibility of cerebral phenylalanine levels in patients with phenylketonuria determined by 1H-MR spectroscopy.

Authors:  R Kreis; K Zwygart; C Boesch; J-M Nuoffer
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8.  Phenylalanine blood levels and clinical outcomes in phenylketonuria: a systematic literature review and meta-analysis.

Authors:  Susan E Waisbren; Kay Noel; Kyle Fahrbach; Catherine Cella; Diana Frame; Alex Dorenbaum; Harvey Levy
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9.  Individual blood-brain barrier phenylalanine transport in siblings with classical phenylketonuria.

Authors:  J Weglage; D Wiedermann; J Denecke; R Feldmann; H G Koch; K Ullrich; H E Möller
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3.  Blood phenylalanine reduction reverses gene expression changes observed in a mouse model of phenylketonuria.

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