Volume 43, Issue 2 pp. 290-296
ORIGINAL ARTICLE

Increased risk of sudden death in untreated primary carnitine deficiency

Jan Rasmussen

Corresponding Author

Jan Rasmussen

Department of Internal Medicine, National Hospital, Torshavn, Faroe Islands

Department of Cardiology, Rigshospitalet University Hospital, Copenhagen, Denmark

Correspondence

Jan Rasmussen, Department of Internal Medicine, National Hospital, Torshavn, Faroe Islands.

Email: [email protected]

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Morten Dunø

Morten Dunø

Department of Clinical Genetics, Centre for Inherited metabolic Diseases, Copenhagen University Hospital, Copenhagen, Denmark

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Allan M. Lund

Allan M. Lund

Department of Clinical Genetics, Centre for Inherited metabolic Diseases, Copenhagen University Hospital, Copenhagen, Denmark

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Ulrike Steuerwald

Ulrike Steuerwald

Department of Occupational and Public Health, Faroese National Health System, Torshavn, Faroe Islands

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Steen-Holger Hansen

Steen-Holger Hansen

Section of Forensic Pathology, Department of Forensic Medicine, University of Copenhagen, Copenhagen, Denmark

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Høgni D. Joensen

Høgni D. Joensen

Retired Chief Medical Officer, Torshavn, Faroe Islands

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Lars Køber

Lars Køber

Department of Cardiology, Rigshospitalet University Hospital, Copenhagen, Denmark

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Olav W. Nielsen

Olav W. Nielsen

Department of Cardiology, Bispebjerg University Hospital, Copenhagen, Denmark

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First published: 01 August 2019
Citations: 25
Communicating Editor: Piero Rinaldo

Abstract

Primary carnitine deficiency (PCD) affects fatty acid oxidation and is associated with cardiomyopathy and cardiac arrhythmia, but the risk of sudden death in PCD is unknown. The Faroe Islands have a high prevalence of PCD, 1:300. This study systematically investigated a possible association between untreated PCD and sudden death in young Faroese subjects. We investigated all medico-legal cases of sudden death between 1979 and 2012 among subjects below the age of 45. Stored biomaterial was examined with molecular genetic analysis to reveal PCD. We compared the prevalence of PCD among sudden death cases with that of the background population (0.23%) to calculate the odds ratio (OR) for sudden death with PCD. Biomaterial was available and genetically analyzed from 53 of 65 sudden death cases (82%) in the Faroe Islands. Six (one male and five females) of the 53 cases were homozygous for the PCD related c.95A>G mutation—a prevalence of 11.3% (95% CI 5%-23%) and an OR of 54.3 (95% CI 21-138, P < .0001) for the association between sudden death and untreated PCD. Only 11 of the 53 sudden death cases were women—of whom five were homozygous for the c.95A>G mutation (45.5%) yielding an OR of 348.8 (95% CI 94-1287, P < .0001) for the association between sudden death and untreated PCD in females. This study showed a strong association between sudden death and untreated PCD, especially in females.

CONFLICT OF INTEREST

The corresponding author and all co-authors would like to declare no conflict of interest with regards to the content presented in this manuscript.

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