Key result
The abstract describes the study design to evaluate the relationship between hyperuricaemia and MACE in 4,290 subjects, but does not report any quantitative results.
Why the study?
Serum uric acid has been proposed as a biomarker to improve cardiovascular risk stratification, but contradictory results exist influenced by sex and age differences.
Does hyperuricaemia predict the incidence of major adverse cardiovascular events in primary care patients without prior cardiovascular disease?
Cohort (n=4,290)
Yes
Does hyperuricaemia predict the incidence of major adverse cardiovascular events in primary care patients without prior cardiovascular disease?
The abstract describes the methodology of a prospective cohort study evaluating the prognostic value of serum uric acid for cardiovascular events in primary care, but does not report the results.
No results reported to guide primary care risk assessment; leaves open whether hyperuricaemia predicts MACE in CVD-free patients.
Atherosclerosis, the pathophysiological basis of cardiovascular disease (CVD), progresses insidiously under the influence of cardiovascular risk factors (CVRFs).1 It is relevant for primary care (PC) to improve the predictive capacity of classical equations due to the underestimation of risk in a non-negligible number of patients.2,3 Serum uric acid (SUA) has been proposed as a potential biomarker to improve cardiovascular risk stratification, but contradictory results have been observed, most likely influenced by the different behaviour of uric acid (UA) depending on sex and age.4,5 The present study aims to evaluate the relationship between UA levels and the incidence of major adverse cardiovascular events (MACE) according to sex and age. A subgroup analysis of the IBERICAN study,6 a prospective cohort of patients recruited from PC centres, was conducted. For this study, 4290 subjects free of prior CVD with baseline UA measurements were included. The sample accumulated a total follow-up of 11 997 person-years (5229 in men and 6768 in women), with a median follow-up of 2.6 years. Hyperuricaemia (HU) was defined using sex-specific cut-off points (≥6 mg/dL in women and ≥7 mg/dL in men). Likewise, the population was stratified into sex-specific quartiles (Q) of SUA: men: Q1 < 4.91 mg/dL; Q2: 4.91–5.85 mg/dL; Q3: 5.86–6.81 mg/dL; and Q4 ≥ 6.82 mg/dL and women: Q1 < 3.81 mg/dL; Q2: 3.81–4.60 mg/dL; Q3: 4.61–5.40 mg/dL; and Q4 ≥ 5.41 mg/dL. The primary outcome variable was the incidence of MACE, which included hospital admission or mortality due to acute myocardial infarction, heart failure, stroke, or peripheral arterial disease.
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Antelo-Pais et al. (2026) conducted a cohort in Cardiovascular risk (n=4,290). Hyperuricaemia vs. Normal uric acid levels was evaluated on Incidence of MACE (hospital admission or mortality due to acute myocardial infarction, heart failure, stroke, or peripheral arterial disease). The abstract describes the study design to evaluate the relationship between hyperuricaemia and MACE in 4,290 subjects, but does not report any quantitative results.
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