Associations between Common and Rare Exonic Genetic Variants and Serum Levels of 20 Cardiovascular-Related Proteins: The Tromsø Study

• Published in: Circulation: Cardiovascular Genetics
• Main Authors: Solomon, Terry, Smith, Erin N., Matsui, Hiroko, Brækkan, Sigrid Kufaas, Wilsgaard, Tom, Njølstad, Inger, Mathiesen, Ellisiv B., Hansen, John-Bjarne, Frazer, Kelly A.
• Format: Article in Journal/Newspaper
• Language: English
• Published: American Heart Association 2016
• Subjects: VDP::Medisinske Fag: 700::Basale medisinske; odontologiske og veterinærmedisinske fag: 710::Medisinsk genetikk: 714; VDP::Medical disciplines: 700::Basic medical; dental and veterinary science disciplines: 710::Medical genetics: 714; biomarker; coronary artery disease; exome; human; protein; venous thromboembolism; Tromsø
• Online Access: https://hdl.handle.net/10037/10554; https://doi.org/10.1161/CIRCGENETICS.115.001327

Published version. Source at http://dx.doi.org/10.1161/CIRCGENETICS.115.001327 Background—Genetic variation can be used to study causal relationships between biomarkers and diseases. Here, we identify new common and rare genetic variants associated with cardiovascular-related protein levels (protein quantitative trait loci [pQTLs]). We functionally annotate these pQTLs, predict and experimentally confirm a novel molecular interaction, and determine which pQTLs are associated with diseases and physiological phenotypes. Methods and Results—As part of a larger case–control study of venous thromboembolism, serum levels of 51 proteins implicated in cardiovascular diseases were measured in 330 individuals from the Tromsø Study. Exonic genetic variation near each protein’s respective gene (cis) was identified using sequencing and arrays. Using single site and gene-based tests, we identified 27 genetic associations between pQTLs and the serum levels of 20 proteins: 14 associated with common variation in cis, of which 6 are novel (ie, not previously reported); 7 associations with rare variants in cis, of which 4 are novel; and 6 associations in trans. Of the 20 proteins, 15 were associated with single sites and 7 with rare variants. cis-pQTLs for kallikrein and F12 also show trans associations for proteins (uPAR, kininogen) known to be cleaved by kallikrein and with NTproBNP. We experimentally demonstrate that kallikrein can cleave proBNP (NTproBNP precursor) in vitro. Nine of the pQTLs have previously identified associations with 17 disease and physiological phenotypes. Conclusions—We have identified cis and trans genetic variation associated with the serum levels of 20 proteins and utilized these pQTLs to study molecular mechanisms underlying disease and physiological phenotypes.