A biallelic variant in COX18 cause isolated Complex IV deficiency associated with neonatal encephalo-cardio-myopathy and axonal sensory neuropathy

• Published in: European journal of human genetics : EJHG 2023-12, Vol.31 (12), p.1414-1420
• Main Authors: Ronchi, Dario, Garbellini, Manuela, Magri, Francesca, Menni, Francesca, Meneri, Megi, Bedeschi, Maria Francesca, Dilena, Robertino, Cecchetti, Valeria, Picciolli, Irene, Furlan, Francesca, Polimeni, Valentina, Salani, Sabrina, Pezzoli, Laura, Fortunato, Francesco, Bellini, Matteo, Piga, Daniela, Ripolone, Michela, Zanotti, Simona, Napoli, Laura, Ciscato, Patrizia, Sciacco, Monica, Mangili, Giovanna, Mosca, Fabio, Corti, Stefania, Iascone, Maria, Comi, Giacomo Pietro
• Format: Article
• Language: English
• Subjects: Antibodies; Biopsy; Cardiac muscle; Cardiomyopathy; Cytochrome; Cytochrome-c oxidase; Cytochrome-c Oxidase Deficiency - genetics; Electron transport; Electron Transport Complex IV - genetics; Electron Transport Complex IV - metabolism; Enzymes; Female; Genetic testing; Genetics; Genomes; HEK293 Cells; Humans; Infant; Medical screening; Mitochondria; Mitochondrial DNA; Mitochondrial Proteins - genetics; Muscular Diseases; Mutation; Myoblasts; Myopathy; Neonates; Neuropathy; Proteins; Skeletal muscle
• ISSN: 1018-4813; 1476-5438; 1476-5438
• DOI: 10.1038/s41431-023-01433-6

Pathogenic variants impacting upon assembly of mitochondrial respiratory chain Complex IV (Cytochrome c Oxidase or COX) predominantly result in early onset mitochondrial disorders often leading to CNS, skeletal and cardiac muscle manifestations. The aim of this study is to describe a molecular defect in the COX assembly factor gene COX18 as the likely cause of a neonatal form of mitochondrial encephalo-cardio-myopathy and axonal sensory neuropathy. The proband is a 19-months old female displaying hypertrophic cardiomyopathy at birth and myopathy with axonal sensory neuropathy and failure to thrive developing in the first months of life. Serum lactate was consistently increased. Whole exome sequencing allowed the prioritization of the unreported homozygous substitution NM_001297732.2:c.667 G > C p.(Asp223His) in COX18. Patient's muscle biopsy revealed severe and diffuse COX deficiency and striking mitochondrial abnormalities. Biochemical and enzymatic studies in patient's myoblasts and in HEK293 cells after COX18 silencing showed a severe impairment of both COX activity and assembly. The biochemical defect was partially rescued by delivery of wild-type COX18 cDNA into patient's myoblasts. Our study identifies a novel defect of COX assembly and expands the number of nuclear genes involved in a mitochondrial disorder due to isolated COX deficiency.