Metabolomics: moving towards personalized medicine
In many fields of medicine there is a growing interest in characterizing diseases at molecular level
with a view to developing an individually tailored therapeutic approach. Metabolomics is a novel
area that promises to contribute significantly to the characterization of various disease phenotypes
and to the identification of personal metabolic features that can predict response to therapies.
Based on analytical platforms such as mass spectrometry or NMR-based spectroscopy, the
metabolomic approach enables a comprehensive overview of the metabolites, leading to the
characterization of the metabolic fingerprint of a given sample. These metabolic fingerprints can
then be used to distinguish between different disease phenotypes and to predict a drug's
effectiveness and/or toxicity.
Several studies published in the last few years applied the metabolomic approach in the field of
pediatric medicine. Being a highly informative technique that can be used on samples collected noninvasively
(e.g. urine or exhaled breath condensate), metabolomics has appeal for the study of
pediatric diseases. Here we present and discuss the pediatric clinical studies that have taken the
metabolomic approach.
BARALDI Eugenio;
CARRARO Silvia;
GIORDANO Giuseppe;
RENIERO Fabiano;
PERILONGO Giorgio;
ZACCHELLO Franco;
2010-01-14
BioMed Central
JRC50460
0022-3476,
http://www.ijponline.net/,
https://publications.jrc.ec.europa.eu/repository/handle/JRC50460,
10.1186/1824-7288-35-30,
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