Aims: In 2003, an Australian woman was convicted by a jury of smothering and killing her four children over a 10-year period. Each child died suddenly and unexpectedly during a sleep period, at ages ranging from 19 days to 18 months. In 2019 we were asked to investigate if a genetic cause could explain the deaths, as part of an inquiry into the mother's convictions. Methods and results: Whole genomes or exomes of the mother and her four children were sequenced. Functional analysis of a novel CALM2 variant was performed by measuring Ca2+-binding affinity, interaction with calcium channels and channel function. We found two children had a novel calmodulin variant (CALM2 G114R) that was inherited maternally. Three genes (CALM1-3) encode identical calmodulin proteins. A variant in the corresponding residue of CALM3 (G114W) was recently reported in a child who died suddenly at age 4 and a sibling who suffered a cardiac arrest at age 5. We show that CALM2 G114R impairs calmodulin's ability to bind calcium and regulate two pivotal calcium channels (CaV1.2 and RyR2) involved in cardiac excitation contraction coupling. The deleterious effects of G114R are similar to those produced by G114W and N98S, which are considered arrhythmogenic and cause sudden cardiac death in children. Conclusion: A novel functional calmodulin variant (G114R) predicted to cause idiopathic ventricular fibrillation, catecholaminergic polymorphic ventricular tachycardia, or mild long QT syndrome was present in two children. A fatal arrhythmic event may have been triggered by their intercurrent infections. Thus, calmodulinopathy emerges as a reasonable explanation for a natural cause of their deaths.

Brohus, M., Arsov, T., Wallace, D., Jensen, H., Nyegaard, M., Crotti, L., et al. (2021). Infanticide vs. inherited cardiac arrhythmias. EUROPACE, 23(3), 441-450 [10.1093/europace/euaa272].

Infanticide vs. inherited cardiac arrhythmias.

Crotti, L;
2021

Abstract

Aims: In 2003, an Australian woman was convicted by a jury of smothering and killing her four children over a 10-year period. Each child died suddenly and unexpectedly during a sleep period, at ages ranging from 19 days to 18 months. In 2019 we were asked to investigate if a genetic cause could explain the deaths, as part of an inquiry into the mother's convictions. Methods and results: Whole genomes or exomes of the mother and her four children were sequenced. Functional analysis of a novel CALM2 variant was performed by measuring Ca2+-binding affinity, interaction with calcium channels and channel function. We found two children had a novel calmodulin variant (CALM2 G114R) that was inherited maternally. Three genes (CALM1-3) encode identical calmodulin proteins. A variant in the corresponding residue of CALM3 (G114W) was recently reported in a child who died suddenly at age 4 and a sibling who suffered a cardiac arrest at age 5. We show that CALM2 G114R impairs calmodulin's ability to bind calcium and regulate two pivotal calcium channels (CaV1.2 and RyR2) involved in cardiac excitation contraction coupling. The deleterious effects of G114R are similar to those produced by G114W and N98S, which are considered arrhythmogenic and cause sudden cardiac death in children. Conclusion: A novel functional calmodulin variant (G114R) predicted to cause idiopathic ventricular fibrillation, catecholaminergic polymorphic ventricular tachycardia, or mild long QT syndrome was present in two children. A fatal arrhythmic event may have been triggered by their intercurrent infections. Thus, calmodulinopathy emerges as a reasonable explanation for a natural cause of their deaths.
Si
Articolo in rivista - Articolo scientifico
Scientifica
BSN; CALM2; Calmodulinopathy; Infanticide; Sudden unexpected death;
English
Brohus, M., Arsov, T., Wallace, D., Jensen, H., Nyegaard, M., Crotti, L., et al. (2021). Infanticide vs. inherited cardiac arrhythmias. EUROPACE, 23(3), 441-450 [10.1093/europace/euaa272].
Brohus, M; Arsov, T; Wallace, D; Jensen, H; Nyegaard, M; Crotti, L; Adamski, M; Zhang, Y; Field, M; Athanasopoulos, V; Baró, I; Ribeiro de Oliveira-Mendes, B; Redon, R; Charpentier, F; Raju, H; Disilvestre, D; Wei, J; Wang, R; Rafehi, H; Kaspi, A; Bahlo, M; Dick, I; Chen, S; Cook, M; Vinuesa, C; Overgaard, M; Schwartz, P
File in questo prodotto:
File Dimensione Formato  
Brohus 2020.pdf

accesso aperto

Tipologia di allegato: Publisher’s Version (Version of Record, VoR)
Dimensione 2.45 MB
Formato Adobe PDF
2.45 MB Adobe PDF Visualizza/Apri

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/10281/297351
Citazioni
  • Scopus 5
  • ???jsp.display-item.citation.isi??? 7
Social impact