Key result
Highest ApoB/ApoA-I quartile linked to ~374% higher ICAS risk in young ischemic stroke patients.
Why the study?
Ischemic stroke incidence among young adults has increased significantly, making the identification of risk factors in this demographic crucial for effective prevention.
Is a higher serum ApoB/ApoA-I ratio associated with intracranial atherosclerotic stenosis in young patients with ischemic stroke?
Observational (n=161)
No
Is a higher serum ApoB/ApoA-I ratio associated with intracranial atherosclerotic stenosis in young patients with ischemic stroke?
Effect estimate: OR 4.743 (95% CI 2.109-10.667)
p-value: p=<0.001
In young adults with ischemic stroke, a higher ApoB/ApoA-I ratio is strongly and independently associated with the presence of intracranial atherosclerotic stenosis.
Should not yet change lipid assessment in young stroke; hypothesis-generating for ICAS risk stratification pending prospective validation.
In recent years, the incidence of ischemic stroke among young adults has increased significantly. Identifying risk factors associated with ischemic stroke in this demographic is crucial for effective prevention. This study aimed to investigate the relationship of the serum apolipoprotein B (ApoB)/apolipoprotein A-I (ApoA-I) ratio with intracranial atherosclerotic stenosis (ICAS) in young patients with ischemic stroke. We collected data from patients with ischemic stroke aged 18 to 45 years. ICAS was assessed using computed tomography angiography (CTA), and serum levels of total cholesterol, triglycerides, high-density lipoprotein cholesterol, low-density lipoprotein cholesterol, ApoA-I, and ApoB were measured. The ApoB/ApoA-I ratio was subsequently calculated. Demographic and clinical characteristics were compared between the ICAS group and the non-ICASs group. Multivariate logistic regression analysis was employed to identify independent risk factors for ICAS in young ischemic stroke patients. A total of 161 young ischemic stroke patients were included, with 89 in the ICAS group and 72 in the non-ICAS group. In a univariate analysis, patients with ICAS had a higher prevalence of diabetes mellitus, smoking, and hyperlipidemia, as well as higher levels of ApoB and a higher ApoB/ApoA-I ratio, but lower levels of HDL-C and ApoA-I compared to those without ICAS. After adjustment for age, sex, smoking, hypertension, diabetes mellitus, and HDL-C, multivariable analyses indicated that ICAS had a dose–response relationship with apoB/apoAI ratio quartiles: the second quartile, OR, 3.051 (95% CI, 1.185 to 7.855); the third quartile, 3.516 (1.504 to 8.219); and the fourth quartile, 4.743 (2.109 to 10.667), when referenced to the first quartile. Our study showed that a higher apoB/apoAI ratio is independently associated with ICAS in young stroke patients, after careful exclusion of alternative arteriopathies and adjustment for confounders. However, findings should be confirmed with vessel wall imaging in future studies.
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Yan et al. (2026) conducted an observational in Ischemic stroke (n=161). ApoB/ApoA-I ratio (highest quartile) vs. ApoB/ApoA-I ratio (lowest quartile) was evaluated on Intracranial atherosclerotic stenosis (ICAS) (OR 4.743, 95% CI 2.109-10.667, p=<0.001). In young patients with ischemic stroke, the highest quartile of the ApoB/ApoA-I ratio was independently associated with an increased risk of intracranial atherosclerotic stenosis (OR 4.743) compared to the lowest quartile.
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