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Diabetic Dead-in-Bed Syndrome: A Possible Link to a Cardiac Ion Channelopathy
Jonathan R Skinner1, Renate Marquis-Nicholson2, Alix Luangpraseuth3
1Cardiac Inherited Disease Group, Auckland City Hospital, Auckland 1148, New Zealand ; Green Lane Paediatric and Congenital Cardiac Services, Starship Children's Hospital, Auckland 1148, New Zealand ; Department of Child Health, University of Auckland, Private Bag 92019, Auckland 1142, New Zealand.
Abstract:
Sudden unexpected nocturnal death among patients with diabetes occurs approximately ten times more commonly than in the general population. Malignant ventricular arrhythmia due to Brugada syndrome has been postulated as a cause, since a glucose-insulin bolus can unmask the Brugada electrocardiographic signature in genetically predisposed individuals. In this report we present a 16-year-old male with insulin-dependent diabetes who died suddenly at night. His diabetes had been well controlled, without significant hypoglycaemia. At autopsy, he had a full stomach and a glucose level of 7 mmol/L in vitreous humor, excluding hypoglycaemia. Genetic analysis of autopsy DNA revealed a missense mutation, c.370A>G (p.Ile124Val), in the GPD1L gene. A parent carried the same mutation and has QT prolongation. Mutations in this gene have been linked to Brugada syndrome and sudden infant death. The patient may have died from a ventricular arrhythmia, secondary to occult Brugada syndrome, triggered by a full stomach and insulin. The data suggest that molecular autopsies are warranted to investigate other cases of the diabetic dead-in-bed syndrome.
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