Journal article
Metabolic syndrome cluster does not provide incremental prognostic information in patients with stable cardiovascular disease: A post hoc analysis of the AIM-HIGH trial
Journal of clinical lipidology, Vol.11(5), pp.1201-1211
09/2017
DOI: 10.1016/j.jacl.2017.06.017
PMCID: PMC5612889
PMID: 28807460
Abstract
Metabolic syndrome (MS) is a well-known risk factor for the development of cardiovascular (CV) disease; yet, controversy persists whether it adds incremental prognostic value in patients with established CV disease.
This study was performed to determine if MS is associated with worse CV outcomes in patients with established CV disease treated intensively with statins.
We performed a post hoc analysis of the Atherothrombosis Intervention in Metabolic Syndrome with Low HDL/High Triglycerides and Impact on Global Health Outcomes trial, in which patients with established CV disease and atherogenic dyslipidemia (n = 3414) were randomly assigned to receive extended release niacin or placebo during a mean 36-month follow-up, to assess whether the presence of MS or the number of MS components contributed to CV outcomes.
The composite primary end point of CV events occurred in 15.1% of patients without MS vs 13.8%, 16.9%, and 16.8% of patients with MS in the subsets with 3, 4, and 5 MS components, respectively (corresponding adjusted hazard ratios 0.9, 1.1, and 1.1 relative to patients without MS), P = .55. Comparing subgroups with 3 vs 4 or 5 MS components, there was no significant difference in either the composite primary end point or secondary end points. Patients with diabetes mellitus had higher event rates, with or without the presence of MS.
The presence of MS was not associated with worse CV outcomes in the AIM-HIGH population. The rate of CV events in statin-treated Atherothrombosis Intervention in Metabolic Syndrome with Low HDL/High Triglycerides and Impact on Global Health Outcomes patients with MS was not significantly influenced by the number of MS components.
•Metabolic syndrome (MS) did not affect progression of atherosclerotic cardiovascular disease (ASCVD).•The number of MS components did not predict cardiovascular outcomes in established ASCVD.•Diabetes mellitus but not MS was associated with higher events in patients with established ASCVD.
Details
- Title: Subtitle
- Metabolic syndrome cluster does not provide incremental prognostic information in patients with stable cardiovascular disease: A post hoc analysis of the AIM-HIGH trial
- Creators
- Radmila Lyubarova - Department of Medicine, Albany Medical Center, Albany Medical College, Albany, NY, USAJennifer G Robinson - Department of Epidemiology, College of Public Health, Carver College of Medicine, University of Iowa, Iowa City, IA, USAMichael Miller - Department of Medicine, University of Maryland Medical Center, Baltimore, MD, USADebra L Simmons - Department of Internal Medicine, University of Utah, Utah Diabetes and Endocrinology Center, Salt Lake City, UT, USAPing Xu - Axio Research LLC, Seattle, WA, USABeth L Abramson - Cardiac Prevention Centre and Women's Cardiovascular Health, St Michael's Hospital, University of Toronto, Toronto, Ontario, CanadaMarshall B Elam - Memphis VA Medical Center, Memphis, TN, USATodd M Brown - Department of Medicine, University of Alabama Health Science Center at Birmingham, Birmingham, AL, USARuth McBride - Axio Research LLC, Seattle, WA, USAJerome L Fleg - Division of Cardiovascular Science, National Institutes of Health, National Heart, Lung and Blood Institute, Bethesda, MD, USAPatrice Desvigne-Nickens - Division of Cardiovascular Science, National Institutes of Health, National Heart, Lung and Blood Institute, Bethesda, MD, USAWoubeshet Ayenew - Hennepin County Medical Center, Minneapolis, MN, USAWilliam E Boden - Department of Medicine, VA New England Healthcare System, Boston, MA, USAAtherothrombosis Intervention in Metabolic Syndrome with Low HDL/High Triglycerides and Impact on Global Health Outcomes (AIM-HIGH) Investigators
- Resource Type
- Journal article
- Publication Details
- Journal of clinical lipidology, Vol.11(5), pp.1201-1211
- DOI
- 10.1016/j.jacl.2017.06.017
- PMID
- 28807460
- PMCID
- PMC5612889
- NLM abbreviation
- J Clin Lipidol
- ISSN
- 1933-2874
- eISSN
- 1876-4789
- Publisher
- Elsevier Inc
- Grant note
- DOI: 10.13039/100000050, name: National Heart, Lung, and Blood Institute, award: U01 HL081616, U01 HL081649
- Language
- English
- Date published
- 09/2017
- Academic Unit
- Epidemiology; Internal Medicine
- Record Identifier
- 9983996069402771
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