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The Intractable Disease Research Center at Juntendo University will conduct broader analyses of mitochondrial genetic data to confirm genetic diagnosis.

TOKYO, Feb. 12, 2024 /PRNewswire/ -- Mitochondrial disease occurs when malfunctioning mitochondria cannot sustain the production of adenosine triphosphate (ATP)—the energy currency of life—in the inner mitochondrial membrane. The loss of this vital molecule has far-reaching consequences that affect various organ systems and can cause psychiatric symptoms, cardiomyopathy, seizures, kidney and liver dysfunction, and hearing loss.

Unfortunately, mitochondrial disease is the most common congenital metabolic condition, with one case detected for every 5000 live births. In 2022, to improve disease surveillance and the understanding of the genetic factors behind the condition, the Japanese Ministry of Health, Labor, and Welfare included mitochondrial genetic testing under medical service fees covered under insurance.

In terms of testing, Juntendo University screens many babies diagnosed with mitochondrial disease each year. Now, the university will use whole genome sequencing, RNA sequencing, and functional analyses to provide finer-grained insights that facilitate more accurate genetic diagnoses.

The program will be feasible mainly due to the endeavors of Professor Yasushi Okazaki's research group at Juntendo University's Intractable Disease Research Center. "Our team has developed a sequencing platform using the mitochondrial disease gene panel based on data collected from analyzing over 600 cases. We can now screen 367 causative genes in a sample by sequencing genes from a patient's nuclear and entire mitochondrial DNA. By enabling us to profile these causative genes in batches, we have increased the efficiency of genetic diagnosis," says Prof. Okazaki.

The data the lab has already generated highlights how insurance-covered mitochondrial disease testing can bear fruit for diagnosis. Having analyzed 449 suspected cases between January 2020 and December 2022, the team could make a genetic diagnosis for 105 cases using gene panel sequencing. In 67 instances, mitochondrial DNA mutations caused mitochondrial disease. Additionally, 38 cases were due to mutations in nuclear genes. Notably, the researchers identified 35 disease cases with gene variants of unknown clinical significance—an area requiring further research to improve the accuracy of diagnosis.

"Moving forward, the insurance coverage for medical expenses will allow us to cast a wider net when screening for suspected cases. There will be two components to the genetic testing: Juntendo University's Clinical Laboratory will conduct gene panel sequencing and report known mutations. When the laboratory identifies unknown mutations with the patient's consent, we will undertake more detailed genomic analyses at the Intractable Disease Research Center," explains Prof. Okazaki.

Professor Kei Murayama's Mitochondrial Disease Research Project will supplement genetic testing. The project is a part of the Japanese Agency for Medical Research and Development's Intractable Disease Practical Application Research Project and aims to address all treatment aspects. In this regard, Prof. Murayama's team commenced mitochondrial disease outpatient care at Juntendo Medical Center's Pediatric and Adolescent Department in July 2023. 

Contact:

Yoshitaka Nakashima

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+81-3-5802-1590

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SOURCE Juntendo University