Genetic Etiology and Evaluation of Sudden Cardiac Death
被引:6
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作者:
Dolmatova, Elena
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机构:
Massachusetts Gen Hosp, Cardiovasc Res Ctr, Charlestown, MA USAMassachusetts Gen Hosp, Cardiovasc Res Ctr, Charlestown, MA USA
Dolmatova, Elena
[1
]
Mahida, Saagar
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机构:
Leeds Gen Infirm, Leeds LS1 3EX, W Yorkshire, EnglandMassachusetts Gen Hosp, Cardiovasc Res Ctr, Charlestown, MA USA
Mahida, Saagar
[2
]
Ellinor, Patrick T.
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机构:
Massachusetts Gen Hosp, Cardiovasc Res Ctr, Charlestown, MA USA
Massachusetts Gen Hosp, Cardiac Arrhythmia Serv, Boston, MA 02114 USAMassachusetts Gen Hosp, Cardiovasc Res Ctr, Charlestown, MA USA
Ellinor, Patrick T.
[1
,3
]
Lubitz, Steven A.
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机构:
Massachusetts Gen Hosp, Cardiovasc Res Ctr, Charlestown, MA USA
Massachusetts Gen Hosp, Cardiac Arrhythmia Serv, Boston, MA 02114 USAMassachusetts Gen Hosp, Cardiovasc Res Ctr, Charlestown, MA USA
Lubitz, Steven A.
[1
,3
]
机构:
[1] Massachusetts Gen Hosp, Cardiovasc Res Ctr, Charlestown, MA USA
[2] Leeds Gen Infirm, Leeds LS1 3EX, W Yorkshire, England
[3] Massachusetts Gen Hosp, Cardiac Arrhythmia Serv, Boston, MA 02114 USA
A wide range of inherited syndromes can result in ventricular arrhythmias and sudden cardiac death (SCD). The natural histories of inherited arrhythmia syndromes are highly variable and current risk stratification techniques are limited. Thus, the management of these conditions can be difficult and often involves a combination of risk assessment, lifestyle modification, cardiac interventions, counselling, and family screening. Recent advances in high throughput sequencing have enabled routine testing in patients with a high clinical index of suspicion for an inherited arrhythmia condition, and cascade screening in relatives of mutation carriers. Given the complexity in screening and data interpretation that has been introduced by recent genomic advances, individuals with inherited arrhythmia syndromes are encouraged to seek care at specialized centers with cardiovascular genetics expertise. In this review, we discuss the etiologies of SCD syndromes and discuss strategies for the evaluation of patients at risk for SCD with a focus on the role of genetic testing and family screening.
机构:
Vanderbilt Univ, Div Med Genet, Dept Med, Nashville, TN 37232 USA
Vanderbilt Univ, Dept Pharmacol, Nashville, TN 37232 USAVanderbilt Univ, Div Med Genet, Dept Med, Nashville, TN 37232 USA