Association between uric acid to lymphocyte ratio and poor functional outcomes in acute ischemic stroke patients

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Authors: Xu Zhu, Yijun Zhang, A N Wang, Xiaoli Zhang, Guoyuan Yu, Shifeng Xiang, Yiping Wu, Xia Meng
Cited by: 0
References: 33

Abstract

Background: Inflammation has an important impact on the pathological progression associated with ischemic stroke. Serum uric acid (UA) to lymphocyte ratio (ULR) is a biomarker that responds to the level of inflammation but is not definitively associated with the clinical outcomes in patients with acute ischemic stroke (AIS). Methods: The data were obtained from the Third China National Stroke Registry (CNSR-III). Enrolled AIS patients were grouped by ULR quartiles at admission. The outcomes were poor functional outcomes (modified Rankin Scale [mRS] score of 3-6 or 2-6) and all-cause mortality at 3 months and 1 year. The associations of ULR with the risk of poor functional outcome and all-cause mortality were analyzed by multivariable logistic regression and Cox proportional hazards regression. Results: A total of 8,241 patients were included from the CNSR-III study. After adjusting for confounders, it was found that patients in the highest ULR quartile had higher mRS scores of 2-6 (odds ratio [OR], 1.33; 95% confidence interval [CI], 1.15-1.53) and 3-6 (OR, 1.35; 95% CI, 1.16-1.57) at the 3-month follow-up. Additionally, the highest ULR quartile was associated with an increased risk of all-cause mortality at the 3-month follow-up (hazard ratio [HR], 1.97; 95%CI, 1.22-3.18). Similar results were observed at the 1-year follow-up. Conclusion: Elevated ULR increased the risks of poorer functional outcomes and all-cause mortality in the AIS patients. However, this observational study was limited by potential unmeasured confounders, selection bias, residual confounding, and restricted generalizability to other populations.

Fields of Study & Subjects

Gout Hyperuricemia Uric Acid Bone and Joint Diseases Spondyloarthritis Studies and Treatments

Publication details

Journal / source
Frontiers in Neurology
Volume
17
Pages
1825152–1825152
Publication date
28 May 2026
Language
EN