Abstract
Objectives
We aimed to investigate the associations between carotid vulnerable plaque features coexisting with cerebral small vessel diseases (CSVDs) and acute ischemic stroke (AIS) and, furthermore, to determine whether coexisting diseases had a stronger association with AIS than a single disease.
Methods
Patients with cerebrovascular symptoms and carotid plaque were recruited from the cross-sectional, multicenter CARE-II study. The population was divided into two groups (AIS and transient ischemic stroke (TIA)). MRI features of carotid plaques (including luminal stenosis and plaque vulnerabilities) and CSVDs (such as white matter hyperintensities (WMHs) and lacunes) were evaluated. Coexisting diseases were defined as the presence of at least one carotid plaque features and one or more CSVDs feature. Multivariate logistic regression was performed to examine the associations between coexisting diseases and AIS.
Results
Of the recruited 634 patients (mean age: 59.1 ± 11.3 years; 429 males), 312 (49.2%) patients had AIS. These subjects had a higher prevalence of carotid vulnerable plaques, lacunes, and moderate-to-severe WMHs (a total Fazekas score of 3–6) than those with TIA (42.6% vs. 29.5%, 59.6% vs. 26.4%, 69.9% vs. 60.6%, respectively, all p < 0.05). Multivariate analysis revealed that carotid plaque features coexisting with lacunes or moderate-to-severe WMHs had a stronger association with AIS compared to carotid lesions alone (all p < 0.05) (i.e., vulnerable plaque coexisting with lacunes vs. vulnerable plaque alone, adjusted odds ratio: 3.67 vs. 1.62).
Conclusions
Carotid vulnerable plaque features coexisting with CSVDs, particularly lacunes, had a stronger association with AIS compared to carotid lesions alone in a large, symptomatic, cohort.
Trial registration
Clinical trial registration URL: http://www.clinicaltrials.gov, unique identifier: NCT02017756
Key Points
• Carotid vulnerable plaque features coexisting with cerebral small vessel diseases, such as lacunes, had a stronger association with acute ischemic stroke compared to single diseases in symptomatic patients.
• A comprehensive assessment of coexisting cerebrovascular diseases may help stratify the risk of acute ischemic stroke.
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Abbreviations
- AIS:
-
Acute ischemic stroke
- BMI:
-
Body mass index
- CARE-II:
-
Chinese Atherosclerosis Risk Evaluation
- CSVDs:
-
Cerebral small vessel diseases
- FC:
-
Fibrous cap
- HDL:
-
High-density lipoprotein
- IPH:
-
Intraplaque hemorrhage
- IQR:
-
Interquartile range
- LDL:
-
Low-density lipoprotein
- LRNC:
-
Lipid-rich necrotic core
- MP-RAGE:
-
Magnetization-prepared rapid acquisition gradient echo
- SD:
-
Standard deviation
- TC:
-
Total cholesterol
- TG:
-
Triglycerides
- TIA:
-
Transient ischemic attack
- WASID:
-
Warfarin-Aspirin Symptomatic Intracranial Disease
- WMHs:
-
White matter hyperintensities
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Acknowledgements
We thank all the CARE-II (Chinese Atherosclerosis Risk Evaluation) investigators for their contributions to the patient recruitment.
Funding
This research was supported by the grants of the National Key R&D Program of China (Grant No. 2017YFC1307900, 2017YFC1307904), National Natural Science Foundation of China (Grant No. 81771825, 81801650, 81571630), Beijing Municipal Science and Technology Commission (Grant No. D171100003017003), and Shanghai Municipal Population and Family Planning Commission (Grant No. 201940060, 20204Y0089).
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The scientific guarantor of this publication is Huilin Zhao.
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The authors of this manuscript declare no relationships with any companies, whose products or services may be related to the subject matter of the article.
Statistics and biometry
No complex statistical methods were necessary for this paper.
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Written informed consent was obtained from all subjects (patients) in this study.
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Institutional review board approval was obtained.
Methodology
• retrospective
• cross-sectional study
• multicenter study
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Li, J., Wu, H., Hang, H. et al. Carotid vulnerable plaque coexisting with cerebral small vessel disease and acute ischemic stroke: a Chinese Atherosclerosis Risk Evaluation study. Eur Radiol 32, 6080–6089 (2022). https://doi.org/10.1007/s00330-022-08757-9
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DOI: https://doi.org/10.1007/s00330-022-08757-9