Bilateral striatal necrosis caused by a founder mitochondrial 14459G > A mutation in two independent Japanese families

• Published in: Journal of the neurological sciences 2017-07, Vol.378, p.177-181
• Main Authors: Hirayanagi, Kimitoshi, Okamoto, Yuji, Takai, Eriko, Ishizawa, Kunihiko, Makioka, Kouki, Fujita, Yukio, Kaneko, Yuka, Tanaka, Makoto, Takashima, Hiroshi, Ikeda, Yoshio
• Format: Article
• Language: English
• Subjects: 14459G > A; Adult; Asian Continental Ancestry Group - genetics; Bilateral striatal necrosis; Corpus Striatum - diagnostic imaging; DNA, Mitochondrial; Family; Heteroplasmy; Homoplasmy; Humans; Japan; Magnetic Resonance Imaging; Male; Mutation; NADH dehydrogenase subunit 6; Necrosis; Neurology; SNP; Striatonigral Degeneration - congenital; Striatonigral Degeneration - diagnostic imaging; Striatonigral Degeneration - genetics; Young Adult
• ISSN: 0022-510X; 1878-5883
• DOI: 10.1016/j.jns.2017.05.015

Abstract Bilateral striatal necrosis (BSN) has many causes and is characterized by unique clinical and neuroradiological features. Herein, we report a clinical and genetic analysis of three BSN cases from two independent Japanese families harboring a mitochondrial DNA (mtDNA) 14459G > A mutation located in a coding region of the NADH dehydrogenase subunit 6 gene. In the first family, two male siblings from non-consanguineous parents exhibited similar phenotypes, with infantile-onset generalized dystonia. A third sporadic case involved a male patient with a comparatively milder phenotype characterized by juvenile-onset mild truncal ataxia and parkinsonism. Cerebral magnetic resonance imaging of these cases revealed abnormal signal intensities along the bilateral putaminal area and enlarged lateral ventricle anterior horns caused by caudate nuclear atrophy, particularly in the sibling pair. The sibling-pair cases shared a homoplasmic 14459G > A mutation, and the sporadic case showed heteroplasmy of the same mutation. Additionally, all three cases harbored the 14605A > G single nucleotide polymorphism, which was previously reported as a rare synonymous variation (4.3%) in a Japanese population. Plasmid sequencing revealed a genetic linkage of these two DNA substitutions, suggesting that the three patients shared a genetic founder. Although our mtDNA analysis was only accessible using leukocytes, clinical severity might be associated with homoplasmy or heteroplasmy. In summary, it is important to evaluate potential mtDNA defects in BSN cases, regardless of familial occurrence.