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Author
- Berstein, Gabriel1
- Brodmerkel, Carrie1
- Campbell, Kim1
- Correa-da Rosa, Joel1
- Curran, Mark1
- Fitz, Lori J1
- Garcet, Sandra1
- Huang, C Chris1
- Kim, Jaehwan1
- Krueger, James G1
- Lee, Julie1
- Li, Katherine1
- Li, Shu1
- Lowes, Michelle A1
- Randazzo, Bruce1
- Suarez-Farinas, Mayte1
- Szapary, Philippe1
- Tomalin, Lewis1
- Valdez, Hernan1
- Wolk, Robert1
Keyword
- PASI2
- tumor necrosis factor2
- 50/75/90% improvement from baseline in Psoriasis Area and Severity Index1
- false discovery rate1
- FCH1
- FDR1
- fold change1
- gene-set variation analysis1
- GSVA1
- HLA1
- HLA-C*06:02-NEG1
- HLA-C*06:02-negative1
- HLA-C*06:02-POS1
- HLA-C*06:02-positive1
- human leukocyte antigen1
- JAK1
- Janus kinase1
- PASI 50/75/701
- T helper type 171
- TH171
- TRANCE1
- tumor necrosis factor-related activation-induced cytokine1
Psoriasis
2 Results
- Original Article Clinical ResearchOpen Archive
Reduction of Inflammatory and Cardiovascular Proteins in the Blood of Patients with Psoriasis: Differential Responses between Tofacitinib and Etanercept after 4 Weeks of Treatment
Journal of Investigative DermatologyVol. 138Issue 2p273–281Published online: September 16, 2017- Jaehwan Kim
- Lewis Tomalin
- Julie Lee
- Lori J. Fitz
- Gabriel Berstein
- Joel Correa-da Rosa
- and others
Cited in Scopus: 32Patients with psoriasis have an increased risk of myocardial infarction, and psoriasis is now recognized as an independent risk factor for coronary heart disease and cardiovascular mortality. To understand the effects of psoriasis medications on systemic inflammation associated with cardiovascular risks, we studied blood proteins related to inflammation and cardiovascular disease archived from a phase 3 clinical trial of tofacitinib and etanercept in adults with moderate-to-severe psoriasis. A total of 157 blood proteins were quantified by a proximity extension assay from 266 patients at baseline and week 4. - Original Article Clinical ResearchOpen Access
HLA-C*06:02 Allele and Response to IL-12/23 Inhibition: Results from the Ustekinumab Phase 3 Psoriasis Program
Journal of Investigative DermatologyVol. 136Issue 12p2364–2371Published online: July 29, 2016- Katherine Li
- C. Chris Huang
- Bruce Randazzo
- Shu Li
- Philippe Szapary
- Mark Curran
- and others
Cited in Scopus: 41Several small studies suggest that the presence of the human leukocyte antigen (HLA)-Cw6 (C*06:02) allele may be a predictor of improved response to ustekinumab. This study was designed to assess the association of the HLA-C*06:02 allele with response to ustekinumab in large cohorts of patients from the phase 3 studies of ustekinumab in moderate-to-severe psoriasis. In this retrospective study, both HLA-C*06:02-positive and -negative patients demonstrated good responses to ustekinumab (86% vs. 76%, respectively, achieved at least a 75% improvement from baseline in Psoriasis Area and Severity Index [PASI 75] at week 24).