Opioids are a treatment option for a variety of chronic pain conditions. But long-term opioid use can be associated with side effects, including hypogonadism. Opioid-induced hypogonadism (OIhG) is associated with the alteration of the hypothalamic-pituitary-gonadal axis (HPG). In males, hypogonadism can result in erectile dysfunction, reduced libido, fatigue, worsening mood, and increased risk of osteoporosis; in females, it can result in changes in the menstrual cycle and reduced libido, among other effects. A current treatment option for these patients is hormone replacement therapy. In this report, we discuss the problem of opioid-induced hypogonadism, and the therapeutic approach and the potential complications of treating pain patients using hormone replacement therapy.
Opioids are an option for pain management for the chronic pain patient, with generally, albeit not always, good effectiveness [
Common OIgH effects experienced by males include reduction in the levels of testosterone, which can lead to effects such as muscle hypotrophy, loss of bone mass, anemia, etc., and/or central effects such as decreased attention, decreased libido, depression, etc. Some common OIgH effects experienced by females include irregular periods and amenorrhea, which is caused by reduced levels of luteinizing hormone, follicle stimulating hormone, oestradiol, and adrenal androgen [
We reviewed publications available in English language using sources such as PubMed, MedLine, and related. We used search terms such as opioid, chronic hypogonadism, hormone replacement therapy, chronic pain, and HPG axis. Additional articles were identified from references therein. All were reviewed for applicability and quality of evidence.
OIgH results from the central suppression of the hypothalamic secretion of gonadotropin-releasing hormone (GnRH) by opioid agonists (endogenous or exogenous) acting at opioid receptors located within the hypothalamus (
Disruption of gonadal hormone balance usually results in physical and mental changes. In a study of 54 males taking opioids, 87% reported severe erectile dysfunction (they had normal erectile function prior to opioid treatment) and/or diminished libido. It was found that 89% of the males had decreased levels of free testosterone, oestradiol, dihydrotestosterone, LH, and FSH [
of menses, an effect that the authors believed to be caused by the recorded reduction in LH, FSH, oestradiol and adrenal androgen [
In another study, 96% and 69% of males and females, respectively, reported decreased libido after being administered opioids for 26 months for non-cancer chronic pain [
When OIhG is diagnosed in chronic pain patients, it might be treated using hormone replacement therapy. Replacement of testosterone or oestradiol may relieve the acute symptoms of OIhG and also prevent the long-term consequences associated with untreated OIhG. Although there is lack of definitive evidence regarding the effectiveness and safety of hormone replacement therapy for OIgH in chronic pain patients, there are sufficient current literature reports of positive results for efficacy and safety to suggest that additional, controlled studies are warranted.
In a study conducted by Daniell et al., testosterone replacement improved sexual function of males with OIhG [
Overall, these studies suggest that testosterone replacement may be a safe and effective treatment option for opioid users. Additional studies are needed.
There is a variety of options to choose from for testosterone replacement therapy, including gels, lotions, creams, intramuscular injections, and implantation devices (every 4 - 6 months). The dosage and treatment regimens of these products vary, but the main goal is to return testosterone level to ~500 ng/dL (the normal range is ~250 - 1000 ng/dL). Patients normally continue on treatment until contradictions or side effects develop (e.g., lower leg edema, breast enlargement, or prostate enlargement with difficulty urinating), but patients can often remain on replacement therapy effectively and safely for many years. Patients usually report improvement in mood, desirable weight loss, rise in testosterone levels, better libido, increased sex drive, better erections, and more energy. The beneficial effects and good safety profile usually translate to high patient satisfaction. The case reports presented below exemplify some positive outcomes associated with testosterone replacement.
Case #1: A 61 year-old man presented with symptoms associated with OIhG. His medical history consisted of depression, insomnia, and anxiety; surgical history consisted of tonsillectomy, a left shoulder open reduction, and right quadrant hernia repair. The patient was diagnosed with chronic low back pain in early 2011 and was taking dilaudid for approximately one year to control back pain. Other medications included well butrin, desoril, and vistaril for depression, insomnia, and anxiety respectively. The patient sought help because of reduced energy, feeling of depression, and lower sexual drive. Testosterone levels, hematocrit level, and PSA level were 188 ng/dL, 42.5% and 1.1 ng/mL respectively. The patient completed a sexual desire inventory questionnaire (score 26) and Becks Depression Inventory Scale (score 16, mild depression) in order to establish baseline values before treatment. The patient was started on 40 mg/day of a testosterone gel. After approximately 2 weeks of treatment, his testosterone levels had risen to 1241 ng/dL; however, the patient did not report feeling much different and the sexual desire inventory (SDI) and Becks depression inventory (BDI) score remained approximately the same (SDI = 23, BDI = 20). At about one month of treatment, his testosterone level was 1154 ng/dL and he began reporting increased energy and increased sexual desire. The SDI score increased to 58, indicating improvement, while the BDI was similar to previous readings. After 2 months of treatment, testosterone level was 737 ng/dL, BDI score 15, and SDI score 78, which correlated with the patient’s description of increased libido. While on treatment, the patient did not have any undesirable side effects and his vital signs remained unchanged. Patient satisfaction was excellent and the patient expressed a desire to continue with longer-term treatment.
Case #2: A 42 year-old man sought help due to decreased sexual desire, fatigue, and lack of muscle strength. His medical history consisted of right knee pain, left side paralysis, spinal cord injury, tracheotomy, anemia, and erectile dysfunction. The patient was diagnosed with osteoarthritis in 2000. He was taking Exalgo, oxycodone, cialis, and iron sulfate supplement for right knee pain, osteoarthritis, erectile dysfunction, and anemia, respectively. Prior to starting testosterone replacement, baseline assessments for total testosterone, hematocrit level, and PSA level were 182 ng/dL, 40.9%, and 0.2 ng/dL. The patient also completed baseline SDI (score 40) and BDI (24, moderately depressed). Based on this information, prescription for 40 mg/day testosterone gel was written. After approximately 2 weeks of treatment, testosterone level was 975 ng/dL and the patient reported feeling a noticeable change in his core muscles, increased energy, feeling rested after sleeping, and an increase in sexual drive. The SDI score increased to 63 and the BDI score decreased to 14. Complaints included nightly calf cramps during first week of medication (that resolved by the end of 2 weeks). After two months of treatment, testosterone level was 1096 ng/dL and the patient continued to notice increase in energy level, increase in sexual desire, and improvement of his left side paralysis. The SDI score was 78 and BDI score was 14. The patient was very satisfied with the treatment and had intentions to continue for a longer term.
Case #3: A 30 year-old morbid obese male chronic pain patient was looking to improve his energy level, weight control, and sexual desire. His medical history consisted of herniated disks, lumbar fusion, tonsillitis, tonsillectomy, cluster headaches, anxiety, right arthroscopic knee surgery, failed back syndrome, degenerative arthritis of the knees, constipation, lower extremity edema, muscle spasms, and neuropathy of the lower extremities. The patient was diagnosed with degenerative disk disease in 2008. Concomitant medications included oxycodone, tizanidine, ibuprofen, verapamil, morphine, xanax, soma, and aquaphor for failed back syndrome, muscle spasms, pain preventative, cluster headaches, degenerative spine disease, anxiety, muscle spasms, and dry skin, respectively. Baseline assessments included total testosterone (17 ng/dL), hematocrit (44.6%), PSA level (0.7 ng/dL), SDI questionnaire (46), and BDI questionnaire (19). The patient was initiated on 40 mg/day testosterone gel and after 2 weeks he noticed a change in his energy and sexual desire. Total testosterone improved to 709 ng/dL. After approximately one month, total testosterone improved to 1269 ng/dL and SDI and BDI improved to 60 and 11, respectively. After approximately two months, total testosterone was 634 ng/dL and SDI and BDI were 59 and 25, respectively. The patient was overall satisfied with the medication and noticed improvement in energy, muscle tone, and sexual desire. The only safety issue reported was dry skin at the application site.
Hormone replacement therapy is not without complications. Men receiving hormone replacement therapy should be monitored for side-effects such as polycythemia, peripheral edema, cardiac and hepatic dysfunction.
Long-term administration of opioids in chronic pain patients can alter the HPG axis in both males and females, resulting in physical and psychological symptoms of OIgH (opioid-induced hypogonadism). Effects of OIgH such as reduced sexual drive, fatigue, and insomnia can lead to a reduction in quality of life and, in combination with the hormonal imbalance, can increase the risk of developing depression and other psychological and physical disorders. Replacement of testosterone in these patients might be a viable option for reversing many of these side effects. Reports from small trials and clinical case reports suggest that androgen replacement therapy might be an effective and safe treatment for long-term pain patients treated with opioids. Large controlled clinical trials are needed.
The authors thank John Bisney of LeQ Medical (Angleton, TX) for his excellent editorial assistance.
The authors declare no conflicts of interest regarding the publication of this paper.
Nalamachu, S., Pergolizzi Jr., J.V., Taylor Jr., R., Quang, J.A.L., Pergolizzi III, J.V. and Raffa, R.B. (2018) Hormone Replacement Therapy for Restoring the HPG Axis in Pain Patients Treated with Long-Term Opioid Analgesics. Pharmacology & Pharmacy, 9, 473-480. https://doi.org/10.4236/pp.2018.911036