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Cord-Blood Lipidome in Progression to Islet Autoimmunity and Type 1 Diabetes.
Lamichhane, Santosh; Ahonen, Linda; Dyrlund, Thomas Sparholt; Dickens, Alex M; Siljander, Heli; Hyöty, Heikki; Ilonen, Jorma; Toppari, Jorma; Veijola, Riitta; Hyötyläinen, Tuulia; Knip, Mikael; Oresic, Matej.
Afiliação
  • Lamichhane S; Turku Centre for Biotechnology, University of Turku and Åbo Akademi University, 20520 Turku, Finland. santosh.lamichhane@utu.fi.
  • Ahonen L; Steno Diabetes Center Copenhagen, 2820 Gentofte, Denmark. la@biosyntia.com.
  • Dyrlund TS; Steno Diabetes Center Copenhagen, 2820 Gentofte, Denmark. thomas@dyrlund.dk.
  • Dickens AM; Turku Centre for Biotechnology, University of Turku and Åbo Akademi University, 20520 Turku, Finland. alex.dickens@utu.fi.
  • Siljander H; Children's Hospital, University of Helsinki, Helsinki University Hospital and Research Program Unit, Diabetes and Obesity, University of Helsinki, 00290 Helsinki, Finland. heli.siljander@helsinki.fi.
  • Hyöty H; Faculty of Medicine and Life Sciences, University of Tampere, Tampere 33014, Finland. heikki.hyoty@uta.fi.
  • Ilonen J; Fimlab Laboratories, Pirkanmaa Hospital District, 33014 Tampere, Finland. heikki.hyoty@uta.fi.
  • Toppari J; Immunogenetics Laboratory, Institute of Biomedicine, University of Turku, 20520 Turku, Finland. jsilonen@utu.fi.
  • Veijola R; Clinical Microbiology, Turku University Hospital, 20014 Turku, Finland. jsilonen@utu.fi.
  • Hyötyläinen T; Institute of Biomedicine, Centre for Integrative Physiology and Pharmacology, University of Turku, 20014 Turku, Finland. jortop@utu.fi.
  • Knip M; Department of Pediatrics, Turku University Hospital, 20521 Turku, Finland. jortop@utu.fi.
  • Oresic M; Department of Pediatrics, PEDEGO Research Unit, Medical Research Centre, University of Oulu, 90014 Oulu, Finland. riitta.veijola@oulu.fi.
Biomolecules ; 9(1)2019 01 21.
Article em En | MEDLINE | ID: mdl-30669674
Previous studies suggest that children who progress to type 1 diabetes (T1D) later in life already have an altered serum lipid molecular profile at birth. Here, we compared cord blood lipidome across the three study groups: children who progressed to T1D (PT1D; n = 30), children who developed at least one islet autoantibody but did not progress to T1D during the follow-up (P1Ab; n = 33), and their age-matched controls (CTR; n = 38). We found that phospholipids, specifically sphingomyelins, were lower in T1D progressors when compared to P1Ab and the CTR. Cholesterol esters remained higher in PT1D when compared to other groups. A signature comprising five lipids was predictive of the risk of progression to T1D, with an area under the receiver operating characteristic curve (AUROC) of 0.83. Our findings provide further evidence that the lipidomic profiles of newborn infants who progress to T1D later in life are different from lipidomic profiles in P1Ab and CTR.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ilhotas Pancreáticas / Diabetes Mellitus Tipo 1 / Sangue Fetal / Lipídeos Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Child / Child, preschool / Female / Humans / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ilhotas Pancreáticas / Diabetes Mellitus Tipo 1 / Sangue Fetal / Lipídeos Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Child / Child, preschool / Female / Humans / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article