#Mitochondria Matter
Facts to know
FAQ
Mitochondrial malfunction, or dysfunction, occurs when these cellular powerhouses fail to produce enough energy for the body to function properly. This can be caused by inherited or spontaneous genetic mutations that disrupt mitochondrial processes, or by environmental factors like toxins, medications, or oxidative stress or as you age. Over time, accumulated damage from these factors can impair mitochondrial function and contribute to a wide range of health issues, from fatigue and muscle weakness to neurodegenerative diseases and organ failure.
Mitochondrial disease and dysfunction are more common than many realize. An estimated 1 in 4,000 individuals has a diagnosed genetic mitochondrial disease, but the true number may be higher due to underdiagnosis and the wide range of potential symptoms. Even more staggering, mitochondrial dysfunction is believed to contribute to a vast array of common diseases, including Alzheimer’s, Parkinson’s, ALS, multiple sclerosis, diabetes, heart disease, and cancer. This means countless individuals are affected, either directly through diagnosed mitochondrial diseases or indirectly through the contribution of mitochondrial dysfunction to their health conditions. Raising awareness and supporting research is crucial to better understand and address this widespread issue.
Adults can certainly have mitochondrial disease and dysfunction. While these conditions are often associated with childhood onset, it’s increasingly recognized that they can also develop or be diagnosed in adulthood. This can happen due to delayed diagnosis, age-related decline in mitochondrial function, acquired mitochondrial dysfunction from environmental factors, or secondary mitochondrial dysfunction stemming from other chronic diseases. The symptoms in adults can range from fatigue and muscle weakness to neurological problems and multi-organ involvement. Early diagnosis and intervention are crucial for managing these conditions and improving quality of life.
Both children and adults are at a high risk for neurological and organ damage during times of extra stress on the body. This includes during and for the two weeks following an illness, starvation, dehydration, surgery, anesthesia, and IV antibiotic.
The prognosis for individuals with mitochondrial diseases varies widely, depending on several factors. While some children and adults experience relatively mild symptoms and lead fulfilling lives, others face more severe challenges, with the potential for significant impact on their health and lifespan. In some cases, children with mitochondrial disease may not survive beyond their teenage years, while adult-onset can lead to rapid deterioration in health and quality of life.
Each individual’s experience is unique, and it’s essential to work closely with healthcare providers to understand the specific prognosis and develop personalized treatment plans.
The exact number of diseases and conditions stemming from mitochondrial dysfunction is vast and continually growing as research progresses. While there are over 40 recognized primary mitochondrial diseases, mitochondrial dysfunction is also a significant contributor to hundreds of other conditions. These include neurodegenerative diseases like Alzheimer’s, ALS, and Parkinson’s, metabolic disorders like diabetes, cardiovascular diseases, neurodevelopmental disorders, and even the aging process itself. As scientists delve deeper into the role of mitochondria in cellular health, the list of associated diseases continues to expand, underscoring the importance of understanding and addressing mitochondrial dysfunction for overall well-being.