Total small vessel disease score and cerebro-cardiovascular events in healthy adults: The Kashima scan study

Author:

Suzuyama Kohei1ORCID,Yakushiji Yusuke1ORCID,Ogata Atsushi2,Nishihara Masashi3,Eriguchi Makoto1,Kawaguchi Atsushi4,Noguchi Tomoyuki5,Nakajima Junko6,Hara Hideo1

Affiliation:

1. Division of Neurology, Department of Internal Medicine, Saga University Faculty of Medicine, Saga, Japan

2. Department of Neurosurgery, Saga University Faculty of Medicine, Saga, Japan

3. Department of Radiology, Saga University Faculty of Medicine, Saga, Japan

4. Education and Research Center for Community Medicine, Saga University Faculty of Medicine, Saga, Japan

5. Department of Radiology, National Hospital Organization Kyushu Medical Center, Fukuoka, Japan

6. Department of Radiology, Yuai-Kai Oda Hospital, Kashima, Japan

Abstract

Background and aims We explored the association between the total small vessel disease score obtained from baseline magnetic resonance imaging and subsequent cerebro-cardiovascular events in neurologically healthy Japanese adults. Methods The presence of small vessel disease features, including lacunae, cerebral microbleeds, white matter changes, and basal ganglia perivascular spaces on magnetic resonance imaging, was summed to obtain a “total small vessel disease score” (range, 0–4). After excluding participants with previous stroke or ischemic heart disease, intracranial artery stenosis (≥50%), or cerebral aneurysm (≥4 mm), a total of 1349 participants (mean age, 57.7 years; range, 22.8–85.0 years; 46.9% male) were classified into three groups by total small vessel disease score: 0 ( n = 984), 1 ( n = 269), and ≥2 ( n = 96). Cerebro-cardiovascular events (i.e., any stroke, transient ischemic attack, ischemic heart disease, acute heart failure, and aortic dissection) were defined as the primary end point. The hazard ratio (HR) of events during follow-up was calculated using Cox proportional hazards modeling with adjustments for age, sex, hypertension, diabetes mellitus, and smoking. Cumulative event-free rates were estimated using the Kaplan–Meier method. Results During follow-up (mean, 6.7 years), 35 cerebro-cardiovascular (16 cerebrovascular) events were identified. Higher small vessel disease score was associated with increased risk of cerebro-cardiovascular events (HR per unit increase, 2.17; 95% confidence interval, 1.36–3.46; P = 0.001). Events were more frequent among participants with higher score ( P < 0.001, log-rank test). Conclusions This study offered additional evidence for the clinical relevance of total small vessel disease score, suggesting the score as a promising tool to predict the risk of subsequent vascular events even in healthy populations.

Publisher

SAGE Publications

Subject

Neurology

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