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Underperformance of clinical risk scores in identifying imaging-based high cardiovascular risk in psoriasis: results from two observational cohorts

Álvaro González‐Cantero, Aarthi Reddy, Amit Dey, Jorge L. González-Calvin, Eric Munger, Justin Rodante, A.I. Sánchez‐Moya, Cristina Pérez‐Hortet, Jorge L. González-Calvin, Martin P. Playford, María G. Barderas, Asunción Ballester, N. Jiménez-Gómez, Pedro Jaén, Marcus Y. Chen, Joel M. Gelfand, Nehal N. Mehta

2020European Journal of Preventive Cardiology22 citationsDOI

Abstract

AIMS: We aimed to evaluate whether traditional risk scores [short-term, 'psoriasis-modified' (multiplied by 1.5) and lifetime] were able to capture high cardiovascular disease (CVD) risk as defined by the presence of atherosclerotic plaques in coronary, femoral, or carotid arteries in psoriasis. METHODS AND RESULTS: We used two prospectives obseravational cohorts. European cohort: femoral and carotid atherosclerotic plaques were evaluated by ultrasound in 73 psoriasis patients. Lifetime CVD risk (LTCVR) was evaluated with QRISK-LT; short-term CVD risk was evaluated with SCORE and psoriasis-modified SCORE. American cohort: 165 patients underwent coronary computed tomography angiography to assess presence of coronary plaques. LTCVR was evaluated with atherosclerotic cardiovascular disease (ASCVD-LT) lifetime; short-term CVD risk was evaluated with ASCVD and psoriasis-modified ASCVD. European cohort: subclinical atherosclerosis was present in 51% of patients. QRISK-LT identified 64% of patients with atherosclerosis missing a high proportion (35%) with atheroma plaque (P < 0.05). The percentage of patients with atherosclerosis identified by QRISK-LT was significantly higher than those detected by SCORE (0%) and modified SCORE (10%). American cohort: subclinical atherosclerosis was present in 54% of patients. ASCVD-LT captured 54% of patients with coronary plaques missing a high proportion (46%) with coronary plaque (P < 0.05). The percentage of patients with atheroma plaques detected with ASCVD and modified ASCVD were only 20% and 45%, respectively. CONCLUSIONS: Application of lifetime, short-term and 'psoriasis-modified' risk scores did not accurately capture psoriasis patients at high CVD risk.

Topics & Concepts

MedicineInternal medicinePsoriasisCohortCardiologyFramingham Risk ScoreSubclinical infectionCoronary atherosclerosisAtheromaCoronary artery diseaseCohort studyAtherosclerotic cardiovascular diseaseDiseaseDermatologyPsoriasis: Treatment and PathogenesisSpondyloarthritis Studies and TreatmentsRheumatoid Arthritis Research and Therapies