Related Experiment Video
Updated: Mar 16, 2026

Reduction in Left Ventricular Wall Stress and Improvement in Function in Failing Hearts using Algisyl-LVR
Published on: April 8, 2013
Allopurinol therapy improves vascular endothelial function in subjects at risk for cardiovascular diseases: a
Wei Xin1, Shuhua Mi1, Zhiqin Lin2
1Department of Cardiology, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.
Aims:
The effect of allopurinol on flow-mediated dilation (FMD), an index of endothelial function in humans, remains inconsistent. We performed a meta-analysis to determine whether allopurinol therapy could improve FMD.
Methods:
Human intervention studies were identified by systematic searches of Medline, Embase, Cochrane's library, and references of related reviews and studies. A random-effect model was applied to estimate the pooled results.
Results:
Ten randomized controlled trials with 594 subjects at risk of cardiovascular risks were included. Results of the meta-analysis indicated that allopurinol therapy significantly improved FMD in these subjects as compared with control groups (WMD=1.67%, 95% CI: 0.83% ~ 2.50%, P<.001; I2 =86%), with no evidence of significant heterogeneity if only double-blinded studies were included (WMD=1.36%, 95% CI: 0.89% ~ 1.83%, P<.001; I2 =21%). Results of metaregression and subgroup analyses suggested that the benefit of allopurinol to FMD seemed to be not related to its uric acid (UA)-lowering action. Moreover, allopurinol therapy may be associated with more remarkable improvement of FMD in subjects with lower serum UA (<7 mg/dL: WMD=2.62%, 95% CI: 1.10% ~ 4.14%), compared to those with higher UA (≥7 mg/dL: WMD=0.87%, 95% CI: 0.37% ~ 1.38%; P for subgroup difference=.03).
Conclusions:
Allopurinol therapy is associated with significantly improved endothelial function in subjects at risk of CVD risks, and the beneficial effects of allopurinol seemed to be more remarkable in patients with normal UA at baseline.
Related Concept Videos
Atherosclerosis III: Management
Peripheral Artery Disease III: Interprofessional Care
Treatment for Pulmonary Arterial Hypertension: Prostacyclin Receptor Agonists
These agonists bind to the IPR receptor situated on the plasma membrane of the pulmonary artery smooth muscle cells. This binding triggers a cascade of reactions known as the GS-AC-cAMP-PKA pathway. This pathway results in the relaxation of smooth muscle...
Treatment for Pulmonary Arterial Hypertension: Endothelin Receptor Antagonists
ETs are synthesized through a complex sequence of enzymatic steps, primarily involving an enzyme referred to as endothelin-converting enzyme...
Treatment for Pulmonary Arterial Hypertension: Phosphodiesterase Inhibitors
Among the PDE5 inhibitors, sildenafil (Revatio) stands out as a competitive and selective inhibitor. It operates by elevating cellular levels of cGMP and augmenting signaling through the cGMP-PKG pathway, promoting vasodilation. Upon oral...
Antiplatelet Drugs: Prostaglandin Synthesis, P2Y12 and Glycoprotein IIb/IIIa Inhibitors
Prostaglandin synthesis inhibitors, exemplified by the widely known aspirin, wield their power by irreversibly acetylating...
