In order to bring you the best possible user experience, this site uses Javascript. If you are seeing this message, it is likely that the Javascript option in your browser is disabled. For optimal viewing of this site, please ensure that Javascript is enabled for your browser.
Did you know that your browser is out of date? To get the best experience using our website we recommend that you upgrade to a newer version. Learn more.

Gout drug reduces adverse events in patients with hyperuricaemia

Renal Failure and Cardiovascular Disease

Munich, Germany – 28 Aug 2018: Uric acid reduction with the gout treatment febuxostat reduces adverse events in elderly patients with hyperuricaemia, according to late breaking research presented today in a Hot Line Session at ESC Congress 2018(1).

Hyperuricaemia, an abnormally high serum uric acid level, causes gout and is associated with coronary artery disease, hypertension, stroke, renal failure, and death. The FREED study(2) examined whether lowering uric acid with febuxostat prevents cerebral, cardiovascular and renal events and death in elderly patients with the condition.

The study enrolled 1,070 patients aged 65 years and older with hyperuricaemia (serum uric acid 7–9 mg/dL) and at risk for cerebral, cardiovascular, or renal events as defined by the presence of hypertension, type 2 diabetes, renal disorder, or a history of cerebral or cardiovascular disease(3).

Patients were randomly assigned in a 1:1 ratio to receive oral febuxostat for 36 months or not. In the febuxostat group, the dose was increased stepwise from 10 to 40 mg per day if tolerated. In the non-febuxostat group, allopurinol 100 mg was considered if serum uric acid was elevated. In both groups, the dose of febuxostat or allopurinol was adjusted to avoid a serum uric acid level less than 2 mg/dL. All patients were advised to consume a healthy diet, quit smoking, and exercise to help manage their hyperuricaemia.

Patients were followed-up for 36 months for the primary endpoint which was a composite of cerebral, cardiovascular, and renal events, and death from any cause. This consisted of death due to cerebral or cardiorenal vascular disease, new or recurring cerebrovascular disease, new or recurring coronary artery disease, cardiac failure requiring hospitalisation, arteriosclerotic disease requiring treatment, renal disease (development of microalbuminuria, progression to overt proteinuria, or worsening of overt proteinuria to ≥300 mg/g albumin/creatinine, doubling of serum creatinine level, progression to end stage renal disease defined as estimated glomerular filtration rate <15 mL/min/1.73 m2), and new atrial fibrillation.

A total of 537 patients received febuxostat and the average dose at the end of the study was 29 mg. Of the 533 patients in the non-febuxostat group, 27% received allopurinol 100 mg. Average serum uric acid levels reached 4.4 mg/dL in the febuxostat group and 6.7 mg/dL in the group not receiving febuxostat.

The primary endpoint occurred in 125 (23%) patients in the febuxostat group and 153 (29%) patients in the non-febuxostat group. Febuxostat significantly reduced the rate of the primary endpoint, with a hazard ratio of 0.75 (95% confidence interval 0.59–0.95, p=0.017) (see figure).

When the individual components of the primary endpoint were analysed separately, the most frequent event was renal impairment, which occurred in 16.2% of the febuxostat group and 20.5% of the non-febuxostat group. Among those with renal impairment, the development of microalbuminuria or mild proteinuria was common in both treatment groups.

Adverse events were observed in 132 (24.6%) patients in the febuxostat group and 135 (25.3%) patients in the non-febuxostat group, with no significant difference between the two groups (p=0.83). Two patients in the febuxostat group died. Also in the febuxostat group, mental disorder, headache, hypertension, abdominal pain, diarrhoea, maculopapular rash, acute kidney injury, and oedema of the extremities occurred in two patients each.

Professor Sunao Kojima, principal investigator, Kawasaki Medical School, Okayama, Japan, said: : “We found that patients receiving febuxostat were 25% less likely to die or experience strokes, heart disease, or kidney disease over a three-year period than patients who did not receive febuxostat. The findings suggest that lowering uric acid with febuxostat provides clinical benefit.”

Figure: Kaplan–Meier curves for the primary composite event

Kojima FREED.png




Notes to editor

SOURCES OF FUNDING: Teijin Pharma Limited.



(1)“FREED - Febuxostat for Cerebral and CaRdiorenovascular Events PrEvEntion StuDy” will be discussed during:

(2)FREED: Febuxostat for Cerebral and CaRdiorenovascular Events PrEvEntion StuDy.

(3)Kojima S, Matsui K, Ogawa H, et al. Rationale, design, and baseline characteristics of a study to evaluate the effect of febuxostat in preventing cerebral, cardiovascular, and renal events in patients with hyperuricemia. J Cardiol. 2017;69:169–175. doi: 10.1016/j.jjcc.2016.02.015.

ESC Press Office
For press enquiries, independent comment on-site, please contact the ESC Press Office at  

To access congress scientific resources visit ESC Congress 365.  

About the European Society of Cardiology

The European Society of Cardiology brings together health care professionals from more than 150 countries, working to advance cardiovascular medicine and help people lead longer, healthier lives.

About ESC Congress 2018

ESC Congress is the world’s largest and most influential cardiovascular event contributing to global awareness of the latest clinical trials and breakthrough discoveries. ESC Congress 2018 takes place 25 to 29 August at the Messe München in Munich, Germany. Explore the scientific programme. More information is available from the ESC Press Office at

This press release accompanies both a presentation and an ESC press conference at the ESC Congress 2018. Edited by the ESC from material supplied by the investigators themselves, this press release does not necessarily reflect the opinion of the European Society of Cardiology. The content of the press release has been approved by the presenter.