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Inflammasome Signaling and Impaired Vascular Health in Psoriasis.
Garshick, Michael S; Barrett, Tessa J; Wechter, Todd; Azarchi, Sarah; Scher, Jose U; Neimann, Andrea; Katz, Stuart; Fuentes-Duculan, Judilyn; Cannizzaro, Maria V; Jelic, Sanja; Fisher, Edward A; Krueger, James G; Berger, Jeffrey S.
Afiliación
  • Garshick MS; From the Center for the Prevention of Cardiovascular Disease, Department of Medicine (M.S.G., E.A.F., J.S.B.), New York University School of Medicine, New York.
  • Barrett TJ; Leon H. Charney Division of Cardiology, Department of Medicine (M.S.G., T.J.B., S.K., E.A.F., J.S.B.), New York University School of Medicine, New York.
  • Wechter T; Leon H. Charney Division of Cardiology, Department of Medicine (M.S.G., T.J.B., S.K., E.A.F., J.S.B.), New York University School of Medicine, New York.
  • Azarchi S; School of Medicine at Stony Brook University, New York (T.W.).
  • Scher JU; Ronald O. Perelman Department of Dermatology (S.A., A.N.), New York University School of Medicine, New York.
  • Neimann A; Division of Rheumatology, Psoriatic Arthritis Center, Department of Medicine (J.U.S.), New York University School of Medicine, New York.
  • Katz S; Ronald O. Perelman Department of Dermatology (S.A., A.N.), New York University School of Medicine, New York.
  • Fuentes-Duculan J; Leon H. Charney Division of Cardiology, Department of Medicine (M.S.G., T.J.B., S.K., E.A.F., J.S.B.), New York University School of Medicine, New York.
  • Cannizzaro MV; Laboratory for Investigative Dermatology, Rockefeller University, New York (J.F.-D., J.G.K.).
  • Jelic S; Department of Dermatology and Venerology, University of Rome Tor Vergata, Italy (M.V.C.).
  • Fisher EA; Division of Pulmonary, Allergy and Critical Care Medicine, Department of Medicine, Columbia University Medical Center, New York (S.J.).
  • Krueger JG; From the Center for the Prevention of Cardiovascular Disease, Department of Medicine (M.S.G., E.A.F., J.S.B.), New York University School of Medicine, New York.
  • Berger JS; Leon H. Charney Division of Cardiology, Department of Medicine (M.S.G., T.J.B., S.K., E.A.F., J.S.B.), New York University School of Medicine, New York.
Arterioscler Thromb Vasc Biol ; 39(4): 787-798, 2019 04.
Article en En | MEDLINE | ID: mdl-30760013
ABSTRACT
Objective- Psoriasis is an inflammatory skin disease which heightens the risk of cardiovascular disease. This study directly investigated vascular endothelial health and systemically altered pathways in psoriasis and matched controls. Approach and Results- Twenty patients (mean age, 40 years; 50% male) with active psoriasis and 10 age-, sex-matched controls were recruited. To investigate systemically alerted pathways, a deep sequencing omics approach was applied, including unbiased blood transcriptomic and targeted proteomic analysis. Vascular endothelial health was assessed by transcriptomic profiling of endothelial cells obtained from the brachial veins of recruited participants. Blood transcriptomic profiling identified inflammasome signaling as the highest differentially expressed canonical pathway ( Z score 1.6; P=1×10-7) including upregulation of CASP5 and interleukin ( IL) -1ß. Proteomic panels revealed IL-6 as a top differentially expressed cytokine in psoriasis with pathway analysis highlighting IL-1ß ( Z score 3.7; P=1.02×10-23) as an upstream activator of the observed upregulated proteins. Direct profiling of harvested brachial vein endothelial cells demonstrated inflammatory transcript (eg, IL-1ß, CXCL10, VCAM-1, IL-8, CXCL1, Lymphotoxin beta, ICAM-1, COX-2, and CCL3) upregulation between psoriasis versus controls. A linear relationship was seen between differentially expressed endothelial inflammatory transcripts and psoriasis disease severity. IL-6 levels correlated with inflammatory endothelial cell transcripts and whole blood inflammasome-associated transcripts, including CASP5 and IL-1ß. Conclusions- An unbiased sequencing approach demonstrated the inflammasome as the most differentially altered pathway in psoriasis versus controls. Inflammasome signaling correlated with psoriasis disease severity, circulating IL-6, and proinflammatory endothelial transcripts. These findings help better explain the heightened risk of cardiovascular disease in psoriasis. Clinical Trial Registration- URL http//www.clinicaltrials.gov . Unique identifier NCT03228017.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Psoriasis / Células Endoteliales / Inflamasomas Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Arterioscler Thromb Vasc Biol Asunto de la revista: ANGIOLOGIA Año: 2019 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Psoriasis / Células Endoteliales / Inflamasomas Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Arterioscler Thromb Vasc Biol Asunto de la revista: ANGIOLOGIA Año: 2019 Tipo del documento: Article