Abstract

Low-phenylalanine diet, the mainstay of treatment for phenylketonuria (PKU), has been shown to increase glycemic index and glycemic load, affecting the availability of substrates for microbial fermentation. Indeed, changes in the PKU gut microbiota compared with healthy controls have been previously reported. In this study we compared the gut microbial communities of children with PKU and with mild hyperphenylalaninemia (MHP, unrestricted diet). For each group, we enrolled 21 children (4–18 years old), for a total dataset of 42 subjects. We assessed dietary intake and performed gut microbiota analysis by sequencing the V3–V4 hypervariable regions of the 16S rRNA gene. Short chain fatty acids (SCFAs) were quantified by gas chromatographic analysis. While alpha-diversity analysis showed no significant differences between PKU and MHP groups, microbial community analysis highlighted a significant separation of the gut microbiota according to both unweighted (p = 0.008) and weighted Unifrac distances (p = 0.033). Major differences were seen within the Firmicutes phylum. Indeed, PKU children were depleted in Faecalibacterium spp. and enriched in Blautia spp. and Clostridium spp (family Lachnospiraceae). We found a divergent response of members of the Firmicutes phylum with respect to daily glycemic index, higher in PKU children. Faecalibacterium prausnitzii, unclassified Ruminococcaceae and, to a lesser extent Roseburia spp. negatively correlated with glycemic index, whereas unclassified Lachnospiraceae were positively associated. Indicator species analysis suggested F. prausnitzii be related to MHP status and Ruminococcus bromii to be associated with PKU. Despite PKU children having a higher vegetable and fiber intake, resembling a vegan diet, their gut microbial profile is different from the microbiota reported in the literature for individuals consuming a high-fiber/low-protein diet. Indeed, beneficial microorganisms, such as F. prausnitzii, considered a biomarker for a healthy status and one of the main butyrate producers, are depleted in PKU gut microbiota. We suggest that both the quality and quantity of carbohydrates ingested participate in determining the observed Firmicutes shifts on the PKU population.

Highlights

  • Phenylketonuria (PKU; OMIM 261600) is an inherited metabolic disorder caused by a mutation in the phenylalanine hydroxylase enzyme (PAH), which converts phenylalanine (Phe) into tyrosine

  • Glycemic index (GI) and glycemic load (GL), evaluated for each meal, were significantly higher in PKU children compared with MHP subjects (p < 0.001)

  • The aim of this study was to investigate the impact of a low-Phe diet on microbial gut community and its possible consequences on PKU patient wellbeing

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Summary

Introduction

Phenylketonuria (PKU; OMIM 261600) is an inherited metabolic disorder caused by a mutation in the phenylalanine hydroxylase enzyme (PAH), which converts phenylalanine (Phe) into tyrosine. Allelic heterogeneity at PAH locus results in a variety of metabolic phenotypes, ranging from mild, moderate and classical PKU (blood Phe levels >360 μmol/L) to mild hyperphenylalaninemia (MHP, blood Phe levels ranging 120–360 μmol/L; Güttler and Guldberg, 1996). A PKU diet, started in the neonatal period and followed lifelong, is characterized by low-protein natural foods (vegetables, fruits) and special low-protein products, which are low-protein variants of some foods (bread, pasta, and biscuits; Giovannini et al, 2012). A PKU diet has been shown to increase glycemic index and glycemic load (Moretti et al, 2017), probably due to special low-protein products frequently being enriched in sugars

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