Differences in faecal microbiome composition between adult patients with UCD and PKU and healthy control subjects

Urea cycle disorders (UCDs) are a group of rare inherited metabolic diseases causing hyperammonemic encephalopathy. Despite intensive dietary and pharmacological therapy, outcome is poor in a subset of UCD patients. Reducing ammonia production by changing faecal microbiome in UCD is an attractive tr...

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Main Authors: C. Timmer, M. Davids, M. Nieuwdorp, J.H.M. Levels, J.G. Langendonk, M. Breederveld, N. Ahmadi Mozafari, M. Langeveld
Format: Article
Language:English
Published: Elsevier 2021-12-01
Series:Molecular Genetics and Metabolism Reports
Subjects:
Gut
Online Access:http://www.sciencedirect.com/science/article/pii/S2214426921000884
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spelling doaj-1dd015315a634f1fa60ece6257b451a22021-09-09T04:27:58ZengElsevierMolecular Genetics and Metabolism Reports2214-42692021-12-0129100794Differences in faecal microbiome composition between adult patients with UCD and PKU and healthy control subjectsC. Timmer0M. Davids1M. Nieuwdorp2J.H.M. Levels3J.G. Langendonk4M. Breederveld5N. Ahmadi Mozafari6M. Langeveld7Department of Dietetics and Nutritional science and Department of Endocrinology and Metabolism, Amsterdam University Medical Centers, Amsterdam, the Netherlands; Corresponding author.Department of Vascular Medicine, Amsterdam University Medical Centers, Amsterdam, the NetherlandsDepartment of Vascular Medicine, Amsterdam University Medical Centers, Amsterdam, the NetherlandsDepartment of Vascular Medicine, Amsterdam University Medical Centers, Amsterdam, the NetherlandsDepartment of Dietetics and Department of Internal Medicine, Center of Lysosomal and Metabolic Diseases, Erasmus University Medical Center, Erasmus MC, Rotterdam, the NetherlandsDepartment of Dietetics and Department of Internal Medicine, Center of Lysosomal and Metabolic Diseases, Erasmus University Medical Center, Erasmus MC, Rotterdam, the NetherlandsDepartment of Dietetics and Department of Internal Medicine, Center of Lysosomal and Metabolic Diseases, Erasmus University Medical Center, Erasmus MC, Rotterdam, the NetherlandsDepartment of Dietetics and Nutritional science and Department of Endocrinology and Metabolism, Amsterdam University Medical Centers, Amsterdam, the NetherlandsUrea cycle disorders (UCDs) are a group of rare inherited metabolic diseases causing hyperammonemic encephalopathy. Despite intensive dietary and pharmacological therapy, outcome is poor in a subset of UCD patients. Reducing ammonia production by changing faecal microbiome in UCD is an attractive treatment approach. We compared faecal microbiome composition of 10 UCD patients, 10 healthy control subjects and 10 phenylketonuria (PKU) patients. PKU patients on a low protein diet were included to differentiate between the effect of a low protein diet and the UCD itself on microbial composition. Participants were asked to collect a faecal sample and to fill out a 24 h dietary journal. DNA was extracted from faecal material, taxonomy was assigned and microbiome data was analyzed, with a focus on microbiota involved in ammonia metabolism.In this study we show an altered faecal microbiome in UCD patients, different from both PKU and healthy controls. UCD patients on dietary and pharmacological treatment had a less diverse faecal microbiome, and the faecal microbiome of PKU patients on a protein restricted diet with amino acid supplementation showed reduced richness compared to healthy adults without a specific diet. The differences in the microbiome composition of UCD patients compared to healthy controls were in part related to lactulose use. Other genomic process encodings involved in ammonia metabolism, did not seem to differ. Since manipulation of the microbiome is possible, this could be a potential treatment modality. We propose as a first next step, to study the impact of these faecal microbiome alterations on metabolic stability. Take home message: The faecal microbiome of UCD patients was less diverse compared to PKU patients and even more compared to healthy controls.http://www.sciencedirect.com/science/article/pii/S2214426921000884MicrobiomeGutFaecalUrea cycle defectPhenylketonuriaHyperammonemia
collection DOAJ
language English
format Article
sources DOAJ
author C. Timmer
M. Davids
M. Nieuwdorp
J.H.M. Levels
J.G. Langendonk
M. Breederveld
N. Ahmadi Mozafari
M. Langeveld
spellingShingle C. Timmer
M. Davids
M. Nieuwdorp
J.H.M. Levels
J.G. Langendonk
M. Breederveld
N. Ahmadi Mozafari
M. Langeveld
Differences in faecal microbiome composition between adult patients with UCD and PKU and healthy control subjects
Molecular Genetics and Metabolism Reports
Microbiome
Gut
Faecal
Urea cycle defect
Phenylketonuria
Hyperammonemia
author_facet C. Timmer
M. Davids
M. Nieuwdorp
J.H.M. Levels
J.G. Langendonk
M. Breederveld
N. Ahmadi Mozafari
M. Langeveld
author_sort C. Timmer
title Differences in faecal microbiome composition between adult patients with UCD and PKU and healthy control subjects
title_short Differences in faecal microbiome composition between adult patients with UCD and PKU and healthy control subjects
title_full Differences in faecal microbiome composition between adult patients with UCD and PKU and healthy control subjects
title_fullStr Differences in faecal microbiome composition between adult patients with UCD and PKU and healthy control subjects
title_full_unstemmed Differences in faecal microbiome composition between adult patients with UCD and PKU and healthy control subjects
title_sort differences in faecal microbiome composition between adult patients with ucd and pku and healthy control subjects
publisher Elsevier
series Molecular Genetics and Metabolism Reports
issn 2214-4269
publishDate 2021-12-01
description Urea cycle disorders (UCDs) are a group of rare inherited metabolic diseases causing hyperammonemic encephalopathy. Despite intensive dietary and pharmacological therapy, outcome is poor in a subset of UCD patients. Reducing ammonia production by changing faecal microbiome in UCD is an attractive treatment approach. We compared faecal microbiome composition of 10 UCD patients, 10 healthy control subjects and 10 phenylketonuria (PKU) patients. PKU patients on a low protein diet were included to differentiate between the effect of a low protein diet and the UCD itself on microbial composition. Participants were asked to collect a faecal sample and to fill out a 24 h dietary journal. DNA was extracted from faecal material, taxonomy was assigned and microbiome data was analyzed, with a focus on microbiota involved in ammonia metabolism.In this study we show an altered faecal microbiome in UCD patients, different from both PKU and healthy controls. UCD patients on dietary and pharmacological treatment had a less diverse faecal microbiome, and the faecal microbiome of PKU patients on a protein restricted diet with amino acid supplementation showed reduced richness compared to healthy adults without a specific diet. The differences in the microbiome composition of UCD patients compared to healthy controls were in part related to lactulose use. Other genomic process encodings involved in ammonia metabolism, did not seem to differ. Since manipulation of the microbiome is possible, this could be a potential treatment modality. We propose as a first next step, to study the impact of these faecal microbiome alterations on metabolic stability. Take home message: The faecal microbiome of UCD patients was less diverse compared to PKU patients and even more compared to healthy controls.
topic Microbiome
Gut
Faecal
Urea cycle defect
Phenylketonuria
Hyperammonemia
url http://www.sciencedirect.com/science/article/pii/S2214426921000884
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