摘要
ABSTRACTBackground and aims Acute ischemic stroke (AIS) is a leading cause of death and long-term disability worldwide. Thromboinflammation plays an important role in the pathophysiology of stroke. The peripheral blood cell count ratios (PBCCR): neutrophil‐to‐lymphocyte ratio (NLR), platelet‐to‐lymphocyte ratio (PLR), and lymphocyte‐to‐monocyte ratio (LMR), are global inflammatory indicators with prognostic value for the clinical outcome after stroke. We aimed to determine the relationship between NLR, PLR, or LMR and the functional outcome three months post-stroke.Methods A prospective, hospital-based study, including 141 participants with AIS, was conducted at a referral stroke center in North-Eastern Bulgaria. The PBCCRs were obtained during the first 24 hours after stroke onset. Stroke severity was measured using the NIHSS scale, and functional outcome was assessed with the modified Rankin Scale (mRS) at discharge and 3 months post-stroke.Results We found significantly lower total lymphocyte counts, and higher NLR, PLR, and C-reactive protein in the poor-outcome group (mRS>3) three months post-stroke. A positive correlation was found between the NIHSS score and mRS score on discharge, NLR, and PLR with the worse outcome on the third month. The receiver operating characteristic (ROC) curves showed the predictability of NLR (AUC, 0.626, 95%CI: 0.524–0.724, p = 0.018), and for PLR– (AUC, 0.613, 95%CI: 0.510–0.716, p = 0.031). The optimal cutoff value for NLR was 2.68 (sensitivity 77.8% and specificity 60.4%), and for PLR - 122.6 (sensitivity 77.8% and specificity 61.5%).Conclusion Neutrophil-to-lymphocyte ratio and platelet-to-lymphocyte ratio are simple, widely available, and cost-effective biomarkers with high prognostic value for the clinical outcome three months post-stroke.KEYWORDS: StrokeIschemic strokeBlood cell countBlood cell count rationeutrophil‐to‐lymphocyte ratioplatelet‐to‐lymphocyte ratiolymphocyte‐to‐monocyte ratioprognosisclinical outcome Disclosure statementNo potential conflict of interest was reported by the author(s).ContributorshipAll authors researched literature and conceived the study. All authors were involved in involved in protocol development, gaining ethical approval, patient recruitment and data analysis. All authors reviewed and edited the manuscript and approved the final version of the manuscript.Data availability statementData sharing not applicable to this article as no datasets were generated or analyzed during the current study.Ethical approvalAll procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.Informed consentAll patients included in the present study signed informed consent on patient selection.GuarantorMihael Tsalta-Mladenov MD, PhD (MihaelTsalta@gmail.com).Additional informationFundingThis research received no specific grant from any funding agency in the public, commercial, or not-for-profit sectors.