Affiliation:
1. Ziekenhuis Netwerk Atwerpen, Antwerp, and University Hospitals Leuven Leuven Belgium
2. University Hospitals Leuven and Skeletal Biology and Engineering Research Centre, KU Leuven Leuven Belgium
Abstract
ObjectiveThe aim of this study was to investigate the prevalence of comorbidities and cardiovascular (CV) risk factors (RFs) in treatment‐naive patients with early psoriatic arthritis (ePsA) and to identify factors that contribute to metabolic burden in ePsA.MethodsThis was an observational longitudinal multicenter cohort study. Clinical and demographic characteristics, CV RFs, and comorbidities were compared in patients newly diagnosed with psoriatic arthritis (PsA) and sex‐ and age‐matched controls. In patients with PsA, comorbidities were reevaluated after one year's follow‐up because the disease activity changed.ResultsSixty‐seven patients with ePsA and 61 healthy volunteers were included. The rate of comorbidities was similar in patients with ePsA and in healthy controls; 82.1% of patients with ePsA had CV RFs at baseline as compared with 62.3% of healthy volunteers (odds ratio [OR] 1.6, 95% confidence interval [CI] 1.14–2.0). Patients with ePsA had higher odds of having multiple (two or more) comorbidities (OR 1.9, 95% CI 1.2–3.0) and multiple CV RFs (OR 2.1, 95% CI 1.3–3.2) than the controls. Comorbidities or CV RFs in patients with ePsA were not influenced by duration of skin psoriasis. Dyslipidemia was the most prevalent comorbidity in the PsA cohort (64.2% vs 39.3% in controls; OR 1.7, 95% CI 1.2–2.5). Patients with ePsA had, on average, above normal body mass index (mean ± SD 28.82 ± 4.5) and a higher rate of obesity (40.3% vs 18.3% in controls; OR 1.9, 95% CI 1.1–3.2). After 1 year, although disease activity scores improved, the proportion of patients with comorbidities and CV RFs did not increase or drop.ConclusionOur data imply that patients with PsA already have higher comorbidities and CV burden at early stages of the disease, suggesting that these are not only a consequence of long‐lasting disease and chronic systemic inflammation.