{"id":770,"date":"2015-06-17T18:41:08","date_gmt":"2015-06-17T18:41:08","guid":{"rendered":"https:\/\/blogs.bmj.com\/jmg\/?p=770"},"modified":"2026-02-25T01:03:30","modified_gmt":"2026-02-25T01:03:30","slug":"rescue-of-primary-ubiquinone-deficiency-due-to-a-novel-coq7-defect-using-24-dihydroxybensoic-acid","status":"publish","type":"post","link":"https:\/\/blogs.bmj.com\/jmg\/2015\/06\/17\/rescue-of-primary-ubiquinone-deficiency-due-to-a-novel-coq7-defect-using-24-dihydroxybensoic-acid\/","title":{"rendered":"Rescue of primary ubiquinone deficiency due to a novel COQ7 defect using 2,4\u2013dihydroxybensoic acid (Contributed by Dr. Christoph Freyer)"},"content":{"rendered":"<p>Coenzyme Q (CoQ10) is an essential mitochondrial electron carrier, redox cofactor and a potent antioxidant in the majority of cellular membranes. A range of metabolic diseases, as well as the ageing process and prolonged statin treatments have been associated with CoQ10 deficiency. Here the first case of a primary CoQ10 defect due to a mutation in COQ7, necessary for CoQ10 biosynthesis, is presented. For accurate diagnosis a novel and highly sensitive method for CoQ10 quantification by UPLC &#8211; mass spectrometry was developed. By applying the COQ10 analogue, 2,4-dihydroxybenzoic acid, a potentially effective treatment strategy for CoQ10 deficiencies is introduced. (<a href=\"http:\/\/jmg.bmj.com\/content\/early\/2015\/06\/16\/jmedgenet-2015-102986\">http:\/\/jmg.bmj.com\/content\/early\/2015\/06\/16\/jmedgenet-2015-102986<\/a> )<!--TrendMD v2.4.8--><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Coenzyme Q (CoQ10) is an essential mitochondrial electron carrier, redox cofactor and a potent antioxidant in the majority of cellular membranes. A range of metabolic diseases, as well as the ageing process and prolonged statin treatments have been associated with CoQ10 deficiency. Here the first case of a primary CoQ10 defect due to a mutation [&#8230;]<\/p>\n<p><a class=\"btn btn-secondary understrap-read-more-link\" href=\"https:\/\/blogs.bmj.com\/jmg\/2015\/06\/17\/rescue-of-primary-ubiquinone-deficiency-due-to-a-novel-coq7-defect-using-24-dihydroxybensoic-acid\/\">Read More&#8230;<\/a><\/p>\n","protected":false},"author":123,"featured_media":0,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[],"class_list":["post-770","post","type-post","status-publish","format-standard","hentry","category-uncategorized"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.6 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Rescue of primary ubiquinone deficiency due to a novel COQ7 defect using 2,4\u2013dihydroxybensoic acid (Contributed by Dr. Christoph Freyer) - JMG Contact blog<\/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:\/\/blogs.bmj.com\/jmg\/2015\/06\/17\/rescue-of-primary-ubiquinone-deficiency-due-to-a-novel-coq7-defect-using-24-dihydroxybensoic-acid\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Rescue of primary ubiquinone deficiency due to a novel COQ7 defect using 2,4\u2013dihydroxybensoic acid (Contributed by Dr. Christoph Freyer) - JMG Contact blog\" \/>\n<meta property=\"og:description\" content=\"Coenzyme Q (CoQ10) is an essential mitochondrial electron carrier, redox cofactor and a potent antioxidant in the majority of cellular membranes. A range of metabolic diseases, as well as the ageing process and prolonged statin treatments have been associated with CoQ10 deficiency. 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