Transthyretin Amyloidosis Therapies: Guiding the Future



Document title: Transthyretin Amyloidosis Therapies: Guiding the Future
Journal: Revista de investigación clínica
Database: PERIÓDICA
System number: 000453018
ISSN: 0034-8376
Authors: 1
Institutions: 1Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Departamento de Neurología, Ciudad de México. México
Year:
Season: Sep-Oct
Volumen: 73
Number: 5
Pages: 310-315
Country: México
Language: Inglés
Document type: Artículo
Approach: Aplicado, descriptivo
English abstract Transthyretin (TTR) amyloidosis (ATTR) is a progressive condition characterized by multiorgan accumulation of amyloid deposits composed of transthyretin (TTR) fibrils. Over the past decades, despite being a rare disease, ATTR amyloidosis has enabled top-tier therapeutics. In the 90s, organ transplantation was the mainstream therapeutic option and fostered distinct approaches, such as combined liver-heart transplant and domino (sequential) liver transplantation. Likewise, several TTR molecule stabilizers were developed successfully. Over the past decade, oriented genetic therapies emerged to prevent, control, and, surprisingly, reverse amyloid deposition. Silencing the TTR gene using different strategies is flourishing, and ongoing trials continue to evaluate diverse approaches to optimize their application. The following perspective describes the currently available treatments for ATTR amyloidosis and the prospects on the potential application of these strategies in other medical fields
Disciplines: Medicina
Keyword: Metabolismo y nutrición,
Terapéutica y rehabilitación,
Amiloidosis,
Transtiretina,
Nanopartículas lípidicas,
Medicina genómica
Keyword: Metabolism and nutrition,
Therapeutics and rehabilitation,
Amyloidosis,
Transthyretin,
Lipid nanoparticles,
Genomic medicine
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