Prevention & lipidsResearch article

Urate-lowering therapy in cardiovascular pharmacotherapy: from Mendelian randomization data to cardio–renal–metabolic risk modulation

Eur Heart J Cardiovasc PharmacotherPublished

  • review

Authors' conclusion

Serum uric acid is a cardio-renal-metabolic biomarker and a plausible therapeutic target in selected cardio-renal-metabolic phenotypes. However, evidence does not support routine ULT for CV prevention in asymptomatic hyperuricaemia. Urate-lowering therapy should remain focused on gout and symptomatic hyperuricaemia, with phenotype-guided strategies to identify patients with asymptomatic hyperuricemia most likely to benefit.

Study context

Population
Studies of serum uric acid, hyperuricaemia and urate-lowering therapy in cardiovascular risk

Main finding

As reported in the abstract

Prevalence of hyperuricaemia
  • Hyperuricaemia is prevalent and rising, often closely accompanying obesity, hypertension, diabetes, and chronic kidney disease (CKD)

Further findings

Serum uric acid (SUA) and cardiovascular (CV) outcomes

Higher SUA correlates with coronary artery disease, heart failure, stroke, cardio-renal-metabolic syndromes, and mortality, with non-linear risk relationships and sex- and age-specific thresholds

Mendelian randomization

Modest causal contribution of genetically elevated SUA to blood pressure, coronary disease, and advanced CKD

CV events with urate-lowering therapy (ULT)

No consistent reduction in CV events when ULT is added to guideline-directed therapy in asymptomatic hyperuricaemia, stable ischaemic heart disease, chronic heart failure, or CKD
Observational data suggest long-term, adequately dosed xanthine oxidase inhibitors (XOIs) and high cumulative uricosuric exposure may reduce coronary risk

Original publication

Urate-lowering therapy in cardiovascular pharmacotherapy: from Mendelian randomization data to cardio–renal–metabolic risk modulation. Eur Heart J Cardiovasc Pharmacother. Published 17 June 2026. doi:10.1093/ehjcvp/pvag042

Summarised from the published abstract; every number is checked against it