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      Exploring the Role of Different Neonatal Nutrition Regimens during the First Week of Life by Urinary GC-MS Metabolomics

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          Abstract

          In this study, a gas-chromatography mass spectrometry (GC-MS) metabolomics study was applied to examine urine metabolite profiles of different classes of neonates under different nutrition regimens. The study population included 35 neonates, exclusively either breastfed or formula milk fed, in a seven-day timeframe. Urine samples were collected from intrauterine growth restriction (IUGR), large for gestational age (LGA), and appropriate gestational age (AGA) neonates. At birth, IUGR and LGA neonates showed similarities in their urine metabolite profiles that differed from AGA. When neonates started milk feeding, their metabolite excretion profile was strongly characterized by the different diet regimens. After three days of formula milk nutrition, urine had higher levels of glucose, galactose, glycine and myo-inositol, while up-regulated aconitic acid, aminomalonic acid and adipic acid were found in breast milk fed neonates. At seven days, neonates fed with formula milk shared higher levels of pseudouridine with IUGR and LGA at birth. Breastfed neonates shared up-regulated pyroglutamic acid, citric acid, and homoserine, with AGA at birth. The role of most important metabolites is herein discussed.

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          Fetal origins of coronary heart disease.

          The fetal origins hypothesis states that fetal undernutrition in middle to late gestation, which leads to disproportionate fetal growth, programmes later coronary heart disease. Animal studies have shown that undernutrition before birth programmes persisting changes in a range of metabolic, physiological, and structural parameters. Studies in humans have shown that men and women whose birth weights were at the lower end of the normal range, who were thin or short at birth, or who were small in relation to placental size have increased rates of coronary heart disease. We are beginning to understand something of the mechanisms underlying these associations. The programming of blood pressure, insulin responses to glucose, cholesterol metabolism, blood coagulation, and hormonal settings are all areas of active research.
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            Metabonomics: a platform for studying drug toxicity and gene function.

            The later that a molecule or molecular class is lost from the drug development pipeline, the higher the financial cost. Minimizing attrition is therefore one of the most important aims of a pharmaceutical discovery programme. Novel technologies that increase the probability of making the right choice early save resources, and promote safety, efficacy and profitability. Metabonomics is a systems approach for studying in vivo metabolic profiles, which promises to provide information on drug toxicity, disease processes and gene function at several stages in the discovery-and-development process.
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              Type 2 (non-insulin-dependent) diabetes mellitus: the thrifty phenotype hypothesis.

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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                Int J Mol Sci
                Int J Mol Sci
                ijms
                International Journal of Molecular Sciences
                MDPI
                1422-0067
                22 February 2016
                February 2016
                : 17
                : 2
                : 265
                Affiliations
                [1 ]Neonatal Intensive Care Unit, Puericulture Institute and Neonatal Section, Azienda Ospedaliera Universitaria, University of Cagliari, 09042 Monserrato, Italy; angelicadessi@ 123456hotmail.it (A.D.); andrea.schirru.as@ 123456gmail.com (A.S.); vafanos@ 123456tiscali.it (V.F.)
                [2 ]Department of Life and Environmental Sciences, University of Cagliari, Via Ospedale 72, 09124 Cagliari, Italy; a-murgia@ 123456hotmail.it
                [3 ]Neonatal Intensive Unit and Neonatal Pathology, “S. Giovanni Calibita” Hospital, Fatebenefratelli Isola Tiberina, 00186 Rome, Italy; rocco.agostino@ 123456uniroma1.it (R.A.); mpattumelli@ 123456gmail.com (M.G.P.)
                [4 ]Department of Chemical and Geological Sciences, University of Cagliari, 09042 Monserrato, Italy; scano@ 123456unica.it
                Author notes
                [* ]Correspondence: caboni@ 123456unica.it ; Tel.: +39-070-6758-617; Fax: +39-070-6758-612
                Article
                ijms-17-00265
                10.3390/ijms17020265
                4783994
                26907266
                bafdc54b-d19e-47b7-8057-9d76e315a392
                © 2016 by the authors; licensee MDPI, Basel, Switzerland.

                This article is an open access article distributed under the terms and conditions of the Creative Commons by Attribution (CC-BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 12 January 2016
                : 16 February 2016
                Categories
                Article

                Molecular biology
                breastfeeding,formula milk,metabonomics,iugr,lga,aga,myo-inositol,glycine,pseudouridine
                Molecular biology
                breastfeeding, formula milk, metabonomics, iugr, lga, aga, myo-inositol, glycine, pseudouridine

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