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    • Psoriasis
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    • Research Article2

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    • Bissonnette, Robert1
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    • 18-fluoro-2-deoxy-d-glucose1
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    • Original Article Clinical Research: Therapeutics
      Open Access

      Impact of Secukinumab on Endothelial Dysfunction and Other Cardiovascular Disease Parameters in Psoriasis Patients over 52 Weeks

      Journal of Investigative Dermatology
      Vol. 139Issue 5p1054–1062Published online: November 30, 2018
      • Esther von Stebut
      • Kristian Reich
      • Diamant Thaçi
      • Wolfgang Koenig
      • Andreas Pinter
      • Andreas Körber
      • and others
      Cited in Scopus: 114
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        Psoriasis increases the risk of cardiovascular (CV) disease. Secukinumab, a fully human monoclonal antibody against IL-17A, shows significant efficacy in psoriasis, but effects on CV markers are unknown. CARIMA (Evaluation of Cardiovascular Risk Markers in Psoriasis Patients Treated with Secukinumab) was a 52-week, randomized, double-blind, placebo-controlled, exploratory trial in patients with moderate to severe plaque psoriasis without clinical CV disease. Patients were randomly assigned to receive 300 mg or 150 mg secukinumab until week 52 or to receive placebo until week 12 and then 300 mg or 150 mg secukinumab until week 52.
        Impact of Secukinumab on Endothelial Dysfunction and Other Cardiovascular Disease Parameters in Psoriasis Patients over 52 Weeks
      • Original Article Clinical Research
        Open Archive

        TNF-α Antagonist and Vascular Inflammation in Patients with Psoriasis Vulgaris: A Randomized Placebo-Controlled Study

        Journal of Investigative Dermatology
        Vol. 137Issue 8p1638–1645Published online: March 9, 2017
        • Robert Bissonnette
        • François Harel
        • James G. Krueger
        • Marie-Claude Guertin
        • Malorie Chabot-Blanchet
        • Juana Gonzalez
        • and others
        Cited in Scopus: 73
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          Vascular inflammation is increased in patients with psoriasis. This randomized, double-blind, multicenter study evaluated the effects of tumor necrosis factor-α antagonist adalimumab on vascular inflammation in patients with psoriasis. A total of 107 patients were randomized (1:1) to receive adalimumab for 52 weeks or placebo for 16 weeks followed by adalimumab for 52 weeks. Vascular inflammation was assessed with positron emission tomography-computed tomography. There were no differences in the change from baseline in vessel wall target-to-background ratio (TBR) from the ascending aorta (primary endpoint) (adalimumab: TBR = 0.002, 95% confidence interval [CI] = –0.048 to 0.053; placebo: TBR = –0.002, 95% CI = –0.053 to 0.049; P = 0.916) and the carotids (adalimumab: TBR = 0.031, 95% CI = –0.005 to 0.066; placebo: TBR = 0.018, 95% CI = –0.019 to 0.055; P = 0.629) at week 16 between adalimumab and placebo.
          TNF-α Antagonist and Vascular Inflammation in Patients with Psoriasis Vulgaris: A Randomized Placebo-Controlled Study
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