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Abstract Details

Whole Exome and Whole Genome Sequencing for the Diagnosis of Mitochondrial Diseases in Critically Ill Children
Child Neurology and Developmental Neurology
S8 - State of the Art Diagnostics in Child Neurology (3:42 PM-3:54 PM)
002
Whole exome sequencing (WES) and whole genome sequencing (WGS) are increasingly used to diagnose mitochondrial diseases. However, the incidence of mitochondrial disease in critically ill patients using WGS or WES remains underreported, and the diagnostic yield of WGS or WES compared to other sequencing methodologies for mitochondrial disease is not well understood.
To assess the yield and utility of WGS/WES in the diagnosis of rare mitochondrial disorders in critically ill children. 
We conducted a single center retrospective cohort study of all participants under 6 years from 1/1/2018-1/1/2023 with a clinical and/or molecularly confirmed diagnosis of mitochondrial disease. We evaluated the proportion of participants who presented to the neonatal or pediatric ICU and characterized their clinical features and genetic testing results. 
Of the 22 participants (11 males, 50%) who met inclusion criteria, 12 (54%) presented critically ill; 7 (58%) in the NICU, 5 (42%) in the PICU; 2 (9%) were deceased at time of writing. 19 participants (86%) had confirmed molecular diagnosis (mean age of diagnosis 1.4 years), 11 who were critically ill. Among the 19 participants with a molecular diagnosis, 13 (68%) were diagnosed by WES or WGS platforms that include mtDNA sequencing. 6/19 (32%) had a pathogenic mtDNA variant, while 13/19 (68%) had pathogenic nDNA variants. Of the mtDNA variants identified, 5/6 presented critically ill. Of the 12 critically ill patients, 10 (91%) received a molecular diagnosis on WGS or WES; 6 of these 10 patients (60%) underwent other genetic tests which did not reveal a molecular diagnosis. Of the 10 non-critically ill patients, 3 (30%) received a diagnosis on WGS or WES, 2 (66%) of whom had at least one other genetic test that did not yield a result. 
WGS/WES has high diagnostic yield in critically ill patients with mitochondrial disease. 
Authors/Disclosures
Mallory Owen (Rady Children's Hospital)
PRESENTER
Dr. Owen has nothing to disclose.
No disclosure on file
Richard Haas No disclosure on file
Jennifer Yang (Rady Childrens Hospital/UCSD) Dr. Yang has received personal compensation in the range of $5,000-$9,999 for serving as an Editor, Associate Editor, or Editorial Advisory Board Member for Sanofi. The institution of Dr. Yang has received research support from Pediatric Epilepsy Research Foundation. The institution of Dr. Yang has received research support from UCB.