» Articles » PMID: 28345429

Uric Acid Therapy Improves the Outcomes of Stroke Patients Treated with Intravenous Tissue Plasminogen Activator and Mechanical Thrombectomy

Overview
Journal Int J Stroke
Publisher Sage Publications
Date 2017 Mar 28
PMID 28345429
Citations 40
Authors
Affiliations
Soon will be listed here.
Abstract

Background Numerous neuroprotective drugs have failed to show benefit in the treatment of acute ischemic stroke, making the search for new treatments imperative. Uric acid is an endogenous antioxidant making it a drug candidate to improve stroke outcomes. Aim To report the effects of uric acid therapy in stroke patients receiving intravenous thrombolysis and mechanical thrombectomy. Methods Forty-five patients with proximal vessel occlusions enrolled in the URICO-ICTUS trial received intravenous recombinant tissue plasminogen activator within 4.5 h after stroke onset and randomized to intravenous 1000 mg uric acid or placebo (NCT00860366). These patients also received mechanical thrombectomy because a brain computed tomogaphy angiography confirmed the lack of proximal recanalization at the end of systemic thrombolysis. The primary outcome was good functional outcome at 90 days (modified Rankin Score 0-2). Safety outcomes included mortality, symptomatic intracerebral bleeding, and gout attacks. Results The rate of successful revascularization was >80% in the uric acid and the placebo groups but good functional outcome was observed in 16 out of 24 (67%) patients treated with uric acid and 10 out of 21 (48%) treated with placebo (adjusted Odds Ratio, 6.12 (95% CI 1.08-34.56)). Mortality was observed in two out of 24 (8.3%) patients treated with uric acid and one out of 21 (4.8%) treated with placebo (adjusted Odds Ratio, 3.74 (95% CI 0.06-226.29)). Symptomatic cerebral bleeding and gout attacks were similar in both groups. Conclusions Uric acid therapy was safe and improved stroke outcomes in stroke patients receiving intravenous thrombolysis followed by thrombectomy. Validation of this simple strategy in a larger trial is urgent.

Citing Articles

The hazards of chasing subgroups in neutral stroke trials.

Bath P, Howard G, Hacke W Neurol Res Pract. 2025; 7(1):17.

PMID: 40069910 DOI: 10.1186/s42466-025-00369-0.


Targeting uric acid: a promising intervention against oxidative stress and neuroinflammation in neurodegenerative diseases.

Xu L, Li C, Wan T, Sun X, Lin X, Yan D Cell Commun Signal. 2025; 23(1):4.

PMID: 39754256 PMC: 11699683. DOI: 10.1186/s12964-024-01965-4.


The Therapeutic Effects of SP-8356, a Verbenone Derivative, with Multimodal Cytoprotective Mechanisms in an Ischemic Stroke Rat Model.

Song H, Jin S, Lee S, Jalin A, Roh K, Kim W Int J Mol Sci. 2024; 25(23).

PMID: 39684478 PMC: 11641512. DOI: 10.3390/ijms252312769.


Nanotechnology approaches to drug delivery for the treatment of ischemic stroke.

Peng B, Mohammed F, Tang X, Liu J, Sheth K, Zhou J Bioact Mater. 2024; 43:145-161.

PMID: 39386225 PMC: 11462157. DOI: 10.1016/j.bioactmat.2024.09.016.


Stroke: Evolution of newer treatment modalities for acute ischemic stroke.

Nag D, Swain A, Sahu S, Sen B, Vatsala , Parween S World J Clin Cases. 2024; 12(28):6137-6147.

PMID: 39371560 PMC: 11362888. DOI: 10.12998/wjcc.v12.i28.6137.