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

Author:

Gonzalez-Cantero Alvaro1,Reddy Aarthi S2,Dey Amit K2,Gonzalez-Cantero Jorge3,Munger Eric2,Rodante Justin2,Sanchez-Moya Ana I4,Perez-Hortet Cristina4,Gonzalez-Calvin Jorge L5,Playford Martin P2,Barderas María G6,Ballester Asunción1,Jimenez-Gomez Natalia1,Jaén Pedro1,Chen Marcus Y2,Gelfand Joel M7,Mehta Nehal N2

Affiliation:

1. Department of Dermatology, Hospital Universitario Ramón y Cajal, Madrid, Spain

2. Section of Inflammation and Cardiometabolic Diseases, National Heart, Lung and Blood Institute, National Institutes of Health, 10 Center Drive, Clinical Research Center, Room 5-5140, Bethesda, MD 20892, USA

3. Department of Radiology, Gregorio Marañon Hospital, Madrid, Spain

4. Department of Dermatology, Complejo Hospitalario de Toledo, Toledo, Spain

5. Department of Gastroenterology, University Hospital San Cecilio, Granada, Spain

6. Department of Vascular Physiopathology, Hospital Nacional de Parapléjicos (HNP), SESCAM, Toledo, Spain

7. Department of Dermatology, University of Pennsylvania, Philadelphia, PA, USA

Abstract

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.

Funder

National Heart, Lung and Blood Institute (NHLBI) Intramural Research Program

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine,Epidemiology

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