Proteinuria Predicts Resistance to Antiplatelet Therapy in Ischemic Stroke

被引:0
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作者
Gemlyn George
Nikul Patel
Cecilia Jang
David Wheeler
Sridhara S. Yaddanapudi
Jonathan Dissin
Ramani Balu
Janani Rangaswami
机构
[1] Einstein Medical Center,Department of Internal Medicine
[2] Einstein Medical Center,Department of Neurosciences
[3] University of Pennsylvania,Division of Neurocritical Care, Department of Neurology, Perelman School of Medicine
[4] Hospital of the University of Pennsylvania,Department of Neurology
[5] Sidney Kimmel College of Thomas Jefferson University,undefined
[6] Delaware Valley Nephrology Associates,undefined
来源
Translational Stroke Research | 2018年 / 9卷
关键词
Stroke; Proteinuria; Platelet reactivity;
D O I
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中图分类号
学科分类号
摘要
The occurrence of a stroke while on antiplatelet agents presents a therapeutic dilemma. One of the main causes for recurrent strokes is antiplatelet resistance more commonly known as high on treatment platelet reactivity (HTPR). Prior studies have established that proteinuria is associated with HTPR following myocardial infarction. Here, we investigated whether dipstick proteinuria correlates with HTPR in patients presenting with stroke. We performed a retrospective cohort analysis of 102 patients admitted for a recurrent ischemic stroke that had either a VerifyNow aspirin or VerifyNow clopidogrel laboratory test performed to assess platelet reactivity. Dipstick proteinuria was defined as > 30 mg/dl (2+ or more). HTPR was defined as an aspirin resistance unit > 550 for aspirin and a P2Y12 reactivity unit > 208 for clopidogrel. Patients with proteinuria on dipstick were significantly more likely to have HTPR to either aspirin (p value 0.017) or clopidogrel (p value 0.017). After controlling for age, smoking, diabetes, hypertension, CAD and GFR, proteinuria was an independent predictor of HTPR for patient taking aspirin (p = 0.025). Platelet resistance is an entity that undermines the activity of antiplatelet agents in reducing stroke risk. Here, we demonstrate an association with increased platelet reactivity and proteinuria. This highlights a potential new therapeutic target in reducing future stroke risk.
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页码:130 / 134
页数:4
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