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Author
- An, Ping1
- Arnett, Donna K1
- Aslibekyan, Stella1
- Borecki, Ingrid1
- Bray, George A1
- Cuervo, Marta1
- Dave, Tushar1
- Feitosa, Mary F1
- Felix, Janine F1
- Franco, Oscar H1
- Frazier-Wood, Alexis C1
- Geng, Xin1
- Goni, Leticia1
- Heianza, Yoriko1
- Hidalgo, Bertha1
- Hofman, Albert1
- Hopkins, Paul N1
- Huang, Tao1
- Irvin, Marguerite R1
- Jaddoe, Vincent WV1
- Latsuzbaia, Ardashel1
- Martínez, J Alfredo1
- Mitchell, Braxton D1
- Ordovas, Jose M1
- Province, Michael A1
Keyword
- low density lipoprotein2
- clinical trials1
- diet and dietary lipids1
- dyslipidemias1
- epidemiology1
- gene-diet interaction1
- genetic risk score1
- high density lipoprotein1
- high-density lipoprotein1
- high-fat diet1
- lipid metabolism1
- low-density lipoprotein1
- melatonin receptor 1B1
- postprandial lipemia1
- rare variant1
- triglyceride1
- triglycerides1
- weight-loss intervention1
- whole-exome sequencing1
JLR Patient-Oriented and Epidemiological Research
3 Results
- Patient-Oriented and Epidemiological ResearchOpen Access
An exome-wide sequencing study of lipid response to high-fat meal and fenofibrate in Caucasians from the GOLDN cohort
Journal of Lipid ResearchVol. 59Issue 4p722–729Published online: January 20, 2018- Xin Geng
- Marguerite R. Irvin
- Bertha Hidalgo
- Stella Aslibekyan
- Vinodh Srinivasasainagendra
- Ping An
- and others
Cited in Scopus: 5Our understanding of genetic influences on the response of lipids to specific interventions is limited. In this study, we sought to elucidate effects of rare genetic variants on lipid response to a high-fat meal challenge and fenofibrate (FFB) therapy in the Genetics of Lipid Lowering Drugs and Diet Network (GOLDN) cohort using an exome-wide sequencing-based association study. Our results showed that the rare coding variants in ITGA7, SIPA1L2, and CEP72 are significantly associated with fasting LDL cholesterol response to FFB (P = 1.24E-07), triglyceride postprandial area under the increase (AUI) (P = 2.31E-06), and triglyceride postprandial AUI response to FFB (P = 1.88E-06), respectively. - 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.