Tumor necrosis factor-α inhibitor-induced psoriasis: Systematic review of clinical features, histopathological findings, and management experience
Tumor necrosis factor-α (TNF-α) inhibitors have been reported to induce new-onset psoriasis. To better define the demographic, clinical features, and treatment approach of TNF-α inhibitor-induced psoriasis. Systematic review of published cases of TNF-α inhibitor-induced psoriasis. We identified 88 a...
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Published in | Journal of the American Academy of Dermatology Vol. 76; no. 2; pp. 334 - 341 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
01.02.2017
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Subjects | |
Online Access | Get full text |
ISSN | 0190-9622 1097-6787 |
DOI | 10.1016/j.jaad.2016.08.012 |
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Abstract | Tumor necrosis factor-α (TNF-α) inhibitors have been reported to induce new-onset psoriasis.
To better define the demographic, clinical features, and treatment approach of TNF-α inhibitor-induced psoriasis.
Systematic review of published cases of TNF-α inhibitor-induced psoriasis.
We identified 88 articles with 216 cases of new-onset TNF-α inhibitor-induced psoriasis. The mean age at psoriasis onset was 38.5 years. The most common underlying diseases were Crohn disease (40.7%) and rheumatoid arthritis (37.0%). Patients underwent TNF-α therapy for an average of 14.0 months before psoriasis onset with 69.9% of patients experiencing onset within the first year. The majority of patients received skin-directed therapy, though patients who discontinued TNF therapy had the greatest resolution of symptoms (47.7%) compared with those who switched to a different TNF agent (36.7%) or continued therapy (32.9%).
Retrospective review that relies on case reports and series.
While TNF-α inhibitor cessation may result in resolution of induced psoriasis, lesions may persist. Decisions regarding treatment should be weighed against the treatability of TNF-α inhibitor-induced psoriasis, the severity of the background rheumatologic or gastrointestinal disease, and possible loss of efficacy with cessation followed by retreatment. Skin-directed therapy is a reasonable initial strategy except in severe cases. |
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AbstractList | Tumor necrosis factor-α (TNF-α) inhibitors have been reported to induce new-onset psoriasis.
To better define the demographic, clinical features, and treatment approach of TNF-α inhibitor-induced psoriasis.
Systematic review of published cases of TNF-α inhibitor-induced psoriasis.
We identified 88 articles with 216 cases of new-onset TNF-α inhibitor-induced psoriasis. The mean age at psoriasis onset was 38.5 years. The most common underlying diseases were Crohn disease (40.7%) and rheumatoid arthritis (37.0%). Patients underwent TNF-α therapy for an average of 14.0 months before psoriasis onset with 69.9% of patients experiencing onset within the first year. The majority of patients received skin-directed therapy, though patients who discontinued TNF therapy had the greatest resolution of symptoms (47.7%) compared with those who switched to a different TNF agent (36.7%) or continued therapy (32.9%).
Retrospective review that relies on case reports and series.
While TNF-α inhibitor cessation may result in resolution of induced psoriasis, lesions may persist. Decisions regarding treatment should be weighed against the treatability of TNF-α inhibitor-induced psoriasis, the severity of the background rheumatologic or gastrointestinal disease, and possible loss of efficacy with cessation followed by retreatment. Skin-directed therapy is a reasonable initial strategy except in severe cases. Background Tumor necrosis factor-α (TNF-α) inhibitors have been reported to induce new-onset psoriasis. Objective To better define the demographic, clinical features, and treatment approach of TNF-α inhibitor-induced psoriasis. Methods Systematic review of published cases of TNF-α inhibitor-induced psoriasis. Results We identified 88 articles with 216 cases of new-onset TNF-α inhibitor-induced psoriasis. The mean age at psoriasis onset was 38.5 years. The most common underlying diseases were Crohn disease (40.7%) and rheumatoid arthritis (37.0%). Patients underwent TNF-α therapy for an average of 14.0 months before psoriasis onset with 69.9% of patients experiencing onset within the first year. The majority of patients received skin-directed therapy, though patients who discontinued TNF therapy had the greatest resolution of symptoms (47.7%) compared with those who switched to a different TNF agent (36.7%) or continued therapy (32.9%). Limitations Retrospective review that relies on case reports and series. Conclusion While TNF-α inhibitor cessation may result in resolution of induced psoriasis, lesions may persist. Decisions regarding treatment should be weighed against the treatability of TNF-α inhibitor-induced psoriasis, the severity of the background rheumatologic or gastrointestinal disease, and possible loss of efficacy with cessation followed by retreatment. Skin-directed therapy is a reasonable initial strategy except in severe cases. |
Author | Leon, Argentina Brown, Gabrielle Liao, Wilson Matro, Rebecca Wang, Eva Wehner, Mackenzie Haemel, Anna Linos, Eleni Huynh, Monica |
Author_xml | – sequence: 1 givenname: Gabrielle surname: Brown fullname: Brown, Gabrielle organization: Department of Dermatology, University of California, San Francisco, California – sequence: 2 givenname: Eva surname: Wang fullname: Wang, Eva organization: Department of Dermatology, University of California, San Francisco, California – sequence: 3 givenname: Argentina surname: Leon fullname: Leon, Argentina organization: Department of Dermatology, University of California, San Francisco, California – sequence: 4 givenname: Monica surname: Huynh fullname: Huynh, Monica organization: Department of Dermatology, University of California, San Francisco, California – sequence: 5 givenname: Mackenzie surname: Wehner fullname: Wehner, Mackenzie organization: Department of Dermatology, University of California, San Francisco, California – sequence: 6 givenname: Rebecca surname: Matro fullname: Matro, Rebecca organization: Department of Gastroenterology, University of California, San Francisco, California – sequence: 7 givenname: Eleni surname: Linos fullname: Linos, Eleni organization: Department of Dermatology, University of California, San Francisco, California – sequence: 8 givenname: Wilson surname: Liao fullname: Liao, Wilson organization: Department of Dermatology, University of California, San Francisco, California – sequence: 9 givenname: Anna surname: Haemel fullname: Haemel, Anna email: Anna.Haemel@ucsf.edu organization: Department of Dermatology, University of California, San Francisco, California |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/27720274$$D View this record in MEDLINE/PubMed |
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Keywords | medication side effect CD IL etanercept infliximab AZA adverse event certolizumab MeSH tumor necrosis factor-α inhibitor adalimumab golimumab UC RA IFN-α MTX AS IL-23R TH TNF-α tumor necrosis factor-α-induced psoriasis psoriasis ankylosing spondylitis methotrexate interleukin-23 receptor interferon α ulcerative colitis interleukin T helper azathioprine rheumatoid arthritis medical subject headings Crohn disease tumor necrosis factor-α T H |
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Snippet | Tumor necrosis factor-α (TNF-α) inhibitors have been reported to induce new-onset psoriasis.
To better define the demographic, clinical features, and treatment... Background Tumor necrosis factor-α (TNF-α) inhibitors have been reported to induce new-onset psoriasis. Objective To better define the demographic, clinical... |
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SubjectTerms | adalimumab Adolescent Adult adverse event Aged Aged, 80 and over certolizumab Child Dermatology Drug Eruptions - diagnosis Drug Eruptions - etiology Drug Eruptions - therapy etanercept Female golimumab Humans infliximab Male medication side effect Middle Aged psoriasis Psoriasis - chemically induced Psoriasis - diagnosis Psoriasis - therapy Tumor Necrosis Factor-alpha - antagonists & inhibitors tumor necrosis factor-α inhibitor tumor necrosis factor-α-induced psoriasis Young Adult |
Title | Tumor necrosis factor-α inhibitor-induced psoriasis: Systematic review of clinical features, histopathological findings, and management experience |
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