PMID- 37111220 OWN - NLM STAT- MEDLINE DCOM- 20230501 LR - 20230501 IS - 2072-6643 (Electronic) IS - 2072-6643 (Linking) VI - 15 IP - 8 DP - 2023 Apr 21 TI - Blood and Tissue Advanced Glycation End Products as Determinants of Cardiometabolic Disorders Focusing on Human Studies. LID - 10.3390/nu15082002 [doi] LID - 2002 AB - Cardiometabolic disorders are characterised by a cluster of interactive risk determinants such as increases in blood glucose, lipids and body weight, as well as elevated inflammation and oxidative stress and gut microbiome changes. These disorders are associated with onset of type 2 diabetes mellitus (T2DM) and cardiovascular disease (CVD). T2DM is strongly associated with CVD. Dietary advanced glycation end products (dAGEs) attributable from modern diets high in sugar and/or fat, highly processed foods and high heat-treated foods can contribute to metabolic etiologies of cardiometabolic disorders. This mini review aims to determine whether blood dAGEs levels and tissue dAGEs levels are determinants of the prevalence of cardiometabolic disorders through recent human studies. ELISA (enzyme-linked immunosorbent assay), high-performance liquid chromatography (HPLC), liquid chromatography-mass spectrometry (LC-MS) and gas chromatography-mass spectrometry (GC-MS) for blood dAGEs measurement and skin auto fluorescence (SAF) for skin AGEs measurement can be used. Recent human studies support that a diet high in AGEs can negatively influence glucose control, body weight, blood lipid levels and vascular health through the elevated oxidative stress, inflammation, blood pressure and endothelial dysfunction compared with a diet low in AGEs. Limited human studies suggested a diet high in AGEs could negatively alter gut microbiota. SAF could be considered as one of the predictors affecting risks for cardiometabolic disorders. More intervention studies are needed to determine how dAGEs are associated with the prevalence of cardiometabolic disorders through gut microbiota changes. Further human studies are conducted to find the association between CVD events, CVD mortality and total mortality through SAF measurement, and a consensus on whether tissue dAGEs act as a predictor of CVD is required. FAU - Kim, Yoona AU - Kim Y AUID- ORCID: 0000-0002-3924-8543 AD - Department of Food and Nutrition, Institute of Agriculture and Life Science, Gyeongsang National University, 501 Jinju-daero, Jinju 52828, Gyeongsangnam-do, Republic of Korea. LA - eng GR - NRF-2022R1F1A1063108./National Research Foundation of Korea (NRF)/ PT - Journal Article PT - Review DEP - 20230421 PL - Switzerland TA - Nutrients JT - Nutrients JID - 101521595 RN - 0 (Glycation End Products, Advanced) RN - 0 (Dietary Advanced Glycation End Products) SB - IM MH - Humans MH - *Diabetes Mellitus, Type 2 MH - Glycation End Products, Advanced/metabolism MH - Risk Factors MH - Diet MH - Inflammation MH - Dietary Advanced Glycation End Products MH - *Cardiovascular Diseases/etiology PMC - PMC10144557 OTO - NOTNLM OT - cardiometabolic disorders OT - dietary advanced glycation end products OT - skin auto fluorescence COIS- The authors declare no conflict of interest. EDAT- 2023/04/28 06:41 MHDA- 2023/05/01 06:42 PMCR- 2023/04/21 CRDT- 2023/04/28 01:45 PHST- 2023/04/04 00:00 [received] PHST- 2023/04/18 00:00 [revised] PHST- 2023/04/20 00:00 [accepted] PHST- 2023/05/01 06:42 [medline] PHST- 2023/04/28 06:41 [pubmed] PHST- 2023/04/28 01:45 [entrez] PHST- 2023/04/21 00:00 [pmc-release] AID - nu15082002 [pii] AID - nutrients-15-02002 [pii] AID - 10.3390/nu15082002 [doi] PST - epublish SO - Nutrients. 2023 Apr 21;15(8):2002. doi: 10.3390/nu15082002.