A Patient Centered Approach to the Treatment of Hypogonadism: Consensus Recommendations from an Expert Panel Richard Sadovsky, MD Associate Professor of Family Medicine, Department of Family Medicine, SUNY-Downstate Medical Center, Brooklyn, New York
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A Patient Centered Approach to the Treatment of Hypogonadism:
Consensus Recommendations from an Expert Panel
Richard Sadovsky, MDAssociate Professor of Family Medicine,
Department of Family Medicine,SUNY-Downstate Medical Center,
Brooklyn, New York
Disclosures
Richard Sadovsky has served as a consultant forEndo Pharmaceuticals and, Eli Lilly & Co.
All conflicts of interest have been resolved according to the NJAFP Conflict of Interest Policy
This program has been made possible through an unrestricted educational grant from Abbott Laboratories.
Describe Your Practice
1. I do not, and have no plans to treat hypogonadism
2. I have not treated hypogonadism but I am considering doing so
3. I treat men for primary, but not secondary, hypogonadism
4. I routinely treat men for hypogonadism but would like more guidance on diagnosis and treatment options
5. I routinely treat men for hypogonadism and am comfortable with my knowledge about the subject
Learning Objectives
At the conclusion of this program you should be able to:
1. Identify patients for assessment of serum testosterone levels to determine if testosterone replacement therapy (TRT) is indicated
2. Recognize link between hypogonadism and obesity, diabetes, and other chronic conditions
3. Articulate current opinions about relationship between TRT and prostate cancer
4. Follow evidence-based practice for the treatment of hypogonadism
5. Understand the role of patient-centered, culturally appropriate communication in arriving at shared decisions about TRT
Overview
• TRT is becoming more popular• New TRT formulations are available• Men are more comfortable seeking counsel for
sexual dysfunctions• Low T is associated with increased risk of CVD• Physicians increasingly likely to encounter men
presenting with symptoms of low T• Family physicians must remain current in their
knowledge
Dandona P, Rosenberg M. A practical guide to male hypogonadism in the primary care setting. Int J Clin Pract. 2010;64:682-696.
Overview
This program will review:
• Testosterone physiology
• Symptoms of low T
• Treatment options
• Possible risks and benefits of TRT
• Consensus recommendations
Pop Quiz
Q: Free (unbound) testosterone represents approximately what fraction of total serum testosterone?a. 1-2 %b. 10-20%c. 45%d. 65%
Pop Quiz
Answer: 1-2%
Dandona P, Rosenberg M. A practical guide to male hypogonadism in the primary care setting. Int J Clin Pract. 2010;64:682-696.
Testosterone Physiology
• Testosterone levels peak ~ 20 yrs, then decline ~1%/yr.
• Normal T levels are regulated by hypothalamic-pituitary-testicular axis
• Dysfunction manifests as different forms of hypogonadism
Dandona P, Rosenberg M. A practical guide to male hypogonadism in the primary care setting. Int J Clin Pract. 2010;64:682-696.
Biochemical Definition of Hypogonadism
• Hypogonadism refers to any state of reduced testicular function, impaired sperm production, and low T
• Agreement on two thresholds for total testosterone (TT): >350 ng/dL (normal) and <230 ng/dL (low)
• Borderline TT : 230 – 345 ng/dL
Buvat J, Maggi M, Guay A, Torres LO. Standard Operating Procedures for Diagnosing and Treating Testosterone Deficiency in Men. Journal of Sexual Medicine. In press.
• Mixed: defects at both levels Examples: aging, alcohol abuse, chronic infections
Dandona P, Rosenberg M. A practical guide to male hypogonadism in the primary care setting. Int J Clin Pract. 2010;64:682-696.
Clinical Definition of Hypogonadism
• Requires below-normal TT and signs/ symptoms
• MMAS, using this definition, found prevalence in general population ranging from 7% (ages 48-59) to 23% (ages 70-80)
• No evidence that prevalence differs between racial and ethnic groups
Araujo AB, O’Donnell AB, Brambilla DJ, et al. Prevalence and Incidence of Androgen Deficiency in Middle-Aged and Older Men: Estimates from the Massachusetts Male Aging Study. J Clin Endocrinol Metab.2004;89:5920-5926.
Nomenclature
• Terms used to describe primarily age-related, below-normal T-levels with associated clinical symptoms:
Miner MM. Low Testosterone Medscape CME Expert Column Series. Issue 2: Screening and Workup for Testosterone Deficiency. 2011. Available at: http://www.medscape.org/viewarticle/749240?src=emailthis
Expert Panel Recommendation
TD does not always need to be treated first in patients with associated
comorbidities. To the extent testosterone levels can be raised by successful treatment or resolution of comorbid
conditions, these approaches should be attempted first.
TD and Cardiovascular Disease
• Recent observational studies suggest that lower T is associated with higher risk of CVD
• No randomized controlled trials of TRT and CVD
• Routine testosterone measurement is not recommended for men with cardiovascular disease unless they also have symptoms of TD
Buvat J, Maggi M, Gooren L, et al. Endocrine Aspects of Male Sexual Dysfunctions. J Sex Med. 2010;7:1627-1656.
TD and Erectile Dysfunction
• ED is a common “portal” to T assessment
• Relationship between ED and TD often unclear
• TD usually only one element of ED in older patients
• ED may be caused by vascular or smooth muscle dysfunctions, which is why TRT is generally ineffective for treating ED
• There may be a beneficial synergy between TRT and phosphodiesterase inhibitors in men with both ED and TD
Buvat J, Maggi M, Gooren L, et al. Endocrine Aspects of Male Sexual Dysfunctions. J Sex Med. 2010;7:1627-1656.
TD Screening Guidelines
• 2010 Endocrine Society Guidelines recommend against screening non-symptomatic patients for TD
• Testing reserved for men with signs/symptoms
• Serum TT levels should be taken in a.m.
• Positive findings must be repeated
• T levels should not be assessed during times of patient illness, malnutrition, or other physiologic stressors
Buvat J, Maggi M, Guay A, Torres LO. Standard Operating Procedures for Diagnosing and Treating Testosterone Deficiency in Men. Journal of Sexual Medicine. In press.
TD Symptoms and Signs
• TD is a challenging diagnosis
• Some signs/symptoms are much more suggestive of
TD than others
Bhasin S, et al. J Clin Endocrinol Metab. 2010;95(6): 2536-2559.
Symptoms & Signs More Specific to TD
Incomplete or delayed sexual development
Reduced sexual desire (libido) and activity
Decreased spontaneous erections
Breast discomfort, gynecomastia
Loss of axillary and pubic hair, reduced shaving
Very small (<5 mL) or shrinking testes
Inability to father children, low or zero sperm count
Hot flushes, sweats
TD Symptoms and Signs
• TD is a challenging diagnosis
• Some signs/symptoms are much more suggestive of
TD than others
Bhasin S, et al. J Clin Endocrinol Metab. 2010;95(6): 2536-2559.
Symptoms & Signs Less Specific to TD
Decreases energy, motivation, and initiative
Feeling sad or blue, depressed mood, dysthymia
Poor concentration and memory
Sleep disturbance, increased sleepiness
Mild anemia
Reduced muscle bulk and strength
Increased body fat, body mass index
Diminished physical or work performance
Height loss, low trauma fracture, low BMD
Expert Panel Recommendation
Family physicians should probe for non-
physiological causes of low libido by asking
questions such as, “Are you still sexually attracted
to your partner?” or “Are you comfortable with
your sexuality?”
Referral to therapy may be appropriate
if non-medical factors are involved.
Prostate Cancer and Testosterone
• Recent analyses refute earlier positive associations between T levels and risk of prostate cancer
• Most observational studies found no correlation
• Case-control studies find correlations between PC and low T
• Low T also associated with high Gleason scores, more advanced stages, higher recurrence rates, and worse survival rates
Herman LM, Miner MM, Quallich SA. Practicing Clinicians Exchange. 2010;1(2):1-8.
Endogenous Hormones and Prostate Cancer Collaborative Group. J Natl Cancer Inst. 2008;100:170-183.
Morgentaler A, Rhoden EL. Urology. 2006;68:1263–1267.
Morgentaler A. Eur Urol. 2007;52:623–625.
Prostate Cancer and Testosterone
• T suppression can reduce prostate growth and symptoms in locally advanced and metastatic prostate cancer
• Explanation: PC may be very sensitive to changes in serum T at low concentrations but insensitive at higher concentrations
• Currently no conclusive evidence that TRT in testosterone-deficient men increases PC risk
• TRT may, however, stimulate growth of metastatic prostatic cancers
Buvat J, Maggi M, Gooren L, et al. Endocrine Aspects of Male Sexual Dysfunctions. J Sex Med. 2010;7:1627-1656.
Dandona P, Rosenberg M. A practical guide to male hypogonadism in the primary care setting. Int J Clin Pract. 2010;64:682-696.
Prostate Cancer and Testosterone
• International guidelines: hypogonadal men w/Hx of PC and no residual disease may be considered for TRT
• AUA suggests urological consult prior to TRT if: PSA > 4 ng/mL PSA > 3 ng/mL in high-risk men (i.e. African-
Americans, men w/family history of PC) PSA velocity change is 0.75 ng/mL or more in 1 yr.
Carroll P, Coley C, McLeod D et al. Prostate-specific antigen best practice policy – part I: early detection and diagnosis of prostate cancer. Urology. 2001;57:217–224.
TRT Contraindications
• Metastatic prostate cancer• Breast cancer• Patient desire to maintain fertility
• Moderate-high risk of adverse outcomes: Unevaluated prostate nodule or induration PSA > 4ng/mL or > 3 ng/mL in high-risk men Hematocrit >50% Severe LUTS Uncontrolled or poorly-controlled heart failure
Bhasin S, et al. J Clin Endocrinol Metab. 2010;95(6): 2536-2559.
TRT Goals
• Safe restoration of normal physiologic T levels
• Reduction or elimination of symptoms
• Target T levels vary—most authors suggest a mid-range value of ~500 ng/dL
• For T injections, ES recommends 350-750 ng/dL at midpoint between injections
• Dose escalations beyond normal range are not recommended
Bhasin S, et al. J Clin Endocrinol Metab. 2010;95(6): 2536-2559.
Dandona P, Rosenberg M. A practical guide to male hypogonadism in the primary care setting. Int J Clin Pract. 2010;64:682-696.
TRT and Therapeutic Lifestyle Changes
• T levels have a synergistic relationship with lifestyle issues such as obesity, lack of exercise, and diabetes
• T levels often rise after weight loss• Important to address T-related health issues
either prior to or concurrent with a trial of TRT• Emerging evidence suggests TRT may have
positive synergistic effect on therapeutic lifestyle changes
Niskanen L, et al. Changes in sex hormone-binding globulin and testosterone during weight loss and weight maintenance in abdominally obese men with the metabolic syndrome. Diabetes Obes Metab. 2004;6:208-215.
Heufelder AE, et al. Fifty-two-week treatment with diet and exercise plus transdermal testosterone reverses the metabolic syndrome and improves glycemic control in men with newly diagnosed type 2 diabetes and subnormal plasma testosterone. J Androl. 2009;30:726-733.
Expert Panel Recommendation
Family physicians considering TRT for a patient
should incorporate therapeutic lifestyle changes
such as weight loss with exercise, healthy
dietary choices, and avoidance of smoking, into
the overall treatment plan.
Diagnosis and Management of TD
Buvat J, Maggi M, Gooren L, et al. Endocrine Aspects of Male Sexual Dysfunctions. J Sex Med. 2010;7:1627-1656.
TRT Formulations Available in US
Potential Adverse Effects of TRT
• AEs associated with all types of TRT: Erythrocytosis
Acne and oily skin
Reduced sperm production and fertility
• Less common AEs: Gynecomastia
Exacerbation of male pattern balding
Growth of breast cancer
Induction or worsening of obstructive sleep apnea
Bhasin S, et al. J Clin Endocrinol Metab. 2010;95(6): 2536-2559.
Monitoring Patients on TRT
Expert Panel Recommendation
Initial treatment with TRT should be viewed as a trial of therapy, with continuation dependent on
satisfactory response and an absence of adverse effects.
Patients should be evaluated 3-6 months after treatment start. If symptoms have not improved, or if unacceptable adverse effects are apparent,
treatment should be withdrawn. If symptoms have improved and therapy is well-tolerated,
patients should be evaluated annually.
Patient-Centered Management of TD
Suggestions for improving patient care: Ask patients about the non-medical aspects of
their lives
Provide culturally-specific educational materials written or produced at an appropriate reading level
Consider adopting the “medical home” model of health care delivery
Set small, easily-achievable goals for lifestyle changes
Make follow-up calls
Expert Panel Recommendation
Family physicians must take the time to clearly
explain to patients the risks and benefits of TRT,
Brad agrees to a trial of a 1.62% testosterone gel. As part of the “prescription” you strongly urge Brad to become more physically active and lose at least 10 pounds.
Question 2: Before he begins TRT, whatadditional test should you order for Brad?
a) Repeat TTb) Hematocritc) LHd) Prolactine) All of the above
Case Study #1: Brad
Brad agrees to a trial of a 1.62% testosterone gel. As part of the “prescription” you strongly urge Brad to become more physically active and lose at least 10 pounds.
Question 2: Before he begins TRT, whatadditional test should you order for Brad?
a) Repeat TTb) Hematocritc) LHd) Prolactine) All of the above
Answer: E
Case Study #1: Brad
At 3 mo. follow-up, Brad reports he is walking daily, eating better, has lost 9 pounds and his blood pressure is lower. His overall energy level is higher, he says, and he and his wife are having more regular sex.
Question 3: If at Brad’s next follow-upappointment his hematocrit is found to be56%, what course of action is indicated?
a) No change in Brad’s regimen is indicated since his hematocrit level is not above the recommended cut-off point for stopping TRT.
b) Brad’s TRT can continue, but he should be advised to drink plenty of fluids to avoid dehydration.
c) Brad’s TRT can continue, but his hematocrit level should be re-checked in 3 weeks to see if it has declined to a safer level.
d) Brad’s TRT should be stopped or decreased, his hematocrit should be monitored, and the dose of T adjusted until it is in the normal range.
Case Study #1: Brad
Question 3: If at Brad’s next follow-upappointment his hematocrit is found to be56%, what course of action is indicated?
a) No change in Brad’s regimen is indicated since his hematocrit level is not above the recommended cut-off point for stopping TRT.
b) Brad’s TRT can continue, but he should be advised to drink plenty of fluids to avoid dehydration.
c) Brad’s TRT can continue, but his hematocrit level should be re-checked in 3 weeks to see if it has declined to a safer level.
d) Brad’s TRT should be stopped or decreased, his hematocrit should be monitored, and the dose of T adjusted until it is in the normal range.
Answer: D
Case Study #2: Dominic
Age: 17
Complaint: Mother concerned he is not developing secondary sex characteristics
Physical exam: little facial or body hair, slightly enlarged breasts, and under-sized and firm testicles for his age.
History: Dominic is successful in school, though he prefers non-athletic extracurricular activities and is prone to a depressed mood.
Case Study #2: Dominic
Question 1: Dominic’s presentationis consistent with which clinical condition?
a) Hypogonadotropic hypogonadism
b) Klinefelter’s Syndrome
c) Fragile X Syndrome
d) Edwards Syndrome
Case Study #2: Dominic
Question 1: Dominic’s presentationis consistent with which clinical condition?
a) Hypogonadotropic hypogonadism
b) Klinefelter’s Syndrome
c) Fragile X Syndrome
d) Edwards Syndrome
Answer: B
Case Study #2: Dominic
Karyotype confirms XXY chromosomal pattern of Klinefelter’s Syndrome. Dominic’s TT level is found to be 225 ng/dL.
Question 2: Testosterone replacement therapy is likely to induce secondary sex characteristics in Dominic, may improve his mood, and may have a beneficial effect on other health parameters. What parameter, however, is TRT not likely to improve?
a) Sexual functionb) Muscle massc) Fertilityd) Libido
Case Study #2
Karyotype confirms XXY chromosomal pattern of Klinefelter’s Syndrome. Dominic’s TT level is found to be 225 ng/dL.
Question 2: Testosterone replacement therapy is likely to induce secondary sex characteristics in Dominic, may improve his mood, and may have a beneficial effect on other health parameters. What parameter, however, is TRT not likely to improve?
a) Sexual functionb) Muscle massc) Fertilityd) Libido
Answer: C
Conclusions
• TD is a complex, multi-factorial disease state bi-directionally related to several common conditions
• Because signs and symptoms of TD may be non-specific a diagnosis of TD must be made cautiously
• Prior to (or concurrent with) a trial of TRT, family physicians should encourage therapeutic lifestyle changes
• Decisions about TRT must rest on good patient education about risks and benefits
Conclusions
• New TRT formulations and delivery systems may allow more accurate dosing and may reduce risk of adverse events
• Long-term, high-quality data documenting the benefits and risks of TRT are lacking
• Nonetheless, available knowledge and guidelines can allow providers to assess and treat TD with greater confidence
Discussion
Post-Presentation Question
1. I do not, and have no plans to treat hypogonadism.
2. I have not treated hypogonadism but I am considering doing so now.
3. I treat men with primary hypogonadism and am considering also treating men with secondary hypogonadism.
4. While I currently treat hypogonadism, I may change my approach to treatment following this presentation.
5. I routinely treat men for hypogonadism and this presentation confirmed that I do not need to change my treatment method.