Abstract

Acute statin therapy improves neurologic outcome and diminishes infarct growth in animal models of stroke. Clinical studies suggest that premorbid and early statin use is associated with improved outcome after major stroke. We studied the association between statin therapy and radiographic and clinical outcomes in patients with high-risk TIA and minor stroke. Patients with high-risk TIA and minor stroke (NIHSS ≤3) were prospectively enrolled within 24 hours of symptom onset. Patients were followed clinically for 3 months, and a subset had a repeat MR imaging at 90 days. Of 418 patients, 23% were prescribed statins before their stroke. Statins were continued in 20% and initiated in 42%. Patients on prior statin therapy were older and more hypertensive, treated with aspirin, and more likely to have symptomatic carotid disease compared with those not on statin. Adjusting for these differences, prior statin treatment was not associated with DWI positivity (adjusted OR = 1.3; 95% CI, 0.77-2.1; P = .32) or smaller median baseline infarct volume, 1.1 mL (interquartile range = 4) versus 1 mL (interquartile range = 2.5; P = .56). Early or continued treatment with statins did not improve the risk of clinical deterioration (adjusted OR = 0.66; 95% CI, 0.27-1.6; P = .35) or poor functional outcome at 3 months (adjusted OR = 0.66; 95% CI, 0.35-1.24; P = .19). Prestroke or early-stroke statin therapy was not associated with a reduction in the number of DWI lesions, infarct volume, or improved clinical or functional outcome at 3 months. The effect of acute statin treatment in patients with ischemic stroke/TIA remains unclear and needs further investigation.

Highlights

  • BACKGROUND AND PURPOSEAcute statin therapy improves neurologic outcome and diminishes infarct growth in animal models of stroke

  • Prestroke or early-stroke statin therapy was not associated with a reduction in the number of DWI lesions, infarct volume, or improved clinical or functional outcome at 3 months

  • The functional outcome of patients randomized to early statin treatment versus placebo was no different in a pilot randomized controlled trial.[6]

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Summary

Methods

Patients with high-risk TIA and minor stroke (NIHSS Յ3) were prospectively enrolled within 24 hours of symptom onset. Patients were followed clinically for 3 months, and a subset had a repeat MR imaging at 90 days. Patients We included patients who underwent MR imaging in the study entitled CT and MR Imaging in the Triage of TIA and Minor Cerebrovascular Events to Identify High Risk Patients (CATCH).[17] The methods of the CATCH study have previously been published. Patients with high-risk TIA (focal weakness or speech disturbance lasting Ն5 minutes) or minor ischemic stroke (with an initial National Institute of Health Stroke Scale score of Յ3) were prospectively enrolled. All patients underwent MR imaging, standard clinical and demographic information was recorded, and secondary stroke-prevention measures were implemented in accordance with current practice guidelines.[18]

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