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Published on: January 18, 2018
ApoB/ApoA-I ratio in young patients with ischemic cerebral stroke or peripheral arterial disease
Adriano Paula Sabino1, Marinez De Oliveira Sousa, Luciana Moreira Lima
1Faculty of Pharmacy, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil, University Hospital-Federal University of Minas Gerais Belo Horizonte, MG, Brazil.
Insights
In young patients, elevated levels of C-reactive protein (hs-CRP) and the apolipoprotein B/apolipoprotein A-I (ApoB/ApoA-I) ratio are independently linked to increased risks of ischemic stroke (IS) and peripheral arterial disease (PAD). These markers indicate significant lipid and inflammatory changes.
Area of Science:
- Cardiovascular Medicine
- Clinical Chemistry
- Vascular Biology
Background:
- Dyslipidemia is a known risk factor for atherothrombotic diseases, but its specific association with vascular diseases beyond myocardial infarction, particularly in younger individuals, requires further clarification.
- Established risk factors like smoking and hypertension are well-documented, yet the role of lipid and apolipoprotein profiles in young patients with ischemic cerebral stroke (IS) and peripheral arterial disease (PAD) remains less defined.
Purpose of the Study:
- To investigate the relationship between lipid and apolipoprotein profiles and the occurrence of IS and PAD in young patients.
- To identify specific biomarkers associated with increased risk of IS and PAD in this demographic, considering inflammatory markers.
Main Methods:
- Analysis of plasma levels of high-sensitivity C-reactive protein (hs-CRP), total cholesterol (TC), HDLc, LDLc, triglycerides (TG), apolipoproteins A-I (ApoA-I), and apolipoproteins B (ApoB) in 81 young patients with IS or PAD and 167 controls.
- Statistical analysis was performed to compare profiles between groups and to identify independent risk factors after adjusting for covariates including age, sex, smoking, hypertension, and various lipid parameters.
Main Results:
- Significant differences in hs-CRP, TC, HDLc, LDLc, TG, ApoA-I, ApoB levels, and the ApoB/ApoA-I ratio were observed between patients with IS/PAD and controls.
- After adjustment for confounding factors, hs-CRP, ApoB, and the ApoB/ApoA-I ratio remained independently associated with an increased risk of IS or PAD.
Conclusions:
- Elevated ApoB/ApoA-I ratio and hs-CRP levels are significant independent predictors of IS and PAD in young patients.
- These findings highlight the importance of assessing lipid and apolipoprotein profiles, alongside inflammatory markers, for risk stratification of vascular diseases in younger populations.
Abstract:
Although smoking and hypertension are classic risk factors for atherothrombotic diseases, the relationship of dyslipidemia and vascular diseases, other than myocardial infarction, is less clearly established, especially in young subjects. In the current study, a detailed analysis of the lipid and apolipoprotein profiles was conducted in young patients of ischemic cerebral stroke (IS) and peripheral arterial disease (PAD). Plasma levels of C-reactive protein (hs-CRP), total cholesterol (TC), high-density lipoprotein cholesterol (HDLc), low-density lipoprotein cholesterol (LDLc), triglycerides (TG), and apolipoproteins A-I (ApoA-I) and apolipoproteins B (ApoB), which include the ApoB/ApoA-I ratio, were analyzed in a group of 81 patients who presented with IS (n = 46) or PAD (n = 35) as well as in 167 control subjects. Significant differences were observed for hs-CRP, TC, HDLc, LDLc, TG, ApoA-I, and ApoB levels, as well as for the ApoB/ApoA-I ratio, between the control and the IS or PAD groups. However, after adjustment for sex, age, smoking, hypertension, hs-CRP, and dyslipidemia (LDLc, TC, HDLc, TG, ApoA, ApoB, and ApoB/ApoA-I ratio), hs-CRP, ApoB, and the ApoB/ApoA-I ratio were independently associated with increased risks of IS or PAD. Increased ApoB/ApoA-I ratio and hs-CRP levels are independently associated with occurrence of IS and PAD in young patients and are significant markers of alterations on lipid and apolipoproteic profiles and inflammatory responses, respectively, in these patients.
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