{"id":59446,"date":"2023-05-09T16:41:51","date_gmt":"2023-05-09T11:11:51","guid":{"rendered":"https:\/\/johnsonfrancis.org\/professional\/?p=59446"},"modified":"2023-05-09T18:57:34","modified_gmt":"2023-05-09T13:27:34","slug":"what-is-mitochondrial-cardiomyopathy","status":"publish","type":"post","link":"https:\/\/johnsonfrancis.org\/professional\/what-is-mitochondrial-cardiomyopathy\/","title":{"rendered":"What is Mitochondrial Cardiomyopathy?"},"content":{"rendered":"<p><iframe loading=\"lazy\" width=\"560\" height=\"315\" src=\"https:\/\/www.youtube.com\/embed\/aViLjQfrhMY\" title=\"YouTube video player\" frameborder=\"0\" allow=\"accelerometer; autoplay; clipboard-write; encrypted-media; gyroscope; picture-in-picture; web-share\" allowfullscreen=\"\"><\/iframe><\/p>\n<h2><span style=\"color: #008000;\">What is Mitochondrial Cardiomyopathy?<\/span><\/h2>\n<p>Mitochondria have two genomes &#8211; mitochondrial and nuclear. Mitochondrial disease could be due to mutations of nuclear or mitochondrial DNA. Mitochondrial DNA is inherited maternally while nuclear DNA has Mendelian inheritance, which could be dominant or recessive [1]. It may be noted in about one in 5000 live births. Cardiac involvement in mitochondrial disease seldom occurs in isolation and is often part of multiorgan dysfunction [2]. Mitochondria being part of the cellular respiratory chain, tissues with high energy requirements like heart, muscle, kidneys and endocrine system are often involved in mitochondrial disease [1]. Cardiac manifestations described in mitochondrial disease include hypertrophic and dilated cardiomyopathy, arrhythmias, left ventricular noncompaction and heart failure. These could worsen during a metabolic crisis [2].<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-59449 size-full\" src=\"https:\/\/johnsonfrancis.org\/professional\/wp-content\/uploads\/2023\/05\/What-is-Mitochondrial-Cardiomyopathy.jpg\" alt=\"What is Mitochondrial Cardiomyopathy\" width=\"1200\" height=\"896\" srcset=\"https:\/\/johnsonfrancis.org\/professional\/wp-content\/uploads\/2023\/05\/What-is-Mitochondrial-Cardiomyopathy.jpg 1200w, https:\/\/johnsonfrancis.org\/professional\/wp-content\/uploads\/2023\/05\/What-is-Mitochondrial-Cardiomyopathy-300x224.jpg 300w, https:\/\/johnsonfrancis.org\/professional\/wp-content\/uploads\/2023\/05\/What-is-Mitochondrial-Cardiomyopathy-1024x765.jpg 1024w, https:\/\/johnsonfrancis.org\/professional\/wp-content\/uploads\/2023\/05\/What-is-Mitochondrial-Cardiomyopathy-768x573.jpg 768w\" sizes=\"auto, (max-width: 1200px) 100vw, 1200px\" \/><\/p>\n<p id=\"p-13\">Mitochondrial crisis can be precipitated by stressors like febrile illness or surgery and can lead to acute heart failure. Kearns-Sayre syndrome is a well known mitochondrial disease with progressive external ophthalmoplegia and cardiac conduction defects. Family history of maternal inheritance of multisystem disease is an indicator for mitochondrial disease. Gold standard for diagnosis of mitochondrial disease is muscle biopsy. Management of mitochondrial disease and cardiomyopathy are mostly supportive. They should avoid medications which are likely to interfere with mitochondrial function and precipitate a crisis.<\/p>\n<p><span style=\"color: #0000ff;\"><strong>References<\/strong><\/span><\/p>\n<ol>\n<li>Limongelli G, Masarone D, Pacileo G. <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/27821705\/\">Mitochondrial disease and the heart<\/a>. Heart. 2017 Mar;103(5):390-398. doi: 10.1136\/heartjnl-2015-308193. Epub 2016 Nov 7. PMID: 27821705.<\/li>\n<li>Meyers DE, Basha HI, Koenig MK. <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/24082366\/\">Mitochondrial cardiomyopathy: pathophysiology, diagnosis, and management<\/a>. Tex Heart Inst J. 2013;40(4):385-94. PMID: 24082366; PMCID: PMC3783139.<\/li>\n<\/ol>\n","protected":false},"excerpt":{"rendered":"<p>What is Mitochondrial Cardiomyopathy? Mitochondria have two genomes &#8211; mitochondrial and nuclear. Mitochondrial disease could be due to mutations of nuclear or mitochondrial DNA. Mitochondrial DNA is inherited maternally while nuclear DNA has Mendelian inheritance, which could be dominant or recessive [1]. It may be noted in about one in 5000 live births. Cardiac involvement [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":59449,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"nf_dc_page":"","footnotes":""},"categories":[9],"tags":[],"class_list":["post-59446","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-general"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.9 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>What is Mitochondrial Cardiomyopathy? - All About Cardiovascular System and Disorders<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/johnsonfrancis.org\/professional\/what-is-mitochondrial-cardiomyopathy\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"What is Mitochondrial Cardiomyopathy? - All About Cardiovascular System and Disorders\" \/>\n<meta property=\"og:description\" content=\"What is Mitochondrial Cardiomyopathy? Mitochondria have two genomes &#8211; mitochondrial and nuclear. Mitochondrial disease could be due to mutations of nuclear or mitochondrial DNA. Mitochondrial DNA is inherited maternally while nuclear DNA has Mendelian inheritance, which could be dominant or recessive [1]. It may be noted in about one in 5000 live births. 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