Onset of effects of testosterone treatment and time span

[Charger Hemi]

I found this research paper and I wanted to share it. I had to remove the introduction and references due to number of characters limitation for the thread.

Onset of effects of testosterone treatment and time span until maximum effects are achieved, Saad F et al.
Table 1
Observed mean range of changes in selected measurable outcomes of testosterone administration to hypogonadal men in reviewed studies.
Outcome Values (range)
Muscle mass (kg) 0.4 to 16.4

Strength (1 repetition max) (11–20)

Leg press strength (kg) 11.6 to 76.5
Composite strength (%) 14 to 35
Isokinetic power torque (Nm) 4.7 to 9.6
Handgrip (kg) 3.5 to 5.3
Bone mineral density

Femoral neck (g/cm2) 0.01 to 0.03
Lumbar spine
g/cm2 0.04 to 0.1
(%) 5 to 8.6
Body composition

Total mass (kg) −3.2 to 1.69
Fat mass (kg) −0.4 to −5.7
Effects on lipids (mmol/l)
Total cholesterol −0.4 to −0.23
Triglycerides −0.98 to 0.1
HDL cholesterol −0.05 to 0.692
LDL cholesterol −0.39 to −0.05
Glycemic control

Glucose (mmol/l) −0.22 to −6.5
Insulin (mIU/l) −0.5 to −14.0
HOMA index −0.72 to −4.2
HbA1c (%) −0.2 to −6.3
Cardiovascular effects (mmHg)

Systolic BP −0.5 to −7
Diastolic BP −0.5 to −7
Pulse pressure −1.9 to −2.6
Pulse wave velocity 0.2 to −0.7
Augmentation index −1.2 to −4.3
Flow mediated dilatation (%) 1.8 to 2.6
Inflammatory markers (pg/dl)

IL6 −0.02 to 1.6
IL1β −0.2
IL10 −0.15
hs-CRP −0.43 to −1.1
TNF-α (mg/dl) 6.1 to −3.1
Effects on erythropoiesis

Hematocrit (%) 1.0 to 6.5
Hemoglobin (g/dl) 0.5 to 3.5
Effects on prostate

PSA (ng/ml) −0.2 to 0.8
Prostate volume (cm3) 0 to 10.1


Time-course of effects on muscle mass/strength
In a series of studies, Bhasin et al. (8) have demonstrated that upon testosterone administration, there is a positive correlation between blood testosterone concentrations and leg press strength, thigh, and quadriceps muscle volume, and, further, levels of hemoglobin and IGF1. In a later study, the same group of authors concluded that the anabolic response to testosterone can largely be predicted by the dose administered (9). If the dose administered is too low, no effects may be demonstrable (10). Recent studies of the effects of testosterone on muscle mass/strength are mostly short term. In a study that combined testosterone with GH, total lean body mass increased, as did appendicular lean tissue. Composite maximum voluntary strength of upper and lower body muscles had increased after 16 weeks (11). A study investigating the effect of a 12-week long-acting testosterone administration on maximal exercise capacity and muscle strength found an increase in quadriceps isometric strength, maximal voluntary contraction, and isokinetic strength (peak torque) (12). Testosterone administration for 20 weeks was associated with dose-dependent increases in skeletal muscle mass, leg strength, and power (13). In a study of 180 days of treatment with a 1% testosterone gel preparation (50 or 100 mg/day, contained in 5 or 10 g gel), mean muscle strength in the leg press exercise increased by 90 days and had not improved further at 180 days (14). A study similar in design found an increase in lean body mass and an improvement of lower limb muscle strength after 6 months (15). Another study using high doses of testosterone gel (starting dose 100 mg/day with possible up-titration to 150 mg/day) observed significant increases in leg press strength, chest press strength, and stair climbing power with a load within 6 months (16). A study administering testosterone enanthate , 200 mg/2 weeks observed major effects to occur over the first 12 months of testosterone administration, thereafter minor increases could be observed (17). It can be concluded that the effects of testosterone on muscle strength are demonstrable after 12–20 weeks and that depending on the achieved testosterone levels , the maximum effects are attained after 6 or 12 months. The data are summarized in Fig. 1.



Figure 1
Time-course on body composition and strength.


Time-course of effects on bone mineral density
The effects of testosterone on bone mineral density are in part mediated by estrogens, derived from testosterone via aromatization (18). Testosterone improves bone mineral density at the lumbar spine compared with placebo, but at the femoral neck improvements are less certain (19). Testosterone produces a consistent reduction in bone resorption markers (20). Effects on bone mineral density have been shown in studies of 6 months duration (21, 22), 8 months duration (23), or 1 year duration (24). From studies analyzing the effects of testosterone administration over as long as 36 months (25, 26) an increase was observed over that time period and it did not become clear whether the maximum effects of testosterone improving bone mineral have been attained after 36 months. The data are summarized in Fig. 1.


Time-course of effects on body composition
Testosterone plays a significant role in obesity, glucose homeostasis, and lipid metabolism (27). At the cellular level there is now insight into the effects of androgen deprivation/administration on fat and muscle mass. Testosterone regulates lineage determination in mesenchymal pluripotent cells by promoting their commitment to the myogenic lineage and inhibiting their differentiation into the adipogenic lineage through an androgen receptor-mediated pathway. The observation that differentiation of pluripotent cells is androgen dependent provides a unifying explanation for the reciprocal effects of androgens on muscle and fat mass in men (28, 29). Upon testosterone administration there is a decrease in fat mass and an increase in lean body mass and the net result is often, but not always, that total body weight does not show major changes. An increase in total mass was found after 3 months (14) and an increase in weight in elderly men after 3 months (30). A decrease in weight has been observed after 3 months (31) and 6 months (17), with further progressive decrease over 24 months (32). An increase in total body mass, lean body mass, and a decrease in fat mass were found after 3 months (14, 30) or 6 months (17). A decrease in fat mass has been widely reported after 3 months (14, 30, 31) or 6 months (17), and a decrease in percent fat mass equally after 3 months (14, 31).
It is now commonly accepted that a preferential accumulation of fat in the abdominal region is associated with an increased risk of type 2 diabetes mellitus and cardiovascular disease, not only in obese subjects but even in non-obese subjects (33). Therefore, the effects on trunk fat, often measured as changes in waist circumference (34), are very relevant effects of testosterone treatment. A decrease in trunk fat or waist circumference was noted in a number of studies after 3 months (35, 36) with continuous decline over 24 months (32) and a decrease in the waist hip ratio after 3 months (31, 36) or after 6 months and 30 weeks respectively (17). A continued decline up to 110 weeks was reported (37). Body mass index as a widely used measure of body composition declined after 6 months with further improvement during an observation period of 2 years (32). The data are summarized in Fig. 1.



Time-course of effects on lipids
Decreases in serum total cholesterol have been noted as quick as after 4 weeks (38, 39) but most studies have reported a decrease after 3 months (35, 36). A decrease after 24 weeks was observed in a recent study (40), others have found this to occur after 9 months (41) or 12 months (42) with a maximum reached after 12 months (32).
The decrease in serum triglycerides follows a similar pattern: after 4 weeks (38), after 3 months (35), and with further decrease over 9 months (41) or 12 months (43).
The decrease in low-density lipoprotein cholesterol seems somewhat slower: after 3 months (35), after 40–44 weeks, (44) or after 12 months (42) with a maximum observed after 24 months (32).
Studies have found both an increase and decrease in high-density lipoprotein cholesterol. An increase was found to occur after 3 months increasing further during 12 months (43), after 6 months, (35) or close to 1 year (44). Continuous increase was observed over 24 months (32). The data are summarized in Fig. 2.



Figure 2
Time-course on lipids.

Time-course of effects on glycemic control
Several studies indicate that upon testosterone administration, serum glucose is reduced after 3 months in men with impaired glucose tolerance (31, 36, 43). In a recent study, this was observed after 24 weeks only in men with baseline glucose >110 ng/ml (6.6 mmol/l) but not significantly in men whose baseline glucose levels were <110 ng/ml (6.6 mmol/l) (40). An early study reported a decrease in glucose and glucose disposal rate after 9 months (41).
A decrease in serum proinsulin and insulin was noted after 3 months (43) or 6 months (45), and a decrease in homeostasis model assessment index of insulin resistance (HOMA-IR) after 3 months (36) or 6 months (45–47).
A decline in HbA1c was observed after 3 months (31, 36, 43) with further decrease after 12 months (43).
Low serum testosterone levels are associated with an adverse metabolic profile which may be explained by the observation that low testosterone levels and impaired mitochondrial function promote insulin resistance in men (48). And indeed, in an experimental study, stimulation of endogenous testosterone was shown to increase insulin sensitivity within 48 h (49).
Recently, it has been demonstrated that the interplay between insulin sensitivity, triglyceride levels, and androgens is practically immediate, as it occurs within a week, and is not facilitated by changes in body composition alone. Concomitantly increasing testosterone and decreasing estradiol (E2) levels had positive effects on both postprandial triglyceride handling and insulin sensitivity in elaborate clamp models during manipulation of these serum sex steroid levels (50). The effects on postprandial triglyceride handling can therefore be observed in line with previous results and seem to be of relevance for metabolic risk (51, 52). An improvement in insulin sensitivity upon testosterone administration resulted in reduced fasting glucose and insulin levels within a single week (50), corroborating the former reports about an increase in insulin sensitivity upon stimulation of endogenous testosterone within 48 h (49) and an acute reduction in insulin sensitivity 2 weeks after discontinuing testosterone replacement in severely hypogonadal men (53).
Such observations are most likely attributed to testosterone-induced changes in lipid metabolism and/or altered postreceptor insulin signaling in muscle (54) and also improved insulin sensitivity enhancing muscle lipid uptake (55). Furthermore, the aforementioned intervention increased the response of postprandial glucose-dependent insulinotropic polypeptide (GIP) release (50). Effects of sex steroids on GIP had not been reported before. This is of specific interest, as action of GIP is not limited to pancreatic cells and may affect lipid homeostasis (56) and intestinal glucose transport (57). The data are summarized in Fig. 3.


Figure 3
Time-course on glucose and insulin.


Time-course of effects on blood pressure and other cardiovascular effects
In some studies a decline in diastolic blood pressure has been observed, after 3–9 months (22, 35, 41, 44) and in some studies in systolic blood pressure also (35, 44). Maximum effects were observed after 12 months (35). A decrease in the resting heart rate occurred after 40–44 weeks (44). A decrease in arterial stiffness measured as pulse wave velocity was measurable after 48 h (58) and in large artery compliance after 3 months (58). Several studies have been conducted in men with heart disease. In men with chronic stable angina pectoris the increase in time to 1 mm ST segment depression was noticeable after 14 weeks (59). The ischemic threshold had increased after 4 weeks (38). Exercise capacity in men with chronic heart failure increased after 12 weeks (60), whereas the cardiac index (cardiac output related to body surface) had already increased after 180 min. In men with coronary artery disease flow-mediated vasodilatation was observed after 12 weeks (61).


Time-course of effects on inflammatory factors/endothelial markers
Low sex hormone levels are associated with inflammation (62). Already after 3 weeks of testosterone administration, a decline was noted in IL6 (63) and in another study after 16 weeks (64). A decrease in C-reactive protein (CRP) was observed after 3 weeks (63) and in other studies after 3 months (32, 43). In a study in patients with Crohn's disease, CRP levels continued to decline over 24 months (65). A decrease in tumor necrosis factor α and in interleukin 1β was noted after 4 weeks (39). Asymmetric dimethylarginine is an endogenous NO synthase inhibitor and appears to decline upon testosterone administration after 10 days (66) or after 4 weeks (67).


Time-course of effects on sexual parameters
Effects on libido
Effects on libido, sexual desire, sexual thoughts and fantasies and satisfaction with sexual life manifest themselves rather rapidly: after 3 weeks (68) or 30 days (14). Some studies have measured these effects only after 3 months (31).

Effects on erection/ejaculation
Effects on erection also appear rather rapidly: after 3 weeks (68). Increase in morning erections occur after 3 weeks (68). An increase in percentage of full erections and sexual performance and satisfaction with erections was noticed after 30 days (14, 69), an increase of ejaculations and sexual activity after 2 weeks (70) and 3 weeks respectively (68). In patients with veno-occlusive dysfunction, testosterone undecanoate restored erectile function after a minimum of 3 months and a maximum of 11.5 months (71).
The International Index of Erectile Function is a reliable, self-administered measure of erectile function that is cross-culturally valid and psychometrically sound, with the sensitivity and specificity for detecting treatment-related changes in patients with erectile dysfunction. It has five domains: erectile function, orgasmic function, sexual desire, intercourse satisfaction, and overall satisfaction. Increases in the IIEF erectile function have been noted after 3 months (35, 40) but increases in IIEF sexual desire, intercourse satisfaction, and overall satisfaction appear already after 6 weeks (40). Maximal effects are usually achieved after 3–6 months (72) but may take even up to 1 year in individual cases (71). The data are summarized in Fig. 4.


Figure 4
Time-course on sexual parameters.

Time-course of effects on quality of life
The St Louis University Androgen Deficiency in Aging Male (ADAM) is a screening tool for hypogonadism in older males. An improvement was noted after 1 month of testosterone treatment (38). The Aging Males' Symptom (AMS) questionnaire is a 17-item scale assessing health-related quality of life and symptoms in aging men (e.g. somato-vegetative, psychological, and sexual symptoms) (73). Improvements on scores on the AMS have been noted after 1 month (38), 6 weeks (40) to 3 months on treatment with parenteral testosterone undecanoate (35) or after 9 months on testosterone gel (74) continuing over a total of 18 months (74).


Time-course of effects on psychological variables
Several studies report an improvement in depression after 3 weeks (68) or 1 month (38). Increase in good mood and a decrease in bad mood were noted after 3 weeks (68) or after 30 days (14). There was also an increase in motivation after 30 days which was maintained thereafter (14). Two studies using the Hamilton Depression Rating Scale found an improvement in depression after 6 weeks (75) or 8 weeks (76). A number of psychological variables (increase in sociability, decrease in anxiety, increase in concentration, and self-confidence) were apparent after 3 weeks (68). A decrease in fatigue and listlessness was found after 1 month (31) or 6 weeks (68). A transient increase in anger/hostility was found in eugonadal men whose testosterone levels were raised above normal after 2 weeks (77).
In a larger set of severely depressed men (n=2×50), effects of testosterone replacement therapy (TRT) by gel versus placebo were observed within 6 weeks. The effect was not consistent within the whole group of patients. It is likely that, in severe clinical depression, the receptiveness for testosterone effects depends on the overall pattern of disturbed neurotransmitters, especially noradrenaline and serotonin, and also baseline testosterone concentrations (78). It is very likely that the positive effects of testosterone on depressive symptoms start as early as after 3–6 weeks, but will most likely take 18–30 weeks to find the patient with a significant improvement. A recent study in hypogonadal men receiving i.m. testosterone undecanoate demonstrated such effects. It is remarkable that effects were more pronounced in men with the lowest baseline testosterone levels (79).
Similarly, effects of testosterone administration in hypogonadal men on the ability to process spatial data of visual content were observed within 2 weeks of treatment (80). These effects are obviously directly related to testosterone and not its aromatization product E2, as it was later confirmed in a placebo-controlled trial involving an aromatase inhibitor combined with testosterone administration in hypogonadal men. These patients exhibited a markedly improved spatial working memory within 3 weeks, improving further until week six (81).


Time-course of effects on erythropoiesis
The effects of testosterone on red blood cell formation (hemoglobin and hematocrit) are dose dependent (14, 82, 83) while higher age is also a factor (44). The effects are apparent after 3 months (14, 35, 40) and a maximum is reached after 9–12 months (35). The data are summarized in Fig. 5.


Figure 5
Time-course on hematocrit and prostate.


Time-course of effects on the prostate
In hypogonadal men treated with testosterone, levels of PSA rise usually up to levels of eugonadal men (84). Upon judging the time-course of effects of testosterone on the prostate, it is of note that aging itself is a factor in the rise of both prostate volume and PSA (84), and there is no endpoint in the effects of testosterone on the prostate. A rise in PSA levels was noticed after 6 months, whereafter over the following 24 months there was no significant further increase (85). Other studies have found a rise of PSA levels after 3 months (40), some only after 12 months (43). An increase in prostate volume was noted after 3 months (86) and after 12 months (44). One study over 24 months found no significant increase in both PSA and prostate volume. In a study of 123 subjects over 42 months of testosterone gel application, there was significant increase in serum PSA over the first 6 months and then no further significant increases with continued testosterone treatment was found (87). In a study of 81 hypogonadal men (mean age 56.8 years) followed for a mean (range) of 33.8 (6–144) months PSA levels did not increase significantly at 1-year intervals for 5 years (88). The data are summarized in Fig. 5.


Discussion
This is a systematic analysis of the time-course of the spectrum of biological effects of testosterone on the various target systems. The authors view this as a worthwhile endeavor for a number of reasons. Attending physicians can prepare their patients for the intervening time periods before effects of testosterone can be experienced. Studies investigating the effects of testosterone have to take this time-course into consideration to design the duration of studies to be able to have quantifiable measurements.
It is of note that almost none of the quoted studies had been specifically designed to assess the time-course of effects. Some studies measure effects of testosterone only after 3 months (31), and, particularly, effects on libido and erections have occurred well before this time span (14, 68).
We noticed considerable differences in the occurrence of effects of testosterone. Effects on libido and other psychological variables and effects on vasculature occur rather rapidly. It may well be that these effects are not mediated via the classical androgen receptor but through other mechanisms like effects on membranes (6, 7). Also effects on erection occur rather rapidly and may be partially explained by non-genomic effects on vascular penile erectile tissue (89).
The effects of testosterone on glycemic control and variables clustered in the metabolic syndrome occur somewhat slower, but there is evidence that acute testosterone fall during deprivation therapy is directly related to a worsening in insulin sensitivity (53). However, in a recent study, the authors were not able to substantiate their earlier finding (90) and hypothesize insulin resistance associated with chronic low testosterone levels may be largely driven by decreased fat-free mass, increased percent body fat, and/or other metabolic regulatory factors. This may also apply to other factors of the metabolic syndrome. Testosterone inhibits the expression of the activity of lipoprotein lipase, the main enzymatic regulator of triglyceride uptake in the fat cell, preferentially in abdominal fat (28, 29). Several studies have indeed confirmed that testosterone treatment reduces waist circumference which, in its simplicity, appears to be a valid parameter of the degree of visceral obesity (91). In our own studies, signs and symptoms of the metabolic syndrome improved substantially following administration of long-acting testosterone undecanoate (32, 35, 92) and improvements in glycemic control and lipids parallel improvements in body composition.
The effects of testosterone on muscle and bone involve protein synthesis and are a result of genomic actions of testosterone and, therefore, rather slow.
Apart from reviewing the onset of effects of testosterone treatment in hypogonadal men, it would also be possible to look at the onset of symptoms of testosterone deficiency in patients on androgen deprivation therapy (ADT), standard treatment for men with advanced prostate cancer. ADT causes unfavorable changes in body composition, insulin resistance and other risk factors for cardiometabolic diseases leading to an increased incidence of cardiovascular diseases and type 2 diabetes (for review (93, 94)). However, deprivation of testosterone and the time-dependent effects thereof might be totally different from the onset of testosterone action in testosterone treatment, even in the same parameter. Therefore, it was decided to restrict this paper to aspects of testosterone treatment.
Finally, in the present analysis it was attempted to select those studies of testosterone treatment that provided adequate doses/delivery of testosterone. It is obvious that sub-optimal therapeutic regimens or, alternatively, inappropriate patient selection (eugonadal or men with biochemical but not clinical hypogonadism) may show different time-course of effects.
In conclusion, this analysis tries to chart the differences in time periods after which biological effects of testosterone administration in hypogonadal men occur. This may add to a better understanding of the physiology of androgen action. Earlier studies have shown that there are thresholds for the various actions testosterone: in other words signs and symptoms of testosterone deficiency appear at different threshold values of circulating testosterone. The above results call for a well-designed study that charts the time required to restore an androgen-dependent function with the optimal circulating testosterone for that specific androgen-dependent function. These studies are not easy to perform. Ideally, they should measure at what serum levels of testosterone , all androgen-dependent biological functions are restored. Some biological functions, like erectile functions are composite in nature, and next to testosterone, endothelial function and psychological factors are equally relevant (2). A major problem is the so-called late onset hypogonadism: the decline in serum testosterone with aging. It is still hotly debated whether this is a true form of hypogonadism, or a decline of serum testosterone associated with the progressive accumulation of health problems with aging (95, 96), but rather independently of the process of aging itself. Though small-scale studies show benefits and acceptable risks of treating elderly men with lower than normal testosterone levels (46, 97), a verdict can only be reached with large-scale studies including 5000 men over 5 years (95), for which presently the funding is not available. There is a degree of consensus that elderly men with serum testosterone clearly below the reference ranges and persistent clear clinical signs of hypogonadism may justifiably be treated (98, 99), but there remains a large degree of dissent.

[MuscleScience]

Thanks for posting that.

[Simon1972]

http://www.nebido.com/tools/index.ph...x/effects-tool

This is a tool that uses the info contained in that study. Have a look and play around.

[hammerheart]

Someday TRT will work for me too...

I'm not talking about subjective feeling of well being but objective signs, take for example erection strength - I still remember as a 20-22 years old I had rock hard boners that actually hurt, are they gone forever? My erections on TRT are s**t poor, the only stuff that helped is thyroid hormone and selegiline.

[Simon1972]

my understanding is DHT causes stronger erections, are you on creams bizarro?
L-Arginine supplementation is also indicated in the same. Supplement that for a while see what happens...

[hammerheart]

my understanding is DHT causes stronger erections, are you on creams bizarro?

Nope I have been on nebido for more than a year and since April on Test E, 100mg E4D.

Never checked for DHT. With AIs I got (soft) morning boners and that's all.


I tried AAKG to no avail. My real question is whether it could be a problem in the penile tissue. I know DHT is needed to maintain the thing healthy and nebido was inconsistent, so pephaps I just have to wait?

[Charger Hemi]

Testosterone Effects Tool

This is a tool that uses the info contained in that study. Have a look and play around.

Thanks, Simon. Nice tool. There is more useful information there.

[macmathews]

Nope I have been on nebido for more than a year and since April on Test E, 100mg E4D.

Never checked for DHT. With AIs I got (soft) morning boners and that's all.


I tried AAKG to no avail. My real question is whether it could be a problem in the penile tissue. I know DHT is needed to maintain the thing healthy and nebido was inconsistent, so pephaps I just have to wait?

Have you tried a lower dose of T ?? Your taking like 190mg /week..
I have read and heard of some doing better on between 50-100mg/week

Mac

[hammerheart]

Have you tried a lower dose of T ?? Your taking like 190mg /week..
I have read and heard of some doing better on between 50-100mg/week

Mac

I just started the month other, I wasn't expecting anything spectacular anyway.

About dosage, I went through any possible range when I was on nebid, and nothing changed. It's not about T levels.

I will be checking hormones again in July, including DHT if possible (it's pricey). I will eventually lower dosage if T levels are way too high.