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

被引:3113
作者
Ference, Brian A. [1 ]
Ginsberg, Henry N. [2 ]
Graham, Ian [3 ]
Ray, Kausik K. [4 ]
Packard, Chris J. [5 ]
Bruckert, Eric [6 ]
Hegele, Robert A. [7 ]
Krauss, Ronald M. [8 ]
Raal, Frederick J. [9 ]
Schunkert, Heribert [10 ,11 ]
Watts, Gerald F. [12 ]
Boren, Jan [13 ]
Fazio, Sergio [14 ]
Horton, Jay D. [15 ,16 ]
Masana, Luis [17 ]
Nicholls, Stephen J. [18 ]
Nordestgaard, Borge G. [19 ,20 ,21 ,22 ]
van de Sluis, Bart [23 ]
Taskinen, Marja-Riitta [24 ,25 ]
Tokgozoglu, Lale [26 ]
Landmesser, Ulf [27 ,28 ]
Laufs, Ulrich [29 ]
Wiklund, Olov [30 ,31 ]
Stock, Jane K. [32 ]
Chapman, M. John [33 ,34 ]
Catapano, Alberico L. [35 ,36 ]
机构
[1] Wayne State Univ, Sch Med, Div Cardiovasc Med, Div Translat Res & Clin Epidemiol, Detroit, MI 48202 USA
[2] Columbia Univ, Irving Inst Clin & Translat Res, New York, NY USA
[3] Trinity Coll Dublin, Dublin, Ireland
[4] Imperial Coll, Imperial Ctr Cardiovasc Dis Prevent, Dept Primary Care & Publ Hlth, London, England
[5] Univ Glasgow, Coll Med Vet & Life Sci, Glasgow, Lanark, Scotland
[6] Hop La Pitie, AP HP, ICAN Inst CardioMetab & Nutr, Dept Endocrinol Metab,INSERM UMRS1166, Paris, France
[7] Univ Western Ontario, Schulich Sch Med & Dent, Robarts Res Inst, Dept Med, London, ON, Canada
[8] Childrens Hosp Oakland, Res Inst, Dept Atherosclerosis Res, Oakland, CA 94609 USA
[9] Univ Witwatersrand, Fac Hlth Sci, Johannesburg, South Africa
[10] Tech Univ Munich, Deutsch Herzzentrum Munchen, D-80636 Munich, Germany
[11] Partner Site Munich Heart Alliance, DZHK, D-81377 Munich, Germany
[12] Univ Western Australia, Royal Perth Hosp, Sch Med & Pharmacol, Ctr Cardiovasc Med,Lipid Disorders Clin, Perth, WA, Australia
[13] Univ Gothenburg, Sahlgrenska Univ Hosp, Dept Mol & Clin Med, Wallenberg Lab, Gothenburg, Sweden
[14] Oregon Hlth & Sci Univ, Dept Med, Knight Cardiovasc Inst, Ctr Prevent Cardiol, Portland, OR 97201 USA
[15] Univ Texas Southwestern Med Ctr Dallas, Dept Mol Genet, Dallas, TX USA
[16] Univ Texas Southwestern Med Ctr Dallas, Dept Internal Med, Dallas, TX USA
[17] Univ Rovira & Virgili, Res Unit Lipids & Atherosclerosis, C Sant Llorenc 21, Reus 43201, Spain
[18] Univ Adelaide, South Australian Hlth & Med Res Inst, Adelaide, SA, Australia
[19] Copenhagen Univ Hosp, Dept Clin Biochem, Copenhagen, Denmark
[20] Copenhagen Univ Hosp, Herlev & Gentofte Hosp, Copenhagen Gen Populat Study, Copenhagen, Denmark
[21] Univ Copenhagen, Fac Hlth & Med Sci, Copenhagen, Denmark
[22] Copenhagen Univ Hosp, Frederiksberg Hosp, Copenhagen City Heart Study, Copenhagen, Denmark
[23] Univ Groningen, Univ Med Ctr Groningen, Dept Pediat, Mol Genet Sect, Antonius Deusinglaan 1, NL-9713 AV Groningen, Netherlands
[24] Univ Helsinki, Cent Hosp, Helsinki, Finland
[25] Univ Helsinki, Diabet & Obes Heart & Lung Ctr, Res Programs Unit, Helsinki, Finland
[26] Hacettepe Univ, Ankara, Turkey
[27] Charite Univ Med Berlin CBF, Dept Cardiol, Hindenburgdamm 30, D-12203 Berlin, Germany
[28] DZHK, BIH, Berlin, Germany
[29] Univ Klinikum Saarlandes, Kardiol Angiol & Internist Intensivmed, Klin Innere Med 3, Homburg, Germany
[30] Univ Gothenburg, Dept Mol & Clin Med, Gothenburg, Sweden
[31] Sahlgrens Univ Hosp, Dept Cardiol, Gothenburg, Sweden
[32] European Atherosclerosis Soc, Gothenburg, Sweden
[33] INSERM, Dyslipidemia & Atherosclerosis Res, Paris, France
[34] Univ Paris 06, Pitie Salpetriere Univ Hosp, Paris, France
[35] Univ Milan, Dept Pharmacol & Biomol Sci, Milan, Italy
[36] IRCCS Multimed, Milan, Italy
关键词
Atherosclerosis; Cardiovascular disease; Low-density lipoprotein; Mendelian randomization; Clinical trials; Statin; Ezetimibe; PCSK9; Causality; Recommendations; CORONARY-HEART-DISEASE; FAMILIAL HYPERCHOLESTEROLEMIA; STATIN THERAPY; MENDELIAN RANDOMIZATION; LDL CHOLESTEROL; GENERAL-POPULATION; RISK; ASSOCIATION; RETENTION; EZETIMIBE;
D O I
10.1093/eurheartj/ehx144
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Aims To appraise the clinical and genetic evidence that low-density lipoproteins (LDLs) cause atherosclerotic cardiovascular disease (ASCVD). Methods and results We assessed whether the association between LDL and ASCVD fulfils 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.
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收藏
页码:2459 / 2472
页数:14
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