Hypogonadism and erectile dysfunction as harbingers of systemic disease
Review Article

Hypogonadism and erectile dysfunction as harbingers of systemic disease

Kelly A. Chiles1,2

1Department of Urology, George Washington University, Washington, DC, USA; 2Weill Cornell Medical College, New York, NY, USA

Correspondence to: Kelly A. Chiles, MD, MSc. Department of Urology, George Washington University Medical Faculty Associates, 2300 M Street, NW, Suite 210, Washington, DC 20037, USA. Email: kchiles@mfa.gwu.edu.

Abstract: Prescription sales of Testosterone and erectile aids such as phosphodiesterase-5 inhibitors are at an all-time high, underscoring the importance of hypogonadism (HG) and erectile dysfunction (ED) to men’s health. The effect of these debilitating conditions has a major impact on the quality of men’s lives. Some risk factors for HG or ED including aging, obesity, smoking, and a sedentary lifestyle. Notably, these are the same risk factors for several other medical co-morbidities that contribute to significant morbidity and mortality in men. HG and ED often co-exist with cardiovascular disease, diabetes, and osteoporosis. This review will explore these three co-morbidities that overlap with HG and ED, and will provide a review of their relationship with each other.

Keywords: Testosterone; erectile dysfunction (ED); cardiovascular disease; diabetes; osteoporosis

Submitted Mar 02, 2016. Accepted for publication Mar 02, 2016.

doi: 10.21037/tau.2016.03.05


Today’s global population has never been older than it is now, nor is it as old as it will be tomorrow. As the age of the population is advancing, so must our knowledge of age-related physiologic changes and disease processes. Harman et al. looked at the change in free and total Testosterone (fT and tT, respectively) in eight hundred and ninety healthy men ranging in age from their twenties to their eighties (1). Using <325 ng/dL as their definition of hypogonadism (HG), they found increasing prevalence of HG with age. Twelve percent of men in their fifties qualified as HG, and the rates of low tT for men in their sixties, seventies, and eighties were 19%, 28%, and 49%, respectively. Naturally, these numbers are not meant to suggest that all of these men have symptoms of HG, as the study was only looking at lab values and subjective outcomes were not available. Instead, these data provide a framework for appreciating how prevalent low tT is in the aging male population.

It has been equally well-established that erectile dysfunction (ED) also increases with age. Johannes et al. sought to determine the incidence of ED from the Massachusetts Male Aging Study (MMAS) (2). These authors found that there will be 26 new cases of ED per 1,000 men, which translates to just over 617,000 cases of ED in the United States annually. Notably, these rates are likely underestimated because of the limitations of the population enrolled in the MMAS. The prevalence of ED is even more impressive because of the cumulative nature of chronic conditions. Feldman et al. determined, again from data accumulated by the MMAS, that the prevalence of ED in men aged forty to 69 years old is 52% (3). Importantly, this study also demonstrated the overlap that ED has with multiple other medical co-morbidities. For example, ED was more likely in diabetics and men with heart disease. The overlap that HG and ED have with other systemic diseases is not surprising when considering the overlap in common risk factors each entity shares. Advancing age, for example, clearly increases the prevalence of these chronic conditions, as does smoking and a sedentary lifestyle. This review will focus on three of the most common co-morbidities which overlap with HG and ED, and will provide a review of the relationships of these entities with each other.

Cardiovacular disease

Few controversies within the field of andrology have garnered more public attention in the past few years than the question of whether testosterone is poison or panacea regarding cardiovascular health in men. Much of this controversy stems from a retrospective study by Vigen et al. that sought to look at the outcomes of veterans who were hypogonadal (defined in this study as tT less than 300 ng/dL) (4). Hypogonadal men who elected to fill one prescription of any form of testosterone supplementation (TS) were compared to hypogonadal men who chose not to supplement. The authors looked at all-cause mortality, myocardial infarction (MI) and stroke, and concluded that TS increased the rates of adverse events in hypogonadal men; this conclusion was only possible because they failed to consider several significant methodological flaws within their study design (5). The much-maligned conclusion of these authors has been the subject of multiple editorials and professional society position statements (6). In 2014 an advisory committee of the Federal Drug Administration (FDA) convened in order to assess whether or not the safety of TS had been adequately established. The committee concluded, and the FDA ultimately agreed, that T formulations required a change in labeling to reflect what they considered a “signal” within the literature that there may be some degree of cardiovascular risk associated with TS (7).

The controversy regarding TS safety must not be confused with the role HG plays in men’s cardiovascular health. The question that the FDA would like answer through carefully designed, well-controlled clinical trials is whether or not TS worsens clinically relevant outcomes such as all-cause mortality or thrombotic events. This is not to suggest that there is any confusion regarding whether hypogonadal men have worse outcomes compared to their (non-supplemented) eugonadal counterparts, because several decades worth of research firmly support this concept. Shores et al. retrospectively analyzed a population of Veterans, and categorized them as having low testosterone (defined as tT <250 ng/dL or fT <0.75 ng/dL; n=166) or not (n=692) (8). The mean ± standard deviation (SD) follow-up was 4.3±1.78 years. These authors found that low T was associated with increased mortality [hazard ratio, 1.88 (95% CI, 1.34–2.63)]. Corona et al. performed a meta-analysis to look at low T as a risk factor for cardiovascular mortality (9). These authors included seventy articles [1969–2011] in their analysis. They found that men in cross-sectional studies with cardiovascular disease had lower T levels, and in longitudinal studies men with lower T levels had increased all-cause and cardiovascular mortality compared to controls.

Erectile function is another facet of men’s health that allows a window into overall CV health. Vasculogenic ED can reside on the same spectrum as other atherosclerotic disorders, such as coronary artery disease and MIs (10). It is well-established that ED often precedes CVD. Montorsi et al. investigated men who had angiographically proven coronary artery disease (11). Of 300 men included in this study, 147 (49%) were identified as having ED prior to their acute coronary event. Even more revealing was their finding that the mean time from onset of ED to development of symptomatic coronary artery disease was only 39 months (range, 1–168). Furthermore, Mulhall et al. studied 49 men with documented vasculogenic ED and no history of coronary artery disease, and found that 20% had abnormal stress echocardiograms, which was over 6 times the incidence found in age-matched, healthy historical controls (12). Vlachopoulos et al. looked at the prevalence of asymptomatic coronary artery disease in men with organic ED (13). Of 47 men who underwent cardiac testing, 9 (19%) of men had silent coronary artery disease documented by angiography.

The “artery size hypothesis” possibly explains the temporal relationship between ED and vascular disease (14). This hypothesis suggests that because atherosclerosis functions to narrow lumens, the narrowest lumens (e.g., the penile or cavernosal arteries) will preferentially be affected before larger vessels such as the coronary arteries. The relationship of ED to CVD is so strong that the Princeton III guidelines state that any man with organic ED should be considered to be at risk for a major adverse CV event (MACE) within 5 years of the onset of ED (15). Furthermore, these guidelines recommend that men with ED should undergo a CV risk assessment as preventative measures. Importantly, the relationship of ED and MACE appears strongest in younger men, and these men are increasingly being identified as the subset that may hold the greatest risk of MACE (16,17).


Diabetes is an expanding health threat with an increasing prevalence world-wide (18). The strong relationship between diabetes and ED is not surprising given the number of risk factors which they share, such as obesity and aging. Anywhere from 35–90% of diabetics eventually suffer from ED (19,20). Men with diabetes not only have more severe ED, but they also have the greatest concomitant decrease in quality of life, and the poorest response to medical management (21). Bacon et al. used the Health Professionals Follow-up study cohort to try to determine the relative risk (RR) of ED in diabetics compared to non-diabetics (22). Over 30,000 men were queried regarding erectile function and their self-reported health information. The RR of ED in diabetics was 1.32 (95% CI, 1.3–1.4). They also demonstrated that the RR for type I diabetics was 3.0 (95% CI, 1.5–5.9), and 1.3 (95% CI, 1.1–1.5) for type II diabetics. The risk of ED increased with increasing time since diagnosis of diabetes. Mazzilli et al. sought to determine how many men with ED suffered from diabetes (23). They found that of 934 men with ED, 182 (19.5%) had diabetes. Increasing age was associated with increased prevalence of diabetes in their population.

An interesting and equally important question to answer is whether or not ED can be used to identify men with impaired insulin sensitivity that would therefore be at risk for developing diabetes. The association between ED and impaired fasting glucose or pre-diabetes is not well defined. Deutsch et al. looked at the results of an oral glucose challenge in 58 men with ED compared to 131 controls (24). These authors identified that seven (12%) of their subjects with ED were diabetic, no one in the control group had diabetes, and there was no difference between the groups in incidence of impaired glucose tolerance. Ettala et al. similarly questioned if they could identify pre-diabetics from screening men with ED (25). They enrolled 926 men, and challenged them with an oral glucose tolerance test. Using the results of the International Index of Erectile Function questionnaire, they determined that 516 (56%) had ED. There was no association between presence or severity of ED and the result of the glucose challenge.

Low T is also associated with diabetes. Ding et al. performed a meta-analysis to discern the relationship between endogenous hormone levels and diabetes (26). After identifying 43 articles used for this analysis, data from 6,427 men was pooled. They found that tT was significantly lower in diabetic men (mean −76.6 ng/dL, 95% CI, −99.4 to −53.6). Furthermore, men with higher tT (range, 449.6-605.2 ng/dL) had a lower RR of diabetes (RR 0.58, 95% CI 0.39–0.87). El Saghier et al. also looked at the relationship between T level and ED in diabetic men (27). They found that almost 90% of men with low T had ED, while only 30% of men with normal T had ED. Also, tT was lower in diabetic men with ED compared to men without ED. Muraleedharan et al. looked at the clinical implications of low T in diabetics (28). These authors looked at 581 men that they followed for a mean ± SD of 5.8±1.3 years. They show that mortality is increased in the men with tT <300 ng/dL (17.2%) compared to men with normal T levels (9%; P=0.003). Interestingly, unlike ED, low T does appear to have a correlation with impaired fasting glucose. Yeap et al. looked at 2,470 non-diabetic men, and demonstrated that lower T levels are related to insulin resistance (29).

Bone and muscle health

The effects of T level on lean muscle mass and bone health are increasingly being appreciated. Finkelstein et al. sought to demonstrate the role that endogenous T plays in maintaining bone health and muscle mass in an elegantly designed clinical trial (30). They treated 198 healthy men with a gonadotropin releasing hormone agonist in order to suppress endogenous T and estradiol production. Men were then randomized to receive either placebo or increasing concentrations of exogenous T. After 4 months, men with lower serum tT saw a decrease in lean muscle mass and strength as well as increased adiposity. The implications of the decreased bone density are significant because of the associated risk of osteopenia and osteoporosis. Although decreased bone density is traditionally thought to affect women, the risk to men is real and likely underappreciated. Up to one third of fractures occur in men, and the fracture-related morbidity and mortality is higher in men than in women (31). The Third National Health and Nutrition Examination Survey (NHANES III) was used to look at the association between decreased bone mineral density and fT and tT levels (32). Paller et al. demonstrated an increased risk of osteopenia in men in the lowest quartile of fT (odds ratio 3.82, 95% CI, 1.87–7.78). Interestingly, they were not able to identify this same increased risk of decreased bone mineral density when looking at tT, suggesting nuanced roles of the various T iterations and the importance of sex hormone binding globulin. The NHANES III was also used in a separate study to determine the relationship between fT and tT and frailty (33). Interestingly, this study also revealed that fT had a positive association with frailty although again tT did not reach statistical significance. Tuck et al. looked at the relationship between fT, tT, and symptomatic vertebral fractures (34). They too found that fT was lower in the men with fractures compared to controls, and did not find any difference in tT levels between the two groups. Declining sex hormone levels also contribute to frailty in the aging male by effects on muscle mass (35). Schaap et al. looked at 623 men enrolled in the Longitudinal Aging Study of Amsterdam, and found that fT and tT were positively associated with increased muscle strength and mobility (36).

Recently, the relationship between osteoporosis and ED has also been questioned. Dursun et al. looked at 95 men with ED and 82 men with normal erectile function (37). They found lower bone mineral density in the men with ED compared to control. Naturally, work remains to be done to elucidate the mechanism of such an association, and evaluating the role that T level plays in this relationship is paramount. Lee et al. looked at the relationship between sexual dysfunction and frailty in 1,504 men involved in the European Male Aging Study (38). Frailty was not only associated with increased risk of ED, but with greater distress associated with sexual dysfunction.


HG and ED overlap with multiple significant co-morbidities that affect men’s health, including CVD, DM, and bone/muscle mass decline. This association, however, must not be confused with causation as very little high quality research has been performed which can help elucidate the temporal relationship of these associated entities. Appreciating that our knowledge is still quite limited in our understanding of the mechanisms of these disease processes allows healthcare workers to appreciate the need for additional research.

Several important take-home messages, however, are quite clear. ED, particularly in a young man, could be a warning sign for occult CVD. The lag time between ED and symptomatic cardiac disease provides healthcare providers with a window of opportunity for intervention and possibly prevention. The overlap between HG and ED with DM should also be appreciated because of the common risk factors which contribute to the individual development of each of these disease processes. In addition, hormonal changes and ED can translate to increased frailty and declining quality of life in men.

Thoughtful consideration of HG and ED as harbingers of other systemic diseases will help improve the care we can provide men. Healthcare providers invested in men’s health need to be aware of these associations in order to appropriately screen patients or make appropriate referrals as needed.


Funding: Dr. Chiles is a National Institutes of Health KL2 scholar, and is supported by the Weill Cornell Medical College Clinical and Translational Science Center award number KL2TR000458 from the NIH National Center for Advancing Translational Science.


Conflicts of Interest: The author has no conflicts of interest to declare.

Disclaimer: The content is solely the responsibility of the author and does not necessarily represent the official view of the NIH.


  1. 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;86:724-31. [Crossref] [PubMed]
  2. Johannes CB, Araujo AB, Feldman HA, et al. Incidence of erectile dysfunction in men 40 to 69 years old: longitudinal results from the Massachusetts male aging study. J Urol 2000;163:460-3. [Crossref] [PubMed]
  3. Feldman HA, Goldstein I, Hatzichristou DG, et al. Impotence and its medical and psychosocial correlates: results of the Massachusetts Male Aging Study. J Urol 1994;151:54-61. [PubMed]
  4. Vigen R, O'Donnell CI, Barón AE, et al. Association of testosterone therapy with mortality, myocardial infarction, and stroke in men with low testosterone levels. JAMA 2013;310:1829-36. [Crossref] [PubMed]
  5. Morgentaler A, Kacker R. Andrology: Testosterone and cardiovascular risk--deciphering the statistics. Nat Rev Urol 2014;11:131-2. [Crossref] [PubMed]
  6. Morgentaler A, Traish A, Kacker R. Deaths and cardiovascular events in men receiving testosterone. JAMA 2014;311:961-2. [Crossref] [PubMed]
  7. Nguyen CP, Hirsch MS, Moeny D, et al. Testosterone and "Age-Related Hypogonadism"--FDA Concerns. N Engl J Med 2015;373:689-91. [Crossref] [PubMed]
  8. Shores MM, Matsumoto AM, Sloan KL, et al. Low serum testosterone and mortality in male veterans. Arch Intern Med 2006;166:1660-5. [Crossref] [PubMed]
  9. Corona G, Rastrelli G, Monami M, et al. Hypogonadism as a risk factor for cardiovascular mortality in men: a meta-analytic study. Eur J Endocrinol 2011;165:687-701. [Crossref] [PubMed]
  10. Corona G, Fagioli G, Mannucci E, et al. Penile doppler ultrasound in patients with erectile dysfunction (ED): role of peak systolic velocity measured in the flaccid state in predicting arteriogenic ED and silent coronary artery disease. J Sex Med 2008;5:2623-34. [Crossref] [PubMed]
  11. Montorsi F, Briganti A, Salonia A, et al. Erectile dysfunction prevalence, time of onset and association with risk factors in 300 consecutive patients with acute chest pain and angiographically documented coronary artery disease. Eur Urol 2003;44:360-4; discussion 364-5. [Crossref] [PubMed]
  12. Mulhall JP. Defining and reporting erectile function outcomes after radical prostatectomy: challenges and misconceptions. J Urol 2009;181:462-71. [Crossref] [PubMed]
  13. Vlachopoulos C, Rokkas K, Ioakeimidis N, et al. Prevalence of asymptomatic coronary artery disease in men with vasculogenic erectile dysfunction: a prospective angiographic study. Eur Urol 2005;48:996-1002; discussion 1002-3. [Crossref] [PubMed]
  14. Montorsi P, Ravagnani PM, Galli S, et al. The artery size hypothesis: a macrovascular link between erectile dysfunction and coronary artery disease. Am J Cardiol 2005;96:19M-23M. [Crossref] [PubMed]
  15. Nehra A, Jackson G, Miner M, et al. The Princeton III Consensus recommendations for the management of erectile dysfunction and cardiovascular disease. Mayo Clin Proc 2012;87:766-78. [Crossref] [PubMed]
  16. Miner M, Seftel AD, Nehra A, et al. Prognostic utility of erectile dysfunction for cardiovascular disease in younger men and those with diabetes. Am Heart J 2012;164:21-8. [Crossref] [PubMed]
  17. Jackson G. Prevention of cardiovascular disease by the early identification of erectile dysfunction. Int J Impot Res 2008;20 Suppl 2:S9-14. [Crossref] [PubMed]
  18. Danaei G, Finucane MM, Lu Y, et al. National, regional, and global trends in fasting plasma glucose and diabetes prevalence since 1980: systematic analysis of health examination surveys and epidemiological studies with 370 country-years and 2·7 million participants. Lancet 2011;378:31-40. [Crossref] [PubMed]
  19. Castela Â, Costa C. Molecular mechanisms associated with diabetic endothelial-erectile dysfunction. Nat Rev Urol 2016. [Epub ahead of print]. [Crossref] [PubMed]
  20. Malavige LS, Levy JC. Erectile dysfunction in diabetes mellitus. J Sex Med 2009;6:1232-47. [Crossref] [PubMed]
  21. Penson DF, Latini DM, Lubeck DP, et al. Do impotent men with diabetes have more severe erectile dysfunction and worse quality of life than the general population of impotent patients? Results from the Exploratory Comprehensive Evaluation of Erectile Dysfunction (ExCEED) database. Diabetes Care 2003;26:1093-9. [Crossref] [PubMed]
  22. Bacon CG, Hu FB, Giovannucci E, et al. Association of type and duration of diabetes with erectile dysfunction in a large cohort of men. Diabetes Care 2002;25:1458-63. [Crossref] [PubMed]
  23. Mazzilli R, Elia J, Delfino M, et al. Prevalence of Diabetes Mellitus (DM) in a population of men affected by Erectile Dysfunction (ED). Clin Ter 2015;166:e317-20. [PubMed]
  24. Deutsch S, Sherman L. Previously unrecognized diabetes mellitus in sexually impotent men. JAMA 1980;244:2430-2. [Crossref] [PubMed]
  25. Ettala OO, Korhonen PE, Syvänen KT, et al. Erectile dysfunction cannot be used in primary screening of pre-diabetes. Diabetes Res Clin Pract 2015;108:e60-2. [Crossref] [PubMed]
  26. Ding EL, Song Y, Malik VS, et al. Sex differences of endogenous sex hormones and risk of type 2 diabetes: a systematic review and meta-analysis. JAMA 2006;295:1288-99. [Crossref] [PubMed]
  27. El Saghier EO, Shebl SE, Fawzy OA, et al. Androgen Deficiency and Erectile Dysfunction in Patients with Type 2 Diabetes. Clin Med Insights Endocrinol Diabetes 2015;8:55-62. [Crossref] [PubMed]
  28. 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;169:725-33. [Crossref] [PubMed]
  29. Yeap BB, Chubb SA, Hyde Z, et al. Lower serum testosterone is independently associated with insulin resistance in non-diabetic older men: the Health In Men Study. Eur J Endocrinol 2009;161:591-8. [Crossref] [PubMed]
  30. Finkelstein JS, Lee H, Burnett-Bowie SA, et al. Gonadal steroids and body composition, strength, and sexual function in men. N Engl J Med 2013;369:1011-22. [Crossref] [PubMed]
  31. Gielen E, Vanderschueren D, Callewaert F, et al. Osteoporosis in men. Best Pract Res Clin Endocrinol Metab 2011;25:321-35. [Crossref] [PubMed]
  32. Paller CJ, Shiels MS, Rohrmann S, et al. Relationship of sex steroid hormones with bone mineral density (BMD) in a nationally representative sample of men. Clin Endocrinol (Oxf) 2009;70:26-34. [Crossref] [PubMed]
  33. Eichholzer M, Barbir A, Basaria S, et al. Serum sex steroid hormones and frailty in older American men of the Third National Health and Nutrition Examination Survey (NHANES III). Aging Male 2012;15:208-15. [Crossref] [PubMed]
  34. Tuck SP, Scane AC, Fraser WD, et al. Sex steroids and bone turnover markers in men with symptomatic vertebral fractures. Bone 2008;43:999-1005. [Crossref] [PubMed]
  35. O'Connell MD, Wu FC. Androgen effects on skeletal muscle: implications for the development and management of frailty. Asian J Androl 2014;16:203-12. [Crossref] [PubMed]
  36. Schaap LA, Pluijm SM, Smit JH, et al. The association of sex hormone levels with poor mobility, low muscle strength and incidence of falls among older men and women. Clin Endocrinol (Oxf) 2005;63:152-60. [Crossref] [PubMed]
  37. Dursun M, Özbek E, Otunctemur A, et al. Possible association between erectile dysfunction and osteoporosis in men. Prague Med Rep 2015;116:24-30. [Crossref] [PubMed]
  38. Lee DM, Tajar A, Ravindrarajah R, et al. Frailty and sexual health in older European men. J Gerontol A Biol Sci Med Sci 2013;68:837-44. [Crossref] [PubMed]
Cite this article as: Chiles KA. Hypogonadism and erectile dysfunction as harbingers of systemic disease. Transl Androl Urol 2016;5(2):195-200. doi: 10.21037/tau.2016.03.05