Effects of combination lipid therapy on coronary stenosis progression and clinical cardiovascular events in coronary disease patients with metabolic syndrome: a combined analysis of the Familial Atherosclerosis treatment study (FATS), the HDL-Atherosclerosis treatment study (HATS) and the Armed Forces regression Study (AFREGS)
Open accessAbstract
We examined the impact of metabolic syndrome (MS) on coronary stenosis progression and major cardiovascular (CV) events and investigated the mitigating effects of low-density lipoprotein (LDL) cholesterol lowering and LDL cholesterol lowering plus high-density lipoprotein (HDL) cholesterol increasing. This analysis combined individual patient data from 445 subjects who participated in 3 double-blinded, randomized, placebo-controlled trials (FATS, HATS, and AFREGS) comparing intensive lipid therapy to placebos on coronary stenosis progression by quantitative coronary angiography and on major CV events. The primary end points were change in mean proximal coronary diameter stenosis (Delta%S(prox)) over 3 years and the frequency of the predefined composite of coronary artery disease death, nonfatal myocardial infarction, stroke, and revascularization due to worsening ischemia. Patients with MS had 50% more rapid coronary stenosis progression and 64% increased CV event frequency compared to those without. More rapid coronary stenosis progression was significantly and independently associated with a 3.5-fold increased event risk (p <0.001). Combination lipid therapy significantly decreased stenosis progression by 83% (Delta%S(prox) 0.5 vs 2.9, p <0.001) in patients with MS and induced a small net regression in those without (Delta%S(prox) -0.3 vs 2.0, p <0.001). Combination therapy decreased the event rate by 54% (13% vs 28%, p = 0.03) in those with MS and by 82% (3% vs 17%, p = 0.002) without. On average, each 10% decrease in LDL cholesterol or 10% increase in HDL cholesterol was significantly associated with a 0.3 Delta%S(prox) decrease. Each 10% decrease in LDL cholesterol or 10% increase in HDL cholesterol was associated with 11% (p = 0.02) or 22% (p <0.001) event risk decrease. In conclusion, patients with MS have significantly more rapid coronary stenosis progression and a higher frequency of CV events. Greater stenosis progression rate is associated with a higher event rate. LDL cholesterol-lowering and HDL cholesterol-increasing therapies independently and significantly decrease coronary stenosis progression and decrease CV events.
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The statin-bile acid sequestrant combination has been found to reduce atherosclerosis as assessed by coronary angiography.
“The combination has been found to reduce atherosclerosis, as evaluated by coronary angiography.113 -115”
From ESC/EAS Guidelines for the management of dyslipidaemias (2011) · cites this paper as [114]
The combination of a statin and a bile acid sequestrant has been found to reduce atherosclerosis as evaluated by coronary angiography.
“The combination has been found to reduce atherosclerosis, as evaluated by coronary angiography.”
From 2016 ESC/EAS Guidelines for the Management of Dyslipidaemias (2016) · cites this paper as [253]
The combination of a statin and a bile acid sequestrant has been found to reduce atherosclerosis, as evaluated by coronary angiography.
“The combination has been found to reduce atherosclerosis, as evaluated by coronary angiography.253”
From 2016 ESC/EAS Guidelines for the Management of Dyslipidaemias (2016) · cites this paper as [253]
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References 30 · Cited by 48
- Authors
- Zhao, X.-Q., Krasuski, R. A., Baer, J., Whitney, E. J., Neradilek, B., Chait, A., Marcovina, S., Albers, J. J., & Brown, B. G.
- Affiliations
- University of Washington (US)
- Cleveland Clinic (US)
- Emory University (US)
- Corresponding author
- Zhao, Xue-Qiao
- Venue
- The American Journal of Cardiology
- Publisher
- Elsevier BV
- Published
- 2009-12
- Volume
- 104
- Issue
- 11
- Pages
- 1457-1464
- ISSN
- 0002-9149 (ISSN-L)
- PMC
- PMC2829987
- OpenAlex
- W2026824875
- Cited by
- 48
- References
- 30
- Citations by year
- 2025: 1 · 2020: 2 · 2019: 2 · 2017: 2 · 2016: 3 · 2015: 1 · 2014: 4 · 2013: 3 · 2012: 7
- FWCI
- 10.02
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- The American Journal of Cardiology (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health (5r01hl019451-14)
- National Heart, Lung, and Blood Institute (P01HL030086, R01 HL 19451, R01HL049546)
- National Institute of Diabetes and Digestive and Kidney Diseases (DK-35816, DK-17047, P30DK035816, P30DK017047)
- Topics
- Health Sciences › Medicine › Surgery › Lipoproteins and Cardiovascular Health
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes, Cardiovascular Risks, and Lipoproteins
- Health Sciences › Medicine › Surgery › Coronary Interventions and Diagnostics
- Keywords
- metabolic syndrome, coronary stenosis progression, LDL cholesterol lowering, HDL cholesterol elevation, cardiovascular events, coronary artery disease, individual patient data meta-analysis, fats, hats, quantitative coronary angiography, myocardial infarction, stroke, revascularization, statins, ezetimibe
- MeSH terms
- Adult, Aged, Anticholesteremic Agents, Double-Blind Method, Female, Follow-Up Studies, Humans, Cholesterol, HDL, Cholesterol, LDL, Male, Middle Aged, Military Personnel, Research Design, Risk Factors, Severity of Illness Index, Biomarkers, Body Mass Index, Survival Analysis, Randomized Controlled Trials as Topic, Treatment Outcome, Coronary Angiography, Disease Progression, Hydroxymethylglutaryl-CoA Reductase Inhibitors, Coronary Stenosis, Metabolic Syndrome, Atherosclerosis
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