Newly identified loci that influence lipid concentrations and risk of coronary artery disease Article Swipe
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· 2019
· Open Access
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· DOI: https://doi.org/10.17615/kfwc-pe72
To identify genetic variants influencing plasma lipid concentrations, we first used genotype imputation and meta-analysis to combine three genome-wide scans totaling 8,816 individuals and comprising 6,068 individuals specific to our study (1,874 individuals from the FUSION study of type 2 diabetes and 4,184 individuals from the SardiNIA study of aging-associated variables) and 2,758 individuals from the Diabetes Genetics Initiative, reported in a companion study in this issue. We subsequently examined promising signals in 11,569 additional individuals. Overall, we identify strongly associated variants in eleven loci previously implicated in lipid metabolism (ABCA1, the APOA5-APOA4-APOC3-APOA1 and APOE-APOC clusters, APOB, CETP, GCKR, LDLR, LPL, LIPC, LIPG and PCSK9) and also in several newly identified loci (near MVK-MMAB and GALNT2, with variants primarily associated with high-density lipoprotein (HDL) cholesterol; near SORT1, with variants primarily associated with low-density lipoprotein (LDL) cholesterol; near TRIB1, MLXIPL and ANGPTL3, with variants primarily associated with triglycerides; and a locus encompassing several genes near NCAN, with variants strongly associated with both triglycerides and LDL cholesterol). Notably, the 11 independent variants associated with increased LDL cholesterol concentrations in our study also showed increased frequency in a sample of coronary artery disease cases versus controls.
Related Topics
- Type
- article
- Language
- en
- Landing Page
- https://doi.org/10.17615/kfwc-pe72
- OA Status
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- Related Works
- 10
- OpenAlex ID
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Raw OpenAlex JSON
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https://openalex.org/W4298249387Canonical identifier for this work in OpenAlex
- DOI
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https://doi.org/10.17615/kfwc-pe72Digital Object Identifier
- Title
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Newly identified loci that influence lipid concentrations and risk of coronary artery diseaseWork title
- Type
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articleOpenAlex work type
- Language
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enPrimary language
- Publication year
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2019Year of publication
- Publication date
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2019-08-17Full publication date if available
- Authors
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Cristen J. Willer, Serena Sanna, Anne Jackson, Angelo Scuteri, Lori L. Bonnycastle, Robert Clarke, Simon Heath, Nicholas J. Timpson, Samer S. Najjar, Heather M. Stringham, James Strait, William L. Duren, Andrea Maschio, Fabio Busonero, Antonella Mulas, Giuseppe Albai, Amy J. Swift, Mario A. Morken, Narisu Narisu, Derrick Bennett, Sarah Parish, Haiqing Shen, Pilar Galán, Pierre Meneton, Serge Herçberg, Diana Zélénika, Wei-Min Chen, Yun Li, Laura J. Scott, Paul Scheet, Jouko Sundvall, Richard M. Watanabe, Ramaiah Nagaraja, Shah Ebrahim, Debbie A. Lawlor, Yoav Ben‐Shlomo, George Davey Smith, Alan R. Shuldiner, Rory Collins, Richard N. Bergman, Manuela Uda, Jaakko Tuomilehto, Antonio Cao, Francis S. Collins, Edward G. Lakatta, G.M. Lathrop, Michael Boehnke, David Schlessinger, Karen L. Mohlke, Gonçalo R. AbecasisList of authors in order
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YesWhether a free full text is available
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greenOpen access status per OpenAlex
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https://doi.org/10.17615/kfwc-pe72Direct OA link when available
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Coronary artery disease, Internal medicine, Cardiology, Disease, Medicine, BiologyTop concepts (fields/topics) attached by OpenAlex
- Cited by
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0Total citation count in OpenAlex
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10Other works algorithmically related by OpenAlex
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