Genetic maneuvers to ameliorate ventricular function in heart failure: Therapeutic potential and future implications

Fariya Bukhari, Thomas MacGillivnay, Federica del Monte, Roger J. Hajjar

Research output: Contribution to journalReview articlepeer-review

4 Scopus citations

Abstract

Gene therapy to treat heart failure has evolved into a growing field of investigation yielding remarkable results in preclinical models. Whether these results will persist in clinical trials remains to be seen. However, researchers still face a number of obstacles that need to be overcome before this treatment can be employed effectively. Efforts are required to identify better vectors with minimal side effects and maximal efficiency and durability. There is also a need to develop less invasive and more effective techniques to deliver these vectors. This review will discuss different methods to achieve these goals, the various pathologic mechanisms that have been targeted so far and those with strong potential for use in the future.

Original languageEnglish
Pages (from-to)85-97
Number of pages13
JournalExpert Review of Cardiovascular Therapy
Volume3
Issue number1
DOIs
StatePublished - Jan 2005
Externally publishedYes

Keywords

  • Apoptosis
  • Heart failure
  • Ryanodine receptors
  • SERCA
  • Vector delivery
  • β-adrenergic receptor signaling

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