Researchers at the National Institute on Aging ³ have established low testosterone levels in:

• 20% of men over age 60
• 30% of men over age 70
• 50% of men over age 80

These percentages understate the magnitude of this problem as they fail to consider the majority of aging men who fail to achieve optimal testosterone and estrogen balance.

By properly balancing testosterone and estrogen , a reversal in many age-related disorders has been found. This includes improvements in libido, bone density, muscle mass, strength, body composition, mood, red blood cell formation, cognition, quality of life, and cardiovascular disease. ^2,4,5

Yet despite these proven benefits, the FDA recently mandated a black box warning label be affixed to prescription testosterone drugs. ⁶ A black box warning is the strongest possible warning issued by the FDA and impliess erious risks associated with a drug.

This irresponsible and scientifically invalid decision threatens to discourage millions of eligible men from taking advantage of the genuine benefits of testosterone replacement therapy.

The FDA’s decision seems to be based on a small number of poorly designed, poorly conducted studies, some of which appeared to show an increased risk of heart attacks and strokes in men undergoing such therapy. ^7-12 Yet the preponderance of the data shows marked decreases in heart attack and stroke risk in response to higher testosterone levels.

In a large study published in 2015 , men treated with testosterone had a 24% reduction in heart attack risk and a 36% reduction in risk of stroke. ¹³ The most exciting revelation about this new study was that the risk of dying from any cause was 56% lower in treated men whose testosterone blood levels normalized, compared with untreated individuals.

With a wealth of studies showing positive benefits, and in the face of the FDA’s irrational decision based on flawed studies, it is time to review the good science on this issue, and to make balanced recommendations about testosterone replacement therapy.

Benefits of Testosterone Replacement Therapy

Testosterone levels begin a gradual fall as men enter their 30s! ^1,2

This matters because declining testosterone levels are associated with muscle atrophy and weakness, osteoporosis, reduced sexual functioning, increased fat mass, metabolic syndrome, diabetes risk, cognitive impairment, depression, and an increased risk of developing Alzheimer’s disease. ^14-16 Furthermore, men with low levels of testosterone are up to 51% more likely to develop frailty, a condition associated with early death, compared to those with higher levels. ¹⁷

Used appropriately, and with regular blood tests , testosterone replacement therapy can reverse many of these age-related disorders. Testosterone replacement therapy has been shown to improve libido and sexual function, bone density, muscle mass, strength, body composition, mood, red blood cell formation, cognition, and quality of life, as well as reduce cardiovascular disease. ^2,4,5 It has even been suggested that testosterone replacement therapy preserves new brain cell growth in the hippocampus, the main memory area of the brain and the one that loses neurons with age. ¹³

Perhaps most importantly, the life-shortening effects of low testosterone can be substantially reversed by testosterone replacement therapy in many men. By one estimate, testosterone replacement therapy can increase longevity by about 2% per year. ¹⁸ After five years, survival rates are back in line with those of men with normal testosterone levels. ¹⁹

Simply put, testosterone replacement therapy offers a wealth of health benefits for older men. It is approved by the FDA for patients with signs and symptoms of low testosterone who also have documented low blood levels of the hormone. ^13,20 The diagnosis of age-related low testosterone is rising, with an estimated 2.4 million American men 40 through 69 years old suffering from the condition. ^13,21

The FDA’s approval criteria, however, excludes the majority of aging men who could benefit by boosting their testosterone level while suppressing excess estrogen when blood test results indicate.

All of this means that more men than ever could benefit from testosterone replacement. Unfortunately, many of these men—or their doctors—will avoid this beneficial therapy due to the FDA’s recent black box warning.

FDA Sows Seeds of Unnecessary Fear

It seems evident that testosterone replacement therapy offers compelling benefits when given to men with genuine symptoms of age-related testosterone deficiency and documented low blood levels of the hormone.

Yet in mid-2015, when the FDA instituted a black box warning on testosterone replacement therapy for older men, they asserted that neither the safety nor the benefits of such therapy had been established, and cited, in particular, a “ possible increased risk of heart attacks and strokes ” in patients taking testosterone. ⁶

Testosterone cannot be obtained without a prescription. In today’s litigation-prone society, that black box warning is likely to dissuade physicians from prescribing testosterone replacement therapy.

But a careful examination of the published literature tells another story. Properly restoring sex hormone balance in aging men confers protection against heart attack and stroke via multiple mechanisms. The FDA chose to ignore these many studies showing disease risk reduction in men with higher testosterone blood levels.

When researchers evaluate the impact that a drug has on humans, the standard practice is to determine the levels of the drug in plasma or serum after administration of the drug. That common-sense design parameter was lacking in most of the studies on which the FDA based its labeling decision.

FDA actions are supposed to be based on multiple high-quality studies to assess safety and efficacy. ²² This “evidence-based-medicine” approach is now standard in peer-reviewed medical research and policymaking, but it was apparently overlooked by the FDA’s decision-makers.

Instead, studies on which the black box labeling decision was made demonstrate considerable inconsistencies and very small clinically important treatment effects. ^7-12

Of the studies included, only two showed an association between testosterone replacement and increased risk of cardiovascular events. Here is a review of the studies apparently used by the FDA in its labeling decision.

Flawed Study #1

The first study was a retrospective, observational study by Rebecca Vigen, MD, MSCS, and colleagues published in the September 5, 2013, issue of the Journal of the American Medical Association ( JAMA ). The study suggests testosterone therapy may increase risk of death and certain cardiovascular events. ⁷ However, there are several significant shortcomings in the study’s design and methodology, and the results conflict with the existing body of research.

The goal of testosterone restoration in most cases is to restore youthful blood levels of the hormone. Typically, Life Extension ^® suggests men target a blood level of total testosterone between 700 and 900 ng/dL for optimal health.

In studies designed to assess the impact of testosterone replacement therapy, one of the most important considerations is to measure subjects’ blood levels of testosterone regularly throughout the study period. This allows the scientists conducting the study to make sure subjects are taking their testosterone as directed and that their blood levels are rising as expected.

Unbelievably, in the flawed analysis by Vigen and colleagues, only 60% of study subjects receiving testosterone had a follow-up blood test to assess their testosterone levels. Among them, average testosterone levels rose from a very low level of 175.5 ng/dL at baseline to a still far-from-optimal level of 332.2 ng/dL during testosterone therapy.

Raising testosterone levels from a paltry 175.5 ng/dL to only 332.2 ng/dL is unlikely to deliver robust health benefits. In fact, research has shown that restoring testosterone levels to 500 ng/dL or higher is associated with pronounced health benefits, whereas benefits may be less evident at lower levels. ^23,24

One of the biggest perils facing aging men is the conversion of their testosterone into estrogen by the aromatase enzyme. ²⁵

Aromatase converts testosterone and other androgens into estrogen , primarily estradiol. Although some conversion of testosterone to estradiol is essential for health, too much conversion can have devastating consequences for men.

In one study, men with heart failure and high levels of estradiol had an increased risk of death compared to men whose levels of estradiol were in a balanced, middle range of 21.8 to 30.11 pg/mL . ²⁶ These findings support Life Extension ^® ’s suggested optimal estradiol level of 20 to 30 pg/mL . Moreover, excess estrogen promotes abnormal clot formation, ²⁷ and high levels may be associated with an increased risk of stroke. ²⁸

When men take testosterone, there is a propensity for it to be converted into estradiol by aromatase, and this is especially so for aging men. ²⁹ It is therefore important that men undergoing testosterone therapy monitor their estradiol levels regularly and take steps like using an aromatase-inhibiting drug to keep estradiol levels in the optimal range in order to protect against the health detriments of excess estrogen.

In the paper published by Vigen and colleagues, there was no report of the subjects’ estradiol levels. If estradiol was not monitored during testosterone administration, this oversight means that the men receiving testosterone could have experienced a concurrent rise in estradiol levels. This may have compromised their cardiovascular health and could partially account for the increased risk observed in the testosterone-treated group.

Lastly, among the men in this flawed JAMA study, there was a statistically significant difference in baseline testosterone levels between the “testosterone therapy” (treatment) and “no-testosterone” (control) groups.

Among the control group, testosterone levels were higher at baseline ( 206.5 ng/dL ), whereas the average level was significantly lower at baseline ( 175.5 ng/dL ) for those who received a prescription for testosterone.

The treatment group may have had significantly lower levels of testosterone than the control group for years prior to entering the study. The damage caused by years of potentially lower testosterone levels was not accounted for in the study and may have skewed the results.

Flawed Study #2

The second study by William Finkle, PhD, and colleagues was retrospective and observational. The design of this study limits the interpretation of the findings because subjects were treated in a clinical setting and were not randomized to treatment. ⁸

The validity of this study is hampered by several methodological flaws. A striking concern is again the failure of the researchers to account for estradiol levels among the men who received a testosterone prescription. As mentioned previously, aging men quickly convert exogenous testosterone into estradiol via action of the aromatase enzyme. Studies have shown that cardiovascular risk correlates with higher estrogen/estradiol levels among men. ^26,30,31

Aromatase activity increases with age among men, ²⁹ a paradigm whose repercussions are potentially highlighted by this flawed study. Older men (65 years and older) in this study were more likely to experience a non-fatal heart attack after receiving a testosterone prescription than younger men. This is potentially due to increased conversion of the added testosterone medication to estradiol among the older men.

It is concerning that conventional physicians and researchers continue to prescribe men testosterone without monitoring their estradiol levels and, if needed, prescribing an aromatase-inhibiting drug such as anastrozole (Arimidex ^® ).

The researchers specifically acknowledged the potentially harmful cardiovascular-related effects of excess estrogen by stating:

“TT (testosterone therapy) also increases circulating estrogens…which may play a role in the observed excess of adverse cardiovascular-related events, given that estrogen therapy has been associated with this excess in both men and women… The mechanisms linking estrogens to thrombotic events (heart attacks) may be related to markers of activated coagulation, decreased coagulation inhibitors, and activated protein C resistance…”

Unfortunately, despite this acknowledgment, the researchers did not assess estradiol levels.

Interestingly, out of the five observational studies included in the FDA’s decision to add a black label warning to testosterone treatment, the two flawed studies mentioned above apparently were the ones that prompted the decision, as the other two studies in the review showed a statistically significant benefit with testosterone replacement, ^11,12 and the remaining study was inconclusive. ¹⁰

If these were the only studies available to consider, the FDA might be pardoned for making a conservative decision out of an abundance of caution.

But several studies had already been published that showed either no effect, or genuine benefits, of testosterone replacement therapy on men’s cardiovascular risks. Let’s take a look.

Beneficial Studies Ignored by FDA

An observational study published in 2012 demonstrated significant reductions in total mortality in men who received testosterone replacement therapy. ¹¹

This study included 1,031 male veterans aged 40 and older, 398 of whom were treated with testosterone. All of the men had testosterone levels that were less than 251 ng/dL . Among testosterone-treated men, 10.3% died over the course of four years. In the untreated (no testosterone) group, twice that number ( 20.7% ) died during the same period. After statistical adjustment for possible biasing factors, the testosterone-treated men were found to be 39% less likely to die of any cause than were untreated men.

In another study based on a national sample of older Medicare beneficiaries, 6,355 patients received testosterone injections while 19,065 men did not receive treatment. ¹⁰ This study showed no association with risk for myocardial infarction (heart attack) over nearly eight years. In fact, in men who began the study with the highest calculated risk score for heart attack, testosterone therapy was associated with a 31% reduction in risk.

Study Debunks FDA’s Position and Shows Testosterone Benefits Heart Health

For the past 19 years, Life Extension ^® has published numerous articles on the proper use of testosterone restoration therapy. The FDA’s insistence that testosterone drugs carry a black box warning is the antithesis of what the totality of the scientific literature clearly states on this critical issue for aging males.

A large study published in 2015 convincingly demonstrates the FDA’s action of mandating a black box warning is based on junk science.

This study evaluated a cohort of male veterans receiving care at Veterans Health Administration facilities over a 13-year period. ¹³ Unlike many of the previous studies, this one was specifically designed to examine the effects of testosterone replacement therapy on specific cardiovascular outcomes (namely heart attack and stroke) as well as on all-cause mortality.

The most important difference between this and prior studies, in addition to its large size (83,010 total subjects), was that it determined, for each subject, whether blood testosterone levels normalized or not. ¹³ The researchers divided the subjects into three groups:

• Men whose total testosterone was normalized after treatment (43,931 men)
• Men whose total testosterone continued to be low even after treatment (25,701 men), and
• Men who were untreated with testosterone and continued to have low total testosterone (13,378 men).

The researchers then analyzed the rates of heart attack, stroke, and death from any cause between the three groups. ¹³

This unique study design allowed for the first-ever comparison of men who attained normal testosterone levels with those who did not, as well as with those who were never treated at all. For the first time, it was possible to examine actual biological effects of therapy in considering whether such therapy was dangerous.

This is a rational and obvious approach, but one never taken before, including in any of the studies evaluated by the FDA for its ruling.

First, the researchers compared the largest group (men whose testosterone normalized with treatment) to the untreated subjects. They found that the treated group had a 24% reduction in the risk of heart attack and a 36% reduction in the risk of stroke. ¹³ This comparison also revealed that the risk of dying from any cause was a significant 56% lower in treated men whose testosterone levels normalized, compared with untreated individuals.

Researchers also compared the group whose levels were normalized with those who were treated but had not achieved normal levels. In this comparison, the group whose levels were normalized experienced an 18% reduction in the risk of heart attack, a 30% reduction in stroke risk, and a 47% reduced risk of death by all causes compared to those treated with testosterone therapy but who did not achieve normal levels. All of the results were statistically significant.

When comparing the treated group that did not achieve normal testosterone levels with the untreated group, the only significant difference was a modest 16% reduction in all-cause mortality. No changes were seen between these groups in heart attack or stroke risk.

This study was enormous in terms of how many people it studied compared with the studies that preceded it. By tracking actual testosterone levels in response to treatment, the researchers were able to expose what is likely to be the biggest contributor to inconsistent results in previous studies. In those studies, failing to check testosterone blood levels essentially combined responders and non-responders together, leading to a failed study.

Even prior to this compelling and well-designed study based on data reviewed here and elsewhere, Dr. Abraham Morgentaler of Harvard Medical School, a renowned expert on testosterone and men’s health, had concluded that:

“There is no convincing evidence of increased cardiovascular risks with testosterone therapy. On the contrary, there appears to be a strong beneficial relationship between normal testosterone and cardiovascular health that has not yet been widely appreciated.” ³²

An Expert’s Recommendations for Testosterone Replacement Therapy

After a recent World Meeting on Sexual Medicine in Chicago, Dr. Morgentaler summarized expert consensus regarding testosterone replacement therapy, especially in the context of these spurious concerns about cardiovascular health: ³³

1. All experts emphasized the essential role of symptoms for diagnosis of testosterone deficiency. (In other words, a low testosterone level without symptoms should not necessarily require testosterone therapy, but a high or normal level with symptoms should not rule it out.)
2. Blood levels of total testosterone indicating a deficiency are in the 350 to 400 ng/dL range, but free testosterone should also be determined and was recommended by all experts for clinical decision-making.
3. Two tests of testosterone on separate occasions were recommended by most experts.
4. In men with symptoms but with normal total testosterone levels, a therapeutic trial of testosterone therapy, to be continued if beneficial effects are achieved, was considered potentially useful.
5. Recent studies suggesting an elevated cardiovascular risk with testosterone therapy were not found to be credible.

Summary

There is no question that in men with symptoms of testosterone deficiency, testosterone replacement therapy produces substantial benefits. ^13,32,33

But a recent labeling action by the FDA is almost certain to frighten many men and their physicians away from using this important treatment. Unfortunately, this decision was based on junk science purporting to show an increased cardiovascular risk in men using the therapy.

We conducted a careful review of the evidence the FDA used to make this decision, coupled with results from recent large, carefully designed studies. What this shows is that in men who achieve normalization of their testosterone levels on replacement therapy, the risks of cardiovascular disease are not only no higher than average, but are in fact lower.

It is impossible to overstate the importance of:

• Getting hormone blood levels checked (including total and free testosterone and estradiol) for men with symptoms consistent with age-related testosterone deficiency.
• Repeating the tests after several months to determine whether levels are normalized. If levels are not normalized, raising the dose of testosterone and rechecking in another few months is ideal. ¹³

There is no reason to let the FDA’s scare tactics stand in the way of a proven means of improving men’s quality of life, vigor, and sexual performance, while improving their cardiovascular status. All men with symptoms should have their levels checked and start on testosterone replacement therapy as indicated.

It should start with a comprehensive blood test panel that measures all sex hormones, PSA, liver function, and blood cell counts. With the results of this blood test in hand, a competent physician and an empowered patient can together safely restore youthful hormone balance.

References

1. Brawer MK. Testosterone replacement in men with andropause: an overview. Rev Urol. 2004;6(Suppl 6):S9-S15.
2. Kazi M, Geraci SA, Koch CA. Considerations for the diagnosis and treatment of testosterone deficiency in elderly men. Am J Med. 2007;120(10):835-40.
3. Harman SM, Metter EJ, Tobin JD, et al. Longitudinal effects of aging on serum total and free testosterone levels in healthy men. Baltimore Longitudinal Study of Aging. J Clin Endocrinol Metab. 2001;86(2):724-31.
4. Bassil N, Morley JE. Late-life onset hypogonadism: a review. Clin Geriatr Med. 2010;26(2):197-222.
5. Bassil N, Alkaade S, Morley JE. The benefits and risks of testosterone replacement therapy: a review. Ther Clin Risk Manag. 2009;5(3):427-48.
6. Available at: http://www.fda.gov/drugs/drugsafety/ucm436259.htm . Accessed December 15, 2015.
7. Vigen R, O’Donnell CI, Baron AE, et al. Association of testosterone therapy with mortality, myocardial infarction, and stroke in men with low testosterone levels. JAMA. 2013;310(17):1829-36.
8. Finkle WD, Greenland S, Ridgeway GK, et al. Increased risk of non-fatal myocardial infarction following testosterone therapy prescription in men. PLoS One. 2014;9(1):e85805.
9. Xu L, Freeman G, Cowling BJ, et al. Testosterone therapy and cardiovascular events among men: a systematic review and meta-analysis of placebo-controlled randomized trials. BMC Med. 2013;11:108.
10. Baillargeon J, Urban RJ, Kuo YF, et al. Risk of myocardial infarction in older men receiving testosterone therapy. Ann Pharmacother. 2014;48(9):1138-44.
11. Shores MM, Smith NL, Forsberg CW, et al. Testosterone treatment and mortality in men with low testosterone levels. J Clin Endocrinol Metab. 2012;97(6):2050-8.
12. Muraleedharan V, Marsh H, Kapoor D, et al. Testosterone deficiency is associated with increased risk of mortality and testosterone replacement improves survival in men with type 2 diabetes. Eur J Endocrinol. 2013;169(6):725-33.
13. Sharma R, Oni OA, Gupta K, et al. Normalization of testosterone level is associated with reduced incidence of myocardial infarction and mortality in men. Eur Heart J. 2015.
14. Ransome MI. Could androgens maintain specific domains of mental health in aging men by preserving hippocampal neurogenesis? Neural Regen Res. 2012;7(28):2227-39.
15. Moskovic DJ, Araujo AB, Lipshultz LI, et al. The 20-year public health impact and direct cost of testosterone deficiency in U.S. men. J Sex Med. 2013;10(2):562-9.
16. Ungureanu MC, Costache, II, Preda C, et al. Myths and controversies in hypogonadism treatment of aging males. Rev Med Chir Soc Med Nat Iasi. 2015;119(2):325-33.
17. Cawthon PM, Ensrud KE, Laughlin GA, et al. Sex hormones and frailty in older men: the osteoporotic fractures in men (MrOS) study. J Clin Endocrinol Metab. 2009;94(10):3806-15.
18. Comhaire F, Mahmoud A. The andrologist’s contribution to a better life for ageing men: part 1. Andrologia. 2015.
19. Comhaire F. Hormone replacement therapy and longevity. Andrologia. 2015.
20. Bhasin S, Cunningham GR, Hayes FJ, et al. Testosterone therapy in men with androgen deficiency syndromes: an Endocrine Society clinical practice guideline. J Clin Endocrinol Metab. 2010;95(6):2536-59.
21. Araujo AB, O’Donnell AB, Brambilla DJ, et al. Prevalence and incidence of androgen deficiency in middle-aged and older men: estimates from the Massachusetts Male Aging Study. J Clin Endocrinol Metab. 2004;89(12):5920-6.
22. Available at: http://www.dartmouth.edu/~biomed/resources.htmld/guides/ebm_resources.shtml . Accessed December 22, 2015.
23. Aversa A, Bruzziches R, Francomano D, et al. Effects of testosterone undecanoate on cardiovascular risk factors and atherosclerosis in middle-aged men with late-onset hypogonadism and metabolic syndrome: results from a 24-month, randomized, double-blind, placebo-controlled study. J Sex Med. 2010;7(10):3495-503.
24. Ohlsson C, Barrett-Connor E, Bhasin S, et al. High serum testosterone is associated with reduced risk of cardiovascular events in elderly men. The MrOS (Osteoporotic Fractures in Men) study in Sweden. J Am Coll Cardiol. 2011;58(16):1674-81.
25. Jasuja GK, Travison TG, Davda M, et al. Age trends in estradiol and estrone levels measured using liquid chromatography tandem mass spectrometry in community-dwelling men of the Framingham Heart Study. J Gerontol A Biol Sci Med Sci. 2013;68(6):733-40.
26. Jankowska EA, Rozentryt P, Ponikowska B, et al. Circulating estradiol and mortality in men with systolic chronic heart failure. JAMA. 2009;301(18):1892-901.
27. Colmou A. Estrogens and vascular thrombosis. Soins Gynecol Obstet Pueric Pediatr. 1982(16):39-41.
28. Abbott RD, Launer LJ, Rodriguez BL, et al. Serum estradiol and risk of stroke in elderly men. Neurology. 2007;68(8):563-8.
29. Lakshman KM, Kaplan B, Travison TG, et al. The effects of injected testosterone dose and age on the conversion of testosterone to estradiol and dihydrotestosterone in young and older men. J Clin Endocrinol Metab. 2010;95(8):3955-64.
30. Phillips GB, Pinkernell BH, Jing TY. The association of hyperestrogenemia with coronary thrombosis in men. Arterioscler Thromb Vasc Biol. 1996;16(11):1383-7.
31. Phillips GB. Is atherosclerotic cardiovascular disease an endocrinological disorder? The estrogen-androgen paradox. J Clin Endocrinol Metab. 2005;90(5):2708-11.
32. Morgentaler A, Miner MM, Caliber M, et al. Testosterone therapy and cardiovascular risk: advances and controversies. Mayo Clin Proc. 2015;90(2):224-51.
33. Morgentaler A, Khera M, Maggi M, et al. Commentary: Who is a candidate for testosterone therapy? A synthesis of international expert opinions. J Sex Med. 2014;11(7):1636-45.
34. Snyder PJ, Bhasin S, Cunningham GR, et al. Effects of testosterone treatment in older men . NEJM. 2016; 374:611-24.