Literature DB >> 18202211

Causes of death in pedigrees with the 3243A>G mutation in mitochondrial DNA.

K Majamaa-Voltti1, J Turkka, M-L Kortelainen, H Huikuri, K Majamaa.   

Abstract

BACKGROUND: Causes of death of patients with the 3243A>G mutation have been described in case reports or case series with a limited number of subjects.
METHODS: Eighty-two maternally related sibships of 11 families with 3243A>G were included in this survey. The lifespan of each subject in these families was compared with the life expectancy of the general population, adjusted with respect to year of birth and gender. Causes of death were determined among 3243A>G carriers and their first-degree maternal relatives.
RESULTS: We identified 123 deceased subjects in families with 3243A>G and found an excess mortality during the early years of life and young adulthood. The median age at death for 3243A>G carriers and their first-degree maternal relatives was significantly lower than that of the general population. Neurological and cardiovascular diseases made up one-third of the causes of death. Sudden and unexpected death was not uncommon in patients with cardiovascular diseases, diabetes and epilepsy.
CONCLUSIONS: 3243A>G carriers and their first-degree maternal relatives died younger than was predicted by their life expectancy at birth. Neurological disease was the most common cause of death.

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Year:  2008        PMID: 18202211     DOI: 10.1136/jnnp.2007.122648

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN: 0022-3050            Impact factor:   10.154


  11 in total

1.  Myocardial glucose uptake in patients with the m.3243A > G mutation in mitochondrial DNA.

Authors:  Markus M Lindroos; Jussi P Pärkkä; Markku T Taittonen; Patricia Iozzo; Mikko Kärppä; Ilmo E Hassinen; Juhani Knuuti; Pirjo Nuutila; Kari Majamaa
Journal:  J Inherit Metab Dis       Date:  2015-06-26       Impact factor: 4.982

2.  Natural history of MELAS associated with mitochondrial DNA m.3243A>G genotype.

Authors:  P Kaufmann; K Engelstad; Y Wei; R Kulikova; M Oskoui; D M Sproule; V Battista; D Y Koenigsberger; J M Pascual; S Shanske; M Sano; X Mao; M Hirano; D C Shungu; S Dimauro; D C De Vivo
Journal:  Neurology       Date:  2011-11-16       Impact factor: 9.910

3.  Causes of Death in Adults with Mitochondrial Disease.

Authors:  Marlieke Barends; Lotte Verschuren; Eva Morava; Victoria Nesbitt; Doug Turnbull; Robert McFarland
Journal:  JIMD Rep       Date:  2015-09-10

Review 4.  Cardiac involvement in mitochondrial DNA disease: clinical spectrum, diagnosis, and management.

Authors:  Matthew G D Bates; John P Bourke; Carla Giordano; Giulia d'Amati; Douglass M Turnbull; Robert W Taylor
Journal:  Eur Heart J       Date:  2012-08-30       Impact factor: 29.983

5.  Cardiomyopathy is common in patients with the mitochondrial DNA m.3243A>G mutation and correlates with mutation load.

Authors:  Kieren G Hollingsworth; Grainne S Gorman; Michael I Trenell; Robert McFarland; Robert W Taylor; Douglass M Turnbull; Guy A MacGowan; Andrew M Blamire; Patrick F Chinnery
Journal:  Neuromuscul Disord       Date:  2012-04-17       Impact factor: 4.296

6.  Defining cardiac adaptations and safety of endurance training in patients with m.3243A>G-related mitochondrial disease.

Authors:  Matthew G D Bates; Jane H Newman; Djordje G Jakovljevic; Kieren G Hollingsworth; Charlotte L Alston; Pawel Zalewski; Jacek J Klawe; Andrew M Blamire; Guy A MacGowan; Bernard D Keavney; John P Bourke; Andrew Schaefer; Robert McFarland; Julia L Newton; Douglass M Turnbull; Robert W Taylor; Michael I Trenell; Gráinne S Gorman
Journal:  Int J Cardiol       Date:  2013-06-03       Impact factor: 4.164

7.  Sudden adult death syndrome in m.3243A>G-related mitochondrial disease: an unrecognized clinical entity in young, asymptomatic adults.

Authors:  Yi Shiau Ng; John P Grady; Nichola Z Lax; John P Bourke; Charlotte L Alston; Steven A Hardy; Gavin Falkous; Andrew G Schaefer; Aleksandar Radunovic; Saidi A Mohiddin; Matilda Ralph; Ali Alhakim; Robert W Taylor; Robert McFarland; Douglass M Turnbull; Gráinne S Gorman
Journal:  Eur Heart J       Date:  2015-07-17       Impact factor: 29.983

8.  Is 2D speckle tracking echocardiography useful for detecting and monitoring myocardial dysfunction in adult m.3243A>G carriers? - a retrospective pilot study.

Authors:  S Koene; J Timmermans; G Weijers; P de Laat; C L de Korte; J A M Smeitink; M C H Janssen; L Kapusta
Journal:  J Inherit Metab Dis       Date:  2017-01-04       Impact factor: 4.982

9.  Mitochondrial DNA variation in sudden cardiac death: a population-based study.

Authors:  Laura Kytövuori; Juhani Junttila; Heikki Huikuri; Sirkka Keinänen-Kiukaanniemi; Kari Majamaa; Mika H Martikainen
Journal:  Int J Legal Med       Date:  2019-05-31       Impact factor: 2.686

10.  Concentric hypertrophic remodelling and subendocardial dysfunction in mitochondrial DNA point mutation carriers.

Authors:  Matthew G D Bates; Kieren G Hollingsworth; Jane H Newman; Djordje G Jakovljevic; Andrew M Blamire; Guy A MacGowan; Bernard D Keavney; Patrick F Chinnery; Douglass M Turnbull; Robert W Taylor; Michael I Trenell; Grainne S Gorman
Journal:  Eur Heart J Cardiovasc Imaging       Date:  2012-11-04       Impact factor: 6.875

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