| Literature DB >> 28205229 |
Abstract
The major goal of this focused review is to highlight some of the recent advances and remaining open questions about how a mutation in a myofilament protein leads to an increased risk for sudden cardiac death (SCD). The link between myofilaments and SCD has been known for over 25 years, but identifying mutation carriers at risk for SCD is still a challenge and currently the only effective prevention is implantation of a defibrillator (ICD). In addition to recognized risk factors, other contributing factors need to be considered and assessed, e.g. 'microvascular dysfunction', to calibrate individual risk more accurately. Similarly, improving our understanding about the underlying mechanisms of SCD in patients with sarcomeric mutations will also allow us to design new and less invasive treatment options that will minimize risk and hopefully make implantation of an ICD unnecessary.Entities:
Keywords: arcomeric mutations; arrhythmia; hypertrophic cardiomyopathy; microvascular dysfunction; myofilament Ca sensitivity; sudden cardiac death
Mesh:
Year: 2017 PMID: 28205229 PMCID: PMC5471415 DOI: 10.1113/JP273047
Source DB: PubMed Journal: J Physiol ISSN: 0022-3751 Impact factor: 5.182