Objective: To determine the effects of large neutral amino acid (LNAA) supplements on brain and plasma phenylalanine (Phe) levels and other metabolites in early treated subjects with classical phenylketonuria (PKU), and to investigate the relationship between these metabolites and neuropsychological performance.

Methods: This was a prospective, double blind, cross over study consisting of four two-week phases with a 4 week washout period. Sixteen subjects (7 males), with classical PKU were recruited into the study and completed all 4 phases. Each phase consisted of either the LNAA supplement or placebo, and either the patient's usual medical product or not. Subjects were instructed to follow their usual Phe restricted diet, maintain energy intake and complete a 3-day food record during each phase. At the end of each phase, brain Phe and other metabolites were measured by proton magnetic resonance spectroscopy (MRS), and plasma amino acids quantified. A detailed neuropsychological assessment was performed on the same day as the MRS and plasma collection.

Results: There was no correlation between plasma and brain Phe, but few of the plasma Phe readings were over 1200 micromol/L. Plasma Phe decreased with LNAA supplementation when patients were not taking their medical formula. LNAA supplementation had a specific impact on executive functions particularly in verbal generativity and cognitive flexibility. Measures of attention were better on medical product, with or without LNAA supplements.

Conclusions: LNAA supplementation was associated with a trend to a lowering of plasma Phe levels. LNAA supplementation had a specific impact on executive functions particularly in verbal generativity and flexibility. For individuals already complying with diet and PKU medical product, additional supplementation with LNAA is of limited value. LNAA supplementation may be of benefit to those unable to comply with PKU medical product by reducing plasma Phe, perhaps by competing with Phe at the level of transport across the gut.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ymgme.2007.02.002DOI Listing

Publication Analysis

Top Keywords

lnaa supplementation
20
medical product
16
plasma phe
16
lnaa
9
phe
9
effects large
8
large neutral
8
neutral amino
8
amino acid
8
plasma
8

Similar Publications

Plasma essential amino acid levels in first episode psychosis at baseline and after antipsychotic treatment.

Schizophrenia (Heidelb)

November 2024

Department of Anatomy and Cell Biology, Schulich School of Medicine and Dentistry, University of Western Ontario, London, ON, Canada.

Article Synopsis
  • The study analyzed the plasma levels of essential amino acids (EAA) in drug-naïve first episode psychosis (FEP) patients before and after 10 weeks of antipsychotic treatment, compared to a control group of healthy volunteers.
  • Findings showed that baseline levels of several EAAs were higher in FEP patients; after treatment, certain levels increased further in those who responded well to the medication.
  • The research suggests that elevated EAA levels may help meet the increased demands for neurotransmitter production, and that EAAs could potentially enhance the effectiveness of antipsychotic treatments when supplemented.*
View Article and Find Full Text PDF

Emerging biosensors in Phenylketonuria.

Clin Chim Acta

June 2024

University Institute of Pharma Sciences, Chandigarh University, Gharuan, Mohali, Punjab 140413, India. Electronic address:

Phenylketonuria (PKU) is an autosomal recessive metabolic disorder resulting from deficient phenylalanine hydroxylase (PAH) enzyme activity, leading to impaired phenylalanine (Phe) metabolism. This condition can lead to intellectual disability, epilepsy, and behavioural issues. Treatment typically involves strict dietary restrictions on natural protein intake, supplemented with chemically manufactured protein substitutes containing amino acids other than Phe.

View Article and Find Full Text PDF

Genetic etiology and clinical challenges of phenylketonuria.

Hum Genomics

July 2022

Department of Clinical Nutrition, Faculty of Applied Medical Sciences, Umm Al-Qura University, Jeddah, Saudi Arabia.

This review discusses the epidemiology, pathophysiology, genetic etiology, and management of phenylketonuria (PKU). PKU, an autosomal recessive disease, is an inborn error of phenylalanine (Phe) metabolism caused by pathogenic variants in the phenylalanine hydroxylase (PAH) gene. The prevalence of PKU varies widely among ethnicities and geographic regions, affecting approximately 1 in 24,000 individuals worldwide.

View Article and Find Full Text PDF

Dietary and serum tyrosine, white matter microstructure and inter-individual variability in executive functions in overweight adults: Relation to sex/gender and age.

Appetite

November 2022

Department of Neurology, Max Planck Institute for Human Cognitive and Brain Sciences, Leipzig, Germany; Cognitive Neurology, University Medical Center Leipzig, Germany. Electronic address:

Tyrosine (tyr), the precursor of the neurotransmitter dopamine, is known to modulate cognitive functions including executive attention. Tyr supplementation is suggested to influence dopamine-modulated cognitive performance. However, results are inconclusive regarding the presence or strength and also the direction of the association between tyr and cognitive function.

View Article and Find Full Text PDF

Introduction: Management of phenylketonuria (PKU) is mainly achieved through dietary control with limited intake of phenylalanine (Phe) from food, supplemented with low protein (LP) food and a mixture of free synthetic (FS) amino acids (AA) (FSAA). Casein glycomacropeptide (CGMP) is a natural peptide released in whey during cheese making by the action of the enzyme chymosin. Because CGMP in its pure form does not contain Phe, it is nutritionally suitable as a supplement in the diet for PKU when enriched with specific AAs.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!