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?
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
4. Acyl-Carnitines- short and long chain elevations
5. Amino Acids- alanine & alanine/lysine
6. Ammonia
8. Lactate & Lactate/Pyruvate
9. Pyruvate
10. Creatine Kinase
11. Oxidative Stress
12. Folate Receptor Antibodies
13. Mitochondrial and nuclear DNA
14. Mast Cells
15. Inflammation
16. GI Dysfunction – Zonulin and Clostridia
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
Red Light therapy
EXERCISE!
REMOVING the toxic exposures