In one-third of strokes, a definite cause cannot be established. This proposal is for a clinical trial involving patients with a stroke of unknown cause who also have atrial cardiopathy, or abnormal changes in the atrial tissue of the heart. The goal is to compare two different blood-thinning treatments to determine which best prevents recurrent stroke. Under the prevailing clinical paradigm, it is thought that atrial fibrillation?a common disorder of heart rhythm?is required for blood clots to form in the heart's left atrium, from where they can embolize to the brain and cause stroke. Therefore, unless atrial fibrillation is apparent, patients do not receive the types of blood-thinning drugs that best prevent embolic stroke. However, recent research indicates that embolization from the left atrium can occur when there are abnormal changes to atrial tissue and function even before there is atrial fibrillation. These abnormal changes?a condition referred to as atrial cardiopathy? may explain many of the strokes that are currently of unknown cause. Since blood-thinning treatment with an anticoagulant drug such as apixaban has already proven more effective than standard aspirin therapy for preventing stroke from atrial fibrillation, the parallels between atrial fibrillation and atrial cardiopathy suggest that apixaban may also be more effective than aspirin for stroke prevention in patients with atrial cardiopathy and no atrial fibrillation. This application is for a multicenter, biomarker-driven, randomized, double-blind, active-control, phase 3 clinical trial of apixaban versus aspirin in patients who have evidence of atrial cardiopathy and a recent stroke of unknown cause by current criteria. Atrial cardiopathy will be defined as one or more of the following biomarkers: P-wave terminal force in electrocardiogram lead V1 >5,000 V*ms, left atrial size index ?3.0 cm/m2 on echocardiogram, and serum amino terminal pro-B-type natriuretic peptide >250 pg/mL. Standard heart-rhythm monitoring will be performed before enrollment to exclude as thoroughly as possible those patients with atrial fibrillation. Eleven hundred patients will be recruited over 2.5 years at 120 sites in the NINDS StrokeNet consortium. Patients will be followed for a minimum of 1.5 years and a maximum of 4 years for the primary efficacy outcome of recurrent stroke and the primary safety outcomes of major hemorrhage and intracranial hemorrhage.
Specific Aim 1 will test the hypothesis that apixaban is superior to aspirin for the prevention of recurrent stroke in patients with atrial cardiopathy. Validation of this hypothesis would have immediate implications for preventing recurrent stroke by identifying a new group of stroke patients who benefit from anticoagulant therapy.
Specific Aim 2 will test the hypothesis that the efficacy of apixaban over aspirin increases with the severity of atrial cardiopathy. Validation of this hypothesis would help establish atrial cardiopathy as a stroke risk factor, and thus set the stage for future studies to determine the benefit of treating patients with atrial cardiopathy before they ever have a stroke in the first place.

Public Health Relevance

The proposed research is relevant to public health because the discovery of novel and treatable cardiac risk factors for stroke will ultimately improve risk factor screening and stroke prevention efforts, thereby reducing the incidence of a disabling and lethal disease. Thus, the proposed research is relevant to the part of the NINDS's mission that involves reducing the burden of neurological disease by fostering research on the causes and prevention of stroke.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project--Cooperative Agreements (U01)
Project #
5U01NS095869-02
Application #
9476371
Study Section
National Institute of Neurological Disorders and Stroke Initial Review Group (NSD)
Program Officer
Vivalda, Joanna
Project Start
2017-05-01
Project End
2022-04-30
Budget Start
2018-05-01
Budget End
2019-04-30
Support Year
2
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Columbia University (N.Y.)
Department
Neurology
Type
Schools of Medicine
DUNS #
621889815
City
New York
State
NY
Country
United States
Zip Code
10032
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