Please use this identifier to cite or link to this item: https://doi.org/10.1172/jci.insight.126925
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dc.titleLarge-scale lipidomics identifies associations between plasma sphingolipids and T2DM incidence
dc.contributor.authorChew, Wee Siong
dc.contributor.authorTorta, Federico
dc.contributor.authorJi, Shanshan
dc.contributor.authorChoi, Hyungwon
dc.contributor.authorBegum, Husna
dc.contributor.authorSim, Xueling
dc.contributor.authorKhoo, Chin Meng
dc.contributor.authorKhoo, Eric Yin Hao
dc.contributor.authorOng, Wei-Yi
dc.contributor.authorVan Dam, Rob M
dc.contributor.authorWenk, Markus R
dc.contributor.authorTai, E Shyong
dc.contributor.authorHerr, Deron R
dc.date.accessioned2020-06-18T07:10:42Z
dc.date.available2020-06-18T07:10:42Z
dc.date.issued2019
dc.identifier.citationChew, Wee Siong, Torta, Federico, Ji, Shanshan, Choi, Hyungwon, Begum, Husna, Sim, Xueling, Khoo, Chin Meng, Khoo, Eric Yin Hao, Ong, Wei-Yi, Van Dam, Rob M, Wenk, Markus R, Tai, E Shyong, Herr, Deron R (2019). Large-scale lipidomics identifies associations between plasma sphingolipids and T2DM incidence. JCI INSIGHT 4 (13). ScholarBank@NUS Repository. https://doi.org/10.1172/jci.insight.126925
dc.identifier.issn23793708
dc.identifier.issn23793708
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/170375
dc.description.abstractCopyright: © 2019 American Society for Clinical Investigation BACKGROUND. Sphingolipids (SPs) are ubiquitous, structurally diverse molecules that include ceramides, sphingomyelins (SMs), and sphingosines. They are involved in various pathologies, including obesity and type 2 diabetes mellitus (T2DM). Therefore, it is likely that perturbations in plasma concentrations of SPs are associated with disease. Identifying these associations may reveal useful biomarkers or provide insight into disease processes. METHODS. We performed a lipidomics evaluation of molecularly distinct SPs in the plasma of 2302 ethnically Chinese Singaporeans using electrospray ionization mass spectrometry coupled with liquid chromatography. SP profiles were compared to clinical and biochemical characteristics, and subjects were evaluated with follow-up visits for 11 years. RESULTS. We found that ceramides correlated positively but hexosylceramides correlated negatively with BMI and homeostatic model assessment of insulin resistance (HOMA-IR). Furthermore, SPs with a d16:1 sphingoid backbone correlated more positively with BMI and HOMA-IR, while d18:2 SPs correlated less positively, relative to canonical d18:1 SPs. We also found that higher concentrations of 2 distinct SMs were associated with a higher risk of T2DM (HR 1.45 with 95% CI 1.18–1.78 for SM d16:1/18:0 and HR 1.40 with 95% CI 1.17–1.68 for SM d18:1/18:0). CONCLUSIONS. We identified significant associations between SPs and obesity/T2DM characteristics, specifically, those of hexosylceramides, d16:1 SPs, and d18:2 SPs. This suggests that the balance of SP metabolism, rather than ceramide accumulation, is associated with the pathology of obesity. We further identified 2 specific SPs that may represent prognostic biomarkers for T2DM. FUNDING. National University Health System (NUHSRO/2014/085/AF-Partner/01) and the National Research Foundation Investigatorship grant (NRF-NRFI2015-05).
dc.language.isoen
dc.publisherAMER SOC CLINICAL INVESTIGATION INC
dc.sourceElements
dc.subjectScience & Technology
dc.subjectLife Sciences & Biomedicine
dc.subjectMedicine, Research & Experimental
dc.subjectResearch & Experimental Medicine
dc.subjectCERAMIDE
dc.subjectTYPE-2
dc.subjectMETABOLISM
dc.subjectGLYCOSPHINGOLIPIDS
dc.subjectGLUCOSYLCERAMIDE
dc.subjectEXERCISE
dc.subjectREVEALS
dc.subjectADIPOSE
dc.subjectMODELS
dc.subjectMICE
dc.typeArticle
dc.date.updated2020-06-17T04:34:36Z
dc.contributor.departmentANATOMY
dc.contributor.departmentBIOCHEMISTRY
dc.contributor.departmentMEDICINE
dc.contributor.departmentPHARMACOLOGY
dc.contributor.departmentLIFE SCIENCES INSTITUTE
dc.contributor.departmentSAW SWEE HOCK SCHOOL OF PUBLIC HEALTH
dc.description.doi10.1172/jci.insight.126925
dc.description.sourcetitleJCI INSIGHT
dc.description.volume4
dc.description.issue13
dc.published.statePublished
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