Paclitaxel-induced Cardiotoxicity: Mechanisms, Molecular Insights, and Clinical Implications
Year: 2025
Type: article
Abstract: Auto-inflammatory disorders are recognized as significant in impacting the health of patients.The majority of autoinflammatory disorders originate from hereditary abnormalities.One of the most significant auto-inflammatory disorders is Familial Mediterranean Fever, which mostly affects populations originating from the Mediterranean region; particularly those of Sephardic Jewish, Armenian, Arab, and Turkish descent.Familial Mediterranean fever typically manifests in childhood due to genetic mutations, mainly the Mediterranean Fever (MEFV) gene.This gene encodes pyrin, which is essential in regulating inflammation.Defects in this particular gene may contribute to higher levels of inflammation, which in turn can cause recurrent episodes of pain and fever.Colchicine, NSAIDs (nonsteroidal anti-inflammatory medicines), and medications that target cytokines are the only options for therapy.Finding new remedies is one of the challenges confronting medical research.Therefore, it is critical to provide information on the clinical signs, etiology, available treatments, side effects, and diagnosis of this particular kind of congenital auto-inflammatory ailments.Furthermore, how variations in gender and genetics could impact the prevalence and course of familial Mediterranean fever.
Authors: Yasmine M. El-Nagar, Mina Y. George, Sara El Wakeel, Doaa A. Elsherbiny
Institution: Ain Shams University
Language: English
Subfield: Cardiology and Cardiovascular Medicine
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $50
OpenAlex ID: W4415365720
