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- apolipoproteins2
- genetics2
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JLR Patient-Oriented and Epidemiological Research
4 Results
- Patient-Oriented and Epidemiological ResearchOpen Access
Macronutrient-specific effect of the MTNR1B genotype on lipid levels in response to 2 year weight-loss diets
Journal of Lipid ResearchVol. 59Issue 1p155–161Published online: October 31, 2017- Leticia Goni
- Dianjianyi Sun
- Yoriko Heianza
- Tiange Wang
- Tao Huang
- Marta Cuervo
- and others
Cited in Scopus: 14Compelling evidence indicates that lipid metabolism is in partial control of the circadian system. In this context, it has been reported that the melatonin receptor 1B (MTNR1B) genetic variant influences the dynamics of melatonin secretion, which is involved in the circadian system as a chronobiotic. The objective was to analyze whether the MTNR1B rs10830963 genetic variant was related to changes in lipid levels in response to dietary interventions with different macronutrient distribution in 722 overweight/obese subjects from the POUNDS Lost trial. - Patient-Oriented and Epidemiological ResearchOpen Access
Associations of genetic variants for adult lipid levels with lipid levels in children. The Generation R Study
Journal of Lipid ResearchVol. 57Issue 12p2185–2192Published online: October 24, 2016- Ardashel Latsuzbaia
- Vincent W.V. Jaddoe
- Albert Hofman
- Oscar H. Franco
- Janine F. Felix
Cited in Scopus: 7Lipid concentrations are heritable traits. Recently, the number of known genetic loci associated with lipid levels in adults increased from 95 to 157. The effects of these 157 loci have not been tested in children. Considering that lipid levels track from childhood to adulthood, we studied to determine whether these variants already affected lipid concentrations in a large group of 2,645 children with a median age of 6.0 years (95% range 5.7–7.3 years) from the population-based Generation R Study. - Patient-Oriented and Epidemiological ResearchOpen Access
Global molecular analysis and APOE mutations in a cohort of autosomal dominant hypercholesterolemia patients in France
Journal of Lipid ResearchVol. 57Issue 3p482–491Published online: January 22, 2016- René Wintjens
- Dominique Bozon
- Khaldia Belabbas
- Félicien MBou
- Jean-Philippe Girardet
- Patrick Tounian
- and others
Cited in Scopus: 20Autosomal dominant hypercholesterolemia (ADH) is a human disorder characterized phenotypically by isolated high-cholesterol levels. Mutations in the low density lipoprotein receptor (LDLR), APOB, and proprotein convertase subtilisin/kexin type 9 (PCSK9) genes are well known to be associated with the disease. To characterize the genetic background associated with ADH in France, the three ADH-associated genes were sequenced in a cohort of 120 children and 109 adult patients. Fifty-one percent of the cohort had a possible deleterious variant in LDLR, 3.1% in APOB, and 1.7% in PCSK9. - 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.