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Volume 111, Issue 10, Pages 825-828 (December 2009)


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Cerebral microbleeds predict first-ever symptomatic cerebrovascular events

Tomofumi Nishikawaa, Tetsuya UebaaCorresponding Author Informationemail address, Motohiro Kajiwaraa, Ichro Fujisawab, Naomi Miyamatsuc, Kohsuke Yamashitaa

Received 10 November 2008; received in revised form 13 August 2009; accepted 15 August 2009.

Abstract 

Objective

Cerebral microbleeds (CMB) on gradient-echo T2*-weighted magnetic resonance image (MRI) are frequently seen in patients with cerebral diseases. In this observational study we assessed whether CMB are a predictive factor for first-ever cerebrovascular events.

Patients and methods

This study consisted of 698 subjects without a history of symptomatic cerebrovascular events, who received gradient-echo T2*-weighted MRI for 3 months between November 2003 and January 2004 in Kishiwada City Hospital, Osaka, Japan. These subjects were then observed as outpatients for over 3.5 years.

Results

The prevalence of CMB at baseline was 17.0% (119/698) in this population, and the follow-up rate was 51%. A total of 36 first-ever symptomatic cerebrovascular events were observed during the 3 and a half-year follow-up period. First-ever symptomatic cerebrovascular events occurred significantly more frequently in subjects with CMB (15 cases) than those without CMB (21 cases) (p=0.001). Even after adjusting for age, sex and hypertension, it was revealed that the presence of CMB was an independent predictor for the first-ever symptomatic cerebrovascular event by using the Cox proportional hazards model (hazard ratio, 2.87; 95% CI, 1.27–6.48; p=0.01).

Conclusion

The presence of CMB is an independent predictor of first-ever symptomatic cerebrovascular diseases.

a Department of Neurosurgery, Kishiwada City Hospital, 1001 Gakuhara-cho, Kishiwada, Osaka 596-8501, Japan

b Department of Radiology, Kishiwada City Hospital, Osaka, Japan

c Department of Clinical Nursing, Faculty of Medicine, Shiga University of Medical Science, Shiga, Japan

Corresponding Author InformationCorresponding author. Tel.: +81 724 45 1000; fax: +81 724 41 8812.

PII: S0303-8467(09)00225-X

doi:10.1016/j.clineuro.2009.08.011


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