Evidence map›Paper›PMID 30669586›Full record

ArticleInternational journal of molecular sciences2019

Analysis of Mucopolysaccharidosis Type VI through Integrative Functional Metabolomics.

Abdellah Tebani, Lenaig Abily-Donval, Isabelle Schmitz-Afonso, Monique Piraud, Jérôme Ausseil, Farid Zerimech, Carine Pilon, Tony Pereira, Stéphane Marret, Carlos Afonso and 1 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Mucopolysaccharidosis Type VI, an Updated Overview of the Disease.International journal of molecular sciences · 2021
    Review
  13. Review
  14. Article
  15. Article
  16. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Abdellah TebaniDepartment of Metabolic Biochemistry, Rouen University Hospital, 76000 Rouen, France. abdellah.tebani@yahoo.com.ORCID 0000-0002-8901-2678
Lenaig Abily-DonvalNormandie University, UNIROUEN, CHU Rouen, INSERM U1245, 76000 Rouen, France. lenaig.abily-donval@chu-rouen.fr.
Isabelle Schmitz-AfonsoNormandie Univ, UNIROUEN, INSA Rouen, CNRS, COBRA, 76000 Rouen, France. isabelle.schmitz-afonso@univ-rouen.fr.
Monique PiraudService de Biochimie et Biologie Moléculaire Grand Est, Unité des Maladies Héréditaires du Métabolisme et Dépistage Néonatal, Centre de Biologie et de Pathologie Est, Hospices Civils de Lyon, 69002 Lyon, France. monique.piraud@chu-lyon.fr.ORCID 0000-0002-2341-6514
Jérôme AusseilINSERM U1088, Laboratoire de Biochimie Métabolique, Centre de Biologie Humaine, CHU Sud, 80054 Amiens CEDEX, France. jerome.ausseil@chu-amiens.fr.
Farid ZerimechLaboratoire de Biochimie et Biologie Moléculaire, Université de Lille et Pôle de Biologie Pathologie Génétique du CHRU de Lille, 59000 Lille, France. farid.zerimech@chru-lille.fr.
Carine PilonDepartment of Metabolic Biochemistry, Rouen University Hospital, 76000 Rouen, France. Carine.Pilon@chu-rouen.fr.
Tony PereiraDepartment of Pharmacology, Rouen University Hospital, 76000 Rouen, France. Tony.Pereira@chu-rouen.fr.
Stéphane MarretNormandie University, UNIROUEN, CHU Rouen, INSERM U1245, 76000 Rouen, France. stephane.marret@chu-rouen.fr.
Carlos AfonsoNormandie Univ, UNIROUEN, INSA Rouen, CNRS, COBRA, 76000 Rouen, France. carlos.afonso@univ-rouen.fr.ORCID 0000-0002-2406-5664
Soumeya BekriDepartment of Metabolic Biochemistry, Rouen University Hospital, 76000 Rouen, France. soumeya.bekri@chu-rouen.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metabolic phenotyping is poised as a powerful and promising tool for biomarker discovery in inherited metabolic diseases. However, few studies applied this approach to mcopolysaccharidoses (MPS). Thus, this innovative functional approach may unveil comprehensive impairments in MPS biology. This study explores mcopolysaccharidosis VI (MPS VI) or Maroteaux⁻Lamy syndrome (OMIM #253200) which is an autosomal recessive lysosomal storage disease caused by the deficiency of arylsulfatase B enzyme. Urine samples were collected from 16 MPS VI patients and 66 healthy control individuals. Untargeted metabolomics analysis was applied using ultra-high-performance liquid chromatography combined with ion mobility and high-resolution mass spectrometry. Furthermore, dermatan sulfate, amino acids, carnitine, and acylcarnitine profiles were quantified using liquid chromatography coupled to tandem mass spectrometry. Univariate analysis and multivariate data modeling were used for integrative analysis and discriminant metabolites selection. Pathway analysis was done to unveil impaired metabolism. The study revealed significant differential biochemical patterns using multivariate data modeling. Pathway analysis revealed that several major amino acid pathways were dysregulated in MPS VI. Integrative analysis of targeted and untargeted metabolomics data with in silico results yielded arginine-proline, histidine, and glutathione metabolism being the most affected. This study is one of the first metabolic phenotyping studies of MPS VI. The findings might shed light on molecular understanding of MPS pathophysiology to develop further MPS studies to enhance diagnosis and treatments of this rare condition.

Indexed as

MetabolomeMetabolomicsAdolescentAdultAgedChildChild, PreschoolComputational BiologyFemaleHumansMaleMetabolic Networks and PathwaysMiddle AgedMolecular Sequence AnnotationMucopolysaccharidosis VIPhenotypeinherited metabolic diseaseslysosomal storage diseasesMaroteaux–Lamy syndromemass spectrometrymetabolomicsmucopolysaccharidosis type VI

Identifiers

PMID30669586
PMCPMC6359186

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.