Affiliation:
1. Department of Clinical Therapeutics National and Kapodistrian University of Athens School of Medicine Athens Greece
2. School of Biomedical Engineering and Imaging Sciences Kings College London London UK
3. Department of Hygiene and Epidemiology University of Ioannina Medical School Ioannina Greece
Abstract
AbstractBackgroundIn this study we used Mendelian randomization (MR) to investigate the potential causal association of lipoprotein (a) [Lp(a)] levels with pulse wave velocity (PWV).MethodsGenetic variants associated with Lp(a) were retrieved from the UK Biobank GWAS (N = 290,497). A non‐ overlapping GWAS based on a European cohort (N = 7,000) was used to obtain genetic associations with PWV (outcome) and utilized two different measures for the same trait, brachial–ankle (baPWV) and carotid–femoral (cfPWV) PWV. We applied a two‐sample MR using the inverse variance weighting method (IVW) and a series of sensitivity analyses for 170 SNPs that were selected as instrumental variables (IVs).ResultsOur analyses do not support a causal association between Lp(a) and PWV for neither measurement [βiwv(baPWV) = −.0005, p = .8 and βiwv(cfPWV) = −.006, p = .16]. The above findings were consistent across sensitivity analyses including weighted median, mode‐based estimation, MR‐Egger regression and MR‐PRESSO.ConclusionWe did not find evidence indicating that Lp(a) is causally associated with PWV, the gold standard marker of arterial stiffness.
Subject
Clinical Biochemistry,Biochemistry,General Medicine