Targeting Transthyretin - Mechanism-Based Treatment Approaches and Future Perspectives in Hereditary Amyloidosis

Key Information
Source
Journal for Neurochemistry
Year
2020
summary/abstract

The liver-derived, circulating transport protein transthyretin (TTR) is the cause of systemic hereditary (ATTRv) and wild-type (ATTRwt) amyloidosis. TTR stabilization and knockdown are approved therapies to mitigate the otherwise lethal disease course. To date, the variety in phenotypic penetrance is not fully understood. This systematic review summarizes the current literature on TTR pathophysiology with its therapeutic implications. Tetramer dissociation is the rate-limiting step of amyloidogenesis. Besides destabilizing TTR mutations, other genetic (RBP4, APCS, AR, ATX2, C1q, C3) and external (extracellular matrix, Schwann cell interaction) factors influence the type of onset and organ tropism. The approved small molecule tafamidis stabilizes the tetramer and significantly decelerates the clinical course.

Abstract Source
https://onlinelibrary.wiley.com/doi/10.1111/jnc.15233
DOI
10.1111/jnc.15233
Authors
Maike F, Dohrn, Sandra Ihne, Ute Hegenbart, Jessica Medina, Stephan L. Zuchner, Teresa Coelho, Katrin Hahn.
Organisation
RWTH Aachen University, Germany; University Hospital of Würzburg, Germany; Heidelberg University Hospital, Germany; University of Miami, USA; University of Miami, USA; University of Porto, Portugal; Charité University Medicine, Germany