Classification of Covert Brain Infarct Subtype and Risk of Death and Vascular Events

Author:

Gutierrez Jose1,Gil-Guevara Andrea2,Ramaswamy Srinath1,DeRosa Janet1,Di Tullio Marco R.3,Cheung Ken4,Rundek Tatjana567,Sacco Ralph L.567,Wright Clinton B.8,Elkind Mitchell S.V.19

Affiliation:

1. From the Department of Neurology (J.G., S.R., J.D., M.S.V.E.), Mailman School of Public Health, Columbia University, New York, NY

2. Department of Medicine, University of Texas, Galveston (A.G.-G.)

3. Department of Cardiology (M.R.D.T.), Mailman School of Public Health, Columbia University, New York, NY

4. Division of Biostatistics (K.C.), Mailman School of Public Health, Columbia University, New York, NY

5. Departments of Neurology (T.R., R.L.S.), University of Miami Miller School of Medicine, FL

6. Public Health Sciences (T.R., R.L.S.), University of Miami Miller School of Medicine, FL

7. Evelyn F. McKnight Brain Institute (T.R., R.L.S.), University of Miami Miller School of Medicine, FL

8. National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD (C.B.W.).

9. Department of Epidemiology (M.S.V.E.), Mailman School of Public Health, Columbia University, New York, NY

Abstract

Background and Purpose— To test the hypothesis that covert brain infarcts (CBIs) are more likely to be located in noneloquent brain areas compared with clinical strokes and that CBI etiological subtypes carry a differential risk of vascular events compared with people without CBI. Methods— We used brain magnetic resonance imaging from 1290 stroke-free participants in the NOMAS (Northern Manhattan Study) to evaluate for CBI. We classified CBI as cardioembolic (ie, known atrial fibrillation), large artery atherosclerosis (extracranial and intracranial), penetrating artery disease, and cryptogenic (no apparent cause). CBI localized in the nonmotor areas of the right hemisphere were considered noneloquent. We then evaluated risk of events by CBI subtype with adjusted Cox proportional models. Results— At the time of magnetic resonance imaging, 236 participants (18%) had CBI (144 [61%] distal cryptogenic, 29 [12%] distal cardioembolic, 26 [11%] large artery atherosclerosis, and 37 [16%] penetrating artery disease). Smaller (per mm, odds ratio, 0.8 [0.8–0.9]) and nonbrain stem infarcts (odds ratio, 0.2 [0.1–0.6]) were more likely to be covert. During the follow-up period (10.4±3.1 years), 398 (31%) died (162 [13%] of vascular death) and 117 (9%) had a stroke (99 [85%]) were ischemic. Risks of events varied by CBI subtype, with the highest risk of stroke (hazard ratio, 2.2 [1.3–3.7]) and vascular death (hazard ratio, 2.24 [1.29–3.88]) noted in participants with intracranial large artery atherosclerosis-related CBI. Conclusions— CBI can be classified into subtypes that have differential outcomes. Certain CBI subtypes such as those related to intracranial large artery atherosclerosis have a high risk of adverse vascular outcomes and could warrant consideration of treatment trials.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Advanced and Specialized Nursing,Cardiology and Cardiovascular Medicine,Neurology (clinical)

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