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Apremilast as a Potential Targeted Therapy for Metabolic Syndrome in Patients with Psoriasis: An Observational Analysis
Psoriasis (PsO) is a chronic inflammatory dermatosis that often presents with erythematous, sharply demarcated lesions. Although psoriasis is primarily a dermatological disease, its immune-mediated pathogenesis produces systemic effects and is closely associated with various comorbid conditions such...
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Published in: | Pharmaceuticals (Basel, Switzerland) Switzerland), 2024-07, Vol.17 (8), p.989 |
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creator | Campione, Elena Zarabian, Nikkia Cosio, Terenzio Borselli, Cristiana Artosi, Fabio Cont, Riccardo Sorge, Roberto Shumak, Ruslana Gaeta Costanza, Gaetana Rivieccio, Antonia Gaziano, Roberta Bianchi, Luca |
description | Psoriasis (PsO) is a chronic inflammatory dermatosis that often presents with erythematous, sharply demarcated lesions. Although psoriasis is primarily a dermatological disease, its immune-mediated pathogenesis produces systemic effects and is closely associated with various comorbid conditions such as cardiovascular disease (CVD), metabolic syndrome (MetS), and diabetes mellitus type II (DMII). Apremilast, an oral phosphodiesterase 4 (PDE-4) inhibitor, has shown promise in treating moderate-to-severe psoriasis and is associated with potential cardiometabolic benefits. In a 12-month prospective observational study involving 137 patients with moderate-to-severe psoriasis, we assessed changes in psoriasis clinimetric scores and metabolic profiles from baseline (T0) to 52 weeks (T1) to evaluate the efficacy of apremilast. After 52 weeks of apremilast treatment, we documented a statistically significant decrease in low-density lipoprotein (LDL) and total cholesterol, triglycerides, and glucose levels. Our findings even suggest a potential synergistic effect among patients treated with apremilast, alongside concomitant statin and/or insulin therapy. Although the results of our study must be validated on a larger scale, the use of apremilast in the treatment of psoriatic patients with cardio-metabolic comorbidities yields promising results. |
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Although psoriasis is primarily a dermatological disease, its immune-mediated pathogenesis produces systemic effects and is closely associated with various comorbid conditions such as cardiovascular disease (CVD), metabolic syndrome (MetS), and diabetes mellitus type II (DMII). Apremilast, an oral phosphodiesterase 4 (PDE-4) inhibitor, has shown promise in treating moderate-to-severe psoriasis and is associated with potential cardiometabolic benefits. In a 12-month prospective observational study involving 137 patients with moderate-to-severe psoriasis, we assessed changes in psoriasis clinimetric scores and metabolic profiles from baseline (T0) to 52 weeks (T1) to evaluate the efficacy of apremilast. After 52 weeks of apremilast treatment, we documented a statistically significant decrease in low-density lipoprotein (LDL) and total cholesterol, triglycerides, and glucose levels. Our findings even suggest a potential synergistic effect among patients treated with apremilast, alongside concomitant statin and/or insulin therapy. Although the results of our study must be validated on a larger scale, the use of apremilast in the treatment of psoriatic patients with cardio-metabolic comorbidities yields promising results.</description><identifier>ISSN: 1424-8247</identifier><identifier>EISSN: 1424-8247</identifier><identifier>DOI: 10.3390/ph17080989</identifier><identifier>PMID: 39204094</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>apremilast ; Cholesterol ; comorbidities ; Comorbidity ; Cytokines ; Dermatology ; Glucose ; High density lipoprotein ; Insulin ; Lipids ; Lipoproteins ; Medical history ; metabolic syndrome ; Metabolism ; Observational studies ; Patients ; PDE4-inhibitor ; Population ; Psoriasis ; Psoriatic arthritis ; Statins ; Tumor necrosis factor-TNF</subject><ispartof>Pharmaceuticals (Basel, Switzerland), 2024-07, Vol.17 (8), p.989</ispartof><rights>2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2024 by the authors. 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c432t-4e4023fb1899d4afc30d57959ff4fad18131be06404652abfac0a3be0d77f0ab3</cites><orcidid>0000-0003-4025-7882 ; 0000-0003-1970-2670 ; 0000-0002-1115-4270 ; 0000-0001-7447-6798 ; 0000-0001-8697-6896</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/3098041705/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/3098041705?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25731,27901,27902,36989,36990,44566,53766,53768,75096</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39204094$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Campione, Elena</creatorcontrib><creatorcontrib>Zarabian, Nikkia</creatorcontrib><creatorcontrib>Cosio, Terenzio</creatorcontrib><creatorcontrib>Borselli, Cristiana</creatorcontrib><creatorcontrib>Artosi, Fabio</creatorcontrib><creatorcontrib>Cont, Riccardo</creatorcontrib><creatorcontrib>Sorge, Roberto</creatorcontrib><creatorcontrib>Shumak, Ruslana Gaeta</creatorcontrib><creatorcontrib>Costanza, Gaetana</creatorcontrib><creatorcontrib>Rivieccio, Antonia</creatorcontrib><creatorcontrib>Gaziano, Roberta</creatorcontrib><creatorcontrib>Bianchi, Luca</creatorcontrib><title>Apremilast as a Potential Targeted Therapy for Metabolic Syndrome in Patients with Psoriasis: An Observational Analysis</title><title>Pharmaceuticals (Basel, Switzerland)</title><addtitle>Pharmaceuticals (Basel)</addtitle><description>Psoriasis (PsO) is a chronic inflammatory dermatosis that often presents with erythematous, sharply demarcated lesions. 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Our findings even suggest a potential synergistic effect among patients treated with apremilast, alongside concomitant statin and/or insulin therapy. 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subjects | apremilast Cholesterol comorbidities Comorbidity Cytokines Dermatology Glucose High density lipoprotein Insulin Lipids Lipoproteins Medical history metabolic syndrome Metabolism Observational studies Patients PDE4-inhibitor Population Psoriasis Psoriatic arthritis Statins Tumor necrosis factor-TNF |
title | Apremilast as a Potential Targeted Therapy for Metabolic Syndrome in Patients with Psoriasis: An Observational Analysis |
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