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Skin Inflammation, Systemic Inflammation, and Cardiovascular Disease in Psoriasis | Dermatology | JAMA Dermatology | vlog

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Brief Report
DZ𳾲20, 2024

Skin Inflammation, Systemic Inflammation, and Cardiovascular Disease in Psoriasis

Author Affiliations
  • 1Division of Dermatology and Venereology, Department of Medicine, Karolinska Institutet, Stockholm, Sweden
  • 2Dermatology and Venereology Clinic, Karolinska University Hospital, Stockholm, Sweden
  • 3Eli Lilly, Indianapolis, Indiana
  • 4Department of Dermatology, Hospital Universitario Ramon y Cajal, Instituto Ramón y Cajal de Investigación Sanitaria, Madrid, Spain
  • 5Faculty of Medicine, Universidad Francisco de Vitoria, Pozuelo de Alarcón, Madrid, Spain
  • 6Section of Inflammation and Cardiometabolic Diseases, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, Maryland
  • 7Office of Biostatistics Research, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland
  • 8Department of Cardiology, The George Washington University School of Medicine and Health Sciences, Washington, DC
JAMA Dermatol. Published online November 20, 2024. doi:10.1001/jamadermatol.2024.4433
Key Points

Question Does systemic inflammation play a role in the association between skin disease severity and cardiovascular disease (CVD) in psoriasis?

Findings In this cohort study including 769 patients, glycan biomarker of N-acetyl side chains of acute-phase proteins (GlycA), a measure of systemic inflammation, mediated 17% of the association between the Psoriasis Area and Severity Index (PASI)—a measure of skin disease severity—and subclinical atherosclerosis and 37% of the association between PASI and cardiovascular events. The indirect effect was statistically significant in both studies.

Meaning Systemic inflammation may play a role in the association between skin disease severity and CVD in psoriasis.

Abstract

Importance Psoriasis is associated with increased cardiovascular risk, but the underlying pathogenic mechanisms remain unclear. Elucidating these mechanisms can help develop treatment strategies and enhance understanding of the link between peripheral inflammation, such as psoriatic skin lesions, and cardiovascular disease (CVD).

Objective To explore whether systemic inflammation is a mediator of the association between psoriasis skin disease severity and CVD.

Design, Setting, and Participants This cohort study used data from cross-sectional study (Psoriasis Atherosclerosis and Cardiometabolic Disease Initiative [PACI]), which enrolled patients from January 2013 to February 2022, and an inception cohort study (Stockholm Psoriasis Cohort [SPC]), which enrolled patients from January 2000 to December 2005. The PACI enrolled consecutive patients referred by dermatologists in Maryland, and the SPC enrolled consecutive patients referred from a wide range of practices in Sweden. Patients with prevalent psoriasis from the PACI and patients with incident psoriasis from the SPC were included. Data were analyzed from October 2023 to January 2024.

Exposures Psoriasis skin disease severity was measured using the Psoriasis Area and Severity Index (PASI), and systemic inflammation was measured using glycan biomarker of N-acetyl side chains of acute-phase proteins (GlycA). Mediation analysis was performed by evaluating the associations between exposure, mediator, and outcome in patients with first-tertile and third-tertile PASI scores when GlycA level was set at the level observed in patients with first-tertile PASI.

Main Outcomes and Measures Noncalcified coronary burden (NCB) measured using coronary computed tomography angiography in the PACI and hospitalization for CVD or cardiovascular death in the SPC.

Results Of 260 eligible patients from the PACI, 162 (62.3%) were male, and the median (IQR) age was 51 (41-60) years; of 509 eligible patients from the SPC, 237 (46.6%) were male, and the median (IQR) age was 43 (30-57) years. In both studies, PASI was associated with GlycA level and CVD, and GlycA level was associated with CVD. The direct and indirect (through GlycA) effects of PASI on NCB were estimated at 0.94 (95% CI, 0.26-1.74) and 0.19 (95% CI, 0.02-0.47), respectively. The odds ratios for the direct and indirect effects of PASI on cardiovascular events were estimated at 1.23 (95% CI, 0.70-1.92) and 1.16 (95% CI, 1.04-1.42), respectively.

Conclusions and Relevance In this study, skin disease severity measured using PASI was associated with systemic inflammation, and both PASI and systemic inflammation, measured using GlycA levels, were associated with CVD. The association between PASI and CVD may be mediated by systemic inflammation.

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