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Author
- Bissonnette, Robert1
- Chabot-Blanchet, Malorie1
- Delorme, Isabelle1
- Frueh, Jennifer1
- Gonzalez, Juana1
- Gori, Tommaso1
- Guertin, Marie-Claude1
- Harel, François1
- Koenig, Wolfgang1
- Krueger, James G1
- Körber, Andreas1
- Lynde, Charles W1
- Maari, Catherine1
- Mani, Venkatesh1
- Mehta, Nehal N1
- Melzer, Nima1
- Pinter, Andreas1
- Rassaf, Tienush1
- Reich, Kristian1
- Sieder, Christian1
- Tardif, Jean-Claude1
- Thaçi, Diamant1
- von Stebut, Esther1
- Waisman, Ari1
- Yates, Denise1
Keyword
- 18-fluoro-2-deoxy-d-glucose1
- 18FDG1
- CAD1
- cardiovascular1
- CARIMA1
- CI1
- confidence interval1
- coronary artery disease1
- CV1
- Evaluation of Cardiovascular Risk Markers in Psoriasis Patients Treated with Secukinumab1
- flow-mediated dilation1
- FMD1
- high-sensitivity C-reactive protein1
- hs-CRP1
- magnetic resonance imaging1
- MRI1
- PET/CT1
- position emission tomography-computed tomography1
- Psoriasis Area and Severity Index1
- Psoriasis Area Severity Index1
- pulse wave velocity1
- PWV1
- TBR1
Psoriasis
2 Results
- Original Article Clinical Research: TherapeuticsOpen Access
Impact of Secukinumab on Endothelial Dysfunction and Other Cardiovascular Disease Parameters in Psoriasis Patients over 52 Weeks
Journal of Investigative DermatologyVol. 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: 114Psoriasis 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. - Original Article Clinical ResearchOpen Archive
TNF-α Antagonist and Vascular Inflammation in Patients with Psoriasis Vulgaris: A Randomized Placebo-Controlled Study
Journal of Investigative DermatologyVol. 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: 73Vascular 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.