Long-term benefits of atorvastatin on the incidence of cardiovascular events: the ASCOT-Legacy 20-year follow-up
AimsCardiovascular (CV) deaths were reduced by atorvastatin during a 16-year follow-up of participants in the Anglo-Scandinavian Cardiac Outcomes Trial-lipid-lowering arm. We now extend these observations over 20 years and report both non-fatal and fatal CV outcomes.MethodsA cohort of 4605 UK hypert...
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Published in | Heart (British Cardiac Society) Vol. 111; no. 16; pp. 769 - 775 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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England
BMJ Publishing Group Ltd and British Cardiovascular Society
01.08.2025
BMJ Publishing Group LTD |
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Online Access | Get full text |
ISSN | 1355-6037 1468-201X |
DOI | 10.1136/heartjnl-2024-325104 |
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Abstract | AimsCardiovascular (CV) deaths were reduced by atorvastatin during a 16-year follow-up of participants in the Anglo-Scandinavian Cardiac Outcomes Trial-lipid-lowering arm. We now extend these observations over 20 years and report both non-fatal and fatal CV outcomes.MethodsA cohort of 4605 UK hypertensive participants with total cholesterol <6.5 mmol/L (2317 atorvastatin vs 2288 placebo) was followed for up to 21 years (IQR 9.1–19.3). Cox proportional hazard models assessed HRs for non-fatal and fatal CV events. At the end of the original trial (3.3 years), all participants were offered atorvastatin. Lipid profiles were obtained from all subjects 2 years later and from subgroups approximately 9 years post-trial.ResultsPatients allocated to atorvastatin had a significant reduction in non-fatal myocardial infarction (MI) and fatal coronary heart disease (CHD) events (HR (95% CI) 0.81 (0.69 to 0.94, p=0.006)), total coronary events (0.88 (0.80 to 0.98, p=0.017)) and CV deaths (0.86 (0.74 to 0.99, p=0.048)). No significant reduction in heart failure (HF), strokes, total CV events and all-cause mortality was observed.In participants assigned atorvastatin in the trial, 3-year mean low-density lipoprotein-cholesterol was strongly associated with long-term CV outcomes. The HRs per 1 mmol/L decrease were for non-fatal MI and fatal CHD (0.69 (0.57 to 0.85, p<0.001)), total coronary events (0.70 (0.61 to 0.79, p<0.001)), non-fatal and fatal HF (0.68 (0.57 to 0.81, p<0.001)), non-fatal and fatal stroke (0.74 (0.59 to 0.92, p=0.006)), total CV events and procedures (0.74 (0.66 to 0.81, p<0.001)), CV mortality (0.66 (0.55 to 0.81, p<0.001)) and all-cause mortality (0.81 (0.71 to 0.90, p<0.001)).Two years after the trial, approximately two-thirds of subjects in each arm were taking atorvastatin. At this time point and approximately 9 years post-trial, lipid profiles were similar between those formerly assigned atorvastatin or placebo.ConclusionsThese observations provide further evidence for the long-term legacy effects of statins and have implications for the early introduction of statins to prevent CV events and mortality. |
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AbstractList | AimsCardiovascular (CV) deaths were reduced by atorvastatin during a 16-year follow-up of participants in the Anglo-Scandinavian Cardiac Outcomes Trial-lipid-lowering arm. We now extend these observations over 20 years and report both non-fatal and fatal CV outcomes.MethodsA cohort of 4605 UK hypertensive participants with total cholesterol <6.5 mmol/L (2317 atorvastatin vs 2288 placebo) was followed for up to 21 years (IQR 9.1–19.3). Cox proportional hazard models assessed HRs for non-fatal and fatal CV events. At the end of the original trial (3.3 years), all participants were offered atorvastatin. Lipid profiles were obtained from all subjects 2 years later and from subgroups approximately 9 years post-trial.ResultsPatients allocated to atorvastatin had a significant reduction in non-fatal myocardial infarction (MI) and fatal coronary heart disease (CHD) events (HR (95% CI) 0.81 (0.69 to 0.94, p=0.006)), total coronary events (0.88 (0.80 to 0.98, p=0.017)) and CV deaths (0.86 (0.74 to 0.99, p=0.048)). No significant reduction in heart failure (HF), strokes, total CV events and all-cause mortality was observed.In participants assigned atorvastatin in the trial, 3-year mean low-density lipoprotein-cholesterol was strongly associated with long-term CV outcomes. The HRs per 1 mmol/L decrease were for non-fatal MI and fatal CHD (0.69 (0.57 to 0.85, p<0.001)), total coronary events (0.70 (0.61 to 0.79, p<0.001)), non-fatal and fatal HF (0.68 (0.57 to 0.81, p<0.001)), non-fatal and fatal stroke (0.74 (0.59 to 0.92, p=0.006)), total CV events and procedures (0.74 (0.66 to 0.81, p<0.001)), CV mortality (0.66 (0.55 to 0.81, p<0.001)) and all-cause mortality (0.81 (0.71 to 0.90, p<0.001)).Two years after the trial, approximately two-thirds of subjects in each arm were taking atorvastatin. At this time point and approximately 9 years post-trial, lipid profiles were similar between those formerly assigned atorvastatin or placebo.ConclusionsThese observations provide further evidence for the long-term legacy effects of statins and have implications for the early introduction of statins to prevent CV events and mortality. Cardiovascular (CV) deaths were reduced by atorvastatin during a 16-year follow-up of participants in the Anglo-Scandinavian Cardiac Outcomes Trial-lipid-lowering arm. We now extend these observations over 20 years and report both non-fatal and fatal CV outcomes. A cohort of 4605 UK hypertensive participants with total cholesterol <6.5 mmol/L (2317 atorvastatin vs 2288 placebo) was followed for up to 21 years (IQR 9.1-19.3). Cox proportional hazard models assessed HRs for non-fatal and fatal CV events. At the end of the original trial (3.3 years), all participants were offered atorvastatin. Lipid profiles were obtained from all subjects 2 years later and from subgroups approximately 9 years post-trial. Patients allocated to atorvastatin had a significant reduction in non-fatal myocardial infarction (MI) and fatal coronary heart disease (CHD) events (HR (95% CI) 0.81 (0.69 to 0.94, p=0.006)), total coronary events (0.88 (0.80 to 0.98, p=0.017)) and CV deaths (0.86 (0.74 to 0.99, p=0.048)). No significant reduction in heart failure (HF), strokes, total CV events and all-cause mortality was observed.In participants assigned atorvastatin in the trial, 3-year mean low-density lipoprotein-cholesterol was strongly associated with long-term CV outcomes. The HRs per 1 mmol/L decrease were for non-fatal MI and fatal CHD (0.69 (0.57 to 0.85, p<0.001)), total coronary events (0.70 (0.61 to 0.79, p<0.001)), non-fatal and fatal HF (0.68 (0.57 to 0.81, p<0.001)), non-fatal and fatal stroke (0.74 (0.59 to 0.92, p=0.006)), total CV events and procedures (0.74 (0.66 to 0.81, p<0.001)), CV mortality (0.66 (0.55 to 0.81, p<0.001)) and all-cause mortality (0.81 (0.71 to 0.90, p<0.001)).Two years after the trial, approximately two-thirds of subjects in each arm were taking atorvastatin. At this time point and approximately 9 years post-trial, lipid profiles were similar between those formerly assigned atorvastatin or placebo. These observations provide further evidence for the long-term legacy effects of statins and have implications for the early introduction of statins to prevent CV events and mortality. |
Author | MacGregor, Graham Handrean, Soran Heller, Simon Whitehouse, Andrew Stanley, Adrian Rostamian, Somayeh Shakespeare, Carl Collier, David Hildick-Smith, David Dyker, Alexander Kristinsson, Arni Delles, Christian Mackay, Judith Milward, Ann Whiteley, William Aldegather, Jehad Reckless, John Webster, John Eaton, Mike Ariti, Cono Sever, Peter S Thom, Simon Gupta, Ajay Godec, Thomas Poulter, Neil R Stokes, Jacqueline Lip, Greg MacDonald, Tom O’Hare, Paul |
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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/40139683$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1161/CIRCULATIONAHA.115.019014 10.1016/j.jacl.2011.01.006 10.1016/S0140-6736(03)12948-0 10.1016/S0140-6736(18)31776-8 10.1016/S0140-6736(04)16936-5 10.1093/eurheartj/ehm583 10.1161/CIRCULATIONAHA.115.018580 10.1016/j.rec.2021.07.001 10.1016/S0140-6736(11)61125-2 10.1016/S0140-6736(24)00537-3 10.1371/journal.pmed.1001885 10.1097/00004872-200106000-00020 10.1056/NEJMoa2204233 10.1093/eurheartj/ehad814 |
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Contributor | Aldegather, Jehad Reckless, John Webster, John MacGregor, Graham Handrean, Soran Heller, Simon Eaton, Mike Stanley, Adrian Shakespeare, Carl Thom, Simon Collier, David Stokes, Jacqueline Lip, Greg Hildick-Smith, David O'Hare, Paul MacDonald, Tom Dyker, Alexander Kristinsson, Arni Delles, Christian Milward, Ann |
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Keywords | atherosclerosis pharmacology, clinical cardiovascular diseases hyperlipidemias |
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References | Sever, Dahlöf, Poulter (R1) 2003; 361 (R14) 2023; 388 Gupta, Mackay, Whitehouse (R3) 2018; 392 Ford, Murray, McCowan (R8) 2016; 133 Strandberg, Pyörälä, Cook (R10) 2004; 364 Gupta, Whiteley, Godec (R12) 2024; 45 Kostis, Moreyra, Cheng (R7) 2011; 5 Benchimol, Smeeth, Guttmann (R6) 2015; 12 Hague, Simes, Kirby (R9) 2016; 133 Sever, Dahlöf, Poulter (R4) 2001; 19 Rossello, González-Del-Hoyo (R5) 2022; 75 Adler, Coleman, Leal (R13) 2024; 404 (R11) 2011; 378 Sever, Poulter, Dahlof (R2) 2008; 29 |
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Snippet | AimsCardiovascular (CV) deaths were reduced by atorvastatin during a 16-year follow-up of participants in the Anglo-Scandinavian Cardiac Outcomes... Cardiovascular (CV) deaths were reduced by atorvastatin during a 16-year follow-up of participants in the Anglo-Scandinavian Cardiac Outcomes... |
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SubjectTerms | Aged Angina pectoris Anticholesteremic Agents - therapeutic use atherosclerosis Atorvastatin Blood pressure Cardiac risk factors and prevention Cardiovascular disease cardiovascular diseases Cardiovascular Diseases - epidemiology Cardiovascular Diseases - mortality Cardiovascular Diseases - prevention & control Cholesterol Female Follow-Up Studies Heart attacks Heart failure Heptanoic Acids - therapeutic use Humans Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use hyperlipidemias Hypertension Hypertension - complications Hypertension - drug therapy Incidence Lipids Male Middle Aged Mortality pharmacology, clinical Public health Pyrroles - therapeutic use Statins Stroke Time Factors Treatment Outcome United Kingdom - epidemiology |
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Title | Long-term benefits of atorvastatin on the incidence of cardiovascular events: the ASCOT-Legacy 20-year follow-up |
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