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dc.creatorŠarac, Ivana
dc.creatorDebeljak-Martačić, Jasmina
dc.creatorTakić, Marija
dc.creatorStevanović, Vuk
dc.creatorMilešević, Jelena
dc.creatorZeković, Milica
dc.creatorPopović, Tamara B.
dc.creatorJovanović, Jovica
dc.creatorKardum Vidović, Nevena
dc.date.accessioned2023-09-18T12:28:46Z
dc.date.available2023-09-18T12:28:46Z
dc.date.issued2023
dc.identifier.issn2296-861X
dc.identifier.urihttp://rimi.imi.bg.ac.rs/handle/123456789/1345
dc.description.abstractIntroduction: Fatty acids (FAs) composition and desaturase activities can be altered in different metabolic conditions, but the adiposity-independent associations with clinical and biochemical indicators of cardiometabolic risk are still unclear. This study aimed to analyze the associations of FAs composition and estimated desaturase activities with anthropometric, clinical, and biochemical cardiometabolic risk indicators in non-diabetic Serbian women, and to investigate if these associations were independent of the level of adiposity and other confounders. Methods: In 76 non-diabetic, otherwise healthy Serbian women, aged 24-68 years, with or without metabolic syndrome or obesity (BMI=23.6±5.6 kg/m2), FA composition in erythrocyte phospholipids was measured by gas-liquid chromatography. Desaturase activities were estimated from product/precursor FAs ratios (D9D:16:1n-7/16:0; D6D:20:3n-6/18:2n-6; D5D:20:4n-6/20:3n-6). Correlations were made with anthropometric, biochemical (serum glucose, triacylglycerols, LDL-C, HDL-C, ALT, AST, and their ratios) and clinical (blood pressure) indicators of cardiometabolic risk. Linear regression models were performed to test the independence of these associations. Results: Estimated desaturase activities and certain FAs were associated with anthropometric, clinical and biochemical indicators of cardiometabolic risk: D9D, D6D, 16:1n-7 and 20:3n-6 were directly associated, while D5D and 18:0 were inversely associated. However, the associations with clinical and biochemical indicators were not independent of the associations with the level of adiposity, since they were lost after controlling for anthropometric indices. After controlling for multiple confounders (age, postmenopausal status, education, smoking, physical activity, dietary macronutrient intakes, use of supplements, alcohol consumption), the level of adiposity was the most significant predictor of desaturase activities and aforementioned FAs levels, and mediated their association with biochemical/clinical indicators. Vice versa, desaturase activities predicted the level of adiposity, but not other components of cardiometabolic risk (if the level of adiposity was accounted). While the associations of anthropometric indices with 16:1n-7, 20:3n-6, 18:0 and D9D and D6D activities were linear, the associations with D5D activity were the inverse U-shaped. The only adiposity-independent association of FAs profiles with the indicators of cardiometabolic risk was a positive association of 20:5n-3 with ALT/AST ratio, which requires further exploration. Discussion: Additional studies are needed to explore the mechanisms of the observed associations.
dc.publisherFrontiers Media S.A.
dc.relationinfo:eu-repo/grantAgreement/MESTD/Integrated and Interdisciplinary Research (IIR or III)/41030/RS//
dc.relationinfo:eu-repo/grantAgreement/MESTD/inst-2020/200015/RS//
dc.rightsopenAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceFrontiers in Nutrition
dc.subjectdesaturase
dc.subjectfatty acids
dc.subjectcardiometabolic risk
dc.subjectobesity
dc.subjectmetabolic syndrome
dc.subjectadiposity
dc.subjectlipid
dc.subjectwomen
dc.titleAssociations of fatty acids composition and estimated desaturase activities in erythrocyte phospholipids with biochemical and clinical indicators of cardiometabolic risk in non-diabetic Serbian women: the role of level of adiposity
dc.typearticleen
dc.rights.licenseBY
dc.citation.volume10
dc.identifier.doi10.3389/fnut.2023.1065578
dc.identifier.fulltexthttp://rimi.imi.bg.ac.rs/bitstream/id/3087/Associations_of_fatty_acids_composition_and_estimated_pub_2023.pdf
dc.identifier.rcubhttps://hdl.handle.net/21.15107/rcub_rimi_1345
dc.type.versionpublishedVersion


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