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JLR Patient-Oriented and Epidemiological Research
2 Results
- Patient-Oriented and Epidemiological ResearchOpen Access
Epigenome-wide association study of triglyceride postprandial responses to a high-fat dietary challenge
Journal of Lipid ResearchVol. 57Issue 12p2200–2207Published online: October 24, 2016- Chao-Qiang Lai
- Mary K. Wojczynski
- Laurence D. Parnell
- Bertha A. Hidalgo
- Marguerite Ryan Irvin
- Stella Aslibekyan
- and others
Cited in Scopus: 27Postprandial lipemia (PPL), the increased plasma TG concentration after consuming a high-fat meal, is an independent risk factor for CVD. Individual responses to a meal high in fat vary greatly, depending on genetic and lifestyle factors. However, only a few loci have been associated with TG-PPL response. Heritable epigenomic changes may be significant contributors to the unexplained inter-individual PPL variability. We conducted an epigenome-wide association study on 979 subjects with DNA methylation measured from CD4+ T cells, who were challenged with a high-fat meal as a part of the Genetics of Lipid Lowering Drugs and Diet Network study. - Patient-Oriented and Epidemiological ResearchOpen Access
Levels of atherogenic lipoproteins are unexpectedly reduced in interstitial fluid from type 2 diabetes patients
Journal of Lipid ResearchVol. 56Issue 8p1633–1639Published online: June 19, 2015- Johanna Apro
- Paolo Parini
- Anders Broijersén
- Bo Angelin
- Mats Rudling
Cited in Scopus: 6At a given level of serum cholesterol, patients with T2D have an increased risk of developing atherosclerosis compared with nondiabetic subjects. We hypothesized that T2D patients have an increased interstitial fluid (IF)-to-serum gradient ratio for LDL, due to leakage over the vascular wall. Therefore, lipoprotein profiles in serum and IF from 35 T2D patients and 35 healthy controls were assayed using fast performance liquid chromatography. The IF-to-serum gradients for VLDL and LDL cholesterol, as well as for apoB, were clearly reduced in T2D patients compared with healthy controls.