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Common and Low-Frequency Genetic Variants in the PCSK9 Locus Influence Circulating PCSK9 Levels

Chernogubova, Ekaterina (author)
Karolinska Institutet
Strawbridge, Rona (author)
Karolinska Institutet
Mahdessian, Hovsep (author)
Karolinska Institutet
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Malarstig, Anders (author)
Karolinska Institutet
Krapivner, Sergey (author)
Gigante, Bruna (author)
Karolinska Institutet
Hellenius, Mai-Lis (author)
Karolinska Institutet
de Faire, Ulf (author)
Karolinska Institutet
Franco-Cereceda, Anders (author)
Karolinska Institutet
Syvänen, Ann-Christine (author)
Uppsala universitet,Molekylär medicin
Troutt, Jason S. (author)
Konrad, Robert J. (author)
Eriksson, Per (author)
Karolinska Institutet
Hamsten, Anders (author)
Karolinska Institutet
van 't Hooft, Ferdinand M. (author)
Karolinska Institutet
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 (creator_code:org_t)
2012
2012
English.
In: Arteriosclerosis, Thrombosis and Vascular Biology. - 1079-5642 .- 1524-4636. ; 32:6, s. 1526-1534
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Objective- Proprotein convertase subtilisin/kexin type 9 (PCSK9) is a circulating protein that influences plasma low-density lipoprotein concentration and susceptibility to coronary heart disease. Circulating PCSK9 levels show considerable interindividual differences, but the factors responsible for this variation are largely unknown. Methods and Results- We analyzed circulating PCSK9 levels in 4 cohorts of healthy, middle-aged Swedes (n=5722) and found that PCSK9 levels varied over approximate to 50-fold range, showed a positive relationship with plasma low-density lipoprotein-cholesterol concentration, and were associated with plasma triglyceride, fibrinogen, insulin, and glucose concentrations. A genome-wide association study conducted in 2 cohorts (n=1215) failed to uncover common genetic variants robustly associated with variation in circulating PCSK9 level. As expected, the minor allele of the PCSK9 R46L variant was in all cohorts associated with reduced PCSK9 levels and decreased plasma low-density lipoprotein-cholesterol concentrations, but no relationship was observed with the plasma triglyceride concentration. Further mapping of the PCSK9 locus revealed a common polymorphism (rs2479415, minor allele frequency 43.9%), located approximate to 6 kb upstream from PCSK9, which is independently associated with increased circulating PCSK9 levels. Conclusion- Common and low-frequency genetic variants in the PCSK9 locus influence the pronounced interindividual variation in circulating PCSK9 levels in healthy, middle-aged white (predominantly Swedish) subjects.

Keyword

dense mapping
genetic variants
genome-wide association study
low-density lipoprotein cholesterol
proprotein convertase subtilisin/kexin type 9

Publication and Content Type

ref (subject category)
art (subject category)

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