<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Pecze, László</dc:creator>
  <dc:creator>Randi, Elisa B.</dc:creator>
  <dc:creator>Szabo, Csaba</dc:creator>
  <dc:date>2020-11-09</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Clinical observations and preclinical studies both suggest that Down syndrome (DS)  may be associated with significant metabolic and bioenergetic alterations. However,  the relevant scientific literature has not yet been systematically reviewed. The aim of  the current study was to conduct a meta-analysis of metabolites involved in  bioenergetics pathways in DS to conclusively determine the difference between DS  and control subjects. We discuss these findings and their potential relevance in the  context of pathogenesis and experimental therapy of DS. Articles published before  July 1, 2020, were identified by using the search terms “Down syndrome” and  “metabolite name” or “trisomy 21” and “metabolite name”. Moreover, DS-related  metabolomics studies and bioenergetics literature were also reviewed. 41 published  reports and associated databases were identified, from which the descriptive  information and the relevant metabolomic parameters were extracted and analyzed.  Mixed effect model revealed the following changes in DS: significantly decreased ATP,  CoQ10, homocysteine, serine, arginine and tyrosine; slightly decreased ADP;  significantly increased uric acid, succinate, lactate and cysteine; slightly increased  phosphate, pyruvate and citrate. However, the concentrations of AMP, 2,3- diphosphoglycerate, glucose, and glutamine were comparable in the DS vs. control  populations. We conclude that cells of subjects with DS are in a pseudo-hypoxic state:  the cellular metabolic and bio-energetic mechanisms exhibit pathophysiological  alterations that resemble the cellular responses associated with hypoxia, even though  the supply of the cells with oxygen is not disrupted. This fundamental alteration may  be, at least in part, responsible for a variety of functional deficits associated with DS,  including reduced exercise difference, impaired neurocognitive status and  neurodegeneration.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/309167</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/309167/files/sza_mam.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1186/s10020-020-00225-8</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Molecular Medicine. - 2020, vol. 26, no. 1, p. 102</dc:source>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Meta-analysis of metabolites involved in bioenergetic pathways reveals a pseudohypoxic state in Down syndrome</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
