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DOI 10.1007/s00228-023-03576-3

Медицинская библиотека · European journal of clinical pharmacology · 2023

Variation of tafamidis plasma levels during the treatment of TTR amyloidosis patients with Glu89Gln mutation.

Smerikarova M, Bozhanov S, Tournev I, Maslarska V

СтатьяПеревод пока не подготовлен

Аннотация

PURPOSE: The transthyretin kinetic stabilizer tafamidis, used as a first-line therapy of amyloidosis patients, binds selectively to the transthyretin protein structure and thus prevents its dissociation. The limited information regarding tafamidis application in Glu89Gln amyloidosis patients imposed our research team to determine and evaluate its individual mean plasma levels and their biological variation.

METHODS

The present cohort study investigated Bulgarian amyloidosis patients, grouped by gender, age, and therapy duration. A total of sixty patients aged 40-75 years and therapy duration up to 9 years were included. A precise and accurate high-performance liquid chromatography method with ultraviolet detection was used for plasma concentration measurement.

RESULTS

Mean plasma concentrations were 5.13 ± 2.64 µmol/L and showed low intra-individual (18.50%) and high inter-individual variability (51.43%). No significant difference was observed between tafamidis plasma levels and therapy duration with p = 0.5941 (p < 0.05 considered significant), but a significant positive correlation was found between plasma concentration, gender, and age with obtained results about p-value 0.0001 and 0.0235, respectively.

CONCLUSION

The summary results of the study showed differences that may be based on some specific clinical features of the Glu89Gln mutation.

Для цитирования: Smerikarova M, Bozhanov S, Tournev I, Maslarska V. Variation of tafamidis plasma levels during the treatment of TTR amyloidosis patients with Glu89Gln mutation.. European journal of clinical pharmacology. 2023. DOI: 10.1007/s00228-023-03576-3.

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