Effect of 2 Psoriasis Treatments on Vascular Inflammation and Novel Inflammatory Cardiovascular Biomarkers: A Randomized Placebo-Controlled Trial

Psoriasis is a chronic inflammatory disease associated with dyslipidemia, cardiovascular events, and mortality. We aimed to assess and compare the effect of treatment of moderate-to-severe psoriasis with adalimumab or phototherapy on vascular inflammation and cardiovascular biomarkers. Randomized, d...

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Veröffentlicht in:Circulation. Cardiovascular imaging 2018-06, Vol.11 (6), p.e007394-e007394
Hauptverfasser: Mehta, Nehal N, Shin, Daniel B, Joshi, Aditya A, Dey, Amit K, Armstrong, April W, Duffin, Kristina Callis, Fuxench, Zelma Chiesa, Harrington, Charlotte L, Hubbard, Rebecca A, Kalb, Robert E, Menter, Alan, Rader, Daniel J, Reilly, Muredach P, Simpson, Eric L, Takeshita, Junko, Torigian, Drew A, Werner, Thomas J, Troxel, Andrea B, Tyring, Stephen K, Vanderbeek, Suzette Baez, Van Voorhees, Abby S, Playford, Martin P, Ahlman, Mark A, Alavi, Abass, Gelfand, Joel M
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Sprache:eng
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Zusammenfassung:Psoriasis is a chronic inflammatory disease associated with dyslipidemia, cardiovascular events, and mortality. We aimed to assess and compare the effect of treatment of moderate-to-severe psoriasis with adalimumab or phototherapy on vascular inflammation and cardiovascular biomarkers. Randomized, double-blind, trial of adalimumab, phototherapy, and placebo (1:1:1) for 12 weeks, with crossover to adalimumab for 52 weeks total. Outcomes included vascular inflammation by F-fluorodeoxyglucose positron emission tomography/computed tomography and biomarkers of inflammation, insulin resistance, and lipoproteins. Ninety-seven patients were randomized, 92 completed the randomized controlled trial portion; 81 entered the adalimumab extension with 61 completing 52 weeks of adalimumab. There was no difference in change in vascular inflammation at week 12 in the adalimumab group (change compared with placebo, 0.64%; 95% confidence interval, -5.84% to 7.12%) or the phototherapy group (-1.60%; 95% confidence interval, -6.78% to 3.59%) or after 52-week adalimumab treatment (0.02% compared with initiation; 95% confidence interval, -2.85% to 2.90%). Both adalimumab and phototherapy decreased inflammation by serum CRP, interleukin-6. Only adalimumab reduced tumor necrosis factor and glycoprotein acetylation at 12 and 52 weeks. Neither had an impact on metabolic markers (insulin, adiponectin, and leptin). Only phototherapy increased high-density lipoprotein-p at 12 weeks. At 52-week of adalimumab cholesterol efflux and high-density lipoprotein-p were reduced. Adalimumab reduced key markers of inflammation including glycoprotein acetylation compared with phototherapy with no effect on glucose metabolism and vascular inflammation, and potential adverse effects on high-density lipoprotein. Glycoprotein acetylation improvement may partially explain the beneficial effects of adalimumab seen in observational studies. Larger studies with more detailed phenotyping of vascular disease should assess the comparative differences in the effects of adalimumab and phototherapy seen in our study. URL: https://www.clinicaltrials.gov. Unique identifiers: NCT01866592 and NCT01553058.
ISSN:1941-9651
1942-0080
DOI:10.1161/CIRCIMAGING.117.007394