Cord-Blood Lipidome in Progression to Islet Autoimmunity and Type 1 Diabetes

dc.contributor.authorLamichhane Santosh
dc.contributor.authorAhonen Linda
dc.contributor.authorDyrlund Thomas Spartholt
dc.contributor.authorDickens Alex M.
dc.contributor.authorSiljander Heli
dc.contributor.authorHyöty Heikki
dc.contributor.authorIlonen Jorma
dc.contributor.authorToppari Jorma
dc.contributor.authorVeijola Riitta
dc.contributor.authorHyötyläinen Tuulia
dc.contributor.authorKnip Mikael
dc.contributor.authorOresic Matej
dc.contributor.organizationfi=Turun biotiedekeskus|en=Turku Bioscience Centre|
dc.contributor.organizationfi=biolääketieteen laitos|en=Institute of Biomedicine|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code1.2.246.10.2458963.20.18586209670
dc.contributor.organization-code1.2.246.10.2458963.20.77952289591
dc.converis.publication-id39635894
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/39635894
dc.date.accessioned2022-10-28T13:15:34Z
dc.date.available2022-10-28T13:15:34Z
dc.description.abstractPrevious 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.
dc.identifier.jour-issn2218-273X
dc.identifier.olddbid180865
dc.identifier.oldhandle10024/163959
dc.identifier.urihttps://www.utupub.fi/handle/11111/36430
dc.identifier.urlhttps://www.mdpi.com/2218-273X/9/1/33
dc.identifier.urnURN:NBN:fi-fe2021042822080
dc.language.isoen
dc.okm.affiliatedauthorLamichhane, Santosh
dc.okm.affiliatedauthorDickens, Alex
dc.okm.affiliatedauthorIlonen, Jorma
dc.okm.affiliatedauthorToppari, Jorma
dc.okm.affiliatedauthorOresic, Matej
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3111 Biomedicineen_GB
dc.okm.discipline3123 Gynaecology and paediatricsen_GB
dc.okm.discipline3111 Biolääketieteetfi_FI
dc.okm.discipline3123 Naisten- ja lastentauditfi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherMDPI
dc.publisher.countrySwitzerlanden_GB
dc.publisher.countrySveitsifi_FI
dc.publisher.country-codeCH
dc.relation.articlenumberARTN 33
dc.relation.doi10.3390/biom9010033
dc.relation.ispartofjournalBiomolecules
dc.relation.issue1
dc.relation.volume9
dc.source.identifierhttps://www.utupub.fi/handle/10024/163959
dc.titleCord-Blood Lipidome in Progression to Islet Autoimmunity and Type 1 Diabetes
dc.year.issued2019

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