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Primary carnitine deficiency as a potential cause of short QT syndrome

Research output: Contribution to journalReview article

Original languageEnglish
Pages (from-to)10-12
Number of pages3
JournalCardiovascular Research and Medicine
Volume2
Issue number1
DateAccepted/In press - 24 Jul 2018
DatePublished (current) - 27 Jul 2018

Abstract

Congenital forms of short QT syndrome (SQTS) are associated with QT interval abbreviation on the electrocardiogram, with atrial and ventricular arrhythmias and with an increased risk of sudden death. Whilst mutations in a number of ion channel and transporter genes have been identified in SQTS patients, often the underlying basis of the condition is not identified. This article briefly surveys evidence that primary carnitine deficiency (PCD), which arises from mutations in the SLC22A5 gene, may be a cause of SQTS. Experimental evidence linking carnitine deficiency with accelerated repolarization is also discussed and a case made for the imperative for further work to understand underlying mechanisms of low-carnitine induced repolarization abbreviation.

    Research areas

  • Carnitine, OCTN2, hERG, Primary carnitine deficiency, PCD, QT interval, SLC22A5, short QT syndrome, SQTS

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    Rights statement: This is the final published version of the article (version of record). It first appeared online via GAP at http://globalaccesspub.com/open_access/primary_carnitine_deficiency_as_a_potential_cause_of_short_qt_syndrome_CRM . Please refer to any applicable terms of use of the publisher.

    Final published version, 150 KB, PDF document

    Licence: CC BY

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