Evan L. Siegel
New York University
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Publication
Featured researches published by Evan L. Siegel.
Arthritis & Rheumatism | 2016
Laura C. Coates; Arthur Kavanaugh; Philip J. Mease; Enrique R. Soriano; Maria Laura Acosta-Felquer; April W. Armstrong; Wilson Bautista-Molano; Wolf-Henning Boehncke; Willemina Campbell; Alberto Cauli; Luis R. Espinoza; Oliver FitzGerald; Dafna D. Gladman; Alice B. Gottlieb; Philip S. Helliwell; M. Elaine Husni; Thorvardur Jon Love; Ennio Lubrano; Neil McHugh; Peter Nash; Alexis Ogdie; Ana Maria Orbai; Andrew Parkinson; Denis O'Sullivan; Cheryl F. Rosen; Sergio Schwartzman; Evan L. Siegel; Sergio Toloza; William Tuong; Christopher T. Ritchlin
To update the 2009 Group for Research and Assessment of Psoriasis and Psoriatic Arthritis (GRAPPA) treatment recommendations for the spectrum of manifestations affecting patients with psoriatic arthritis (PsA).
The Journal of Rheumatology | 2014
Ana Maria Orbai; Joshua Weitz; Evan L. Siegel; Stefan Siebert; Laura J. Savage; Sibel Zehra Aydin; Jolanda J. Luime; Ori Elkayam; Barbara Neerinckx; Slavo Urbancek; Kurt de Vlam; Christopher T. Ritchlin
Enthesitis is a characteristic feature of psoriatic arthritis (PsA) and is important in disease pathogenesis and classification. Use of clinical outcome measures for enthesitis is heterogeneous, and only 1 measure has been specifically developed and validated in PsA. Ultrasound and magnetic resonance imaging assessments of enthesitis may have advantages over clinical examination but are insufficiently studied. As part of an update of treatment recommendations by the Group for Research and Assessment of Psoriasis and Psoriatic Arthritis (GRAPPA), we performed a systematic literature review and identified randomized controlled trials with enthesitis outcomes in PsA. For each treatment agent we calculated treatment effect sizes (where applicable) and graded the level of evidence.
Arthritis Research & Therapy | 2014
Shawn Rose; Jenny Dave; Corina Millo; Haley B. Naik; Evan L. Siegel; Nehal N. Mehta
IntroductionPsoriasis and psoriatic arthritis (PsA) increase cardiovascular disease (CVD) risk, but surrogate markers for CVD in these disorders are inadequate. Because the presence of sacroiliitis may portend more severe PsA, we hypothesized that sacroiliitis defined by computed tomography (CT) would be associated with increased vascular inflammation defined by 18-fluorodeoxyglucose-positron emission tomography/computed tomography (FDG-PET/CT), which is an established measure of CVD.MethodsParticipants (n = 65) underwent whole-body FDG-PET/CT. Metabolic activity of the aorta was measured using the maximal standardized uptake value (SUVmax), a measure of atherosclerotic plaque activity. The primary outcome was aortic vascular inflammation. Linear regression (with β-coefficients (β) and P-values reported for PsA and sacroiliitis) was used to adjust for CVD risk factors to determine associations of PsA or sacroiliitis with vascular inflammation. Likelihood ratio testing was performed to evaluate the contribution of sacroiliitis to vascular disease estimation compared to the effects of PsA and traditional CVD risk factors.ResultsVascular inflammation (measured as SUVmax) was greater (P < 0.001) in patients with sacroiliitis (mean ± SD = 7.33 ± 2.09) defined by CT compared to those without sacroiliitis (6.39 ± 1.49, P = 0.038). There were associations between PsA and aortic inflammation (β = 0.124, P < 0.001) and between sacroiliitis and aortic inflammation (β = 0.270, P < 0.001) after adjusting for CVD risk factors. Sacroiliitis predicted vascular inflammation beyond PsA and CVD risk factors (χ2 = 124.6, P < 0.001).ConclusionsSacroiliitis is associated with increased vascular inflammation detected by FDG-PET/CT, suggesting that sacroiliac joint disease may identify patients at greater risk for CVD. Large, ongoing prospective studies are required to confirm these findings.
Current Opinion in Rheumatology | 2015
Evan L. Siegel; Ana Maria Orbai; Christopher T. Ritchlin
Purpose of reviewEnthesitis and dactylitis are cardinal manifestations of psoriatic arthritis (PsA), but a limited understanding of underlying pathophysiologic mechanisms has hindered development of targeted therapies. This gap is of clinical relevance because these manifestations are clinically relevant to patients. Herein, we discuss new exciting findings in animal models with enthesitis and dactylitis, summarize developments in clinical and imaging assessments and review recent clinical trial data on the efficacy of targeted therapies for enthesitis and dactylitis. Recent findingsSeveral different animal models reveal that cytokines in the interleukin-23/Th17 pathway and mechanical stress are key events in the development of enthesitis and dactylitis. Elevated levels of interleukin-23, generated in the gut, joint or skin, trigger subsequent tissue inflammation. Both enthesitis and dactylitis involve heterogeneous tissues, associate with specific Class I Major Histocompatibility Complex alleles, and enthesitis may be critical for the development of PsA, although a causal pathway remains unproven. Diagnosis is based on clinical and imaging assessments; however, Power Doppler ultrasound (PDUS) is more sensitive for diagnosis and longitudinal follow-up of enthesitis. Agents targeting tumor necrosis factor, interleukin-12/23, interleukin-17, interleukin-17 receptor (interleukin-17R) and PDE4 are effective therapies for psoriatic enthesitis and dactylitis. SummaryNovel preclinical models established, for the first time, the importance of the interleukin-23/Th17 pathway and mechanical stress in pathogenesis of dactylitis and enthesitis. Advances in imaging, particular (PDUS), may improve sensitivity and specificity for diagnosis and longitudinal assessments. Many targeted therapies are effective for enthesitis and dactylitis.
Arthritis & Rheumatism | 2018
Lihi Eder; Aditya A. Joshi; Amit K. Dey; Richard J. Cook; Evan L. Siegel; Dafna D. Gladman; Nehal N. Mehta
To assess the effect of tumor necrosis factor inhibitors (TNFi) on subclinical cardiovascular disease in patients with psoriatic disease.
JAMA Dermatology | 2018
Adam R. Ford; Michael P. Siegel; Jerry Bagel; Kelly M. Cordoro; Amit Garg; Alice B. Gottlieb; Lawrence Green; Johann E. Gudjonsson; John Koo; Mark Lebwohl; Wilson Liao; Arthur M. Mandelin; Joseph A. Markenson; Nehal N. Mehta; Joseph F. Merola; Ronald Prussick; Caitriona Ryan; Sergio Schwartzman; Evan L. Siegel; Abby S. Van Voorhees; Jashin J. Wu; April W. Armstrong
Importance Psoriasis is a chronic, inflammatory skin disease and has significant associated morbidity and effect on quality of life. It is important to determine whether dietary interventions help reduce disease severity in patients with psoriatic diseases. Objective To make evidence-based dietary recommendations for adults with psoriasis and/or psoriatic arthritis from the Medical Board of the National Psoriasis Foundation. Evidence Review We used literature from prior systematic reviews as well as additional primary literature from the MEDLINE database from January 1, 2014, to August 31, 2017, that evaluated the impact of diet on psoriasis. We included observational and interventional studies of patients with psoriasis or psoriatic arthritis. The quality of included studies was assessed using the Newcastle-Ottawa scale for observational studies and the Cochrane Risk of Bias Tool for interventional studies. We made evidence-based dietary recommendations, which were voted on by the National Psoriasis Foundation Medical Board. Findings We identified 55 studies meeting the inclusion criteria for this review. These studies represent 77 557 unique participants of which 4534 have psoriasis. Based on the literature, we strongly recommend dietary weight reduction with a hypocaloric diet in overweight and obese patients with psoriasis. We weakly recommend a gluten-free diet only in patients who test positive for serologic markers of gluten sensitivity. Based on low-quality data, select foods, nutrients, and dietary patterns may affect psoriasis. For patients with psoriatic arthritis, we weakly recommend vitamin D supplementation and dietary weight reduction with a hypocaloric diet in overweight and obese patients. Dietary interventions should always be used in conjunction with standard medical therapies for psoriasis and psoriatic arthritis. Conclusions and Relevance Adults with psoriasis and/or psoriatic arthritis can supplement their standard medical therapies with dietary interventions to reduce disease severity. These dietary recommendations from the National Psoriasis Foundation Medical Board will help guide clinicians regarding the utility of dietary interventions in adults with psoriatic diseases.
Arthritis & Rheumatism | 2004
Philip J. Mease; Alan Kivitz; Francis X. Burch; Evan L. Siegel; Stanley B. Cohen; Peter Ory; David Salonen; Joel Rubenstein; John T. Sharp; Wayne Tsuji
The Journal of Rheumatology | 2006
Philip J. Mease; Alan Kivitz; Francis X. Burch; Evan L. Siegel; Stanley B. Cohen; Peter Ory; David Salonen; Joel Rubenstein; John T. Sharp; Meleana Dunn; Wayne Tsuji
Arthritis & Rheumatism | 1992
Sharon L. Kolasinski; K A Haines; Evan L. Siegel; Bruce N. Cronstein; Steven B. Abramson
Arthritis | 2015
Laura C. Coates; Arthur Kavanaugh; Philip J. Mease; Enrique R. Soriano; M. Laura Acosta-Felquer; April W. Armstrong; Wilson Bautista-Molano; Wolf-Henning Boehncke; Willemina Campbell; Alberto Cauli; Luis R. Espinoza; Oliver FitzGerald; Dafna D. Gladman; Alice B. Gottlieb; Philip S. Helliwell; M. Elaine Husni; Thorvardur Jon Love; Ennio Lubrano; Neil McHugh; Peter Nash; Alexis Ogdie-Beatty; Ana-Maria Orbai; Andrew Parkinson; Denis O'Sullivan; Cheryl F. Rosen; Sergio Schwartzman; Evan L. Siegel; Sergio Toloza; William Tuong; Christopher T. Ritchlin