Abstract:
BACKGROUND:We characterised the phenotypic consequence of genetic variation at the PCSK9 locus and compared findings with recent trials of pharmacological inhibitors of PCSK9. METHODS:Published and individual participant level data (300,000+ participants) were combined to construct a weighted PCSK9 gene-centric score (GS). Seventeen randomized placebo controlled PCSK9 inhibitor trials were included, providing data on 79,578 participants. Results were scaled to a one mmol/L lower LDL-C concentration. RESULTS:The PCSK9 GS (comprising 4 SNPs) associations with plasma lipid and apolipoprotein levels were consistent in direction with treatment effects. The GS odds ratio (OR) for myocardial infarction (MI) was 0.53 (95% CI 0.42; 0.68), compared to a PCSK9 inhibitor effect of 0.90 (95% CI 0.86; 0.93). For ischemic stroke ORs were 0.84 (95% CI 0.57; 1.22) for the GS, compared to 0.85 (95% CI 0.78; 0.93) in the drug trials. ORs with type 2 diabetes mellitus (T2DM) were 1.29 (95% CI 1.11; 1.50) for the GS, as compared to 1.00 (95% CI 0.96; 1.04) for incident T2DM in PCSK9 inhibitor trials. No genetic associations were observed for cancer, heart failure, atrial fibrillation, chronic obstructive pulmonary disease, or Alzheimer's disease - outcomes for which large-scale trial data were unavailable. CONCLUSIONS:Genetic variation at the PCSK9 locus recapitulates the effects of therapeutic inhibition of PCSK9 on major blood lipid fractions and MI. While indicating an increased risk of T2DM, no other possible safety concerns were shown; although precision was moderate.
journal_name
BMC Cardiovasc Disordjournal_title
BMC cardiovascular disordersauthors
Schmidt AF,Holmes MV,Preiss D,Swerdlow DI,Denaxas S,Fatemifar G,Faraway R,Finan C,Valentine D,Fairhurst-Hunter Z,Hartwig FP,Horta BL,Hypponen E,Power C,Moldovan M,van Iperen E,Hovingh K,Demuth I,Norman K,Steinhagen-doi
10.1186/s12872-019-1187-zsubject
Has Abstractpub_date
2019-10-29 00:00:00pages
240issue
1issn
1471-2261pii
10.1186/s12872-019-1187-zjournal_volume
19pub_type
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pub_type: 临床试验,杂志文章,多中心研究
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