Jim Paoletti BS Pharmacy, FAARM, FIACP, Director of Education, P2P

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presents Converting Patients from Conventional Pioneering Technologies For to Bioidentical Lifestyle Based Medicine Hormone Therapy with Jim Paoletti BS Pharmacy, FAARM, FIACP, Director of Education, P2P

Clinical Consultant and the Director of Education at Power2Practice. 30 years of experience creating and using bio-identical hormone therapies in both retail pharmacy and clinical practice. Nationally recognized expert in pharmacy, BHRT and custom compounding. Previously served as Director of Provider Education for ZRT Laboratory and Education Director for the Professional Compounding Centers of America. Pioneering Technologies For Lifestyle Based Medicine Jim Paoletti BS Pharmacy, FAARM, FIACP Director of Education P2P

Pioneering Technologies For Lifestyle Based Medicine

Conventional HRT Inappropriate dosage route for estrogen Invalid assessment of effects Too much estrogen Inaccurate evaluation of the need for progesterone/progestins Inaccurate, invalid, and inappropriate dosage and monitoring of testosterone replacement in males

CONVENTIONAL FEMALE HRT

Conventional HRT Metabolism of orally administered estradiol Estradiol administered orally is significantly converted to Estrone. Estradiol levels may be normal, but estrone levels are almost always higher than normal pre-menopausal ranges. Increase in 4-catechol-quinoone estrone metabolites that may damage DNA and therefore increase risk of breast cancer. Conjugated Estrogens contain 50% estrone and only 5-19% Estradiol Measuring Estradiol levels does not at all give total picture of estrogen burden. Conjugated Estrogens and Estradiol oral manufactured products provide too much estrogen for all women.

Estradiol (E2), Estrone (E1) and Oral Estrogen Supplementation Serum E2 (pg/ml) Serum E1 (pg/ml) E2/E1 Premenopause 60 60 1 Postmenopause 20 60 0.33 Oral Estradiol 60 300 0.2

Conventional HRT Oral dosage route for estradiol Significantly increased risk of stroke and VTEs compared to sublingual or topical administration. Increased binding proteins SHBG, TBG, CBG. Improper ratio of E1 to E2 created by oral route: When oral estrogen creates a normal level of estradiol, estrone is significantly higher than it should be.

Conventional HRT Inaccurate assessment of effects Misleading levels for oral estradiol Serum testing is not accurate for topical administration Conjugated Estrogens approved for treating hot flashes based only on short term effects No long term studies looking at: Overall effects compared to endogenous functions of estrogen Risk increases associated with oral administration of approved dosages

Too Much Hormone Symptoms of excess hormone may mirror symptoms of deficiency. The symptoms of too much of a hormone can closely mimic the symptoms of too little. May indicate the receptor response to hormone level. Delayed response to excessive hormone.

Response OPTIMAL RECEPTOR RESPONSE X X X X Hormone Level X

Physiologic Dosing Representative of normal endogenous production Based on restoration therapy

Daily Endogenous Production in Women Sex Hormone Follicular Luteal Estradiol 0.036 mg 0.25 mg Progesterone 1 mg 25 mg Testosterone 0.14-0.35 mg 0.13-0.35 mg DHEA 7-8 mg 7-8 mg

Daily Endogenous Production in Men Sex Hormone Testosterone Estradiol DHEA Progesterone Amount 5-6 mg 0.045-0.050 mg 10-18 mg 2-3 mg

Progesterone and Progestins Invalid assumption was/is taught that a woman does not need Progesterone if she no longer has a uterus Progestins only mimic the action natural progesterone in the uterus. Outside of the uterus progestins produce the opposite effect of natural progesterone.

Medroxyprogesterone Acetate (MPA) Vs. Progesterone Progesterone has favorable effects on cardiovascular health, lipid profile, liver function, sleep, mood, CNS, insulin & glucose regulation Medroxyprogesterone Acetate has unfavorable effects on all the above, creating side effects and increased risks

Medroxyprogesterone Acetate (MPA) Vs. Progesterone Progesterone protects against breast cancer while MPA and all progestins significantly increase the risk no matter how long used and what dosage is used. When compared to a MPA-containing regimen, women using progesterone-containing HRT experienced significant improvement in symptoms and 80% reported overall satisfaction. Progesterone is required to maintain pregnancy while MPA is contraindicated in pregnancy.

Conversion to BHRT Considerations in conversion from synthetics to bio-identical hormones: Length of time on synthetics - Estrogen receptors can lose sensitivity due to exposure to high amounts and/or long exposure of estrogen replacement (any type of estrogen). Liver detox

Conversion Considerations - Progesterone Start Progesterone Immediately Discontinue Any Progestin

Conversion Considerations - Progesterone Progesterone affects estrogen effects: Regulates estrogen receptors. Has effects on SHBG, thyroid and cortisol actions all effect estrogen deficiency symptoms. Start progesterone prior to switching from conventional estrogen therapy to bio-identical estrogen.

Conversion to BHRT Address other hormone imbalances that may be adding to symptoms: All endocrine hormones effect estrogen function Insulin resistance, adrenals, thyroid and androgens.

Conversion Considerations - Estrogen Taper off of conventional estrogen: Higher than physiological levels reset the threshold for estrogen need within the brain. - Quick reduction in dosage will cause withdrawal symptoms (severe hot flashes).

Conversion Considerations - Estrogen Taper off of synthetic estrogen: Various protocols have been used: - Reduce estrogen dosage 25% to 50% every two weeks. - Reduce estrogen dosage to one-half the dose every other day for 2-3 weeks, then to one-half dose every day for 2-3 weeks, then one-half dose every other day for 2-3 weeks.

Conversion Considerations - Estrogen Taper off of synthetic estrogen: Protocol that I use Use 1/2 dose every 3rd day for 9-12 days, then 1/2 dose 2 of 3 days for 9-12 days, then 1/2 dose daily for 9 days, then 1/2 dose 2 out of 3 days for 9 days, then 1/2 dose every other day for 8 days My goal to get to Conjugated Estrogen 0.3mg every other day or Estradiol 0.25 mg every other day before changing to Biest 50:50

Decreasing Estrogen Protocol Example

Decreasing Estrogen Protocol Example (continued)

Conversion Considerations - Estrogen High variance of degree of symptoms of withdrawal among individuals Patients should be allowed to decrease dose at a rate that doesn t make them miserable. Some patients have stopped Conjugated Estrogens completely in 1-2 weeks. Some patients have taken up to a year to obtain a low dose. Patients on supraphysiologic doses of estrogen for a long duration may take longer to lower dosages.

CONVENTIONAL MALE HRT

Male HRT Manufactured products provide supraphysiologic doses of testosterone Medical profession told that venous serum levels were appropriate to monitor testosterone levels for topical/transdermal therapies. Manufactures invented the word delivered and redefined the words absorption & bioavailable in explaining monitoring of their products. Young adult males produce 5-10 mg of testosterone daily.

Male HRT Topical application of 25 mg of testosterone is a supraphysiologic dose. Weekly injections may be close to physiologic on the average, but provide supraphysiologic amounts immediately and shortly following the dose. Increase in conversion to Estradiol Increase in potentially dangerous estrogen metabolites

Male BHRT Decreasing supraphysiologic dosage of testosterone in males can lead to withdrawal symptoms. Lethargy, depression, fatigue, erectile dysfunction, even suicidal thoughts. Need to taper down testosterone dose over time.

Male BHRT Tapering Testosterone No established protocols. For patches, I change to topical administration to make tapering easier. I ask patient to stop testosterone until they start feeling worse. Patient then goes back on a reduced dose for no longer than the number of days they went without it. Example: if patient tolerated 6 days off of testosterone, then they take the reduced dose for no more than 6 days, then go off of hormone again. With each stoppage, go back at lower dose, and keep patient on for original number of days. Decrease dose by 20-25% with each reduction until physiologic dose/levels are obtained.

Last Thought For topical administration of hormones, I suggest not to dose every day. To prevent accumulation of hormone. Dose 6 out of 7 days each week, skipping the same day each week. If patient feels worse on day they skip their hormone (rare), then they can try skipping one day every other week, or once a month.

Thank You! Jim Paoletti BS Pharmacy, FAARM, FIACP Director of Education P2P If you would like a copy of this presentation, please contact: 1-855-667-1967 jpaoletti@power2practice.com