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Optimal Control of all Modifiable Vascular Risk Factors Among Patients With Atherosclerotic Disease. A Real-Life
Guillermo Escudero-Sánchez1, Sergio Rico-Martín2, Carmen Sánchez-Bacaicoa3
1Department of Internal Medicine, Hospital Virgen Del Puerto, Cáceres, Spain.
Insights
Maintaining optimal control of vascular risk factors in atherosclerotic cardiovascular disease (ASCVD) patients did not reduce recurrent events or death. Associated conditions, not risk factor control, predicted worse outcomes in ASCVD.
Area of Science:
- Cardiovascular Medicine
- Clinical Research
- Epidemiology
Background:
- Optimal control of vascular risk factors is crucial for managing atherosclerotic cardiovascular disease (ASCVD).
- Uncertainty exists regarding the benefits of sustained, optimal risk factor management in stabilized ASCVD patients.
Purpose of the Study:
- To evaluate the impact of maintaining target levels for classical vascular risk factors on recurrent events and mortality in ASCVD patients.
- To identify factors associated with major adverse cardiovascular events (MACE) and all-cause death in this population.
Main Methods:
- Prospective registry (Factores de Riesgo y ENfermedad Arterial - FRENA) of 4285 outpatients with coronary, cerebrovascular, or peripheral artery disease.
- Analysis of recurrent events and mortality based on sustained control of LDL cholesterol, glucose, blood pressure, and smoking status.
- Multivariable analysis to identify predictors of MACE and all-cause death.
Main Results:
- Only 15% of patients achieved sustained optimal control of all principal risk factors.
- No significant differences in recurrent MACE or death were observed between patients achieving optimal risk factor control and those who did not.
- Known dyslipidemia, polyvascular disease, insulin therapy, and associated conditions were associated with increased MACE risk.
- Associated medical conditions strongly predicted all-cause death.
Conclusions:
- A minority of ASCVD patients achieve sustained optimal risk factor control.
- Current evidence does not demonstrate discernible clinical benefit from achieving optimal control of all risk factors in stabilized ASCVD.
- Physicians may need to adapt intensive, multifactorial therapy based on individual patient factors and associated conditions.
Abstract:
The effects of maintaining all classical, vascular risk factors on target among patients with stabilized atherosclerotic cardiovascular disease (ASCVD) are uncertain. Factores de Riesgo y ENfermedad Arterial (FRENA) was a prospective registry of consecutive outpatients with coronary, cerebrovascular, or peripheral artery disease. We analyzed the incidence of recurrent events and mortality according to sustained, optimal control of principal risk factors including the following: LDL cholesterol, glucose, blood pressure, and smoking. As of December 2018, 4285 stable outpatients were eligible for this study. Over a median follow-up of 21 months, 664 (15%) maintained all risk factors on target (Group 1), while 3621 (85%) did not (Group 2). During follow-up, no differences in recurrent major adverse cardiovascular events (MACEs) or death were observed between groups. On multivariable analysis, patients with previous known dyslipidemia (hazard ratio [HR]: 95% confidence interval (95% CI): ([HR]: 1.20 [95% CI, 1.03-1.40]), polyvascular disease ([HR]: 1.98 [95% CI, 1.69-2.32]), insulin therapy ([HR]: 1.56 [95% CI, 1.24-1.95]) and associated conditions ([HR]: 1.47 [95% CI, 1.24-1.74]) were associated with a higher risk for subsequent MACE. The presence of associated medical conditions was also strongly associated with all-cause death ([HR]: 3.49 [95% CI, 2.35-5.19]). Only a minority of patients with atherosclerotic cardiovascular disease achieved sustained optimal control for all principal risk factors although without discernible clinical, therapeutic benefit. The findings of the present study provide some insights into what factors may be used to guide physicians in adapting intensive, multifactorial therapy to the individual patient in clinical practice.
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