Lipidome as a predictive tool in progression to type 2 diabetes in Finnish men

dc.contributor.authorTommi Suvitaival
dc.contributor.authorIsabel Bondia-Pons
dc.contributor.authorLaxman Yetukuri
dc.contributor.authorPäivi Pöhö
dc.contributor.authorJohn J. Nolan
dc.contributor.authorTuulia Hyötyläinen
dc.contributor.authorJohanna Kuusisto
dc.contributor.authorMatej Orešič
dc.contributor.organizationfi=Turun biotiedekeskus|en=Turku Bioscience Centre|
dc.contributor.organization-code1.2.246.10.2458963.20.18586209670
dc.contributor.organization-code2609201
dc.converis.publication-id29143799
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/29143799
dc.date.accessioned2025-08-28T01:21:28Z
dc.date.available2025-08-28T01:21:28Z
dc.description.abstractBackground. There is a need for early markers to track and predict the development of type 2 diabetes mellitus (T2DM) from the state of normal glucose tolerance through prediabetes. In this study we tested whether the plasma molecular lipidome has biomarker potential to predicting the onset of T2DM.Methods. We applied global lipidomic profiling on plasma samples from well-phenotyped men (107 cases, 216 controls) participating in the longitudinal METSIM study at baseline and at five-year follow-up. To validate the lipid markers, an additional study with a representative sample of adult male population (n = 631) was also conducted. A total of 277 plasma lipids were analyzed using the lipidomics platform based on ultra performance liquid chromatography coupled to time-of-flight mass spectrometry. Lipids with the highest predictive power for the development of T2DM were computationally selected, validated and compared to standard risk models without lipids.Results. A persistent lipid signature with higher levels of triacylglycerols and diacyl-phospholipids as well as lowerlevels of alkylacyl phosphatidylcholines was observed in progressors to T2DM. Lysophosphatidylcholine acyl C18:2 (LysoPC(18:2)), phosphatidylcholines PC(32:1), PC(34:2e) and PC(36:1), and triacylglycerol TG(17:1/18:1/18:2) were selected to the full model that included metabolic risk factors and FINDRISC variables. When further adjusting for BM and age, these lipids had respective odds ratios of 0.32, 2.4, 0.50, 2.2 and 0.31 (all p < 0.05) for progression to T2DM. The independently-validated predictive power improved in all pairwise comparisons between the lipid model and the respective standard risk model without the lipids (integrated discrimination improvement IDI > 0; p < 0.05). Notably, the lipid models remained predictive of the development of T2DM in the fasting plasma glucose-matched subset of the validation study.Conclusion. This study indicates that a lipid signature characteristic of T2DM is present years before the diagnosis and improves prediction of progression to T2DM. Molecular lipid biomarkers were shown to have predictive power also in a high-risk group, where standard risk factors are not helpful at distinguishing progressors from non-progressors.
dc.format.pagerange1
dc.format.pagerange12
dc.identifier.eissn1532-8600
dc.identifier.jour-issn0026-0495
dc.identifier.olddbid207436
dc.identifier.oldhandle10024/190463
dc.identifier.urihttps://www.utupub.fi/handle/11111/51213
dc.identifier.urnURN:NBN:fi-fe2021042718474
dc.language.isoen
dc.okm.affiliatedauthorHyötyläinen, Tuulia
dc.okm.affiliatedauthorOresic, Matej
dc.okm.discipline3111 Biomedicineen_GB
dc.okm.discipline3121 Internal medicineen_GB
dc.okm.discipline3111 Biolääketieteetfi_FI
dc.okm.discipline3121 Sisätauditfi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherW B SAUNDERS CO-ELSEVIER INC
dc.publisher.countryUnited Statesen_GB
dc.publisher.countryYhdysvallat (USA)fi_FI
dc.publisher.country-codeUS
dc.relation.doi10.1016/j.metabol.2017.08.014
dc.relation.ispartofjournalMetabolism
dc.relation.volume78
dc.source.identifierhttps://www.utupub.fi/handle/10024/190463
dc.titleLipidome as a predictive tool in progression to type 2 diabetes in Finnish men
dc.year.issued2018

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