MITO DISEASE - SCIENCE
News: Scientists
are currently preparing for a clinical trial to determine whether mitochondrial
donation is safe and effective, following the passage of a law in Australia in
2022 that will allow for the practice.
 
What’s in the news?
Mitochondrial Donation
 - An IVF-based procedure that prevents the transmission of faulty
     mitochondrial DNA, allowing families to have healthy, genetically related
     children.
 
 - Process:
 
·        
Hormone Injections: Stimulate egg production in both the donor and the affected
individual.
·        
Egg Retrieval: Collect eggs from both the donor and the affected individual using an
ultrasound-guided procedure.
·        
Nuclear DNA Transfer: Extract the nuclear DNA from the affected individual’s egg and insert
it into the donor egg with healthy mitochondria.
·        
Fertilization: Use sperm from the intending father to fertilize the modified donor
egg.
 Legal and Ethical Considerations
 - Maeve's Law: The
     Mitochondrial Donation Law Reform Bill 2021, passed by the Australian
     Senate in 2022, allows mitochondrial donation for research and clinical
     trials under strict regulations.
 
 - Requirements:
 
o   
Facilities must obtain special permits.
o   
Initial licenses for pre-clinical and clinical
trial research to ensure safety and effectiveness.
 
Mitochondrial Disease
 - Mitochondrial diseases are a group of disorders caused by
     dysfunctional mitochondria, the organelles that generate energy for the
     cell.
 
 - These diseases can affect multiple organs and systems, including
     the brain, heart, liver, muscles, kidneys, and endocrine system.
 
 - Affects 1 in every 5,000 people, making it a common inherited
     metabolic condition
 
 Causes
 - Mitochondrial diseases are primarily genetic, resulting from
     mutations in either nuclear DNA (nDNA) or mitochondrial DNA (mtDNA).
 
 - They can be inherited in several ways:
 
 - Autosomal Recessive/Dominant Inheritance: Mutations in nDNA inherited from both or one parent.
 
 - Mitochondrial Inheritance:
     Mutations in mtDNA passed down from the mother.
 
 - De Novo Mutations: New
     mutations that occur spontaneously without a family history
 
 Symptoms
Symptoms of mitochondrial diseases vary widely and
can include:
 - Muscle weakness and exercise intolerance
 
 - Neurological issues such as seizures, migraines, and developmental
     delays
 
 - Cardiomyopathy and other heart issues
 
 - Liver and kidney dysfunction
 
 - Endocrine problems, including diabetes and growth delays
 
 - Gastrointestinal disturbances
 
 - Visual and hearing impairments.
 
 
Types of Mitochondrial Diseases
There are several types of mitochondrial diseases,
each with unique characteristics. Some notable types include:
 - Leigh Syndrome: Severe
     neurological disorder
 
 - MELAS (Mitochondrial Encephalopathy, Lactic Acidosis, and
     Stroke-like episodes)
 
 - MERRF (Myoclonic Epilepsy with Ragged Red Fibers)
 
 - Kearns-Sayre Syndrome
 
 - Barth Syndrome
 
 - Alpers Disease
 
 - Chronic Progressive External Ophthalmoplegia (CPEO)
 
 - Friedreich's Ataxia
 
 Source: https://www.business-standard.com/health/mitochondrial-donation-all-you-need-to-know-about-this-mito-disease-124070800771_1.html