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Novel In Vivo Micro-Computed Tomography Imaging Techniques for Assessing the Progression of Non-Alcoholic Fatty Liver Disease
Published on: March 24, 2023
Psoriasis and Nonalcoholic Fatty Liver Disease
J M Carrascosa1, C Bonanad2, E Dauden3
1Servicio de Dermatologia, Hospital Universitari Germans Trias i Pujol. Universitat Autònoma de Barcelona, Badadalona, España.
Nonalcoholic fatty liver disease (NAFLD) is common in psoriasis patients, linked by inflammation and insulin resistance. Early NAFLD screening is crucial for psoriasis patients, especially with metabolic syndrome, due to shared risks and potential treatment toxicities.
Area of Science:
- Hepatology
- Dermatology
- Metabolic Syndrome
Background:
- Nonalcoholic fatty liver disease (NAFLD) is the most common liver condition in Western countries.
- Psoriasis patients exhibit higher prevalence and severity of NAFLD, with a worse prognosis.
- Chronic inflammation and peripheral insulin resistance are key pathogenic links between psoriasis and NAFLD.
Purpose of the Study:
- To highlight the importance of ruling out NAFLD in psoriasis patients.
- To discuss the implications of co-existing psoriasis and NAFLD on treatment strategies.
- To review the hepatotoxic risks associated with conventional and biologic therapies.
Main Methods:
- Literature review on the association between psoriasis and NAFLD.
- Analysis of pathogenic mechanisms linking the two conditions.
- Evaluation of treatment options and their potential liver toxicity.
Main Results:
- NAFLD should be screened for in psoriasis patients, particularly those with metabolic syndrome or requiring systemic therapy.
- Concomitant psoriasis and NAFLD present treatment challenges due to potential drug-induced liver injury.
- Conventional treatments (e.g., acitretin, methotrexate) and some biologics carry hepatotoxic risks requiring monitoring.
Conclusions:
- Close monitoring is essential for psoriasis patients undergoing systemic treatment due to potential liver toxicity.
- Anti-tumor necrosis factor agents may offer benefits but also carry risks of liver injury.
- Current evidence does not support benefits or adverse effects of anti-p40 or anti-interleukin 17 agents in this context.
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