MITOCHONDRIAL DYSFUNCTION & ASD
What is it?
Mitochondria are distinct cellular organelles that generate adenosine triphosphate (ATP), the energy carrier in most mammalian cells, from adenosine diphosphate by oxidizing glucose and fatty acids. The prevalence of abnormal biomarker values of mitochondrial dysfunction was found to be high in ASD, possibly as high as 80% in the ASD population. Variances and mean values of many mitochondrial biomarkers (lactate, pyruvate, carnitine, and ubiquinone) were significantly different between ASD and controls in one meta-analysis. Some markers correlated with ASD severity.
What Causes it?
Primary- Defect in genetics directly related to the function of mitochondria, producing ATP.
Toxins in the environment impair mitochondrial processes such as methylation, the Krebs cycle, the electron transport chain, and fatty acid oxidation.
What are Associated Conditions?
Seizures
Fatigue
Migraine HAs
Anxiety/Depression
Insomnia
Developmental Regression
Speech/Gross Motor/Fine Motor difficulties
Common Biomarkers Associated with Mitochondrial Dysfunction (No one biomarker exists to confirm diagnosis):
Methylation Redox- Glutathione and cysteine
Carnitine- total and/or free low, high esthers
Coq10
Acyl-Carnitines- short and long chain elevations
Amino Acids- alanine & alanine/lysine
Ammonia
Electron Transport Chain- via mitoswab
Lactate & Lactate/Pyruvate
Pyruvate
Creatine Kinase
Oxidative Stress- such as low glutathione found on OAT
Folate Receptor Antibodies
Mitochondrial and nuclear DNA - gene mutations
Mast Cells
Inflammation- IL10, TNFalpha
GI Dysfunction- i.e., elevated Zonulin, Clostridia, and fungal markers on OAT test, stool test
What Treatments are Available?
Carnitine
Co Q 10 (ubiquinol)
B vitamins (including b1, b2, b6, b9 and b12)
PQQ
Antioxidants such as NAC
Creatine
Minerals such as magnesium and potassium
HBOT
Anti-inflammatories like quercetin and curcumin
Red Light therapy
Exercise
Balancing microbiome
REMOVING the toxic exposures