hcg for HRT

cvictorg

New Member
Can you use just hcg to stimulate the testes to produce more testosterone or do you need some form of testosterone - such as weekly injections of Test Cypionate - in addition to the hcg??

http://www.steroidology.com/forum/anabolic-steroid-forum/135966-opinions-hcg-hrt.html

Regarding HCG and Its Use in Functional Medicine

Human Chorionic Gonadotrophin (HCG) is a hormone found in men and women. Women secrete large amounts of HCG during pregnancy and men secrete large amounts during puberty.

HCG is administered as a form of TRT. HCG is an alternative to standard Testosterone Replacement Therapy in men with low LH and FSH (i.e., secondary hypo-gonadism). To determine if you are a candidate for HCG you must have a blood test showing low Testosterone, & Luteinizing Hormone. This blood test cannot be taken while you're on standard TRT because standard TRT shuts down LH and FSH production and thereby distorts the test results.

Rather than shutting down your body's natural Testosterone production system (like standard TRT does), HCG stimulates it back towards normal function. Your body produces it's own Testosterone.

Some scientists believe that HCG is vastly superior to standard forms of TRT for the following reasons:

1. Better mimics the body's own natural physiologic rhythm of Testosterone production. 2. Easier to maintain normal Testosterone levels when administered properly. 3. More physiologic Testosterone levels minimize excess estradiol production (i.e., reduces aromatization associated with testosterone use).

4. Maintains normal size of testicles (in contrast, standard Testosterone Replacement Therapy shrinks & shuts down the testicles). 5. Stimulates sperm production (thereby increasing/restoring fertility). In contrast, standard Testosterone Replacement Therapy reduces, if not eliminates, sperm production thereby making you infertile.

6. Restores normal function to testicles

7. Restarts the pituitary/hypothalamus axis (see Medline article 4044781). This means that my body is responding to HCG by producing more LH and FSH on the "off days." Some have claimed that HCG can restart your system completely; pituitary/hypothalamus axis is being stimulated to return towards normal function.

The only disadvantage of HCG is that doctors are unaware of this excellent alternative.

The current guidelines of the American Association of Clinical Endocrinologists (AACE) indicate that HCG should only be prescribed when a man is interested in fertility. As a result, most doctors will not prescribe HCG unless you tell them you are currently trying to have children. The AACE guidelines can be found at: www.aace.com/clin/guidelines/hypogonadism.pdf

These guidelines (written in 1996 and updated in 2002) are considered outdated by many practitioners with respect to HCG therapy for the following reasons:

1. The guidelines call for intramuscular HCG injections. Subcutaneous injections are much more convenient, much less painful and equally effective (see discussion below and/or just ask the many men who inject HCG subcutaneously or look at their blood test results).

2. The excessive HCG dosage levels suggested in the guidelines cause a variety of problems. In particular, excessive HCG dosages cause elevated estradiol, which defeats many of the positive effects of increased Testosterone. Scientific studies have demonstrated that HCG dosage levels of about 5,000 IU per week or more administered long-term cause permanent damage to the testicles (see Medline articles 6210708 and 3583230). These studies have shown that such excessive HCG dosages taken long-term result in testicular desensitization (to future stimulation by LH or HCG). In other words, long-term, such excessive dosages of HCG will result in primary hypogonadism!

Each day more and more doctors are becoming more and more aware of the benefits of HCG.

*****************************

Chorionic Gonadotropin Stimulation Test (males < 75 years old)*

Chorionic Gonadotrophin is presently available through most pharmacies or distributors as Profasi, Pregnyl or generic Chorionic Gonadotrophin 10,000 units per 10 cc vial. Various stimulation tests have been described, from high dose, short course testing to more normal physiologic doses over a longer time period. I have found that a typical treatment course for three weeks is best for determining those individuals who will respond well to this type of treatment. It is administered by injection 500 units (0.5 cc) SQ, Monday through Friday for three weeks. Teach patient to self administer with 50 Unit Insulin Syringes with 30 gauge needles in anterior thigh, seated with both hands free to perform the injection. Measure: Testosterone, total and free, plus E2 before starting CG and on the third Saturday AM after 3 weeks of stimulation (salivary testing may be more accurate for adjusting doses). Studies have shown that SQ is equal in efficacy to IM administration.

Results:

1. <20% rise suggests poor testicular reserve of leydig cell function (primary hypo-gonadism or eu-gonadotrophic hypo-gonadism indicating combined central and peripheral factors).

2. 20-50% increase indicates adequate reserve but slightly depressed response, mostly central inhibition but possibly decreased testicular response as well.

3. > 50% increase suggests primarily centrally mediated depression of testicular function.

Options for treatment vary both with the response to CG and patient determined choices.

1. If there is an inadequate response (< 20%), then replacement with testosterone will be indicated.

2. The area in between 20-50% will usually require CG boosting for a period of time, plus natural boosting or "partial" replacement options. I believe that full replacement with exogenous testosterone is always the last option in borderline cases since improvement over time may frequently occur as leydig cell regeneration may actually happen. Much of this is age dependent. Up to age 60, boosting is almost always successful. 60-75 is variable, but will usually be clear by the results of the stimulation test. Also, disease related depression of testosterone output might be reversible with adequate treatment of the underlying process (depression, AMI, obesity, alcohol, deficiency, etc.) This positive effect will not occur if suppressive therapy is instituted in the form of full replacement.

3. If there is an adequate response, >50% rise in testosterone, there is very good leydig cell reserve. Natural boosting or CG therapy will probably be successful in restoring full testosterone output without replacement, a better option over the long term and a more natural restoration of biologic fluctuations for optimal response.

4. Chorionic Gonadotrophin can be self-administered and adjusted according to response. In younger, high output responders (T > 1100ng/dl), CG can be given every third or fourth day at bedtime or in the AM. This also minimizes estrogen conversion. In lower level responders(600-800ng/dl), or those with a higher E2 output associated with full dose CG, 300-500 units can be given Mon-Wed-Fri. At times, sluggish responders may require a higher dose to achieve full Testosterone response. In these cases, the diluent is lowered to 7.5cc or even to 5 cc, which increases the CG concentration 1 - 2 X. This can be administered in variable doses 0.3 - 0.5cc given every 3rd day. Check salivary levels on the day of the next injection, but before the next injection to determine effectiveness and to adjust the dose accordingly. Keep in mind that later as leydig cell restoration occurs, a reduction in dose or frequency of administration may be later needed.

5. Monitor both Testosterone and E2 levels to assess response to treatment after 2 - 3 weeks after change in dose of CG as well as periodic intervals during chronic administration. Sublingual testing is very easy and cost effective. It will also better reflect the true free levels of both estrogens and testosterone. (Pharmasan Labs 888-342-7272 is very good)

6. Adjustment of dosage is a result of symptomatic response and hormone level boosting. It is based on clinical judgement as much as actual hormone levels. Remember that "Normal" ranges are for populations, not individuals!

7. Except for reports of antibodies developing against CG (I have not seen this), there are no adverse effects of chronic CG administration. An additional benefit is the boosting of Growth Hormone output which has also been reported, either as a direct effect of CG or as an effect of increased levels of testosterone.

*Protocol adapted from "The Testosterone Syndrome" by Eugene Shippen, M. D. (M Evans and Co, NY 1998). Posted on ASI with permission of Eugene Shippen, M. D.
 
Self-priming effect of luteinizing hormone-human c... [J Clin Endocrinol Metab. 1985] - PubMed result

Self-priming effect of luteinizing hormone-human chorionic gonadotropin (hCG) upon the biphasic testicular response to exogenous hCG. I. Serum testosterone profile.

The present study was conducted to investigate whether the early (2-8 h) testicular response to a single dose of exogenous hCG depends on previous exposure to LH activity. Four different groups of subjects were studied: 1) four normal adult men [Tanner stage-G5 (T-G5)] and one late pubertal subject (T-G4); 2) normal prepubertal (T-G1) and early- and midpubertal boys (T-G2 and T-G3) (n = 4-6 each); 3) five patients with hypogonadotropic hypogonadism (HH); and 4) two patients with the complete form of the androgen insensitivity syndrome. Each subject received an im injection of hCG (40 IU/kg) on day 1 and blood samples were drawn before and 1-8, 24, 48, and 72 h after injection. At 96 h, a second dose of hCG was given (80 IU/kg) and blood samples were obtained at the same times as after the first hCG dose. Serum testosterone (T) was measured by RIA. The first dose of hCG evoked a biphasic response of serum T in groups T-G2 to T-G5 as well as in the two patients with the complete form of the androgen insensitivity syndrome. The early peak was at 2-7 h, whereas the late T peak was at 48-72 h after injection. In T-G1 children and in patients with HH, the early response did not occur [T-G1, from 129 +/- 43 (SEM) to 288 +/- 127 pg/ml (P greater than 0.05); HH, 79 +/- 18 to 107 +/- 12 (P greater than 0.05) pg/ml], and the late peak was attenuated as compared with the pubertal boys. There were not significant differences in the responses of the T-G1 and the HH groups. After the second dose, all groups had biphasic T responses, although they varied in magnitude. These results demonstrate that previous exposure to LH activity is an obligatory prerequisite for the early peak of the hCG-mediated biphasic testicular response, and that a single dose of hCG has a priming effect that is sufficient to ensure a biphasic response to a second dose of hCG given 96 h later.
 
Back
Top