Cerebral Microbleeds, Vascular Risk Factors, and Magnetic Resonance Imaging Markers: The Northern Manhattan Study

Author:

Caunca Michelle R.12,Del Brutto Victor3,Gardener Hannah12,Shah Nirav4,Dequatre‐Ponchelle Nelly5,Cheung Ying Kuen6,Elkind Mitchell S. V.78,Brown Truman R.9,Cordonnier Charlotte5,Sacco Ralph L.121011,Wright Clinton B.1210

Affiliation:

1. Evelyn F. McKnight Brain Institute and the Neuroscience Program, University of Miami, Miami, FL

2. Department of Neurology, University of Miami Miller School of Medicine, Miami, FL

3. Department of Neurology, The University of Chicago, IL

4. Department of Neurology, University of California, San Francisco, CA

5. Inserm, CHU Lille, U 1171, Degenerative & Vascular Cognitive Disorders, University of Lille, France

6. Department of Biostatistics, Mailman School of Public Health, Columbia University, New York, NY

7. Department of Epidemiology, Mailman School of Public Health, Columbia University, New York, NY

8. Department of Neurology, College of Physicians and Surgeons, Columbia University, New York, NY

9. Department of Radiology and Radiological Science, Medical University of South Carolina, Charleston, SC

10. Department of Public Health Sciences, University of Miami Miller School of Medicine, Miami, FL

11. Department of Human Genetics, University of Miami Miller School of Medicine, Miami, FL

Abstract

Background Cerebral microbleeds ( CMB s) represent intracerebral hemorrhages due to amyloid angiopathy or exposure to modifiable risk factors. Few community‐based stroke‐free studies including blacks and Hispanics have been done. Methods and Results The Northern Manhattan Study ( NOMAS ) is a stroke‐free, racially and ethnically diverse cohort study. Brain MRI was performed in 1290 participants, 925 of whom had available T2* gradient‐recall echo data. We used multivariable logistic regression to examine the association of sociodemographics, vascular risk factors, apolipoprotein E ( APOE ) genotype, and brain MRI markers with CMB presence and location. The prevalence of CMB s in our cohort was 5%. Of the 46 participants with CMB s, 37% had only deep CMB s, 48% had only lobar CMB s, and 15% had CMB s in both locations. The difference in CMB distribution was not statistically significant across race/ethnic group or APOE genotype. In multivariable analyses, age ( OR [95% CI ]: 1.09 [1.04, 1.15]) and SBI s (2.58 [1.01, 6.59]) were positively associated with CMB presence, and diabetes medication use was negatively associated (0.25 [0.07, 0.86]). Conclusions CMB s may represent the severity of vascular disease in this racially and ethnically diverse cohort. Larger studies are needed to elucidate the association between diabetes medication use and CMB presence.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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