Abstract

We evaluated the impact of prestroke glycemic variability estimated by glycated albumin (GA) on symptomatic hemorrhagic transformation (SHT) in patients with intravenous thrombolysis (IVT). Using a multicenter database, we consecutively enrolled acute ischemic stroke patients receiving IVT. A total of 378 patients were included in this study. Higher GA was defined as GA ≥ 16.0%. The primary outcome measure was SHT. Multivariate regression analysis and a receiver operating characteristic curve were used to assess risks and predictive ability for SHT. Among the 378 patients who were enrolled in this study, 27 patients (7.1%) had SHT as defined by the Safe Implementation of Thrombolysis in Stroke-Monitoring Study (SHTSITS). The rate of SHTSITS was higher in the higher GA group than in the lower GA group (18.0% vs. 1.6%, p < 0.001). A higher GA level (GA ≥ 16.0%) significantly increased the risk of SHTSITS (adjusted odds ratio [OR], [95% confidence interval, CI], 12.57 [3.08–41.54]) in the logistic regression analysis. The predictive ability of the GA level for SHTSITS was good (AUC [95% CI]: 0.83 [0.77–0.90], p < 0.001), and the cutoff value of GA in SHT was 16.3%. GA was a reliable predictor of SHT after IVT in acute ischemic stroke in this study.

Highlights

  • We evaluated the impact of prestroke glycemic variability estimated by glycated albumin (GA) on symptomatic hemorrhagic transformation (SHT) in patients with intravenous thrombolysis (IVT)

  • Using a multicenter registry database, we investigated the effects of glycemic variability estimated by GA on SHT and functional outcomes in patients treated with IVT

  • The sensitivity analysis revealed that the impact of the GA/HbA1c ratio and GA in patients treated with IVT and diabetes mellitus (DM) on SHT improved the robustness of our results

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Summary

Introduction

We evaluated the impact of prestroke glycemic variability estimated by glycated albumin (GA) on symptomatic hemorrhagic transformation (SHT) in patients with intravenous thrombolysis (IVT). We consecutively enrolled acute ischemic stroke patients receiving IVT. GA was a reliable predictor of SHT after IVT in acute ischemic stroke in this study. Several previous studies showed that chronic hyperglycemia estimated by glycated hemoglobin (HbA1c) increased the risk of HT and poor functional outcomes after IVT by inducing microvascular ­injury[6,7,8,9]. Glycated albumin (GA) reflects glycemic variability within 4 weeks prior to stroke and may be a useful marker for predicting recent prestroke glycemic v­ ariability[14,15]. Using a multicenter registry database, we investigated the effects of glycemic variability estimated by GA on SHT and functional outcomes in patients treated with IVT

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