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Serum Urate as a Cardiometabolic Risk Enhancer Beyond SCORE2 in Psoriatic Arthritis
Lilyan C Charca1, Marta Loredo2, Estefanía Pardo2
1Rheumatology Section, Fundació Hospital de l'Esperit Sant, 08923 Santa Coloma de Gramenet, Spain.
Insights
Serum urate improves cardiovascular risk prediction in psoriatic arthritis patients beyond the standard SCORE2 assessment. This accessible marker helps identify subclinical atherosclerosis, enhancing risk stratification for better patient management.
Area of Science:
- Rheumatology
- Cardiology
- Biochemistry
Background:
- Cardiovascular risk (CVR) prediction models like SCORE2 may underestimate atherosclerosis in chronic inflammatory diseases.
- Subclinical atherosclerosis detection needs simpler markers for refined risk stratification.
Purpose of the Study:
- To assess if serum urate improves subclinical atherosclerosis detection in psoriatic arthritis (PsA) patients, beyond SCORE2.
- To evaluate serum urate's role in refining CVR stratification in PsA.
Main Methods:
- Cross-sectional study of 250 PsA patients (CASPAR criteria).
- Vascular assessment included ultrasound and radiography for atherosclerotic plaque.
- Multivariable logistic regression and decision curve analysis (DCA) were used.
Main Results:
- Hyperuricemia (21.6%) was linked to higher global plaque prevalence (88.9% vs. 62.8%).
- Serum urate independently predicted global plaque after SCORE2 adjustment (OR 4.23).
- Adding serum urate improved risk reclassification (cfNRI +0.60) in the 50-69 age group.
Conclusions:
- SCORE2 showed discordance with imaging-defined atherosclerosis in PsA patients.
- Serum urate is a valuable, accessible marker for refining CVR stratification.
- This marker can help identify PsA patients needing further vascular assessment.
Abstract:
Background/Objectives: Cardiovascular risk (CVR) prediction using SCORE2 may incompletely capture the burden of subclinical atherosclerosis in patients with chronic inflammatory conditions. Identifying simple, accessible markers to refine risk stratification remains an unmet need. This study aimed to evaluate whether serum urate improves detection of subclinical atherosclerosis beyond SCORE2 in a psoriatic arthritis cohort. Methods: We conducted a cross-sectional study including 250 patients with psoriatic arthritis fulfilling CASPAR criteria. Vascular assessment comprised carotid and femoral ultrasound and abdominal radiography. Atherosclerotic plaque was defined according to Mannheim criteria. The main outcomes were global plaque (≥1 vascular territory) and extended plaque (≥2 territories). Multivariable logistic regression adjusted for SCORE2 categories assessed independent associations. Incremental value was evaluated using decision curve analysis (DCA), category-free net reclassification improvement (cfNRI), and integrated discrimination improvement (IDI). Results: Hyperuricemia prevalence was 21.6%. Patients with hyperuricemia showed a higher prevalence of global plaque (88.9% vs. 62.8%, p < 0.001). After adjustment for SCORE2, serum urate was independently associated with global plaque (OR 4.23, 95% CI 1.26-14.2). Notably, 64.3% of patients classified as low-moderate risk already exhibited plaque. In the 50-69-year subgroup, adding serum urate improved reclassification (cfNRI +0.60; IDI +0.031) and was associated with higher net clinical benefit across decision thresholds. The combined model (SCORE2+HU+cIMT) achieved the highest curves, although with limited incremental gain over HU alone. Conclusions: SCORE2 categories showed substantial discordance with imaging-defined subclinical atherosclerotic burden in this population. Serum urate, an inexpensive and widely available marker, may help refine cardiovascular risk stratification and identify patients who could benefit from further vascular assessment.
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