Shehzad Basaria and Adrian S. Dobs
Division of Endocrinology and Metabolism, Johns Hopkins University, Baltimore, Maryland, USA
Dr Adrian S. Dobs, Division of Endocrinology and Metabolism, Johns Hopkins University, 1830 Monument Street, Suite-328, Baltimore, MD 21287, USA.; E-mail: adobs@welchlink.welch.jhu.
Abstract
‘Andropause’, like menopause, has received significant attention in recent years. It results in a variety of symptoms experienced by the elderly. Many of these symptoms are nonspecific and vague. For this reason, many authors have questioned the value of androgen replacement in this population. Also in dispute is the normal cutoff level for testosterone beyond which therapy should be initiated, and whether to measure free or total testosterone. Testosterone levels decline with age, with the lowest level seen in men older than 70 years. This age-related decline in testosterone levels is both central (pituitary) and peripheral (testes) in origin. With aging, there is also a loss of circadian rhythm of testosterone secretion and a rise in sex hormone binding globulin (SHBG) levels. Total testosterone level is the best screening test for patients with suspected hypogonadism. If the total testosterone concentration is low, free testosterone levels should be obtained. Prostate cancer remains an absolute contraindication to androgen therapy. Testosterone replacement results in an improvement in muscle strength and bone mineral density. Similar effects are observed on the haematopoietic system. Data on cognition and lipoprotein profiles are conflicting. Androgen therapy can result in polycythemia and sleep apnoea. These adverse effects can be deleterious in men with compromised cardiac reserve. We recommend that elderly men with symptoms of hypogonadism and a total testosterone level < 300 ng/dl should be started on testosterone replacement. This review discusses the pros and cons of testosterone replacement in hypogonadal elderly men and attempts to answer some of the unan-swered questions. Furthermore, emphasis is made on the regular follow-up of these patients to prevent the development of therapy-related complications.
Introduction
‘Andropause’ or male climacterium is a term used to describe a collection of symptoms associated with a decline in male gonadal function with aging. At the time of menopause in women, there is an abrupt and complete loss of ovarian function, often leading to a relative sudden onset of drastic symptoms such as hot flashes orflushes, behavioural changes, variations in sleep cycle and dyspareunia. In contrast, men experience a gradual decline in testicular function leading to nonspecific complaints of decreased muscular strength, energy and libido, erectile dysfunction, and depression. Another feature which differentiates andropause from menopause is that the decline in biologically active androgens is only moderate and many elderly men have free androgen levels that are at the lower end of the normal range. In this review we will discuss the actions of testosterone, the changes in testosterone levels associated with aging, and the risks and benefits of testosterone supplementation.
1.Androgen Production and Aging
1.1Normal Metabolism
Testosterone, synthesised and secreted by Leydig cells of the testes,[1] is regulated by a negative feedback system involving the hypothalamus and the pituitary. The testes produce 0.24 mmol/day of testosterone. Testosterone is metabolised to dihydrotestosterone (DHT) by 5α reductase. Most of the circulating testosterone (80%) is bound to sex hormone binding globulin (SHBG). The remaining is bound to albumin and other plasma proteins. Only 2% of total testosterone is free and is bioactive.[2-4] There is a diurnal variation in serum testosterone levels in young men, which is highest at about 08.00 hours and lowest in the late afternoon.[5]
Testosterone secretion begins in utero with a peak in the male fetus at 12 weeks. The second peak occurs after birth. From this time until puberty, the levels are low and equal to the female. At puberty, there is a pulsatile secretion of luteinising hormone (LH) leading to maturity of the Leydig cells resulting in increased testosterone synthesis.
1.2Changes in Hormone Levels With Age
Numerous cross-sectional and longitudinal stud-ies have found that beginning in the fifth decade of life, serum total testosterone levels progressively decline with age with the lowest levels noted in men older than 70 years.[6-10]
Serum SHBG levels increase gradually as a function of age.[11] This effect may be mediated by enhanced estradiol production due to increased adiposity with age. Since most of the testosterone is bound to serum proteins, a decline in levels of free testosterone with increasing age is of greater mag-nitude than that of serum total testosterone.[11,12] Morley et al,.[13] in their longitudinal study of 77 elderly men, showed a significant decline intestos-terone levels with aging. They also observed an increase in gonadotropin and SHBG levels. Fur-thermore, the normal diurnal variation of testoster-one levels observed in young men is lost in elderly men with values throughout the day similar to those of young men at 20.00 hours.[5]
On the other hand, plasma DHT levels do not vary significantly withage.[10] Harman etal.[14] found no effect of age on serum testosterone levels in male members of the Baltimore Longitudinal Study on Aging (BLSA) group. The only drawback of this study was that testosterone levels were checked in the afternoon (14.00 to 15.00 hours), the time when the testosterone levels are at their nadir. Measuring serum testosterone levels in the morning between 06.00 to 08.00 hours may have shown lower values in the older population compared with their younger counterparts.
Testicular function may be affected by many conditions seen more frequently in the elderly such as stress, illness, medications, obesity, malnutrition and psychiatric conditions. Therefore, serum tes-tosterone levels may be even more profoundly sup-pressed in elderly experiencing the above men-tioned conditions than in those who are not.[8-10] However, decreased testosterone levels have also been reported in carefully screened exceptionally healthy elderly men.[15] Morley et al.,[16] in their cross-sectional study of 56 healthy men belonging to different age groups, showed a significant decline in bioavailable testosterone levels with aging.
1.3Mechanism of Age-Related Changes in Hormone Levels
It is generally accepted that the decline in tes-tosterone levels with age is primarily testicular in origin. This belief is supported by the decreased number and volume of Leydig cells,[17-20] impaired testicular perfusion2122 and impaired steroid bio-synthesis in aging men.[23]
Although the above evidence supports testicular failure, several alterations in the hypothalamic- pituitary compartment of the hypothalamic-pituitary- gonadal axis have been noted. These include loss of nycthemeral variations in testosterone levels,[5,24] decreased frequency of large amplitude LH pulses in elderly men[25] and increased sensitivity of the gonadotrophs to sex hormone feedback.[26,27]
Based on the above evidence, it may be concluded that hypogonadism in elderly men is both central and peripheral in origin.
2.Androgens, Target Organs and Elderly Men
2.1Prostate
The development of both benign pro static hyperplasia (BPH) and prostatic cancer requires the presence of functional testes in fetal life, puberty and, at least part of, adulthood.[28] Neither of these conditions occur in men who undergo prepubertal castration. [29] After sexual maturation, both androgens and estrogens are important in maintaining the structure and integrity of the prostate. Although testosterone is the main circulating androgen, a peripheral conversion product, DHT, binds to the main nuclear androgen receptor in sexual tissue.[30-33] DHT is the major androgen for prostatic growth.
The role of androgens in the aetiology of pre-clinical prostate cancer is not known. Hulka et al.[34] showed that there was no statistically signif-icant association between testosterone levels and occurrence of prostatic cancer. Carter et al.[35] also found no significant difference in LH, total testos-terone, free testosterone and SHBG levels between men who developed prostate cancer and those free of disease by evaluating sera collected over many years.
The pathogenesis of BPH is also not completely understood. Contrary to the study by Hulka et al.,[34] Gann et al.[36] failed to show any relation between circulating androgen levels and BPH. On the other hand, a number of studies show improvement in symptoms of patients with BPH when treated with anti-androgens. Finasteride, a 5α reductase inhibitor, has been shown to statistically significantly decrease the size of the prostate,[37] especially in those men who have gland size > 40ml atbaseline.[38] Treatment with other anti-androgens such as flutamide and the gonadotropin releasing hormone (GnRH) agonist nafarelin, have shown similar results.[39,40]
Although it is known that the clinical course of prostate cancer is accelerated by testosterone, its incidence is not increased by its administration.41 The other way to put it would be that testosterone does not cause prostate cancer. There is even no clear evidence that testosterone replacement accel-erates the development of BPH.[42] A recent study showed no symptoms of bladder outlet obstruction in hypogonadal men receiving intramuscular tes-tosterone and followed for 2 years.43 Another study by Tenover[41] in elderly men (mean age 67.5 years) receiving testosterone enanthate 100mg weekly for 3 months, showed no increase in total prostate volume determined by suprapubic ultrasound. Behre et al.[44] showed that men receiving various modalities of testosterone replacement therapy had an increase in prostate size which was comparable with, but not higher than, those in age-matched eu- gonadal men. Another recent study found no abnormal prostate growth in hypogonadal men (aged 21 to 65 years) when treated with transdermal testosterone.45 The mean prostate volume in treated patients was similar to age-matched eugonadal men. The prostate specific antigen (PSA) levels also remained in the normal range. Many other studies have shown no effect of testosterone replacement ther-apy on serum PSA values, changes on prostate ex-amination or prostate volume in elderly men.[46 47]
To summarise, testosterone replacement therapy slightly increases prostate size and increases PSA levels, but they remain within the normal range. However, testosterone therapy remains an absolute contraindication in patients with known prostate cancer (but not for BPH). More long term studies are needed to demonstrate the effect of androgen replacement on benign or malignant growth of the prostate.
2.2Bone
Osteoporosis is a major health problem resulting in more than 1.3 million fractures annually in the US.[48] 20% of all hip fractures occur in men. The hip fracture rates in men increase dramatically after the age of 60 years and double with each decade thereafter. According to the cross-sectional and longitudinal studies, typical bone loss rates for vertebral bone in men (aged 30 to 80 years) have been 1.2 to 2% per year.[49-52] Cortical bone loss is less rapid. Hypogonadism is a well established cause for male osteoporosis[53-55] and a risk factor for fractures.56 Jackson et al.[57] reported testosterone deficiency in 71% of elderly men with hip fractures compared with 32% of controls. Ongphiphadhanakul et al.[58] reported a clear association between decrease in serum free testosterone levels and decline in bone mineral density (BMD) at the femoral neck and Ward’s triangle. Finkelstein et al.[59] showed lower cortical and trabecular bone densities in young hypogonadal men than their age-matched controls. Furthermore, a rapid decline in vertebral bone den-sity after castration or treatment with a GnRH an-alogue illustrates the beneficial role oftestosterone on bone.[60 61] Reversal of hypogonadism is asso-ciated with improvement in bone mass and main-tenance of skeletal integrity.[62]
Loss of bone mass in men becomes more clini-cally significant as they live longer. The work on hypogonadism and male osteoporosis goes back to 1948 when Fuller Albright studied the results of testosterone replacement therapy in a 72-year-old man with osteoporosis. He noted that androgen re-placement resulted in a decline in total calcium ex- cretion.[63] Following in Albright’s footsteps, Laf- ferty treated a 75-year-old osteopenic man with testosterone for 3 months and observed a decrease in urinary calcium excretion and an increase in cal-cium retention.[64]
Oppenheim et al.[65] studied 6 hypogonadal os-teopenic men with a mean age of 61 years. Testos-terone replacement therapy for 6 to 8 months re-sulted in increased spinal BMD in all patients. In her study on 13 elderly men treated with testoster-one enanthate (100 mg/week for 3 months), Ten- over[41] showed significant decline in urinary ex-cretion of hydroxyproline. No changes in serum alkaline phosphatase or osteocalcin levels, or in urinary calcium excretion, were noted in this study. In his 3 -month study, Morley et al.[66] also reported an increase in serum osteocalcin levels in elderly hypogonadal men treated with testosterone. An-other study showed an increase in spinal BMD of 5% and trabecular BMD of 14% in hypogonadal men treated with testosterone.[62] Bone specific al-kaline phosphatase and urinary hydroxyproline levels also decreased significantly.
Behre et al.[68] recently studied the effect of transdermal testosterone on BMD. In this study of 72 hypogonadal men, aged 18 to 74 years, testosterone replacement was given either intramuscularly or transdermally. Significant increases in BMD were seen during the first year of testosterone therapy independent of the route of administration. Long term testosterone therapy maintained BMD in age- dependent reference range. Transdermal testosterone scrotal patches were as effective as intramuscular testosterone in this study.
To summarise, androgens are as important in maintaining BMD in elderly men as they are inyoung hypogonadal men. Long term studies on larger number of elderly men are needed to ascertain whether testosterone replacement therapy can reverse bone loss in this population.
2.3Body Composition
About 50 years ago, Kochakian demonstrated that testosterone increases nitrogen retention in cas-trated male rats.[69] Both cross-sectional and longi-tudinal studies show that aging is accompanied by an increase in upper and central body fat, decreased muscle mass, increased muscle fibrous tissue and decreased muscle strength^70-72 Studies have shown that men with abdominal accumulation of body fat often have low testosterone concentration.73 Marin et al.[74] and Rogers et al.[75] have shown that testosterone induces a decrease in abdominal fat and increases fat free mass male volunteers.
The anabolic effects of androgens have been knownforalongtime.[76] Cell culture studies have shown that androgens stimulate mitosis in myo- blasts.[77-79] In studies of young hypogonadal men, muscle size, strength and lean body mass increase when they are given replacement doses of testos- terone.[80] An increase in muscle protein synthesis, muscle mass and strength is also seen in young eugonadal men given pharmacological doses of testosterone.[81-83]
Several studies in elderly men have evaluated the effect of androgen on body fat, muscle mass and strength. Wang et al.[84 and others showed an increment in lean body mass and leg muscle strength in hypogonadal men after testosterone therapy.[84-86] Brodsky et al.[87] observed an increase in fat free mass, decrease in fat mass and a rise in muscle mass in 5 hypogonadal men on testosterone therapy.
Many studies in elderly men have shown similar results. In a 3 month crossover study of testoster-one replacement in hypogonadal old men (57 to 76 years of age), Tenover[41] demonstrated an increase inbodyweight and leanbody mass with subsequent declines in body fat. Urban et al.[88] showed testos-terone administration increased muscle protein synthesis, muscle strength and mRNA concentra-tion of intramuscular somatomedin-1 in elderly men. In a study by Sih et al.,[89] significant in-creases in upper body strength were seen in elderly hypogonadal men when treated with intramuscular testosterone enanthate for 1 year. The strength was evaluated by measuring hand grip strength. An-other report also showed an increase in muscle functional strength in hypogonadal men (aged 69 to 89 years) on testosterone therapy.[66]
Finally, 2 other studies demonstrated decline in visceral fat with testosterone therapy in patients with acquired hypogonadism[67] and with obesity.[46] Since androgen receptors are present on adipose cells, testosterone may affect adipose metabolism directly by causing increased lipolysis.[90 91]
In summary, the evidence is reasonably robust that testosterone administration in elderly men may decrease body fat, increase muscle mass and enhance skeletal muscle strength. However, whether the increase in muscle strength would be of such magnitude to have a significant clinical impact on patients function and quality of life is a remaining issue.
2.4Lipids
The effect of androgens on the lipid profile is of particular interest amongst physicians because it may explain, in part, the higher prevalence of atherosclerosis and shorter life span of men, relative to women. Epidemiological studies have revealed that high density lipoprotein cholesterol (HDL-C) levels are lower in men and triglyceride (TG) levels are higher compared with premenopausal women.[92 93] In prepubertal children, plasma levels of lipoproteins and TG show no gender difference. In boys during puberty, the HDL-C levels decline, while low density lipoprotein cholesterol (LDL-C) and TG levels increase slightly.[94] After menopause, there is no alteration in HDL-C levels in women, but LDL-C levels rise significantly resulting in a greater incidence of coronary artery disease (CAD) in postmenopausal than premenopausal women.[94] In addition, when young men are given a GnRH antagonist to suppress endogenous testosterone, their mean serum HDL-C levels increase by 20%.[95]
Although all of the above data point towards a negative impact of androgens on lipid profile, Hau- ner et al.[96] showed no significant role of sex ster-oids in the aetiology of CAD in men when assessed angiographically. Barrett-Connor[97] summarised interesting data showing that exogenous testoster-one in physiological doses had no effect onHDL-C levels in clinical trials, while many cross-sectional epidemiological studies find that endogenous tes-tosterone levels are positively associated with HDL-C levels;[98-103]
Data regarding effects of testosterone on cardiovascular risk factors in the elderly are conflicting and few. Administration of non-aromatisable oral androgens like stanozolol or methyltestosterone, cause profound decreases in HDL-C and significant increases in LDL-C.[94] One study showed a 7.6% decrease in HDL-C levels and a 9% rise in the total cholesterol/HDL-C ratio in adult hypogonadal men on testosterone replacement therapy.[104]
Although the above mentioned studies[94 104] re-port adverse effects of testosterone on lipids, other studies suggest otherwise. In one 4-year study in which testosterone cipionate at 25 mg/week was administered intramuscularly, no changes in HDL-, LDL- or total cholesterol were seen.[105] Tenover[41] reported 11% decline in total and LDL cholesterol in elderly hypogonadal men receiving testosterone therapy. Although HDL-C levels also decreased, the decline was insignificant. In their 3 year study, Hajjar et al.[43] also report no increase in angina pectoris, myocardial infarction or strokes in elderly patients on testosterone therapy. Zgliczynski et al.[106] exclusively studied the effects of testoster-one on lipids in hypogonadal men and healthy el-derly men. Testosterone replacement in both groups showed a beneficial effect on lipid metabo-lism as a decline in total cholesterol and athero-genic fractions of LDL-C without significant alter-ations in HDL-C or its subfractions (HDL2-C and HDL3-C).
Cardiovascular disease is a major cause of morbidity and mortality in an elderly population. It is important to study the long term effects of testosterone replacement on plasma lipoproteins and body fat distribution. Only after analysing the incidence of cardiovascular events in elderly men receiving androgens testosterone replacement for extended period, can testosterone replacement be considered safe.
2.5Haematopoiesis
Over the last 3 decades numerous studies have shown that androgens may be beneficial in the treatment of primary anaemias and bone marrow fail- ures.[107] It is a general observation that haemoglobin concentration increases in boys at puberty along with an increase in serum testosterone levels.[108] Adult men also have higher haemoglobin and red blood cell counts than do adult women.[109-110] These differences are not influenced by iron deficiency, pregnancy or blood loss. In addition, hypo- gonadal men have reduced haemoglobin levels compared with their age-matched controls and testosterone replacement restores the level to within the normal range for adult males.[111,112]
With age, haemoglobin and haemocrit (HcT) values decline and mild anaemia is prevalent in elderly men. Healthy older men tend to have slightly lower HcTs than healthy young adult men.[113] This has led many workers to explore the use of testosterone replacement to correct anaemia and also to monitor its complication, mainly polycythemia.
It is well known that testosterone therapy in-creases whole body Hct values.[114] Studies re-viewed by Griggs et al.[82] involving healthy men of different ages supplemented with androgens show a significant increase in Hct. One short term study reported a rise in Hct of up to 7% in hypo- gonadal elderly men receiving testosterone ther- apy.[41] Another long term study in which older men were treated with testosterone for sexual dysfunction for 2 years also demonstrated a increase in Hct.[42] In their study on hypogonadal men, Sih et al.[89] also observed a significant rise in Hct values.
Although a rise in Hct may be beneficial for anaemic patients, polycythemia is a known complication of testosterone therapy.[43] This may have grave consequences in the elderly since increased blood viscosity can result in thromboembolic sequelae such as strokes, and add to cardiac afterload, which an aging heart is not equipped to handle. Hajjar et al.[43] in their study of testosterone therapy in hypogonadal men showed that 24% of the treated individuals developed polycythemia. Phlebotomy and withholding testosterone therapy was required to reverse polycythemia. Another study demonstrated an increase in neurological complications secondary to polycythemia.[115] Drinka et al.[116] have implicated testosterone-induced polycythemia as a risk factor for sleep apnoea in a study on nursing home patients.
Testosterone usually increases the Hct within the normal range, but the risk of polycythemia should always be considered. Since it can add to cardiovascular burden, many authors believe phlebotomy or a decrease in testosterone dose when Hct reaches 51% and to stop treatment if it rises to 54%.[117]
2.6Sexual Function and Cognition
Data on the relationship between androgen lev-els and declining sexual function are conflicting. There is a steady decline in orgasmic frequency and worsening erectile function with aging.[118] In-creased detumescence, decreased vasocongestive responses and an increase in refractory period with aginghave also been reported.[119] Davidson etal.[120] have also shown that there is a decrease in sexual thoughts and enjoyment with age. However, it is important to remember that hypogonadism is the sole cause of erectile dysfunction in only 10% of cases.121 Data on androgen replacement in hypogonadal men reveal that testosterone is necessary for spontaneous erections, normal libido and ejaculation.[122-124] Carani et al.[125] also found that nocturnal erections were substantially less in hypogonadal men in terms of both rigidity and tumescence compared with eugonadal men. Similarly, frequency of ejaculation and ratings of libido significantly increased in patients with hypopituitarism receiving testosterone and gonadotropins compared with those receiving placebo.[126]
One study showed that sexual behaviour is test-osterone dependent and that the individual limit of plasma testosterone level below which sexual be-haviour is impaired lies between 2.0 to 4.5 pg/L.[127] Arver et al.[128] studied the effects of testosterone on sexual function in 37 hypogonadal men aged 21 to 65 years. In this study, patients were treated with intramuscular testosterone, then withdrawn from therapy, and then retreated with transdermal testosterone. During testosterone therapy (both intramuscular and transdermal), the number of erectile events per day, mean duration of events, and mean penile rigidity increased significantly compared with during the testosterone withdrawal period. Furthermore, patients’ libido, arousal, sexual desire, orgasm and satisfaction significantly decreased during testosterone withdrawal and returned with testosterone replacement. Kwan et al.[124] reported similar results, also in hypogonadal men. Recently Morales et al.[129] studied effects of oral testosterone undecanoate on 23 hypogonadal men (aged 30 to 72 years) with impotence. Testosterone replacement produced an improvement in sexual attitudes and performance in 61% of these patients.
Studies have shown an improvement in mood and sense of well being, and decreased anxiety in hypogonadal men receiving testosterone therapy.[130-132] Similarly many studies have reported an increased sense of well being in older men receiving androgen replacement therapy.[46-43] A few reports also report confusion in spatial cognition in the elderly population.[134,135] Janowsky et al.[136] reported that testosterone replacement enhances spatial cognition in elderly men. Similar results were obtained by Orwoll et al.[47] by using transdermal testosterone supplementation in healthy older men. Depression is more prevalent in the elderly population and studies, reviewed by Vogel et al.,[137] have shown that testosterone can has antidepressant properties. However, in their study in men (aged 45 to 74 years) with erectile dysfunction, Schiavi et al.[138] found no effect of biweekly testosterone enanthate administration on the affective state or psychological symptoms.
To summarise, evidence suggests that testosterone therapy in elderly men improves libido and sexual function. It also has a positive effect on spatial cognition and memory.[136]
2.7Sleep Apnoea
Studies investigating androgen replacement and the development of sleep apnoea in the elderly are nonexistent. However, it is known that sleep ap- noea is more common in men than women11391 and is more common in postmenopausal women than premenopausal women.[140] Matsumoto et al.[141] studied the development of obstructive sleep ap- noea (OSA) in 5 hypogonadal men while receiving no therapy and after 6 weeks of intramuscular tes-tosterone enanthate. Hypoxic ventilatory drive de-creased significantly in all patients on testosterone therapy. OSA developed in 1 patient and markedly worsened in another in association with testoster-one administration. There was also a marked de-crease in nocturnal oxygen saturation with the de-velopment of cardiac arrythmias in both these patients.
In summary, the effects of testosterone replace-ment on the development of OSA needs to be stud-ied in elderly men. Since nocturnal arterial desatu-ration is associated with cardiac arrythmias, it may lead to serious consequences in this population be-cause of underlying CAD in many elderly patients.
3.Conclusion
Aging is associated with a decline in Leydig cell mass and free testosterone levels. Parameters such as muscle mass, Hct, and sexual desire and function also decline. Although total testosterone is the best screening test, free testosterone is a better parameter to evaluate elderly men with suspected hypogonadism since total testosterone levels are ef-fected by a rise in SHBG levels with age. Although the number of studies of testosterone replacement in the elderly are limited, an overview of the data favours real potential for androgen therapy in a few areas such as BMD, muscle mass, muscle strength and Hct. Most of the studies also suggest a positive impact on mood and sexual behaviour. Data on the significance of lipid changes with testosterone replacement are conflicting. Although prostate cancer remains an absolute contraindication to testosterone therapy, one can say that testosterone therapy does not cause cancer. Sleep apnoea related to testosterone replacement can result in dire consequences secondary to increased Hct and arrythmias.
Since androgen replacement results in a constel-lation of positive and negative impacts on different body parameters, we do not recommend routine treatment of elderly men with testosterone. How-ever, in elderly men who have manifestations of androgen deficiency and whose serum total testos-terone level is < 300 ng/dl, testosterone adminis-tration is warranted. If treatment is undertaken, the patient should be screened before treatment for Hct and arrythmias, and monitored carefully during therapy.
The development of selective androgen receptor modulators is crucial, since their use may help target areas like bone and muscle tissue while avoiding any hazardous affect on the prostate and lipids. Similarly, it will be useful to explore a combination of testosterone with 5α reductase inhibitors, since DHT is the major androgen in prostate growth. The use of an androgen preparation such as 7α-methyl- 19-nortestosterone, which is aromatised but not 5α reduced, should be also studied in the elderly.
References
Jeffcoate SL, Brocks RV, Lin NY, et al. Androgen production in hypogonadal men. J Endocrinol 1967; 37: 401-11
Wheeler MJ. Determination of bio-available testosterone. Ann Clin Biochem 1995; 32: 345-57
Ekins R. Measurement of free hormones in blood. Endocr Rev 1990; 11: 5-46
Meikel CM. The free hormone hypothesis: a physiologically based mathematical model. Endocr Rev 1989; 10: 232-74
Bremner WJ, Vitiello V, PrinzPN. Loss of circadian rhythmicity in blood testosterone levels with aging in normal men. J Clin Endocrinol Metab 1983; 56: 1278-81
Vermeulen A, Rubens R, Verdonck L. Testosterone secretion and metabolism in male senescence. J Clin Endocrinol Metab 1972; 34: 730-5
Stearns EL, MacDonell JA, Kauffman BJ, et al. Declining testicular function with aging: hormonal and clinical correlates. Am J Med 1974; 57: 761-6
Baker HWG, Burger HG, de Kretser DM, et al. Endocrinology of aging: pituitary testicular axis. Clin Endocrinol (Oxf) 1976; 5: 349-72
Vermeulen A. Androgens in the aging male. J Clin Endocrinol Metab 1991;73:221-4
Gray A, Feldman HA, McKinley JB, et al. Age, disease and changing sex hormone levels in middle-aged men: results of the Massachusetts Male Aging Study. J Clin Endocrinol Metab 1991; 73: 1016-25
Purifoy FE, Koopmans LH, Mayes DM. Age differences in serum androgen levels in normal adult males. Hum Biol 1981; 57: 71
Deslypere JP, Vermeulen A. Leydig cell function in normal men: effect of age, life-style, residence, diet, and activity. J Clin Endocrinol Metab 1984; 59: 955-62
Morley JE, Kaiser FE, Perry IIIHM, et al. Longitudinal changes in testosterone, LH, and FSH in healthy older men. Metabo-lism 1997; 46 (4): 410-3
Harman SM, Tsitouras PD. Reproductive hormones in aging men. I. Measurement of sex steroids, basal luteinizing hormone, and leydig cell response to human chorionic gonadotropin. J Clin Endocrinol Metab 1980; 51: 35-40
Tenover JS, Matsumoto AM, Plymate SR, et al. The effects of aging in normal men on bioavailable testosterone and lutein-izing hormone secretion: response to clomiphine citrate. J ClinEndocrinolMetab 1987;65: 1118-26
Morley JE, Kaiser F, Raum WJ, et al. Potentially predictive and manipulable blood serum correlates of aging in the healthy human male: progressive decreases in bioavailable testosterone, dehydroepiandrosterone sulfate, and the ratio of insulinlike growth factor 1 to growth hormone. Proc Natl Acad Sci 1997; 94: 7537-42
Sniffen RC. The testes. I. The normal testes. Arch Pathol 1950; 50: 259-84
Tillinger KG. Testicular morphology. Acta Endocrinol Suppl (Copenh) 1957; Suppl. 30: 1-192
Harbitz TB. Morphometric study ofLeydig cells in elderly men with special reference to the histology of the prostate. Acta PatholMicrobiol Scand 1973; 81: 301-13
Neaves WB, Johnson L, Porter JC, et al. Leydig cell numbers, daily sperm production and serum gonadotrophin levels in aging men. J Clin Endocrinol Metab 1984; 59: 756-63
Sasano M, Ishyo S. Vascular patterns of the human testes with special reference to its senile changes. Tohoku J Exp Med 1969; 99: 269-80
Suoranta H. Changes in small blood vessels of the adult human testes in relation to age and some pathological conditions. Virchows Arch Pathol Anat Physiol Klin Med 1971; 352: 765-81
Vermeulen A, Desylpere JP. Intratesticular unconjugated steroids in elderly men. J Steroid Biochem 1986; 24: 1079-89
Desylpere JP, Vermeulen A. Leydig cell function in normal men: effect ofage, lifestyle, residence, diet and activity. J Clin Endocrinol Metab 1989; 68: 68-72
Vermeulen A, Desylpere JP, Kaufman JM. Influence of antiopioids and luteinizing hormone pulsatility in aging men. J Clin Endocrinol Metab 1989; 68: 68-72
Winters SJ, Sherins RJ, Troen P The gonadotropin suppressive activity of androgens is increased in elderly men. Metabolism 1984; 33: 1052-9
Desylpere JP, Kaufman JM, Vermeulen T, et al. Influence ofage on pulsatile luteinizing hormone release and responsiveness of the ganadotrophs to sex hormone feedback in men. J Clin Endocrinol Metab 1987; 64: 68-73
McConnell JD. Prostatic growth: new insights into hormonal regulation. Br JUrol 1995; 76 Suppl. 1: 5-10
Horton R. Benign prostatic hyperplasia: a disorder ofandrogen metabolism in the male. J Am Geriatr Soc 1984; 32: 380-85
Wilson JD. Recent studies on the mechanism of action of testosterone. N Engl J Med 1972; 287: 1284-94
Rogers C, Coffey D, Cunha G, et al. Benign prostatic hyperplasia. Vol. II. Bethesda (MD): US Department of Health and Human Service. NIH publication no: 87-2881
McConnell JD. The pathophysiology of BHP J Androl 1991; 12: 356-63
Liao S, Fang S. Receptor proteins for androgens and the mode of action of androgens on gene transcription in ventral prostate. Vitam Horm 1969; 27: 17-26
Hulka BS, Hammond JE, DiFerdinando G, et al. Serum hormone levels among patients with prostatic carcinoma or benign prostatic hyperplasia and clinic controls. Prostate 1987; 11: 171-82
Carter HB, Pearson JD, Metter EJ, et al. Longitudinal evaluation of serum androgen levels in men with and without prostate cancer. Prostate 1995; 27: 25-31
Gann PH, Hennekens CH, Longcope C, et al. A prospective study of plasma hormone levels, nonhormonal factors, and development of benign prostatic hyperplasia. Prostate 1995; 26: 40-9
McConnell JD, Wilson JD, George FW, et al. Finasteride, an inhibitor of 5alpha reductase, suppresses prostatic dihydro-testosterone in men with benign prostatic hyperplasia. J Clin Endocrinol Metab 1992; 74: 505-8
Ekman P Arisk benefit assessment of treatment with Finasteride in benign prostatic hyperplasia. Drug Saf 1998; 18 (3): 161-70
Stone NN, Clejan SJ. Response of prostate volume, prostatespecific antigen, and testosterone to flutamide in men with benign prostatic hyperplasia. J Androl 1991; 12: 376-80
Peters CA, Walsh PC. The effect of nafarelin acetate, a lutein-izing-hormone-releasing hormone agonist, on benign prostatic hyperplasia. N Engl J Med 1987; 317: 599-604
Tenover JS. Effects of testosterone supplementation in the aging male. J Clin Endocrinol Metab 1992; 75: 1092-8
Hartnell J, Korenman SG, Viosca SP Results of testosterone enanthate therapy for hypogonadism in older men. Proceedings of the 72nd Annual Meeting of The Endocrine Society; 1990 Jun; 428
Hajjar RR, Kaiser FE, Morley JE. Outcomes of long-term testosterone replacement in older hypogonadal males: a retro-spective analysis. J Clin Endocrinol Metab 1997; 82: 3793-6
Behre HM, Bohmeyer J, Nieschlag E. Prostate volume in testosterone treated and untreated hypogonadal men in comparison to age-matched normal controls. Clin Endocrinol 1994; 40: 341-9
Meikle AW, Arver S, Dobs AS, et al. Prostate size in hypogonadal men treated with a nonscrotal permeation- enhancedtestosteronetransdermal system. Urology 1997; 49: 191-6
Marin P, Holmang S, Gustafsson C, et al. Androgen treatment of abdominally obese men [abstract]. Obes Res 1993; 1: 245
Orwoll E, Oviatt S, Biddle J, et al. Transdermal testosterone supplementation in normal older men [abstract no. 1071]. Programs and Abstracts of the 74th Annual Meeting of the Endocrine Society; 1992 Jun 24-27; San Antonio, 319
Melton IIILJ. Epidemiology of fractures. In: Riggs BL, Melton III LJ, editors. Osteoporosis, etiology, diagnosis, and man-agement. New York: Raven Press, 1988: 133-54
Genant HK, Cann CE, Pozzi-Mucelli S, et al. Vertebral mineral determination by quantitative CT: clinical feasibility and nor-mative data [abstract]. J Comput Assist Tomogr 1981; 7: 554
Meier DE, Orwoll ES, Jones JM. Marked disparity between trabecular and cortical bone loss with age in healthy men. Ann InternMed 1984; 101: 605-12
Riggs BL, Wahner HW, Dunn WL, et al. Differential changes in bone mineral density of the appendicular and axial skeleton with aging: relationship to spin osteoporosis. J Clin Invest 1981; 67: 328-35
Orwoll ES, Oviatt S, McClung MR, et al. The rate of bone mineral loss in normal men and the effects of calcium and cholecalciferol supplementation. Ann Intern Med 1990; 112: 29-34
Drinka PJ, Bauwens SF. Male osteopenia: a brief review. J Am GeriatrSoc 1987;35:258-61
Seeman E, Melton LJ, O’Fallon WM, et al. Risk factors for spinal osteoporosis in men. Am J Med 1983; 75: 977-83
Smith DAS, Walker MS. Changes in plasma steroids and bone density in Klinefelter’s syndrome. Calcif Tissue Res 1977; 22: 225-8
Lewinnek GE, Kelsey J, White AA, et al. The significance and a comparative analysis of the epidemiology of hip fractures. Clin Orthoped 1980; 152: 35-43
Jackson JA, Riggs MW, Spiekerman AM. Testosterone deficiency as a risk factor for hip fractures in men: a case-control study. Am J Med Sci 1992; 304 (1): 4-8
Ongphiphadhanakul B, Rajatanavin R, Chailurkit L, et al. Serum testosterone and its relation to bone mineral density and body composition in normal males. Clin Endocrinol 1995; 43: 727-33
Finkelstein JS, Klibanski A, Neer RM, et al. Increases in bone density during treatment of men with idiopathic hypogo- nadotropic hypogonadism. J Clin Endocrinol Metab 1989; 69: 776-83
Goldray D, Weisman Y, Jaccard N, et al. Decreased bone density in elderly men treated with gonadotropin-releasing hormone agonist decapeptyl (D-Trp6-GnRH). J Clin Endocrinol Metab 1993; 76: 288-90
Stepan JJ, Lachman M, Zverina J, et al. Castrated men exhibit bone loss: effect of calcitonin treatment on biochemical indices of bone remodelling. J Clin Endocrinol Metab 1989; 69: 523-7
Greenspan SL, Oppenheim DS, Klibanski A. Importance ofgo-nadal steroids to bone mass in men with hyperprolactinemic hypogonadism. Ann Intern Med 1989; 110: 526-31
Albright F, Reifenstein EC. Metabolic bone disease: osteoporosis. In: Williams, editor. The parathyroid glands and metabolic bone disease. Baltimore (MD): Williams and Wilkins, 1948: 145
Lafferty FW, Spencer GE, Pearson OH. Effects of androgens, estrogens and high calcium intakes on bone formation and resorption in osteoporosis. Am J Med 1964; 36: 514-28
Oppenheim D, Klibanski A. Osteopenia in men with acquired hypogonadism: improvement with testosterone replacement [abstract no. 585]. Programs and Abstracts of the 71st Meeting of The Endocrine Society; 1989 Jun: 289
Morley JE, Perry HM, Kaiser FE, et al. Effects oftestosterone replacement therapy in old hypogonadal males: a preliminary study. J Am Geriatr Soc 1993; 41: 149-52
Katznelson L, Finkelstein JS, Schoenfeld DA, et al. Increase in bone density and lean body mass during testosterone admin-istration in men with acquired hypogonadism. J Clin Endocrinol Metab 1996; 81: 4358-65
Behre HM, Kliesch S, Leifke E, et al. Long-term effect oftes-tosterone therapy on bone mineral density in hypogonadal men. J Clin Endocrinol Metab 1997; 82: 2386-90
Kochakian CD. Comparison of protein anabolic property ofvar-ious androgens in the castrated rat. Am J Physiol 1950; 60: 553-8
Forbes GB, Reina JC. Adult lean body mass declines with age: some longitudinal observations. Metabolism 1970; 19: 653-63
Kallman DA, Plato CA, Tobin JD. The role of muscle loss in the age-related decline of grip strength: cross-sectional and longitudinal perspectives. J Gerontol 1990; 45: M82-8
Shimokata H, Tobin JD, Muller DC, et al. Studies in the distribution of body fat. I. Effects of age, sex, and obesity. J Gerontol 1989; 44: M66-73
Seidell JC, Bjorntorp P, Sjostrom L, et al. Visceral fat accumulation in men is positively associated with insulin, glucose and C-peptide levels, but negatively with testosterone levels. Me-tabolism 1990; 39: 897-901
Marin P, Oden B, Bjorntop P. Assimilation and mobilization of triglycerides in subcutaneous abdominal and femoral adipose tissue in vivo in men: effects of androgens. J Clin Endocrinol Metab 1995; 80: 239-43
Rogers MA, Evans WJ. Changes in skeletal muscle with aging: effects of exercise training. Exerc Sport Sci Rev 1993; 21: 65-102
Spencer H, Lewin I, Friedland JA. Actions of androgens and related substances on mineral metabolism and bone [abstract]. Pharmacol Ther 1976; 1: 207
Bergamini E. Testosterone and sugar transport in levator ani muscle of rat. Biochim Biophys Acta 1969; 193: 193-202
Breuer CB, Florini JR. Effects of ammonium sulphate, growth hormone and testosterone propionate on ribonucleic acid polymerase and chromatin activities in rat skeletal muscle. Biochemistry 1966; 5: 3857-65
Powers ML, Florini JR. A direct effect of testosterone on muscle cells in tissue culture. Endocrinology 1975; 97: 1043-7
Bhasin S, Storer TW, Berman N, et al. Anabolic effects of androgens: testosterone increases lean body mass, muscle size and strength in hypogonadal men [abstract]. The 19th Annual Meeting of the American Society of Andrology; 1994 Nov: 40
Friedl KE, Dettori JR, Hannan CJ, et al. Comparison of the effects of high dose testosterone and 19-nortestosterone to a replacement dose of testosterone on strength and body com-position in normal men. J Steroid Biochem Molec Biol 1991; 40: 607-12
Griggs RC, Kingston W, Jozefowics RF, et al. Effect oftestos-terone on muscle mass and muscle protein synthesis. J Appl Physiol 1989; 66:498-503
Young NR, Baker HWG, Liu G, et al. Body composition and muscle strength in healthy men receiving testosterone enanth- ate for contraception. J Clin Endocrinol Metab 1993; 77: 1028-32
Wang C, Eyre DR, Clark R, et al. Sublingual testosterone replacement improves muscle mass and strength, decreases bone resorption, and increases bone formation markers in hypogonadal men: a clinical research center study. J Clin En-docrinol Metab 1996; 81: 3654-62
Bhasin S, Storer T, Strakora J, et al. Testosterone increases lean body mass, muscle size and strength in hypogonadal men [abstract]. Clin Res 1994; 42: 74A
Wong FHW, Pun KK, Wang C. Loss of bone mass in patients with Kleinfelter’s syndrome despite sufficient testosterone re-placement. Osteoporos Int 1993; 7: 281-7
Brodsky IG, Balagopal P, Nair KS. Effects of testosterone replacement on muscle mass and muscle protein synthesis in hypogonadal men: a clinical research study. J Clin Endocrinol Metab 1996; 81: 3469-75
Urban RJ, Bodenburg YH, Gilkison C, et al. Testosterone administration to elderly men increases skeletal muscle strength and protein synthesis. Am J Physiol 1995; 269: E820-26
Sih R, Morley JE, Kaiser FE, et al. Testosterone replacement in older hypogonadal men: a 12-month randomised controlled trial. J Clin Endocrinol Metab 1997; 82: 1661-7
De Pergola G, Xu X, Yang S, et al. Upregulation of androgen receptor binding in male rat fat adipose precursor cells exposed to testosterone: study in a whole cell assay system. J Steroid Biochem Mol Biol 1990; 37: 553-8
Xu X, De Pergola G, Bjorntorp P. The effects of androgens on the regulation oflipolysis in adipose precursor cells. Endocri-nology 1990; 126: 1229-34
US Department of Health, Education and Welfare. The prevalence study. In: Lipid Research Group. The Lipids Research Clinics population studies data book. Vol. 1. Bethesda (MD): US Department of Health, Education and Welfare, 1979. NIH publication no: 79-1527
Heiss G, Johnson NJ, Reiland S, et al. The epidemiology of plasma high density lipoproteins cholesterol levels. Circula-tion 1980; 62 Suppl. 4: 116
Bagatell CJ, Bremner WJ. Androgen and progestagen effects on plasma lipids. Prog Cardiovasc Dis 1995; 38: 255-71
von Eckardstein A, Kliesch S, Nieschlag E, et al. Suppression of endogenous testosterone in young men increases serum levels of high density lipoprotein subclass lipoprotein A-1 and lipoprotein(a). J Clin Endocrinol Metab 1997; 82: 3367-72
Hauner H, Stangl K, Burger K, et al. Sex hormone concentrations in men with angiographically assessed coronary artery disease: relationship to obesity and body fat distribution. Klin Wochenschr 1991; 69 (14): 664-8
Barrett-Connor EL. Testosterone and risk factors for cardiovascular disease in men. Diabete Metab 1995; 21 (3): 156-61
Dai WS, Gutai JP, Kuller LH, et al. Relation between plasma high-density lipoprotein cholesterol and sex hormone con-centrations in men. Am J Cardiol 1984; 53 (9): 1259-63
Zmuda JM, Cauley JA, Kriska A, et al. Longitudinal relation between endogenous testosterone and cardiovascular disease risk factors in middle-aged men: a 13-year follow-up of former Multiple Risk Factor Intervention Trial participants. Am J Epidemiol 1997; 146 (8): 609-17
Zhao Sp, Li XP. The association of low plasma testosterone level with coronary artery disease in Chinese men. Int J Cardiol 1998; 63 (2): 161-4
Barrett-Connor E. Lower endogenous androgen levels and dys-lipidemia in men with non-insulin-dependent diabetes melli-tus. Ann Intern Med 1992; 117(10): 807-11
Khaw KT, Barrett-Connor E. Endogenous sex hormones, high density lipoprotein cholesterol, and other lipoprotein fractions in men. Arterioscler Thromb 1991; 11 (3): 489-94
Freedman DS, O’Brian TR, Flanders WD, et al. Relation of serum testosterone levels to high density lipoprotein choles-terol and other characteristics in men. Arterioscler Thromb 1991; 11 (2): 307-15
Arver S, Dobs AS, Meikle AW, et al. Long-term efficacy and safety of a permeation-enhanced testosterone transdermal system in hypogonadal men. Clin Endocrinol 1997; 47: 727-37
Ellvin FM, Plunkett-Reid K, Rumilla AE. The long-term beneficial effect of low-dose testosterone in the aging male [ab-stract]. Proceedings of the 79th Annual Meeting of the Endocrine Society: 1997 Jun 11-14; Minneapolis, 236
Zgliczynski S, Ossowski M, Slowinska-Srzednicka J, et al. Effect of testosterone replacement therapy on lipids and lipo-proteins in hypogonadal and elderly men. Arteriosclerosis 1996; 121(1): 35-43
Gardner FH, Besa EC. Physiologic mechanisms and the hema-topoeitic effects of the androstanes and their derivatives. Curr Top Hematol 1983; 4: 123-95
Krabbe S, Christensen T, Worm J, et al. Relationship between
haemoglobin and serum testosterone in normal children and adolescents and in boys with delayed puberty. Acta Paediatr Scand 1978; 67: 655-8
Vahlquist B. The cause of the sexual differences in erythrocyte, hemoglobin and serum iron levels in human adults. Blood 1950; 5: 874-5
Williamson CS. Influence of age and sex on hemoglobin: a spectrophotometric analysis of nine hundred and nineteen cases. Arch Intern Med 1916; 18: 505-28
McCullagh EP, Jones R. Effect of androgens on blood counts of men. J Clin Endocrinol 1942; 2: 243-51
Hamilton JB, Bunch LD, Mestler GE, et al. Effect of castration in men upon blood sedimentation rate, hematocrit and hemo-globin. J Clin Endocrinol Metab 1964; 24: 506-11
Garry PJ, Goodwin JS, Hunt WC. Iron status and anemia in the elderly: new findings and a review ofprevious studies. J Am GeriatrSoc 1983;31:389-99
Kennedy BJ, Gilbertsen AS. Increased erythropoiesis induced by androgenic hormone therapy. N Engl J Med 1957; 256: 719-26
Krauss DJ, Taub HA, Lantinga LJ, et al. Risks of blood volume changes in hypogonadal men treated with testosterone en- anthate for erectile impotence. JUrol 1991; 146: 1566-70
Drinka PJ, Jochen AL, Cuisinier M, et al. Polycythemia as a complication of testosterone replacement therapy in nursing home men with low testosterone levels. J Am Geriatr Soc 1995; 43: 899-901
Bhasin S, Bagatell CJ, Bremner WJ, et al. Issues in testosterone replacement in older men. J Clin Endocrinol Metab 1998; 83: 3435-48
Morley JE, Kaiser FE. Sexual function with advancing age. Med Clin North Am 1989; 73: 1483-95
Bhasin S. Androgen treatment of hypogonadal men. J Clin Endocrinol Metab 1992; 74: 1221-5
Davidson JM, Chen JJ, Crapo L, et al. Hormonal changes and sexual function in aging men. J Clin Endocrinol Metab 1983; 57: 71-7
Feldman HA, Goldstein I, Hatzichristou DG, et al. Impotence and its medical and psychological correlates: results of the Massachussetts Male Aging Study. JUrol 1994; 151: 54-61
Bancroft J, Wu FCW. Changes in erectile responsiveness during androgen replacement therapy. Arch Sex Behav 1983; 12: 59-66
Davidson JM, Camargo CA, Smith ER. Effects of androgen on sexual behavior in hypogonadal men. J Clin Endocrinol Metab 1979; 48: 955-8
Kwan M, Greenleaf WJ, Mann J, et al. The nature of androgen action on male sexuality: a combined laboratory-self report study in hypogonadal men. J Clin Endocrinol Metab 1983; 57: 557-62
Carani C, Bancroft J, Granata A, et al. Testosterone and erectile function, nocturnal penile tumescence and rigidity, and erectile response to visual erotic stimuli in hypogonadal and eugonadal men. Psychoneuroendocrinology 1992; 17 (6): 647-54
Clopper RR, Voorhess ML, MacGillivray MH, et al. Psychosexual behavior in hypopituitary men: a controlled comparison of gonadotropin and testosterone replacement. Psycho-neuroendocrinology 1993; 18 (2): 149-61
Salmimies P, Kockott G, Pirke KM. Effects of testosterone replacement on sexual behavior in hypogonadal men. Arch Sex Behav 1982; 11 (4): 345-53
Arver S, Dobs AS, Meikle AW, et al. Improvement of sexual function in testosterone deficient men treated for one year with a permeation enhanced testosterone transdermal system. JUrol 1996; 155: 1604-8
Morales A, Johnston B, Heaton JPW, et al. Testosterone supplementation for hypogonadal impotence: assessment of bio-chemical measures and therapeutic outcomes. J Urol 1997; 157: 849-54
Burris AS, Banks SM, Carter CS, et al. Along term, prospective study of the physiologic and behavioral effects of hormone replacement in untreated hypogonadal men. J Androl 1992; 13: 297-304
Nielson J, Pelsen B, Sorensen K. Follow-up of 30 Klinefelter males treated with testosterone. Clin Genet 1988; 33: 262-9
O’Carroll R, Shapiro C, Bancroft J. Androgens, behavior and nocturnal erection in hypogonadal men: the effects of varying the replacement dose. Clin Endocrinol 1985; 23: 527-38
Albeaux-Fernet M, Bohler CC, Karpas AE. Testicular function in the aging male. In: Greenblatt RB, editor. Aging-geriatric endocrinology. Vol 5. New York: Raven Press, 1978: 210
Benton AL, Eslinger PJ, Danasio AR. Normative observations on neuropsychological test performance in old age. J Clin Neuropsychol 1981; 3: 33-42
Koss E, Haxby JW, DeCarli C, et al. Patterns of performance preservation and loss in healthy aging. Dev Psychol 1991; 7: 99-107
Janowsky JS, Oviatt SK, Carpenter JS, et al. Testosterone administration enhances spatial cognition in older men [abstract no. 340.12]. Programs and Abstracts of the Society for Neu-roscience Annual Meeting; 1991 Nov: 868
Vogel W, Klaiber EL, Broverman DM. The role of the gonadal steroid hormones in psychiatric depression in men and women. Prog Neuropsychopharmacol 1978; 2: 487-90
Schiavi RC, White D, Mandeli J, et al. Effect of testosterone administration on sexual behaviour and mood in men with erectile dysfunction. Arch Sex Behav 1997; 26 (3): 231-41
Block AJ, Boysen PG, Wynne JW, et al. Sleep apnea, hypopnea and oxygen desaturation in normal subjects: a strong male predominance. N Engl J Med 1979; 300: 513-7
Block AJ, Wynne JW, Boysen PG. Sleep-disordered breathing and nocturnal oxygen desaturation in postmenopausal women. Am J Med 1980; 69: 75-9
Matsumoto AM, SandblomRE, SchoeneRB, etal. Testosterone replacement in hypogonadal men: effects on obstructive sleep apnoea, respiratory drives, and sleep. Clin Endocrinol 1985; 22 (6): 713-21