Literature DB >> 27134827

Arrhythmias in MELAS syndrome.

Josef Finsterer1, Sinda Zarrouk-Mahjoub2.   

Abstract

Entities:  

Keywords:  Congenital heart defect; Heart failure; Hypertrabeculation; Non-compaction; Sudden cardiac death

Year:  2016        PMID: 27134827      PMCID: PMC4834673          DOI: 10.1016/j.ymgmr.2016.03.008

Source DB:  PubMed          Journal:  Mol Genet Metab Rep        ISSN: 2214-4269


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Letter to the Editor With interest we read the article by Thomas et al. about a 44 year old female with MELAS syndrome due to the m.3243A > G mutation, which manifested cardiologically as hypertrophic cardiomyopathy and episodes of supraventricular tachycardia requiring atenolol [1]. We have the following comments and concerns. MELAS may be associated with sudden cardiac death [2]. Did the authors consider implantation of a loop-recoder to monitor if there were also ventricular arrhythmias requiring implantation of an ICD? The authors describe hypertrophic cardiomyopathy as progressive [1]. What was the systolic function and wall thickness at the last follow-up? Figure 1B suggests that there is noncompaction of the left ventricular myocardium [1]. Did the authors look for this unclassified cardiomyopathy, which may occur in addition to hypertrophic cardiomyopathy, goes frequently along with late gadolinium enhancement [3], and is most frequently associated with mitochondrial disorders? [4] A heteroplasmy rate of 25% of the m.3243A > G mutation is low. In which tissue was it determined? Blood, muscle, saliva, or urine? Were other tissues investigated for the heteroplasmy rate as well? Was a muscle biopsy carried out? Recurrent stroke-like episodes (SLEs) are reported during the 11 years since diagnosis [1], which are a clinical manifestation of cerebral stroke-like lesions [5]. How many SLEs did the patient experience, in which cerebral region, and why could the remnants not be seen on cerebral MRI, which only showed atrophy and leucencephalopathy? Concerning the initial fall, did the patient loose consciousness, did she experience a tongue bite, or did she experience a secessus urinae/alvi? What were the results of the EEG? Did the patient always experience seizures during SLEs? Were antiepileptic drugs administered? Were other causes of the fall excluded? Overall, this interesting case should be supplemented by results about the heteroplasmy in more than a single tissue, long-term ECG results, and the medication she was taking at last follow-up.
  5 in total

Review 1.  [MELAS sudden death due to paroxysmal arrhythmia].

Authors:  Akira Taniguchi; Takeo Kitagawa; Shigeki Kuzuhara
Journal:  Nihon Rinsho       Date:  2002-04

Review 2.  Cardiogenetics, neurogenetics, and pathogenetics of left ventricular hypertrabeculation/noncompaction.

Authors:  Josef Finsterer
Journal:  Pediatr Cardiol       Date:  2009-01-29       Impact factor: 1.655

3.  Stroke and Stroke-like Episodes in Muscle Disease.

Authors:  Josef Finsterer
Journal:  Open Neurol J       Date:  2012-05-18

4.  Comparison of cardiovascular magnetic resonance characteristics and clinical consequences in children and adolescents with isolated left ventricular non-compaction with and without late gadolinium enhancement.

Authors:  Huaibing Cheng; Minjie Lu; Cuihong Hou; Xuhua Chen; Li Li; Jing Wang; Gang Yin; Xiuyu Chen; Wei Xiangli; Chen Cui; Jianmin Chu; Shu Zhang; Sanjay K Prasad; Jielin Pu; Shihua Zhao
Journal:  J Cardiovasc Magn Reson       Date:  2015-05-30       Impact factor: 5.364

5.  Arrhythmia as a cardiac manifestation in MELAS syndrome.

Authors:  Tamara Thomas; William J Craigen; Ryan Moore; Richard Czosek; John L Jefferies
Journal:  Mol Genet Metab Rep       Date:  2015-06-03
  5 in total
  1 in total

1.  Sea food consumption for improving cardiac and cerebral manifestations of mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes.

Authors:  Fulvio A Scorza; Josef Finsterer
Journal:  Ann Transl Med       Date:  2017-09
  1 in total

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