452
IRUS Total
Downloads
  Altmetric

Low-density lipoproteins cause atherosclerotic cardiovascular disease. 1. Evidence from genetic, epidemiologic and clinical studies A Consensus Statement from the European Atherosclerosis Society Consensus Panel

File Description SizeFormat 
ehx144.pdfPublished version1.23 MBAdobe PDFView/Open
Title: Low-density lipoproteins cause atherosclerotic cardiovascular disease. 1. Evidence from genetic, epidemiologic and clinical studies A Consensus Statement from the European Atherosclerosis Society Consensus Panel
Authors: Ference, BA
Ginsberg, HN
Graham, I
Ray, KK
Packard, CJ
Bruckert, E
Hegele, RA
Krauss, RM
Raal, FJ
Schunkert, H
Watts, GF
Boren, J
Fazio, S
Horton, JD
Masana, L
Nicholls, SJ
Nordestgaard, BG
Van de Sluis, B
Taskinen, M
Tokgozoglu, L
Landmesser, U
Laufs, U
Wiklund, O
Stock, JK
Chapman, MJ
Catapano, AL
Item Type: Journal Article
Abstract: Aim: To appraise the clinical and genetic evidence that low-density lipoproteins (LDL) cause atherosclerotic cardiovascular disease (ASCVD). Methods and Results: We assessed whether the association between LDL and ASCVD fulfills the criteria for causality by evaluating the totality of evidence from genetic studies, prospective epidemiologic cohort studies, Mendelian randomization studies, and randomized trials of LDL-lowering therapies. In clinical studies, plasma LDL burden is usually estimated by determination of plasma LDL cholesterol level (LDL C). Rare genetic mutations that cause reduced LDL receptor function lead to markedly higher LDL-C and a dose-dependent increase in the risk of ASCVD, whereas rare variants leading to lower LDL-C are associated with a correspondingly lower risk of ASCVD. Separate meta-analyses of over 200 prospective cohort studies, Mendelian randomization studies, and randomized trials including more than 2 million participants with over 20 million person-years of follow-up and over 150,000 cardiovascular events demonstrate a remarkably consistent dose-dependent log-linear association between the absolute magnitude of exposure of the vasculature to LDL-C and the risk of ASCVD; and this effect appears to increase with increasing duration of exposure to LDL-C. Both the naturally randomized genetic studies and the randomized intervention trials consistently demonstrate that any mechanism of lowering plasma LDL particle concentration should reduce the risk of ASCVD events proportional to the absolute reduction in LDL-C and the cumulative duration of exposure to lower LDL-C, provided that the achieved reduction in LDL-C is concordant with the reduction in LDL particle number and that there are no competing deleterious off-target effects. Conclusion: Consistent evidence from numerous and multiple different types of clinical and genetic studies unequivocally establishes that LDL causes ASCVD.
Issue Date: 24-Apr-2017
Date of Acceptance: 1-Mar-2017
URI: http://hdl.handle.net/10044/1/45373
DOI: https://dx.doi.org/10.1093/eurheartj/ehx144
ISSN: 1522-9645
Publisher: Oxford University Press (OUP)
Start Page: 2459
End Page: 2472
Journal / Book Title: European Heart Journal
Volume: 38
Issue: 32
Copyright Statement: © The Author 2017. Published on behalf of the European Society of Cardiology. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
Keywords: Science & Technology
Life Sciences & Biomedicine
Cardiac & Cardiovascular Systems
Cardiovascular System & Cardiology
Atherosclerosis
Cardiovascular disease
Low-density lipoprotein
Mendelian randomization
Clinical trials
Statin
Ezetimibe
PCSK9
Causality
Recommendations
CORONARY-HEART-DISEASE
HOMOZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA
CHOLESTEROL-FED RABBITS
STATIN THERAPY
MENDELIAN RANDOMIZATION
LDL CHOLESTEROL
GENERAL-POPULATION
RISK
METAANALYSIS
TRIAL
1102 Cardiovascular Medicine And Haematology
Cardiovascular System & Hematology
Publication Status: Published
Appears in Collections:School of Public Health