Cargando…
Variant rs10911021 that associates with coronary heart disease in type 2 diabetes, is associated with lower concentrations of circulating HDL cholesterol and large HDL particles but not with amino acids
AIMS: An intergenic locus on chromosome 1 (lead SNP rs10911021) was previously associated with coronary heart disease (CHD) in type 2 diabetes (T2D). Using data from the UCLEB consortium we investigated the relationship between rs10911021 and CHD in T2D, whether rs10911021 was associated with levels...
Autores principales: | Beaney, Katherine E., Cooper, Jackie A., McLachlan, Stela, Wannamethee, S. Goya, Jefferis, Barbara J., Whincup, Peter, Ben-Shlomo, Yoav, Price, Jacqueline F., Kumari, Meena, Wong, Andrew, Ong, Ken, Hardy, Rebecca, Kuh, Diana, Kivimaki, Mika, Kangas, Antti J., Soininen, Pasi, Ala-Korpela, Mika, Drenos, Fotios, Humphries, Steve E. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4994200/ https://www.ncbi.nlm.nih.gov/pubmed/27549350 http://dx.doi.org/10.1186/s12933-016-0435-0 |
Ejemplares similares
-
Impaired HDL2-mediated cholesterol efflux is associated with metabolic syndrome in families with early onset coronary heart disease and low HDL-cholesterol level
por: Paavola, Timo, et al.
Publicado: (2017) -
Marginal role for 53 common genetic variants in cardiovascular disease prediction
por: Morris, Richard W, et al.
Publicado: (2016) -
Commentary: Big data bring big controversies: HDL cholesterol and mortality
por: Ala-Korpela, Mika, et al.
Publicado: (2021) -
Quantitative high-throughput metabolomics: a new era in epidemiology and genetics
por: Ala-Korpela, Mika, et al.
Publicado: (2012) -
Trans-ancestry Fine Mapping and Molecular Assays Identify Regulatory Variants at the ANGPTL8 HDL-C GWAS Locus
por: Cannon, Maren E., et al.
Publicado: (2017)