Bone Density

Male and female patients face bone-density issues. Calcium is not the solitary answer, since it cannot be deposited or stored without the correct hormonal milieu. Other factors play a role in bone density, such as nutrition, exercise, lifestyle choices (cigarettes, excessive alcohol), family history, race (Caucasian, Hispanic and Asian). Review current research and medical articles on bone density to offer your patients a wider prospective.


Mortality Greater for Hip Fracture Than Breast Cancer in Elderly Women.pdf

Older women are at greater risk for death after hip fracture than after breast cancer, according to a presentation at the American Geriatrics Society (AGS) annual meeting held in Seattle, Washington. The investigators suggest that increased awareness of mortality associated with hip fracture is needed to improve preventive measures.
Barclay, L. (2007, May 18). Mortality greater for hip fracture than breast cancer in elderly women [Electronic version]. Medscape Medical News. Retrieved May 31, 2007.

Once-Yearly Zoledronic Acid for Treatment of Postmenopausal Osteoporosis.pdf

In this double-blind, placebo-controlled trial, 3889 patients (mean age, 73 years) were randomly assigned to receive a single 15-minute infusion of zoledronic acid (5 mg) and 3876 were assigned to receive placebo at baseline, at 12 months, and at 24 months; the patients were followed until 36 months. It concluded that once-yearly infusion of zoledronic acid during a 3-year period significantly reduced the risk of vertebral, hip, and other fractures.
Black, D.M., Delmas, P.D., Eastell, R., Reid, I.R., Boonen, S., Cauley, J.A., et al. (2007). Once-yearly zoledronic acid for treatment of postmenopausal osteoporosis [Electronic version]. The New England Journal of Medicine, 356(18), 1809-1822. Retrieved May 14, 2007.

Endogenous Hormones, Muscle Strength, and Risk of Fall-Related Fractures in Older Women.pdf

This study showed that in 75-year-old women higher serum estradiol concentration and greater muscle strength were independently associated with a low incidence of fall-related limb fractures even after adjustment for bone density. Our results suggest that hormonal status and muscle strength have their own separate mechanisms protecting from fall-related fractures. This finding is of importance in developing preventive strategies, but calls for further study.
Sipila, S., Heikkinen, E., Cheng, S., Suominen, H., Saari, P., Kovanen, V., et al. (2006). Endogenous hormones, muscle strength, and risk of fall-related fractures in older women [Electronic version]. The Journals of Gerentology, Series A, Biological Sciences and Medical Sciences, 61(1), 92-96. Retrieved May 14, 2007.

Don’t Call it Male Menopause.pdf

As men start to age, their bodies also start to undergo major changes. They don't get hot flashes, but they do experience hormonal, physiological and chemical shifts that can affect many aspects of their lives. This article suggests that you can call it aging; just don't call it male menopause.
Yara, S. (2006, September 28). Don’t call it male menopause [Electronic version]. Forbes.com Website. Retrieved May 2, 2007.

NAMS Updates Recommendations on Diagnosis and Management of Osteoporosis in Postmenopausal Women.pdf

To address the need for standards of care as they relate to menopause-associated health conditions, the North American Menopause Society (NAMS) has updated its evidence-based guidelines on the diagnosis, prevention, and treatment of osteoporosis in postmenopausal women. The full report was published in the May/June 2006 issue of Menopause.
Armstrong, C. (2006, November 1). NAMS updates recommendations on diagnosis and management of osteoporosis in postmenopausal women [Electronic version]. American Family Physician, 74(9). Retrieved November 2, 2006.

New Studies Point to Effects of Growth Hormone on Osteoporosis and Amino Acid Levels on Hip Fracture Risk.pdf

The administration of growth hormone improves the sensitivity of women with osteoporosis to their own circulating parathyroid hormone, leading to an increase in bone formation and an improvement in bone mineral balance, according to a new study released at ENDO 2006, the 88th Annual Meeting of The Endocrine Society. The research may lead the way to improved treatment for women who are endangered by thinning bones.
(2006, June 27). New studies point to effects of growth hormone on osteoporosis and amino acid levels on hip fracture risk [Electronic version]. The Endocrine Society. Retrieved July 18, 2006.

Risk Factors of Cardiovascular Disease in GH-Deficient Adults with Hypopituitarism: A Preliminary Report.pdf

This study concluded that an atherogenic lipid profile, insulin resistance, obesity, and increased body and trunk fat in GHD adults may cause the higher risk of cardiovascular disease in these patients. GHD adults should receive human recombinant GH along with conventional replacement therapy. This may be a useful method in protecting against early onset of atherosclerosis, metabolic disturbances, and osteoporosis, especially in young patients.
Bohdanowicz-Pawlak, A., Szymczak, J., Bladowska, J., Bednarek-Tupikowska, G., Bidzinska, B. & Milewicz, A. (2006). Risk factors of cardiovascular disease in GH-deficient adults with hypopituitarism: a preliminary report [Electronic version]. Medical Science Monitor, 12(2), CR75-80. Epub January 26, 2006. Retrieved November 14, 2006.

Prevalence of Hypogonadism in Males Aged at Least 45 Years: The HIM study.pdf

According to this study, based on TT concentration, the prevalence of hypogonadism in men reporting to primary care offices was estimated to be 38.7%. The medical conditions that occurred significantly more frequently among hypogonadal men than eugonadal men included increased BMI, hypertension, hyperlipidaemia, diabetes, and asthma or COPD. As men age, they are susceptible to conditions that share many of the same symptoms similar to hypogonadism. The presence of these conditions may, in effect, mask underlying hypogonadism and negatively impact quality of life.
Mulligan, T., Frick, M.F., Zuraw, Q.C., Stemhagen, A. & McWhirter, C. (2006). Prevalence of hypogonadism in males aged at least 45 years: the HIM study [Electronic version]. International Journal of Clinical Practice, 60(7), 762-769. Retrieved November 27, 2006.

DHEA in Elderly Women and DHEA or Testosterone in Elderly Men.pdf

This study concluded that neither DHEA nor low-dose testosterone replacement in elderly people has physiologically relevant beneficial effects on body composition, physical performance, insulin sensitivity, or quality of life.
Nair, K.S., Rizza, R.A., O'Brien, P., Dhatariya, K., Short, K.R., Nehra, A., et al. (2006). DHEA in elderly women and DHEA or testosterone in elderly men [Electronic version]. The New England Journal of Medicine, 355(16), 1647-1659. Retrieved November 27, 2006.

Experts Consider HT for Younger Women.pdf

Questions still persist after the release of the July 2002 Women’s Health Initiative findings regarding hormone therapy.  Researchers have been looking at the data to see if certain changes in dosage or initiation age could still provide benefits to women.
Elliott, V.S., (2005, February 28). Experts consider HT for younger women [Electronic version]. American Medical News, pp. 19-20.  Retrieved April 28, 2005.

Study Links Fat Distribution and Not Body Weight as an Indicator of Cardiovascular Disease Risk.pdf

GE Healthcare, a unit of General Electric Company (NYSE: GE), announced that the company’s Lunar Prodigy bone density system was used in a groundbreaking study to evaluate body composition and fat distribution in the body as an important indicator of risk of cardiovascular disease.  The study was presented at the 27th Annual Meeting of the American Society for Bone and Mineral Research meeting in Nashville, TN, September 23-27.
(2005, September 23). Study links fat distribution and not body weight as an indicator of cardiovascular disease risk [Electronic version]. (PDF)

GE Healthcare Announces Most Extensive Body Composition Reference Database in China.pdf

GE Healthcare, a unit of General Electric Company (NYSE: GE), announced that the company has developed the most extensive body composition reference database to evaluate total body composition in Chinese women. The reference database provides improved confidence for Chinese physicians in evaluating clinical conditions such as obesity, eating disorders, diseases that cause muscle wasting, and conditions that may increase the risk of diabetes and heart disease. The new reference database was presented at the 27th Annual Meeting of the American Society for Bone and Mineral Research meeting in Nashville, TN September 23-27.
(2005, September 23). GE Healthcare announces most extensive body composition reference database in China [Electronic version]. (PDF)

Hormone Therapy Reduces Fracture Risk.pdf

A positive link between hormone replacement therapy (HRT) and the reduction of risk for bone fractures in postmenopausal women was recently discovered by British researchers. This article summarizes their findings, published in the Journal of the American Medical Association (JAMA), revealing the significant increase in protection against bone fracture for women using hormone replacement therapy (HRT).
Gordon, S. (2004, May 11). Hormone therapy reduces fracture risk [Electronic version]. HealthDay News. Retrieved June 15, 2004.

Exogenous Testosterone or Testosterone with Finasteride Increases Bone Mineral Density in Older Men with Low Serum Testosterone.pdf

The results of this study demonstrate that T therapy in older men with low serum T increases vertebral and hip BMD over 36 months, both when administered alone and when combined with F. This finding suggests that dihydrotestosterone is not essential for the beneficial effects of T on BMD in men. In addition, the concomitant administration of F with T appears to attenuate the impact of T therapy on prostate size and PSA and might reduce the chance of benign prostatic hypertrophy or other prostate-related complications in older men on T therapy. These findings have important implications for the prevention and treatment of osteoporosis in older men with low T levels.
Amory, J.K., Watts, N.B., Easley, K.A., Sutton, P.R., Anawalt, B.D., Matsumoto, A.M., et al. (2004). Exogenous testosterone or testosterone with finasteride increases bone mineral density in older men with low serum testosterone [Electronic version]. The Journal of Clinical Endocrinology and Metabolism, 89(2), 503-510. Retrieved November 21, 2005.

Effects of Conjugated Equine Estrogen in Postmenopausal Women with Hysterectomy: The Women's Health Initiative Randomized Controlled Trial.pdf

According to this study, the use of CEE increases the risk of stroke, decreases the risk of hip fracture, and does not affect CHD incidence in postmenopausal women with prior hysterectomy over an average of 6.8 years. A possible reduction in breast cancer risk requires further investigation. The burden of incident disease events was equivalent in the CEE and placebo groups, indicating no overall benefit. Thus, CEE should not be recommended for chronic disease prevention in postmenopausal women.
Anderson, G.L., Limacher, M., Assaf, A.R., Bassford, T., Beresford, S.A., Blac,, H., et al. (2004). Effects of conjugated equine estrogen in postmenopausal women with hysterectomy: the Women's Health Initiative Randomized Controlled Trial [Electronic version]. The Journal of the American Medical Association, 291(14), 1701-1712. Retrieved November 21, 2005.

Safety and Adverse Effects of Androgens: How to Counsel Patients.pdf

In short-term clinical trials of androgen replacement in women, several benefits have been shown, including improved libido, bone mineral density and body composition.  While androgen therapy for women is relatively new, it is receiving more attention.
Basaria, S. & Dobs, A.S. (2004). Safety and adverse effects of androgens: how to counsel patients [Electronic version]. Mayo Clinic Proceedings, 79(4 Suppl.), S25-32. Retrieved May 18, 2005.

Formulations and Use of Androgens in Women.pdf

The use of androgen therapy for postmenopausal women is discussed in this article. It suggests that the goal of androgen treatment should be to achieve normal premenopausal levels of testosterone, thus limiting adverse effects and adverse experiences.
Chu, M.C. & Lobo, R.A. (2004). Formulations and use of androgens in women. [Electronic version]. Mayo Clinic Proceedings, 79(4 Suppl.), S3-7. Retrieved May 18, 2005.

The Women’s Health Initiative 2004 – Review and Critique.pdf

This article reviews the published results from the Women’s Health Initiative (WHI) and their various interpretations. The WHI was designed to define the risks and benefits of interventions, notably hormone therapy, to potentially prevent heart disease, breast and colorectal cancer, and osteoporotic fractures in postmenopausal women.
Goldman, J.A. (2004). The Women’s Health Initiative 2004 – Review and Critique [Electronic version]. Medscape General Medicine, 6(3). Retrieved September 27, 2005.

Potential Anabolic Effects of Androgens on Bone.pdf

With the decrease of estrogen at menopause, the need for androgens increases in post-menopausal women.  Androgens also appear to be important for the bone health of women who are pre-menopausal.
Kearns, A.E. & Khosla, S. (2004). Potential anabolic effects of androgens on bone [Electronic version]. Mayo Clinic Proceedings, 79(4 Suppl.), S14-18. Retrieved May 18, 2005.

Review of the Book The Sexy Years: Discover the Hormone Connection: The Secret to Fabulous Sex, Great Health, and Vitality, for Women and Men.pdf

Review by Amazon.com of Suzanne Somers’ book The Sexy Years: Discover the Hormone Connection: The Secret to Fabulous Sex, Great Health, and Vitality, for Women and Men.
Lightner, J. (2004). [Review of the book The sexy years: Discover the hormone connection: the secret to fabulous sex, great health, and vitality, for women and men]. Retrieved September 10, 2004.

Recombinant Human Chorionic Gonadotropin But Not Dihydrotestosterone Alone Stimulates Osteoblastic Collagen Synthesis in Older Men with Partial Age-Related Androgen Deficiency.pdf

In this study, bone resorption was not accelerated during unchanged (DHT) or increased (rhCG) E2 levels, suggesting that minimal E2 levels are needed to maintain stable resorption, although direct androgen receptor-mediated effects cannot be excluded. If androgen supplementation is required for aging men, aromatizable androgens with sufficient endogenous estrogenic activity may have the most beneficial effects on bone.
Meier, C., Liu, P.Y., Ly, L.P., de Winter-Modzelewski, J., Jimenez, M., Handelsman, D.J., et al. (2004). Recombinant human chorionic gonadotropin but not dihydrotestosterone alone stimulates osteoblastic collagen synthesis in older men with partial age-related androgen deficiency [Electronic version]. The Journal of Clinical Endocrinology and Metabolism, 89(6), 3033-3041. Retrieved November 21, 2005.

Risks of Testosterone-Replacement Therapy and Recommendations for Monitoring.pdf

According to this study, hypogonadism affects an estimated 2 million to 4 million men in the United States; its prevalence increases with age. However, it has been estimated that only 5 percent of affected men currently receive treatment. Recent interest in testosterone therapy has been fueled not only by increased medical awareness of the effects of hypogonadism, but also by media attention regarding hormone-replacement therapy in both men and women, the marketing of new topical testosterone formulations, and the desire of "baby boomers" to maintain vigor and health into their more mature years.
Rhoden, E.L. & Morgentaler, A. (2004). Risks of testosterone-replacement therapy and recommendations for monitoring [Electronic version]. The New England Journal of Medicine, 350(5), 482-492. Retrieved September 27, 2005.

Testosterone Treatment Improves Body Composition and Sexual Function in Men with COPD, in a 6-Month Randomized Controlled Trial.pdf

This article concludes that administration of a low-dose testosterone to men with COPD for 26 weeks was associated with improvement of body composition, better erectile function and sexual quality of life. Furthermore, there were no clinical or biochemical side effects.
Svartberg, J., Aasebo, U., Hjalmarsen, A., Sundsfjord, J. & Jorde, R. (2004). Testosterone treatment improves body composition and sexual function in men with COPD, in a 6-month randomized controlled trial [Electronic version]. Respiratory Medicine, 98(9), pp. 906 - 913. Retrieved September 10, 2004.

Effects of Growth Hormone Replacement on Parathyroid Hormone Sensitivity and Bone Mineral Metabolism.pdf

The results of this study demonstrate that GH may have a regulatory role in bone mineral metabolism, and our data provide a possible underlying mechanism for the development of osteoporosis in AGHD patients. The changes observed after GHR may further explain the beneficial effects of GHR on bone mineral density that have consistently been reported.
Ahmad, A.M., Thomas, J., Clewes, A., Hopkins, M.T., Guzder, R., Ibrahim, H., et al. (2003). Effects of growth hormone replacement on parathyroid hormone sensitivity and bone mineral metabolism [Electronic version]. The Journal of Clinical Endocrinology and Metabolism, 88(6), 2860-2868. Retrieved December 7, 2005.

Deterioration of Trabecular Architecture in Hypogonadal Men.pdf

This study concluded that male hypogonadism is associated with marked deterioration of trabecular architecture and to a greater degree than bone densitometry of the spine and hip suggests.
Benito, M., Gomberg, B., Wehrli, F.W., Weening, R.H., Zemel, B., Wright, A.C., et al. (2003). Deterioration of trabecular architecture in hypogonadal men [Electronic version]. The Journal of Clinical Endocrinology and Metabolism, 88(4), 1497-1502. Retrieved December 7, 2005.

Effects of Estrogen Plus Progestin on Risk of Fracture and Bone Mineral Density: The Women's Health Initiative Randomized Trial.pdf

This study demonstrates that estrogen plus progestin increases BMD and reduces the risk of fracture in healthy postmenopausal women. The decreased risk of fracture attributed to estrogen plus progestin appeared to be present in all subgroups of women examined. When considering the effects of hormone therapy on other important disease outcomes in a global model, there was no net benefit, even in women considered to be at high risk of fracture.
Cauley, J.A., Robbins, J., Chen, Z., Cummings, S.R., Jackson, R.D., LaCroix, A.Z., et al. (2003). Effects of estrogen plus progestin on risk of fracture and bone mineral density: The Women's Health Initiative Randomized Trial [Electronic version]. The Journal of the American Medical Association, 290(13), 1729-1738. Retrieved December 7, 2005.

Hormone Replacement Therapy in Rheumatoid Arthritis is Associated with Lower Serum Levels of Soluble IL-6 Receptor and Higher Insulin-Like Growth Factor 1.pdf

The aim of this study was to investigate the effects of HRT on the serum levels of hormones and cytokines regulating bone turnover in 88 postmenopausal women with active rheumatoid arthritis (RA) randomly allocated to receive HRT plus calcium and vitamin D3 or calcium and vitamin D3 alone for 2 years.
D'Elia, H.F., Mattsson, L.A., Ohlsson, C., Nordborg, E. & Carlsten, H. (2003). Hormone replacement therapy in rheumatoid arthritis is associated with lower serum levels of soluble IL-6 receptor and higher insulin-like growth factor 1 [Electronic version]. Arthritis Research & Therapy, 5(4), R202-209. Epub 2003, May 1. Retrieved October 25, 2005.

Growth Hormone Predicts Bone Density in Elderly Women.pdf

According to this study, evidence is accumulating that the risk of osteoporosis may be influenced by environmental factors during intrauterine and early postnatal life; such programming might be mediated through modification of the GH/IGF-1 axis during critical periods in its development.
Dennison, E.M., Hindmarsh, P.C., Kellingray, S., Fall, C.H. & Cooper, C. (2003). Growth hormone predicts bone density in elderly women [Electronic version]. Bone, 32(4), 434-440. Retrieved December 7, 2005.

The Effect of Cessation of Growth Hormone (GH) Therapy on Bone Mineral Accretion in GH-Deficient Adolescents at the Completion of Linear Growth.pdf

These preliminary data suggest that, in adolescent patients with severe GHD, discontinuation of GH at completion of growth may limit the attainment of peak bone mass in this patient group. This may predispose to clinically significant osteopenia in later adult life.
Drake, W.M., Carroll, P.V., Maher, K.T., Metcalfe, K.A., Camacho-Hubner, C., Shaw, N.J., et al.  (2003). The effect of cessation of growth hormone (GH) therapy on bone mineral accretion in GH-deficient adolescents at the completion of linear growth [Electronic version]. The Journal of Clinical Endocrinology and Metabolism, 88(4), 1658-1663. Retrieved December 7, 2005.

American Association of Clinical Endocrinologists Medical Guidelines for Clinical Practice for Growth Hormone Use in Adults and Children -- 2003 Update.pdf

This report is based on a thorough review of published studies of the safety and efficacy of GH therapy in children and adults. Summarized herein are the indications for GH use in adults and children, the conditions for which GH use has been investigated but is not approved, and the potential adverse effects of GH therapy. The authors believe that these guidelines will help clinical endocrinologists in the treatment of patients with recombinant GH.
Gharib, H., Cook, D.M., Saenger, P.H., Bengtsson, B.A., Feld, S., et al. (2003). American Association of Clinical Endocrinologists medical guidelines for clinical practice for growth hormone use in adults and children -- 2003 update [Electronic version]. Endocrine Practice: Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists, 9(1), 64-76. Retrieved September 19, 2005.

Growth Hormone Increases Bone Mineral Content in Postmenopausal Osteoporosis: A Randomized Placebo-Controlled Trial.pdf

This study concluded that bone mineral content increased to 14% with GH treatment on top of HRT and calcium/vitamin D in postmenopausal women with osteoporosis. There seems to be a delayed, extended, and dose-dependent effect of GH on bone. Thus, GH could be used as an anabolic agent in osteoporosis.
Landin-Wilhelmsen, K., Nilsson, A., Bosaeus, I. & Bengtsson, B.A. (2003). Growth hormone increases bone mineral content in postmenopausal osteoporosis: a randomized placebo-controlled trial [Electronic version]. Journal of Bone Mineral Research, 18(3), 393-405. Retrieved December 7, 2005.

Seeking the Optimal Target Range for Insulin-Like Growth Factor 1 During the Treatment of Adult Growth Hormone Disorders.pdf

The aim of this study was to identify a range of IGF-I values commensurate with GHD, which could be used to determine the risk of functional GHD during the treatment of adult GH disorders.
Mukherjee, A., Monson, J.P., Jonsson, P.J., Trainer, P.J. & Shalet, S.M. on behalf of KIMS International Board. (2003). Seeking the optimal target range for insulin-like growth factor 1 during the treatment of adult growth hormone disorders [Electronic version]. The Journal of Clinical Endocrinology and Metabolism, 88(12), 5865-5870. Retrieved December 7, 2005.

Endogenous Hormones and Bone Turnover Markers in Pre- and Perimenopausal Women: SWAN.pdf

This study tested the hypothesis that higher serum osteocalcin and urinary N-telopeptide of type I collagen (NTx) concentrations would be found in women with increasing cycle irregularity or increased follicle stimulating hormone concentrations. It concluded that in these pre- and early perimenopausal women, higher FSH concentrations, but not other serum reproductive hormone concentrations, are positively associated with greater bone turnover prior to the last menstrual period.
Sowers, M.R., Greendale, G.A., Bondarenko, I., Finkelstein, J.S., Cauley, J.A., Neer, R.M., et al. (2003). Endogenous hormones and bone turnover markers in pre- and perimenopausal women: SWAN [Electronic version]. Osteoporosis International, 14(3), 191-197. Epub April 11, 2003. Retrieved November 27, 2006.

Can Growth Hormone Prevent Aging?.pdf

This article cites the article by Rudman et al. that appeared in the Journal in 1990 that reported the effect on body composition of administering human growth hormone for six months to 12 older men. This article incited a proliferation of "antiaging" clinics and lay publications, such as "Grow Young with HGH," extolling the benefits of growth hormone in reversing or preventing aging.
Vance, M.L. (2003). Can growth hormone prevent aging? [Electronic version]. The New England Journal of Medicine, 348(9), 779-780. Retrieved October 31, 2005.

Recombinant Human Growth Hormone Treatment in Elderly Patients Undergoing Elective Total Hip Replacement.pdf

This study concluded that in elderly patients undergoing total hip replacement, preoperative GH treatment results in improvements in lean body mass and skeletal muscle mass that are sufficient to offset postoperative losses.  The treatment may also preserve or improve muscle strength and postoperative walking ability.
Weissberger, A.J., Anastasiadis, A.D., Sturgess, I., Martin, F.C., Smith, M.A. & Sonksen, P.H. (2003). Recombinant human growth hormone treatment in elderly patients undergoing elective total hip replacement [Electronic version]. Clinical Endocrinology (Oxford), 58(1), 99-107. Retrieved May 17, 2005.

Single and Combined Effects of Growth Hormone and Testosterone Administration on Measures of Body Composition, Physical Performance, Mood, Sexual Function, Bone Turnover, and Muscle Gene Expression in Healthy Older Men.pdf

This study examined the effects of GH and/or testosterone (T) administration on body composition, performance, mood, sexual function, bone turnover, and muscle-gene expression in healthy older men. It concluded that 1 month of GH and/or T administration improves certain measures of balance and physical performance in older men and increases muscle IGF-I gene expression.
Brill, K.T., Weltman, A.L., Gentili, A., Patrie, J.T., Fryburg, D.A., Hanks, J.B., et al. (2002). Single and combined effects of growth hormone and testosterone administration on measures of body composition, physical performance, mood, sexual function, bone turnover, and muscle gene expression in healthy older men [Electronic version]. The Journal of Clinical Endocrinology and Metabolism, 87(12), 5649-5657. Retrieved January 4, 2006.

Shouldn't Adults with Growth Hormone Deficiency Be Offered Growth Hormone Replacement Therapy?.pdf

This analysis should encourage reluctant practitioners to at least consider growth hormone replacement therapy for patients with definite growth hormone deficiency--that is, patients with symptomatic panhypopituitarism.
Cook, D.M. (2002). Shouldn't adults with growth hormone deficiency be offered growth hormone replacement therapy? [Electronic version]. Annals of Internal Medicine, 137(3), 197-201. Retrieved September 26, 2005

Bone Alterations in Patients with Idiopathic Hypercalciuria and Calcium Nephrolithiasis.pdf

This study concluded that altered bone metabolism and overall bone loss were found only in the patients with FH. Overloading of acid valences, perhaps of dietary origin, could be the pathogenic factor responsible.
Tasca, A., Cacciola, A., Ferrarese, P., Ioverno, E., Visona, E., Bernardi, C., et al. (2002). Bone alterations in patients with idiopathic hypercalciuria and calcium nephrolithiasis [Electronic version]. Urology, 59(6), 865-869. Retrieved May 21, 2003.

Effects of Low-Carbohydrate High Protein Diets on Acid-Base Balance, Stone-Forming Propensity, and Calcium Metabolism.pdf

This study concluded that consumption of an LCHP diet for 6 weeks delivers a marked acid load to the kidney, increases the risk for stone formation, decreases estimated calcium balance, and may increase the risk for bone loss.
Reddy, S.T., Wang, C.Y., Sakhaee, K., Brinkley, L., & Pak, C.Y. (2002). Effects of low-carbohydrate high protein diets on acid-base balance, stone-forming propensity, and calcium metabolism [Electronic version]. American Journal of Kidney Disease, 40(2), 265-274. Retrieved May 21, 2003.

Dehydroepiandrosterone Supplementation and Bone Turnover in Middle-Aged to Elderly Men.pdf

This study concluded that oral DHEA does not affect bone turnover in middle-aged to elderly men when used for a 6-month period at doses targeted to restore circulating levels of the steroid to that seen in young adults.
Kahn, A.J., Halloran, B., Wolkowitz, O. & Brizendine, L. (2002). Dehydroepiandrosterone supplementation and bone turnover in middle-aged to elderly men [Electronic version]. The Journal of Clinical Endocrinology and Metabolism, 87(4), 1544-1549. Retrieved December 7, 2005.

Use of Site-Specific Antibodies to Characterize the Circulating Form of Big Insulin-Like Growth Factor II in Patients with Hepatitis C-Associated Osteosclerosis.pdf

Hepatitis C-associated osteosclerosis (HCAO) is a rare syndrome of adult-onset osteosclerosis. An understanding of the factor(s) leading to the stimulation of bone formation in these patients may provide novel anabolic approaches for the treatment of osteoporosis.
Khosla, S., Ballard, F.J. & Conover, C.A. (2002). Use of site-specific antibodies to characterize the circulating form of big insulin-like growth factor II in patients with hepatitis C-associated osteosclerosis [Electronic version]. The Journal of Clinical Endocrinology and Metabolism, 87(8), 3867-3870. Retrieved October 3, 2005.

Bone Loss Following Hypogonadism in Men with Prostate Cancer Treated with GnRH Analogs.pdf

These findings of this study demonstrate a significant loss of bone in men with prostate cancer after receiving GnRH therapy and suggest that the total hip and radius are the preferred sites for monitoring bone loss in older men. In addition, markers of bone resorption may be helpful. 
Mittan, D., Lee, S., Miller, E., Perez, R.C., Basler, J.W. & Bruder, J.M. (2002). Bone loss following hypogonadism in men with prostate cancer treated with GnRH analogs [Electronic version]. The Journal of Clinical Endocrinology and Metabolism, 87(8), 3656-3661. Retrieved December 7, 2005.

Hormone Replacement Therapy, Insulin Sensitivity, and Abdominal Obesity in Postmenopausal Women.pdf

The authors concluded that postmenopausal women taking oral estrogen or those taking a combination of estrogen and HRT are more insulin-resistant than women not on HRT, even when women are of comparable total and abdominal adiposity.
Ryan, A.S., Nicklas, B.J. & Berman, D.M. (2002). Hormone replacement therapy, insulin sensitivity, and abdominal obesity in postmenopausal women [Electronic version]. Diabetes Care, 25(1), 127-133. Retrieved January 19, 2006.

Dietary Indoles and Isothiocyanates That Are Generated from Cruciferous Vegetables Can Both Stimulate Apoptosis and Confer Protection Against DNA Damage in Human Colon Cell Lines.pdf

According to this study, neither ICZ alone nor SUL alone were able to confer the same degree of protection against DNA damage produced by BaP as they achieved in combination. Similar results were obtained with H(2)O(2) as the genotoxic agent. Together, these phytochemicals may prevent colon tumorigenesis by both stimulating apoptosis and enhancing intracellular defenses against genotoxic agents.
Bonnesen, C., Eggleston, I.M. & Hayes, J.D. (2001). Dietary indoles and isothiocyanates that are generated from cruciferous vegetables can both stimulate apoptosis and confer protection against DNA damage in human colon cell lines [Electronic version]. Cancer Research, 61(16), 6120-6130. Retrieved May 21, 2003.

Association of IGF-I Levels with Muscle Strength and Mobility in Older Women.pdf

This article summarizes that in a study population including frail and healthy older women, low IGF-I levels were associated with poor knee extensor muscle strength, slow walking speed, and self-reported difficulty with mobility tasks. These findings suggest a role for IGF-I in disability as well as a potential target population for interventions to raise IGF-I levels.
Cappola, A.R., Bandeen-Roche, K., Wand, G.S., Volpato, S. & Fried, L.P. (2001). Association of IGF-I levels with muscle strength and mobility in older women [Electronic version]. The Journal of Clinical Endocrinology and Metabolism, 86(9), 4139-4146. Retrieved September 28, 2005.

Effects of 6 Years of Growth Hormone (GH) Treatment on Bone Mineral Density in GH-Deficient Adults.pdf

This study concluded that GH therapy in GH-deficient adults is able to progressively increase BMD and bone area at the lumbar spine over a period of at least 6 years. However, the authors state that their study has several limitations, making it necessary to confirm these findings in further long-term studies.
Clanget, C., Seck, T., Hinke, V., Wuster, C., Ziegler, R. & Pfeilschifter, J. (2001). Effects of 6 years of growth hormone (GH) treatment on bone mineral density in GH-deficient adults [Electronic version]. Clinical Endocrinology (Oxf.), 55(1), 93-99. Retrieved January 18, 2006.

Personal Business; Trying to Roll Back the Biological Clock, for a Price.pdf

This article, written soon after September 11th, says that Americans have been re-evaluating their priorities since the attacks, and for some people that means paying closer attention to their health. There has even been a rise in interest in so-called anti-aging clinics.  It discusses several clinics, including Cenegenics.
Siwolop, S. (2001, October 21). Personal business; trying to roll back the biological clock, for a price [Electronic version]. The New York Times. Retrieved October 31, 2005.

Bone Mineral Density Response to Estrogen Replacement in Frail Elderly Women: A Randomized Controlled Trial.pdf

This study concluded that in physically frail elderly women, 9 months of HRT significantly increased BMD compared with placebo in clinically important skeletal regions. Further studies are needed to determine whether these osteogenic effects of HRT in elderly women are associated with a reduction in osteoporotic fractures.
Villareal, D.T., Binder, E.F., Williams, D.B., Schechtman, K.B, Yarasheski, K.E. & Khort, W.M. (2001). Bone mineral density response to estrogen replacement in frail elderly women: a randomized controlled trial [Electronic version]. The Journal of the American Medical Association, 286(7), 815-820. Retrieved December 14, 2006.

Oral Estrogen Antagonizes the Metabolic Actions of Growth Hormone in Growth Hormone-Deficient Women.pdf

According to this study, oral estrogen antagonizes several of the metabolic actions of GH. It may aggravate body composition abnormalities already present in GHD women and attenuate the beneficial effects of GH therapy. Estrogen replacement in GHD women should be administered by a nonoral route.
Wolthers, T., Hoffman, D.M., Nugent, A.G., Duncan, M.W., Umpleby, M. & Ho, K.K. (2001). Oral estrogen antagonizes the metabolic actions of growth hormone in growth hormone-deficient women [Electronic version]. American Journal of Physiology, 281(6), E1191-1196. Retrieved January 19, 2006.

Hormone Replacement Therapy Produced Net Harm, Consistent with the Observational Data.pdf

This article states that women with or at high risk of coronary heart disease should not start HRT. There is a risk that women without coronary heart disease might experience even greater net harm from HRT. The late benefit is necessarily limited, as it cannot exceed the event rate. The mechanism of the early loss is unknown; if it were reduced proportionately less than the late benefit, considerable net harm could result.
Blakely, J.A. (2000). Hormone replacement therapy produced net harm, consistent with the observational data [Electronic version]. Archives of Internal Medicine, 160(19), 2897-2900. Retrieved October 3, 2005.

Testosterone Therapy in Men: An Update.pdf

This article discusses that because testosterone levels decline with age, and aging is accompanied by body changes including loss of muscle and increases in fat, there is great interest in the potential benefits of testosterone administration in elderly men.
Katznelson, L. (2000, Winter). Testosterone therapy in men: an update [Electronic version]. MGH Neuroendocrine Clinical Center Newsletter Bulletin, 6(2). Retrieved September 14, 2005.

Growth Hormone - Hormone Replacement for the Somatopause?.pdf

According to this article, the fall in GH secretion seen with ageing coincides with changes in body composition and lipid metabolism that are similar to those seen in adults with GH deficiency. In elderly subjects, although GH secretion is markedly reduced, remaining GH secretion correlates closely with body composition (particularly with lean body mass and inversely with central abdominal fat).
Savine, R. & Sonksen, P. (2000). Growth hormone - hormone replacement for the somatopause? [Electronic version]. Hormone Research, 53(Suppl. 3), 37-41. Retrieved January 18, 2006.

Measures of Bioavailable Serum Testosterone and Estradiol and Their Relationships with Muscle Strength, Bone Density, and Body Composition in Elderly Men.pdf

In this cross-sectional study in healthy elderly men, non-SHBG-bound T seems to be the best parameter for serum levels of bioactive T, which seems to play a direct role in the various physiological changes that occur during aging. A positive relation with muscle strength and BMD and a negative relation with fat mass was found. In addition, both serum E1 and E2 seem to play a role in the age-related bone loss in elderly men, although the cross-sectional nature of the study precludes a definitive conclusion. Non-SHBG-bound E2 seems to be the best parameter of serum bioactive E2 in describing its positive relation with BMD.
van den Beld, A.W., de Jong, F.H., Grobbee, D.E., Pols, H.A. & Lamberts, S.W. (2000). Measures of bioavailable serum testosterone and estradiol and their relationships with muscle strength, bone density, and body composition in elderly men [Electronic version]. The Journal of Clinical Endocrinology and Metabolism, 85(9), 3276-3282. Retrieved October 3, 2005.

Nutritional, Respiratory, and Psychological Effects of Recombinant Human Growth Hormone in Patients Undergoing Abdominal Aortic Aneurysm Repair.pdf

This pilot study indicates that rhGH administered preoperatively has beneficial effects on skeletal muscle and respiratory function and may be more useful than postoperative rhGH administration alone.
Barry, M.C., Mealy, K., O'Neill, S., Hughes, A., McGee, H., Sheehan, S.J., et al. (1999). Nutritional, respiratory, and psychological effects of recombinant human growth hormone in patients undergoing abdominal aortic aneurysm repair [Electronic version]. Journal of Parenteral and Enteral Nutrition, 23(3), 128-135. Retrieved January 4, 2006.

Bone Loss is Correlated to the Severity of Growth Hormone Deficiency in Adult Patients with Hypopituitarism.pdf

This study concluded that a significant reduction of BMD associated with abnormalities of bone turnover parameters was found only in patients with very severe or severe GHD, whereas normal BMD values were found in non-GHD hypopituitary patients. These abnormalities were consistently present in all patients with GHD regardless of the presence of additional hormone deficits, suggesting that GHD plays a central role in the development of osteopenia in hypopituitary patients.
Colao, A., Di Somma, C., Pivonello, R., Loche, S., Aimaretti, G., Cerbone, G., et al. (1999). Bone loss is correlated to the severity of growth hormone deficiency in adult patients with hypopituitarism [Electronic version]. The Journal of Clinical Endocrinology and Metabolism, 84(6), 1919-1924. Retrieved September 28, 2005.

Hip Fracture Patients, a Group of Frail Elderly People with Low Bone Mineral Density, Muscle Mass and IGF-I Levels.pdf

This study found a lower IGF-I level and lower bone and lean body mass in hip fracture patients than in an age-matched group of patients. This sign of catabolism seems to continue postoperatively, with a significant decrease of both BMD and lean body mass possibly indicating GH/IGF-I therapy together with adequate nutrition to preserve bone and muscle losses in elderly patients with hip fractures.
Hedstrom, M. (1999). Hip fracture patients, a group of frail elderly people with low bone mineral density, muscle mass and IGF-I levels [Electronic version]. Acta Physiologica Scandinavica, 167(4), 347-350. Retrieved September 28, 2005.

Effects of Two Years of Growth Hormone (GH) Replacement Therapy on Bone Metabolism and Mineral Density in Childhood and Adulthood Onset GH Deficient Patients.pdf

The aim of this study was to evaluate bone metabolism and mass before and after 2 years of GH replacement therapy in adults with childhood or adulthood onset GH deficiency. It concluded that patients with childhood or adulthood onset GH deficiency have osteopenia that can be improved by long-term treatment with GH.
Longobardi, S., Di Rella, F., Pivonello, R., Di Somma, C., Klain, M., Maurelli, L., et al. (1999). Effects of two years of growth hormone (GH) replacement therapy on bone metabolism and mineral density in childhood and adulthood onset GH deficient patients [Electronic version]. Journal of Endocrinological Investigation, 22(5), 333-339. Retrieved September 28, 2005.

Effect of Testosterone Treatment on Bone Mineral Density in Men Over 65 Years of Age.pdf

This study found that increasing the serum testosterone concentrations of normal men over 65 yr of age to the midnormal range for young men did not increase lumbar spine bone density overall, but did increase it in those men with low pretreatment serum testosterone concentrations.
Snyder, P.J., Peachey, H., Hannoush, P., Berlin, J.A., Loh, L., Holmes, J.H., et al. (1999). Effect of testosterone treatment on bone mineral density in men over 65 years of age [Electronic version]. The Journal of Clinical Endocrinology and Metabolism, 84(6), 1966-1972. Retrieved November 30, 2006.

Effect of Recombinant Human Growth Hormone in Elderly Osteoporotic Women.pdf

The results of this study indicate that GH attenuates the decrease in muscle strength and bone mass as well as the gain of abdominal fat with ageing in elderly women. The present data provide useful information about the application of GH treatment in elderly women.
Sugimoto, T., Nakaoka, D., Nasu, M., Kanzawa, M., Sugishita, T. & Chihara, K. (1999). Effect of recombinant human growth hormone in elderly osteoporotic women [Electronic version]. Clinical Endocrinology (Oxford), 51(6), 715-724. Retrieved September 28, 2005.

Effects of 42 Months of GH Treatment on Bone Mineral Density and Bone Turnover in GH-Deficient Adults.pdf

This study concluded that GH treatment in GH-deficient adults increased BMD for up to 30-36 months, with a plateau thereafter. Concurrently with the plateau in BMD the bone turnover rate normalized. From the skeletal point of view GH-deficient patients exhibiting osteopenia or osteoporosis should be considered as candidates for GH supplementation of at least 3-4 years.
Valimaki, M.J., Salmela, P.I., Salmi, J., Viikari, J., Kataja, M., Turunen, H., et al. (1999). Effects of 42 months of GH treatment on bone mineral density and bone turnover in GH-deficient adults [Electronic version]. European Journal of Endocrinology/European Federation of Endocrine Societies, 140(6), 545-554. Retrieved September 28, 2005.

A Randomized Controlled Trial of Four Doses of Transdermal Estradiol for Preventing Postmenopausal Bone Loss.pdf

This study concluded that transdermal E2 at doses of 0.025, 0.05, 0.06, and 0.1 mg/day effectively prevented bone loss in postmenopausal women.
Weiss, S.R., Ellman, H. & Dolker, M. (1999). A randomized controlled trial of four doses of transdermal estradiol for preventing postmenopausal bone loss. Transdermal Estradiol Investigator Group [Electronic version]. Obstetrics and Gynecology, 94(3), 330-336. Retrieved September 14, 2005.

Growth Hormone Deficiency in Adulthood and the Effects of Growth Hormone Replacement: A Review.pdf

The importance of GH throughout adult life is now unequivocally accepted.  GH deficiency is recognized to result in alterations in body composition, physical performance, psychological well-being, and substrate metabolism.  Many of these alterations can be improved or corrected with GH replacement.  The prospect of GH replacement becoming routine, however, does raise a number of issues.
Carroll, P.V., Christ, E.R., Bengtsson, B.A., Carlsson, L., Christiansen, J.S., et al.  (1998). Growth hormone deficiency in adulthood and the effects of growth hormone replacement: A review [Electronic version]. The Journal of Clinical Endocrinology & Metabolism, 83(2), 382-395. Retrieved May 17, 2005.

Effect of Long-Term Growth-Hormone Substitution Therapy on Bone Mineral Density and Parameters of Bone Metabolism in Adult Patients with Growth Hormone Deficiency.pdf

This study concluded that GH replacement therapy in adult patients with GHD over a period of 18 months causes a pronounced increase in bone turnover mainly during the first 12 months of therapy and increases BMD of the lumbar spine and the femoral neck after 18 months.
Kotzmann, H., Riedl, M., Bernecker, P., Clodi, M., Kainberger, F., Kaider, A., et al. (1998).  Effect of long-term growth-hormone substitution therapy on bone mineral density and parameters of bone metabolism in adult patients with growth hormone deficiency [Electronic version]. Calcified Tissue International, 62(1), 40-46. Retrieved January 18, 2006.

Growth Hormone and Mild Exercise in Combination Markedly Enhance Cortical Bone Formation and Strength in Old Rats.pdf

The effects of a combination of mild exercise and GH injections on bone were studied in old female rats. This study showed that GH injections and mild exercise in combination modulate and increase further the formation and strength of cortical bone in old female rats.
Oxlund, H., Andersen, N.B., Ortoft, G., Orskov, H. & Andreassen, T.T. (1998). Growth hormone and mild exercise in combination markedly enhance cortical bone formation and strength in old rats [Electronic version]. Endocrinology, 139(4), 1899-1904. Retrieved September 28, 2005.

Effects of Physiologic Growth Hormone Therapy on Bone Density and Body Composition in Patients with Adult-Onset Growth Hormone Deficiency. A Randomized, Placebo-Controlled Trial.pdf

According to this study, growth hormone administered to men with adult-onset growth hormone deficiency at a dose adjusted according to serum IGF-1 levels increases bone density and stimulates bone turnover, decreases body fat and increases lean mass, and is associated with a low incidence of side effects.
Baum, H.B., Biller, B.M., Finkelstein, J.S., Cannistraro, K.B., Oppenhein, D.S., Schoenfeld, D.A., et al. (1996).  Effects of physiologic growth hormone therapy on bone density and body composition in patients with adult-onset growth hormone deficiency. A randomized, placebo-controlled trial [Electronic version]. Annals of Internal Medicine, 125(11), 883-890. Retrieved September 28, 2005.

Relationship Between Baseline Insulin-Like Growth Factor-I (IGF-I) and Femoral Bone Density in Women Aged Over 70 Years: Potential Implications for the Prevention of Age-Related Bone Loss.pdf

The data from this study support the hypothesis that circulating IGF-I not only reflects the integrated growth hormone secretion but also has a direct role in the endocrine regulation of bone remodeling. The present findings support the need for further studies to assess the potential of IGF-I in attenuating age-related femoral bone loss.
Boonen, S., Lesaffre, E., Dequeker, J., Aerssens, J., Nijs, J., Pelemans, W., et al. (1996). Relationship between baseline insulin-like growth factor-I (IGF-I) and femoral bone density in women aged over 70 years: potential implications for the prevention of age-related bone loss [Electronic version]. Journal of the American Geriatrics Society, 44(11), 1301-1306. Retrieved January 19, 2006.

Increase of Bone Mineral Density and Anabolic Variables in Patients with Rheumatoid Arthritis Resistant to Methotrexate After Cyclosporin A Therapy.pdf

This study concluded that patients with active RA, even in the early phases, lose bone very rapidly. Effective control of systemic inflammation allowed a rapid rescue of BMD, at least in the short term. This happened with a simultaneous increase in some anabolic variables such as IGF-1, BGP, and DHEAS.
Ferraccioli, G., Casatta, L. & Bartoli, E. (1996). Increase of bone mineral density and anabolic variables in patients with rheumatoid arthritis resistant to methotrexate after cyclosporin A therapy [Electronic version]. The Journal of Rheumatology, 23(9), 1539-1542. Retrieved October 25, 2005.

Growth Hormone Therapy for Protein Catabolism.pdf

GH and IGF-1 have shown remarkable consistency of effect in a wide range of catabolic conditions, including improved net protein synthesis and preserving lean body mass.
Jenkins, R.C. & Ross, R.J. (1996). Growth hormone therapy for protein catabolism [Electronic version]. Monthly Journal of the Association of Physicians, 89(11), 813-819. Retrieved May 17, 2005.

Two Years of Growth Hormone (GH) Treatment Increases Bone Mineral Content and Density in Hypopituitary Patients with Adult-Onset GH Deficiency.pdf

According to this study, two years of GH treatment induced a sustained increase in overall bone remodeling activity, which resulted in a net gain in BMD that was more marked in those subjects with a low pretreatment z-score.
Johannsson, G., Rosen, T., Bosaeus, I., Sjostrom, L. & Bengtsson, B.A. (1996). Two years of growth hormone (GH) treatment increases bone mineral content and density in hypopituitary patients with adult-onset GH deficiency [Electronic version]. The Journal of Clinical Endocrinology and Metabolism, 81(8), 2865-2873. Retrieved January 18, 2006.

Cyclosporin A Increases Somatomedin C Insulin-Like Growth Factor I Levels in Chronic Rheumatic Diseases.pdf

This study concluded that the effects of CysA on IGF-I may explain some of the clinical, immunologic, and metabolic results during CysA treatment of rheumatic diseases.
Ferraccioli, G., Guerra, P., Rizzi, V. & Bartoli, E. (1995). Cyclosporin A increases somatomedin C insulin-like growth factor I levels in chronic rheumatic diseases [Electronic version]. The Journal of Rheumatology, 22(6), 1060-1064. Retrieved October 25, 2005.

Consequences of Growth Hormone Deficiency in Adults and the Benefits and Risks of Recombinant Human Growth Hormone Treatment. A Review Paper.pdf

According to this study, growth hormone deficiency (GHD) in adults is now recognized as a specific clinical syndrome with characteristic symptoms and signs. Thus, the patients are overweight, have an abnormal body composition (excess body fat and a decrease in the extracellular water volume) and a low bone mineral content compared to normals.
Rosen, T., Johannsson, G., Johansson, J.O. & Bengtsson, B.A. (1995). Consequences of growth hormone deficiency in adults and the benefits and risks of recombinant human growth hormone treatment. A review paper [Electronic version]. Hormone Research, 43(1-3), 93-99. Retrieved January 25, 2006.

Comparison of Oral Estrogens and Estrogens Plus Androgen on Bone Mineral Density, Menopausal Symptoms, and Lipid-Lipoprotein Profiles in Surgical Menopause.pdf

This study concludes that oral estrogen-androgen increased vertebral bone mineral density compared with pre-treatment values and relieved somatic symptoms. Safety indices, including lipoprotein levels, indicated that the combination was well tolerated over the 2 years of treatment.
Watts, N.B., Notelovitz, M., Timmons, M.C., Addison, W.A., Wiita, B. & Downey, L.J. (1995). Comparison of oral estrogens and estrogens plus androgen on bone mineral density, menopausal symptoms, and lipid-lipoprotein profiles in surgical menopause [Electronic version]. Obstetrics and Gynecology, 85(4), 529-537. Retrieved October 3, 2005.

Advances in Recombinant Human Growth Hormone Replacement Therapy in Adults.pdf

According to this article, it is now apparent that acquired GH deficiency is associated with significant changes in body composition, bone density, lipid metabolism, cardiovascular function and physical performance. In addition, new information is now available on the use of low doses of recombinant human growth hormone (rhGH) to reverse the negative effects of GH deficiency in adults.
Grinspoon, S. (1994). Advances in recombinant human growth hormone replacement therapy in adults [Electronic version]. MGH Neuroendocrine Clinical Center Bulletin, 2. Retrieved January 19, 2006.

Short and Long-Term Effects of Growth Hormone Treatment on Bone Turnover and Bone Mineral Content in Adult Growth Hormone-Deficient Males.pdf

The data of this study show that administration of substitutive doses of growth hormone to GH-deficient adult males activates bone turnover for a period of at least one year and suggests that this may have a beneficial effect on bone mass in these patients.
Vandeweghe, M., Taelman, P. & Kaufman, J.M. (1993). Short and long-term effects of growth hormone treatment on bone turnover and bone mineral content in adult growth hormone-deficient males [Electronic version]. Clinical Endocrinology (Oxford), 39(4), 409-415. Retrieved July 25, 2003.

Increased Bone Density After Recombinant Human Growth Hormone (GH) Therapy in Adults with Isolated GH Deficiency.pdf

According to this study, no significant changes occurred in bone mineral measurements during 6 months of placebo therapy. Midthigh muscle and fat cross-sectional area increased and decreased, respectively, during the active treatment phase. These results demonstrate that GH plays an important role in maintaining the integrity of the adult skeleton.
O’Halloran, D.J., Tsatsoulis, A., Whitehouse, R.W., Holmes, S.J., Adams, J.E., & Shalet, S.M. (1993). Increased bone density after recombinant human growth hormone (GH) therapy in adults with isolated GH deficiency [Electronic version]. The Journal of Clinical Endocrinology and Metabolism, 76(5), 1344-1348. Retrieved July 21, 2003. 

Treatment of Adults with Growth Hormone (GH) Deficiency with Recombinant Human GH.pdf

The results of this study show that GH replacement in GHD adults results in marked alterations in body composition, fat distribution, and bone and mineral metabolism and reduces psychiatric symptoms. Finally, the authors conclude that the observed beneficial effects of replacement therapy with GH are of sufficient magnitude to consider treatment of GHD adults.
Bengtsson, B.A., Eden, S., Lonn, L., Kvist, H., Stokland, A., Lindstedt, G., et al. (1993). Treatment of adults with growth hormone (GH) deficiency with recombinant human GH [Electronic version]. The Journal of Clinical Endocrinology and Metabolism, 76(2), 309-317. Retrieved July 21, 2003.

Potent Effect of Recombinant Growth Hormone on Bone Mineral Density and Body Composition in Adults with Panhypopituitarism.pdf

Six patients between the ages of 21and 50 with human growth hormone (hGH) deficiency and hypopituitarism were treated with human growth hormone (hGH) supplementation and modulation.  After one year, all subjects reported having an improved sense of well-being with increased working capacity and a noticeable increase in bone density. The beneficial effects of human growth hormone (hGH) supplementation and modulation indicate that this treatment be considered for any adult with hypopituitarism or human growth hormone (hGH) deficient adult, irrespective of age. 
Degerblad, M., Elgindy, N., Hall, K., Sjoberg, H.E. & Thoren, M. (1992). Potent effect of recombinant growth hormone on bone mineral density and body composition in adults with panhypopituitarism [Electronic version]. Acta Endocrinol (Copenhagen), 126(5), 387-393. Retrieved July 22, 2003.

The Effect of Growth Hormone Administration in Growth Hormone Deficient Adults on Bone, Protein, Carbohydrate and Lipid Homeostasis, as Well as on Body Composition.pdf

This study concluded that therapy with growth hormone for 6 months in a dose varying between 6 and 25 micrograms/kg/day increased lean body mass and decreased fat mass. The sense of general well-being improved in most patients. Furthermore, growth hormone treatment increased bone turnover without a measurable increase in bone density, caused some minor changes in lipid and carbohydrate metabolism, and increased the metabolism of thyroxine to T3.
Binnerts, A., Swart, G.R., Wilson, J.H., Hoogerbrugge, N., Pols, H.A., Birkenhager, J.C., et al. (1992). The effect of growth hormone administration in growth hormone deficient adults on bone, protein, carbohydrate and lipid homeostasis, as well as on body composition [Electronic version]. Clinical Endocrinology (Oxford), 37(1), 79-87. Retrieved July 25, 2003.

Androgen Treatment of Middle-Aged, Obese Men: Effects on Metabolism, Muscle and Adipose Tissues.pdf

This pilot investigation was conducted to explore the relationship between androgens and glucose tolerance in obese men and to select an optimal mode for androgen treatment. The results suggest that T administration to middle-aged, obese man may have beneficial effects.
Marin, P., Krotkiewski, M. & Bjorntorp, P. (1992). Androgen treatment of middle-aged, obese men: effects on metabolism, muscle and adipose tissues [Electronic version]. The European Journal of Medicine, 1(6), 329-336. Retrieved October 3, 2005.

Increase in Bone Mass After One Year of Percutaneous Oestradiol and Testosterone Implants in Post-Menopausal Women Who Have Previously Received Long-Term Oral Oestrogens.pdf

This study concluded that subcutaneous oestradiol and testosterone implants will result in an increase in bone mass even after many years of oral oestrogen replacement therapy.
Savvas, M., Studd, J.W., Norman, S., Leather, A.T., Garnett, T.J. & Fogelman, I. (1992). Increase in bone mass after one year of percutaneous oestradiol and testosterone implants in post-menopausal women who have previously received long-term oral oestrogens [Electronic version]. British Journal of Obstetrics and Gynaecology, 99(9), 757-760. Retrieved October 3, 2005.

Effects of Testosterone and Venesection on Spinal and Peripheral Bone Mineral in Six Hypogonadal Men with Hemochromatosis.pdf

To measure the effect of testosterone replacement and venesection on spinal and peripheral bone mineral this study prospectively examined six hypogonadal men and six eugonadal men with idiopathic hemochromatosis for 24 months. The data suggest that bone mineral increases in the lumbar spine and in the forearm in hypogonadal men with hemochromatosis treated by testosterone replacement and venesection.
Diamond, T., Stiel, D. & Posen, S. (1991). Effects of testosterone and venesection on spinal and peripheral bone mineral in six hypogonadal men with hemochromatosis [Electronic version]. Journal of Bone and Mineral Research, 6(1), 39-43. Retrieved October 26, 2005.

Effects of Human Growth Hormone in Men Over 60 Years Old.pdf

This landmark study concluded that diminished secretion of growth hormone is responsible in part for the decrease of lean body mass, the expansion of adipose-tissue mass, and the thinning of the skin that occur in old age.
Rudman, D., Feller, A.G., Nagraj, H.S., Gergans, G.A., Lalitha, P.Y., Goldberg, A.F., et al. (1990). Effects of human growth hormone in men over 60 years old [Electronic version]. The New England Journal of Medicine, 323(1), 1-6. Retrieved January 31, 2007.

Sex Hormones and Skin Collagen Content in Postmenopausal Women.pdf

The implication from the findings in this study is that oestrogen or testosterone, or both, prevents the decrease in skin collagen content during the aging process.  It concludes that it protects skin in the same way as it protects bone in menopausal women.  Skin biopsy specimens were taken from the participants.
Brincat, M., Moniz, C.F., Studd, J.W., Darby, A.J., Magos, A. & Cooper, D. (1983). Sex hormones and skin collagen content in postmenopausal women [Electronic version]. British Medical Journal, 287(6402), 1337-1338. Retrieved May 18, 2005.

Growth and Mitotic Rate of the Proximal Tibial Epiphyseal Plate in Hypophysectomized Rats Given Estradiol and Human Growth Hormone.pdf

The results of this study on rats injected with human growth hormone (hGH) and/or estradiol indicate that human growth hormone (hGH) supplementation and modulation does promote growth of the epiphyseal cartilage, therefore improving bone density. 
Gustafsson, P.O., Kasstrom, H., Lindberg, L. & Olsson, S.E. (1975). Growth and mitotic rate of the proximal tibial epiphyseal plate in hypophysectomized rats given estradiol and human growth hormone [Electronic version]. Acta Radiol Suppl., 344, 69-74. Retrieved July 22, 2003.