DEPRESSION. William J. Walsh, Ph.D.



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Transcription:

DEPRESSION. William J. Walsh, Ph.D.

Depression Database More than 3,000 patients diagnosed with clinical depression, > 250,000 assays of blood and urine, 50 to 150 symptoms or traits recorded for each patient.

Database Studies A wide range of abnormal chemistries and behaviors were observed in the depressive population. 5 chemical classifications (phenotypes) were identified, representing 95% of depressives. Distinctive symptoms and traits were identified for each depression group.

Chemical Classification of Depression 38% Undermethylation 20% Folate Deficiency 17% Copper Overload 15% Elevated Pyrroles 5% Toxic Metal Overload

Implications of Database Findings Depression is a name given to a variety of different mood disorders. Each depression phenotype has unique chemical imbalances and symptoms. Different treatment approaches are needed for these disorders.

A 25-Year Mystery! Folic Acid is a very-effective methylating agent. Undermethylated depressed patients are intolerant to folates. Overmethylated depressives thrive on folates. WHY?

Mystery Solved by Epigenetic Science Folic Acid generates acetylase enzymes that alter histones & promote expression of SERT. SERT increases serotonin reuptake, thus reducing serotonin activity. For low-serotonin depressives, the harmful impact of folic acid at the synapse exceeds the benefits of normalizing methylation.

Epigenetics of Methyl and Folate SAMe modifies histones to block production of transporter proteins: This reuptake inhibition increases activity of serotonin & dopamine. Folates have the opposite effect on histones and lower serotonin and dopamine activity.

Nutrients That Increase Serotonin Neurotransmission S-Adenosyl Methionine (SAMe) Methionine Tryptophan 5-HTP

Nutrients That Decrease Dopamine Neurotransmission Folic Acid Niacin or Niacinamide DMAE or Choline Manganese

Nutrients That Decrease Norepinephrine Neurotransmission GABA Folic Acid Niacin or Niacinamide Pantothenic Acid Zinc

Five Depression Phenotypes 1. Undermethylation 2. Low Folate 3. Copper Overload 4. Pyrrole Disorder 5. Toxic Metal Overload

Phenoptype #1 Undermethylated Depression Elevated Blood Histamine Low SAMe/SAH Ratio Low Basophils Low Serotonin Activity

Symptoms & Traits Undermethylated Depression OCD tendencies Seasonal affective disorder Competitive & perfectionistic SSRI medications usually effective Calm exterior, but inner tension Strong willed High libido Seasonal allergies

Useful Nutrients Undermethylated Depression SAMe Methionine Calcium Magnesium Zinc, Trimethylglycine (TMG) Vitamins B-6, C, E Inositol

Phenotype #2 Low-Folate Depression Low Serum Folates Low Blood Histamine Elevated SAMe/SAH Ratio Elevated Dopamine & Norepinephrine

Symptoms and Traits of Low-Folate Depression Tendency for high anxiety, panic Non-competitive in sports or games Absence of inhalent allergies Food/chemical sensitivities Adverse reaction to SSRI medications High musical or artistic ability Underachievement Sleep disorder Low libido

Useful Nutrients For Low-Folate Depression Folic Acid B-12 GABA DMAE Manganese Niacin or Niacinamide Vitamins A, B-6, C, E Zinc

Phenotype #3 High-Copper Depression Elevated Serum Copper Insufficient Serum Ceruloplasmin Zinc Depletion Low Metallothionein Activity Elevated Norepinephrine & Adrenaline

Norepinephrine Synthesis

Symptoms and Traits of High-Copper Depression More than 95% are female Inability to eliminate excess copper High anxiety Tendency for post-partum depression Onset during hormonal event (puberty, birth control, pregnancy, menopause) Estrogen intolerance Tinnitis (ringing in the ears) Sensitive skin, intolerance to cheap metals.

Useful Nutrients for High-Copper Depression Zinc Vitamin B-6 MT-Promotion Nutrients Manganese (avoid if undermethylated) Selenium Vitamin C Vitamin E

Decoppering Protocol Issues The excess copper departs via the blood stream. Gradual introduction of zinc is recommended to minimize copper elevations in blood & increased irritability and anxiety during early treatment. Zinc dosages should be increased to tolerance.

Depression Phenotype #4 Pyrrole Disorder Elevated urine pyrroles Zinc deficiency Vitamin B-6 deficiency Severe oxidative stress Low serotonin & GABA

Pyrrole Depression Severe mood swings Poor stress control Extreme anxiety Poor short-term memory, reading disorder, absence of dream recall Sensitivity to light, noise Poor immune function Very poor morning appetite Abnormal fat distribution, Inability to tan.

Treatment of Pyrrole Disorder Zinc Therapy Supplements of B-6, P-5-P Omega-6 (Primrose Oil, Borage Oil) Biotin

Toxic Metal Depression Absence of trauma or emotional triggers Abdominal distress Unrelenting depression Cognitive deficits (children only) Metallic taste in mouth, bad breath Irritability, anger Food sensitivities High oxidative stress

Useful Nutrients: Toxic Metal Depression Zinc Manganese Glutathione Selenium MT-Promotion Nutrients Calcium (lead poisoning) Vitamin C Vitamin E

Open-Label Outcome Studies 20% non-compliance rate 85% of compliant patients report improvement and reduced medication needs Many reports of zero depression without medication support.

Treatment Time Frames Pyrrole Disorder: 1-4 weeks to achieve full effect. Copper Overload: No progress until week 3; 60-90 days to normalize blood Cu levels. Low Folates: Clear improvement by week 4; 3-6 months to achieve full effect. Undermethylation: No progress until month 2; 6-12 months to achieve full effect.

THANK YOU! William J. Walsh, PhD Walsh Research Institute www.walshinstitute.org