Targeted Therapeutics for Transthyretin Cardiac Amyloidosis
- PMID: 30664380
- PMCID: PMC6438186
- DOI: 10.1161/CIRCULATIONAHA.118.037593
Targeted Therapeutics for Transthyretin Cardiac Amyloidosis
Abstract
Despite the availability of proven treatments for some patients with heart failure (HF), many patients—particularly those with HF and preserved ejection fraction (HFpEF)—remain difficult to treat, resulting in persistently high morbidity and mortality in the majority of HF patients. The lack of effective treatments, disappointing results of many HF randomized clinical trials (RCT), and variable treatment responses even for proven therapies are all possible reasons for the poor prognosis of HF patients. In the context of this backdrop, it is not surprising that there has been growing interest and enthusiasm for “precision medicine” in order to improve outcomes for patients who suffer from the HF syndrome.,
Keywords: Editorials; amyloidosis; heart failure; precision medicine.
Comment on
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Effects of Patisiran, an RNA Interference Therapeutic, on Cardiac Parameters in Patients With Hereditary Transthyretin-Mediated Amyloidosis.Circulation. 2019 Jan 22;139(4):431-443. doi: 10.1161/CIRCULATIONAHA.118.035831. Circulation. 2019. PMID: 30586695 Clinical Trial.
References
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- Pitt GS. Cardiovascular precision medicine: hope or hype? Eur Heart J. 2015;36:1842–1843. - PubMed
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- Senn S Individual Therapy: New Dawn or False Dawn? Ther Innov Regul Sci. 2001;35:1479–1494.
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