Key result
Higher serum calprotectin linked to ~3-fold higher odds of carotid plaque in psoriatic arthritis.
Why the study?
Whether calprotectin could play a role in augmenting cardiovascular risk in patients with psoriatic arthritis remains uncertain.
Are serum calprotectin levels associated with subclinical atherosclerosis and arterial stiffness in patients with psoriatic arthritis?
Cross-Sectional (n=78)
No
Are serum calprotectin levels associated with subclinical atherosclerosis and arterial stiffness in patients with psoriatic arthritis?
Odds Ratio: 3.19 (95% CI 1.22–8.38)
p-value: p=0.018
Serum calprotectin levels are independently associated with the presence of carotid plaque and increased carotid intima-media thickness in patients with psoriatic arthritis, suggesting its potential as a biomarker for cardiovascular risk stratification.
Calprotectin may support cardiovascular risk stratification in psoriatic arthritis; leaves open clinical utility and requires prospective validation.
Background Whether calprotectin could play a role in augmenting cardiovascular (CV) risk in patients with psoriatic arthritis (PsA) remains uncertain. The aim of this study is to elucidate the association between serum calprotectin and subclinical atherosclerosis and arterial stiffness in patient with PsA. Method Seventy-eight PsA patients (age: 52±10 years, 41 [52.6%] male) without CV disease were recruited into this cross-sectional study. Carotid intima-media thickness (cIMT) and the presence of plaque were determined by high-resolution ultrasound. Arterial stiffness was measured by brachial-ankle PWV (baPWV) and augmentation index (AIx) Calprotectin levels in serum were quantified by enzyme-linked immunosorbent assay. Results 29/78 (37.2%) of patient had carotid plaque (CP+ group). Serum calprotectin levels were significantly higher in the CP+ group (CP- group: 564.6 [329.3-910.5] ng/ml; CP+ group: 721.3 [329.3-910.5] ng/ml, P=0.005). Serum calprotectin level correlated with C-reactive protein (CRP) (r=0.244, P =0.033) and PsA disease duration (r=0.245, P =0.030). Using multivariate logistic regression analysis, the levels of Ln-calprotectin were significantly associated with the presence of CP (OR: 3.19, 95% confidence interval [CI]: [1.22, 8.38]; P=0.018), and mean cIMT (β: 0.35, 95% CI [0.02, 0.68]; P=0.038) after adjusting for baseline covariates. The optimal cut-offs for discriminating patients with and without CP were calprotectin >569ng/ml (AUC: 0.688; sensitivity: 79%; specificity: 51%; P=0.006) and FRS >9% (AUC: 0.645; sensitivity: 62%; specificity: 67%; P=0.033). Conclusion Serum calprotectin level may be a good biomarker for CV risk stratification in PsA. Further studies are required to confirm whether this pathway is associated with CV events in PsA.
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T et al. (2022) conducted a cross-sectional in Psoriatic Arthritis (n=78). Serum calprotectin level vs. Lower serum calprotectin levels was evaluated on Presence of carotid plaque (OR 3.19, 95% CI 1.22-8.38, p=0.018). Higher log-transformed serum calprotectin levels were independently associated with the presence of carotid plaque in patients with psoriatic arthritis (OR 3.19).
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