Usefulness of Magnetic Resonance Spectroscopy for the Initial Diagnosis of Mitochondrial DNA-Associated Leigh Syndrome

Purpose Diagnosing Leigh syndrome (LS), a representative mitochondrial disease, remains challenging. Mitochondrial DNA (mtDNA)-associated LS, which is maternally inherited, has relatively well-known genetic variants. We evaluated the usefulness of brain magnetic resonance spectroscopy (MRS) for the...

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Main Authors: Ji-Hoon Na (Author), Je Hee Shin (Author), Hyunjoo Lee (Author), Young-Mock Lee (Author)
Format: Book
Published: Korean Child Neurology Society, 2022-01-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Ji-Hoon Na  |e author 
700 1 0 |a Je Hee Shin  |e author 
700 1 0 |a Hyunjoo Lee  |e author 
700 1 0 |a Young-Mock Lee  |e author 
245 0 0 |a Usefulness of Magnetic Resonance Spectroscopy for the Initial Diagnosis of Mitochondrial DNA-Associated Leigh Syndrome 
260 |b Korean Child Neurology Society,   |c 2022-01-01T00:00:00Z. 
500 |a 2635-909X 
500 |a 2635-9103 
500 |a 10.26815/acn.2021.00542 
520 |a Purpose Diagnosing Leigh syndrome (LS), a representative mitochondrial disease, remains challenging. Mitochondrial DNA (mtDNA)-associated LS, which is maternally inherited, has relatively well-known genetic variants. We evaluated the usefulness of brain magnetic resonance spectroscopy (MRS) for the initial diagnosis of mtDNA-associated LS using data from LS patients. Methods The study involved LS patients who visited Gangnam Severance Hospital between 2006 and 2018. Based on patients' clinical findings, genetic evaluations, brain magnetic resonance imaging, and brain MRS findings, 24 mtDNA-associated and 49 gene-negative LS patients were included in the current study. Lactate peaks and decreased N-acetyl aspartate (NAA) peaks in brain MRS were compared between both groups. Results In total, 11 mtDNA mutation subtypes were detected. Our findings showed a higher proportion of brain MRS abnormalities in mtDNA-associated LS patients than in gene-negative LS patients, but no statistically significant differences were observed between the two groups (lactate peak, P=0.080; decreased NAA peak, P=0.115). Conclusion Brain MRS is currently limited as an initial diagnostic test for mtDNA-associated LS. However, it may be a useful non-invasive test for the follow-up evaluation of mtDNA-associated LS treatment. Ultra-high-field MRS technology is expected in the future. 
546 |a EN 
546 |a KO 
690 |a mitochondrial diseases 
690 |a leigh disease 
690 |a magnetic resonance spectroscopy 
690 |a lactates 
690 |a Internal medicine 
690 |a RC31-1245 
690 |a Neurosciences. Biological psychiatry. Neuropsychiatry 
690 |a RC321-571 
690 |a Neurology. Diseases of the nervous system 
690 |a RC346-429 
655 7 |a article  |2 local 
786 0 |n Annals of Child Neurology, Vol 30, Iss 1, Pp 17-23 (2022) 
787 0 |n http://www.annchildneurol.org/upload/pdf/acn-2021-00542.pdf 
787 0 |n https://doaj.org/toc/2635-909X 
787 0 |n https://doaj.org/toc/2635-9103 
856 4 1 |u https://doaj.org/article/ce271786dcc24b1b97d0de6eaf62a8f0  |z Connect to this object online.