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Status: Bibliographieeintrag

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Verfasst von:Vries, Paul S. de [VerfasserIn]   i
 Brown, Michael R. [VerfasserIn]   i
 Bentley, Amy R. [VerfasserIn]   i
 Sung, Yun J. [VerfasserIn]   i
 Winkler, Thomas W. [VerfasserIn]   i
 Ntalla, Ioanna [VerfasserIn]   i
 Schwander, Karen [VerfasserIn]   i
 Kraja, Aldi T. [VerfasserIn]   i
 Guo, Xiuqing [VerfasserIn]   i
 Franceschini, Nora [VerfasserIn]   i
 Cheng, Ching-Yu [VerfasserIn]   i
 Sim, Xueling [VerfasserIn]   i
 Vojinovic, Dina [VerfasserIn]   i
 Huffman, Jennifer E. [VerfasserIn]   i
 Musani, Solomon K. [VerfasserIn]   i
 Li, Changwei [VerfasserIn]   i
 Feitosa, Mary F. [VerfasserIn]   i
 Richard, Melissa A. [VerfasserIn]   i
 Noordam, Raymond [VerfasserIn]   i
 Aschard, Hugues [VerfasserIn]   i
 Jonas, Jost B. [VerfasserIn]   i
Titel:Multiancestry genome-wide association study of lipid levels incorporating gene-alcohol interactions
Verf.angabe:Paul S. de Vries, Michael R. Brown, Amy R. Bentley, Yun J. Sung, Thomas W. Winkler, Ioanna Ntalla, Karen Schwander, Aldi T. Kraja, Xiuqing Guo, Nora Franceschini, Ching-Yu Cheng, Xueling Sim, Dina Vojinovic, Jennifer E. Huffman, Solomon K. Musani, Changwei Li, Mary F. Feitosa, Melissa A. Richard, Raymond Noordam, Hugues Aschard et al.
E-Jahr:2019
Jahr:January 29, 2019
Umfang:22 S.
Fussnoten:Gesehen am 04.10.2019
Titel Quelle:Enthalten in: American journal of epidemiology
Ort Quelle:Oxford : Oxford Univ. Press, 1921
Jahr Quelle:2019
Band/Heft Quelle:188(2019), 6, Seite 1033-1054
ISSN Quelle:1476-6256
Abstract:A person's lipid profile is influenced by genetic variants and alcohol consumption, but the contribution of interactions between these exposures has not been studied. We therefore incorporated gene-alcohol interactions into a multiancestry genome-wide association study of levels of high-density lipoprotein cholesterol, low-density lipoprotein cholesterol, and triglycerides. We included 45 studies in stage 1 (genome-wide discovery) and 66 studies in stage 2 (focused follow-up), for a total of 394,584 individuals from 5 ancestry groups. Analyses covered the period July 2014-November 2017. Genetic main effects and interaction effects were jointly assessed by means of a 2-degrees-of-freedom (df) test, and a 1-df test was used to assess the interaction effects alone. Variants at 495 loci were at least suggestively associated (P < 1 x 10(-6)) with lipid levels in stage 1 and were evaluated in stage 2, followed by combined analyses of stage 1 and stage 2. In the combined analysis of stages 1 and 2, a total of 147 independent loci were associated with lipid levels at P < 5 x 10(-8) using 2-df tests, of which 18 were novel. No genome-wide-significant associations were found testing the interaction effect alone. The novel loci included several genes (proprotein convertase subtilisin/kexin type 5 (PCSK5), vascular endothelial growth factor B (VEGFB), and apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1 (APOBEC1) complementation factor (A1CF)) that have a putative role in lipid metabolism on the basis of existing evidence from cellular and experimental models.
DOI:doi:10.1093/aje/kwz005
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: https://doi.org/10.1093/aje/kwz005
 Volltext: https://academic.oup.com/aje/article/188/6/1033/5304469
 DOI: https://doi.org/10.1093/aje/kwz005
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:alcohol consumption
 blood-lipids
 cholesterol
 consumption
 coronary-heart-disease
 density-lipoprotein cholesterol
 gene-environment interactions
 gene-lifestyle interactions
 genome-wide association studies
 hdl cholesterol
 individuals
 lipids
 low-frequency
 metaanalysis
 plasma
 triglycerides
 vegf-b
K10plus-PPN:1678136336
Verknüpfungen:→ Zeitschrift

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