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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00006824naa a2200913 4500
001oai:DiVA.org:umu-100162
003SwePub
008150224s2014 | |||||||||||000 ||eng|
009oai:lup.lub.lu.se:52bd9e1a-b683-4679-8363-e90894aeece0
024a https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-1001622 URI
024a https://doi.org/10.1016/S2213-8587(14)70146-92 DOI
024a https://lup.lub.lu.se/record/46151542 URI
040 a (SwePub)umud (SwePub)lu
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Forouhi, Nita G.4 aut
2451 0a Differences in the prospective association between individual plasma phospholipid saturated fatty acids and incident type 2 diabetes :b the EPIC-InterAct case-cohort study
264 1c 2014
338 a electronic2 rdacarrier
520 a Background Conflicting evidence exists regarding the association between saturated fatty acids (SFAs) and type 2 diabetes. In this longitudinal case-cohort study, we aimed to investigate the prospective associations between objectively measured individual plasma phospholipid SFAs and incident type 2 diabetes in EPIC-InterAct participants. Methods The EPIC-InterAct case-cohort study includes 12 403 people with incident type 2 diabetes and a representative subcohort of 16 154 individuals who were selected from a cohort of 340 234 European participants with 3 . 99 million person-years of follow-up (the EPIC study). Incident type 2 diabetes was ascertained until Dec 31, 2007, by a review of several sources of evidence. Gas chromatography was used to measure the distribution of fatty acids in plasma phospholipids (mol%); samples from people with type 2 diabetes and subcohort participants were processed in a random order by centre, and laboratory staff were masked to participant characteristics. We estimated country-specific hazard ratios (HRs) for associations per SD of each SFA with incident type 2 diabetes using Prentice-weighted Cox regression, which is weighted for case-cohort sampling, and pooled our findings using random-effects meta-analysis. Findings SFAs accounted for 46% of total plasma phospholipid fatty acids. In adjusted analyses, different individual SFAs were associated with incident type 2 diabetes in opposing directions. Even-chain SFAs that were measured (14: 0 [myristic acid], 16: 0 [palmitic acid], and 18: 0 [stearic acid]) were positively associated with incident type 2 diabetes (HR [95% CI] per SD difference: myristic acid 1.15 [95% CI 1.09-1.22], palmitic acid 1.26 [1.15-1.37], and stearic acid 1.06 [1.00-1.13]). By contrast, measured odd-chain SFAs (15: 0 [pentadecanoic acid] and 17: 0 [heptadecanoic acid]) were inversely associated with incident type 2 diabetes (HR [95% CI] per 1 SD difference: 0.79 [0.73-0.85] for pentadecanoic acid and 0.67 [0.63-0.71] for heptadecanoic acid), as were measured longer-chain SFAs (20: 0 [arachidic acid], 22:0 [behenic acid], 23:0 [tricosanoic acid], and 24:0 [lignoceric acid]), with HRs ranging from 0.72 to 0.81 (95% CIs ranging between 0.61 and 0.92). Our findings were robust to a range of sensitivity analyses. Interpretation Different individual plasma phospholipid SFAs were associated with incident type 2 diabetes in opposite directions, which suggests that SFAs are not homogeneous in their effects. Our findings emphasise the importance of the recognition of subtypes of these fatty acids. An improved understanding of differences in sources of individual SFAs from dietary intake versus endogenous metabolism is needed.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicinx Endokrinologi och diabetes0 (SwePub)302052 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Clinical Medicinex Endocrinology and Diabetes0 (SwePub)302052 hsv//eng
700a Koulman, Albert4 aut
700a Sharp, Stephen J.4 aut
700a Imamura, Fumiaki4 aut
700a Kroger, Janine4 aut
700a Schulze, Matthias B.4 aut
700a Crowe, Francesca L.4 aut
700a Huerta, Jose Maria4 aut
700a Guevara, Marcela4 aut
700a Beulens, Joline W. J.4 aut
700a van Woudenbergh, Geertruida J.4 aut
700a Wang, Laura4 aut
700a Summerhill, Keith4 aut
700a Griffin, Julian L.4 aut
700a Feskens, Edith J. M.4 aut
700a Amiano, Pilar4 aut
700a Boeing, Heiner4 aut
700a Clavel-Chapelon, Francoise4 aut
700a Dartois, Laureen4 aut
700a Fagherazzi, Guy4 aut
700a Franks, Paul W.u Lunds universitet,Umeå universitet,Medicin,Lund University, Malmö, Sweden,Genetisk och molekylär epidemiologi,Forskargrupper vid Lunds universitet,Genetic and Molecular Epidemiology,Lund University Research Groups4 aut0 (Swepub:lu)med-plf
700a Gonzalez, Carlos4 aut
700a Jakobsen, Marianne Uhre4 aut
700a Kaaks, Rudolf4 aut
700a Key, Timothy J.4 aut
700a Khaw, Kay-Tee4 aut
700a Kuhn, Tilman4 aut
700a Mattiello, Amalia4 aut
700a Nilsson, Peteru Lund University,Lunds universitet,Internmedicin - epidemiologi,Forskargrupper vid Lunds universitet,Internal Medicine - Epidemiology,Lund University Research Groups4 aut0 (Swepub:lu)medf-pni
700a Overvad, Kim4 aut
700a Pala, Valeria4 aut
700a Palli, Domenico4 aut
700a Quiros, J. Ramon4 aut
700a Rolandsson, Olovu Umeå universitet,Allmänmedicin4 aut0 (Swepub:umu)olro0005
700a Roswall, Nina4 aut
700a Sacerdote, Carlotta4 aut
700a Sanchez, Mara-Jose4 aut
700a Slimani, Nadia4 aut
700a Spijkerman, Annemieke M. W.4 aut
700a Tjonneland, Anne4 aut
700a Tormo, Maria-Jose4 aut
700a Tumino, Rosario4 aut
700a van der A, Daphne L.4 aut
700a van der Schouw, Yvonne T.4 aut
700a Langenberg, Claudia4 aut
700a Riboli, Elio4 aut
700a Wareham, Nicholas J.4 aut
710a Umeå universitetb Medicin4 org
773t LANCET DIABETES & ENDOCRINOLOGYg 2:10, s. 810-818q 2:10<810-818x 2213-8587x 2213-8595
856u https://umu.diva-portal.org/smash/get/diva2:790584/FULLTEXT01.pdfx primaryx Raw objecty fulltext:print
856u https://portal.research.lu.se/files/6549248/8147275x primaryx freey FULLTEXT
856u http://www.ncbi.nlm.nih.gov/pubmed/25107467?dopt=Abstractx freey FULLTEXT
856u http://dx.doi.org/10.1016/S2213-8587(14)70146-9x freey FULLTEXT
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-100162
8564 8u https://doi.org/10.1016/S2213-8587(14)70146-9
8564 8u https://lup.lub.lu.se/record/4615154

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