Testosterone Enanthate and Relationships: How TRT Affects Intimacy, Mood, and Daily Life

Hormone therapy clinical care image for Testosterone Enanthate and Relationships: How TRT Affects Intimacy, Mood, and Daily Life

At a glance

  • Standard dose / 50 to 200 mg IM every 1 to 2 weeks (Endocrine Society guideline recommendation)
  • Libido improvement onset / 3 to 6 weeks after first injection in most hypogonadal men
  • Erectile function response / 6 to 12 weeks for full benefit; IIEF score gains of 3 to 5 points in RCTs
  • Mood normalization / depressive symptom reduction measurable by week 6 in testosterone-deficient men
  • Partner awareness rate / fewer than 40% of partners receive formal education about TRT side effects per survey data
  • Trough variability / TE peaks at 24 to 72 hours post-injection and troughs before the next dose, creating a 7 to 14 day mood/libido cycle
  • Hematocrit risk / polycythemia (hematocrit >54%) reported in up to 6.7% of TE users; requires monitoring
  • Fertility warning / exogenous testosterone suppresses LH and FSH, reducing sperm production within 6 to 8 weeks
  • Injection-site reactions / occur in roughly 11% of patients; rotation technique reduces incidence

What Testosterone Enanthate Actually Does to Your Body and Brain

Testosterone enanthate is a long-acting esterified form of testosterone that releases active hormone over 7 to 14 days after a single intramuscular injection. For men diagnosed with hypogonadism (morning serum total testosterone persistently below 300 ng/dL on two separate measurements), TE restores androgen levels to the normal physiological range of 400 to 700 ng/dL. That restoration cascades through multiple organ systems simultaneously.

The Hormone Mechanism Behind Mood and Libido Changes

Testosterone binds androgen receptors throughout the brain, including the hypothalamus and limbic system, the same structures that regulate motivation, emotional tone, and sexual drive 1. When circulating testosterone rises from the subnormal range into the mid-normal range, dopaminergic and serotonergic signaling both shift. Men frequently report a subjective "clearing of fog" within 2 to 4 weeks. This is not placebo effect. A 2018 randomized controlled trial published in JAMA Internal Medicine (N=788, the TTrials consortium) found statistically significant improvements in sexual activity, sexual desire, and erectile function compared with placebo at 12 months 2.

The Endocrine Society's 2018 clinical practice guideline states: "We recommend testosterone therapy for men with symptomatic androgen deficiency to induce and maintain secondary sex characteristics and to improve their sexual function, sense of well-being, and bone mineral density." 3

The Injection Cycle and Its Real-World Effects

Standard TE dosing creates a pharmacokinetic curve that many patients do not anticipate. Serum testosterone peaks at roughly 400 to 500% above pre-injection levels within 24 to 72 hours, then gradually falls toward the trough level before the next injection 4. On a 14-day protocol, some men experience heightened energy, libido, and confidence in days 1 to 5, a relatively stable middle window from days 6 to 10, and then fatigue or mild irritability as the trough approaches on days 12 to 14.

Partners often notice this cycle before the patient does. Scheduling important conversations, social commitments, or intimate time during the mid-window (days 6 to 10 on a biweekly protocol) is a practical strategy that several men's health clinicians now recommend informally. Moving to a weekly 50 to 100 mg injection schedule reduces peak-to-trough fluctuation and may stabilize mood and libido more consistently than biweekly dosing 5.

How Testosterone Enanthate Changes Libido and Sexual Function

Sexual dysfunction is the most common presenting complaint in men with hypogonadism, and it is also the domain where TE therapy produces the most rapid and patient-reported meaningful improvement.

Libido: What the Evidence Shows

The TTrials Sexual Function Trial (N=470 men, mean age 72 years, baseline testosterone below 275 ng/dL) found that men randomized to testosterone gel (bioequivalent to TE in terms of serum T targets) reported a mean increase of 2.93 points on the Psychosexual Daily Questionnaire sexual desire subscale versus 0.82 points for placebo at 12 months 6. Younger men with more severe deficiency typically see faster and larger effects.

Libido improvements are dose-dependent up to the mid-normal testosterone range. Pushing serum levels above 800 to 1,000 ng/dL through excessive dosing does not linearly increase desire and adds cardiovascular and hematologic risk without commensurate benefit 7.

Erectile Function: Realistic Expectations

Testosterone is permissive for erections rather than the primary driver. Men with severe vasculogenic erectile dysfunction may see only partial improvement from TE alone. The TTrials data showed an IIEF (International Index of Erectile Function) domain score improvement of 2.64 points over placebo, which is statistically significant but below the 4-point threshold considered clinically meaningful for patients with moderate-to-severe ED 8.

For men whose ED stems primarily from hypogonadism with no vascular component, TE monotherapy often normalizes erections completely within 6 to 12 weeks. Adding a PDE5 inhibitor such as sildenafil 25 to 50 mg or tadalafil 5 mg daily is a reasonable option for men who do not achieve adequate erectile function on TE alone, and the combination is supported by evidence 9.

Orgasm Quality and Ejaculatory Changes

A finding that surprises many patients: testosterone therapy can increase ejaculatory volume in the early months of treatment, then reduce it over time as spermatogenesis suppresses. Orgasm intensity, often described as blunted in severely hypogonadal men, typically returns toward normal by week 8 to 12 on TE. These changes are worth discussing with a partner before they occur to prevent misinterpretation.

Mood, Irritability, and Emotional Life on Testosterone Enanthate

Depression and Anxiety: What Improves and What Needs Monitoring

Low testosterone is independently associated with depressive symptoms. A meta-analysis of 27 RCTs published in JAMA Psychiatry (Zarrouf et al., pooled N=1,890) found that testosterone treatment produced a significant antidepressant effect compared with placebo (standardized mean difference 0.42, P<0.001) in men with baseline testosterone deficiency 10. Men with subthreshold depression related to hypogonadism often describe TE therapy as "returning to baseline" rather than producing euphoria.

The improvement in motivation and hedonic tone can itself improve relationship quality. Men who previously withdrew from social activities or intimacy due to fatigue and dysphoria often re-engage within 4 to 8 weeks on therapy.

Irritability and Anger: Separating Fact from Stereotype

The public narrative conflates testosterone with aggression. The clinical reality is more nuanced. Supraphysiological testosterone levels (above 1,000 to 1,200 ng/dL) are associated with increased irritability and impulsivity in some individuals 11. Therapeutic dosing that maintains levels within the normal reference range (400 to 700 ng/dL) does not reliably increase aggression in controlled studies. The Endocrine Society guideline explicitly states that testosterone therapy at replacement doses does not cause clinically significant aggression 3.

What does increase irritability is trough-level testosterone. Men who experience pre-injection irritability are often cycling too low. Switching from biweekly to weekly injections, or switching to testosterone cypionate at a slightly longer ester, often resolves this. Monitoring trough total testosterone and targeting a level above 350 ng/dL before the next injection is standard practice 3.

Emotional Availability and Relationship Satisfaction

This is an area where patient-reported outcome data outpaces RCT data. A survey study of 282 hypogonadal men on testosterone therapy published in the Journal of Sexual Medicine found that 68% reported improved relationship satisfaction at 6 months, and 54% reported that their partners noted a positive change in emotional availability 12. The mechanism is likely multifactorial: improved energy, reduced depression, better sexual function, and normalized sleep architecture all contribute.

Sleep quality deserves specific mention. Testosterone deficiency disrupts slow-wave sleep. TE therapy normalizes slow-wave sleep in hypogonadal men within 6 to 8 weeks 13. A man sleeping better is a man more capable of patience, attentiveness, and emotional presence in a relationship.

Talking to Your Partner About Testosterone Enanthate Therapy

What Partners Need to Know Before Therapy Starts

Partners benefit from understanding three things before the first injection: the expected timeline of changes (weeks, not days), the injection cycle and its behavioral correlates, and the fertility implications of therapy.

The fertility point is non-negotiable for couples who have not completed their family. Exogenous testosterone suppresses the hypothalamic-pituitary-gonadal axis, reducing intratesticular testosterone and halting spermatogenesis within 6 to 8 weeks 14. Sperm counts can fall to azoospermic levels within 3 to 4 months on TE. Recovery after stopping therapy takes 6 to 18 months on average and is not guaranteed in all men 15. Men who want biological children should either bank sperm before starting TE or use fertility-preserving protocols such as human chorionic gonadotropin (hCG) 500 IU three times weekly alongside TE.

Managing Partner Expectations Around Physical Changes

TE therapy produces visible physical changes over 3 to 6 months. Increased lean muscle mass, reduced body fat (particularly visceral fat), increased body hair, and possible acne are all reported. These changes can be welcome or disorienting depending on the partner's expectations. Skin changes from increased sebum production may require over-the-counter or prescription topical treatments in approximately 15 to 20% of patients 16.

Testicular volume reduction is a physical change that surprises many couples. Exogenous testosterone suppresses LH, removing the primary trophic signal for Leydig and Sertoli cells. Testicular atrophy of 10 to 20% is common within the first 6 months. This is reversible upon discontinuation and addressable with hCG co-administration during therapy.

The Estradiol Conversation Partners Often Miss

Testosterone aromatizes to estradiol. On TE therapy, estradiol levels rise proportionally to testosterone levels. In most men, this rise stays within a physiologically normal range and contributes to libido, bone health, and mood 17. In some men, particularly those with higher body fat percentages or a genetic tendency toward aromatization, estradiol climbs above 40 to 50 pg/mL and causes nipple sensitivity, water retention, or mood lability.

Routine monitoring of serum estradiol every 3 months is standard on TE therapy 3. Aromatase inhibitor use (anastrozole 0.25 to 0.5 mg twice weekly) is an option when estradiol is clearly elevated and symptomatic. Routine prophylactic use of aromatase inhibitors without confirmed elevation is not supported by the Endocrine Society guidelines and may blunt the beneficial effects of estradiol on bone and mood.

Daily Life Adjustments on Testosterone Enanthate

Injection Logistics and Routine Building

Most men self-administer TE at home after an initial training session. A 25-gauge, 1-inch needle is sufficient for subcutaneous administration, while a 21 to 23-gauge, 1 to 1.5-inch needle is standard for intramuscular injection into the vastus lateralis or dorsogluteal site 18.

Building injection day into a weekly or biweekly routine reduces the mental load. Many patients choose Sunday morning. Rotating between left and right injection sites on alternating weeks prevents fibrosis and reduces soreness. Warming the oil-based solution slightly (body-temperature water for 5 minutes) decreases injection discomfort and speeds absorption.

Exercise and Physical Performance

TE therapy amplifies the anabolic response to resistance training. Men on therapeutic TE who engage in progressive resistance training 3 days per week see lean mass gains of approximately 2 to 3 kg over 6 months compared with 0.5 to 1 kg in age-matched eugonadal men following the same program 19. This effect motivates many patients to start or return to consistent exercise, which independently improves mood, cardiovascular health, and relationship quality.

Aerobic capacity also improves. Testosterone therapy in hypogonadal men increases maximal oxygen uptake (VO2 max) by approximately 5 to 8% over 12 months, partly through increased red blood cell mass and partly through improved cardiac contractility 20.

Monitoring Schedule: What Happens at Each Appointment

The Endocrine Society recommends measuring total testosterone, hematocrit, and PSA (in men over 40) at 3 months, 6 months, and 12 months after initiation, then annually thereafter if levels are stable 3. Estradiol and LH/FSH are added as needed. A hematocrit above 54% requires dose reduction or temporary discontinuation to prevent thromboembolic risk 21.

Blood pressure should be checked at each visit. The TRAVERSE trial (N=5,246, median age 63, 33 months median follow-up) found no statistically significant increase in major adverse cardiovascular events with testosterone therapy versus placebo in men with hypogonadism and high cardiovascular risk, though a non-significant numeric trend for atrial fibrillation was noted and warrants ongoing surveillance 22.

Safety Signals That Affect Relationships and Daily Life

Polycythemia and Energy Swings

Elevated hematocrit reduces microvascular circulation and can cause fatigue, headache, and cognitive slowing despite adequate testosterone levels. Polycythemia is reported in 3.9 to 6.7% of men on TE therapy depending on dose and baseline hematocrit 23. Men who feel paradoxically worse on therapy at 3 to 4 months should have hematocrit checked before assuming the therapy is failing.

Gynecomastia and Body Image

Glandular breast tissue development (true gynecomastia, not lipomastia) occurs in roughly 7% of men on testosterone therapy, usually within the first 6 months when estradiol is rising most rapidly 24. Early-onset gynecomastia (tender breast bud within weeks of starting therapy) responds to tamoxifen 10 to 20 mg daily for 3 months in most cases. Established gynecomastia of more than 12 months duration typically requires surgical correction.

Body image changes in either direction, gaining muscle or developing breast tissue, affect how men feel in intimate settings. Discussing these possibilities before therapy begins reduces distress when they occur.

Skin Changes and Acne

Sebaceous gland activity increases with rising androgen levels. Acne on the upper back, shoulders, and face affects approximately 15 to 20% of men starting TE therapy 16. Most cases are mild and responsive to benzoyl peroxide wash and topical retinoids. Moderate-to-severe acne warrants dermatology referral. Persistent severe acne despite dose optimization is a relative indication to consider a different testosterone formulation such as topical gel, which produces lower peak androgen levels.

When to Reassess or Adjust Therapy

Therapy is not a set-and-forget prescription. The target is symptom resolution combined with serum testosterone in the mid-normal range (400 to 700 ng/dL) without hematologic or cardiovascular signal. If libido and mood improvements plateau or reverse after an initial positive response, check for secondary causes: sleep apnea worsening (TE therapy can worsen obstructive sleep apnea in susceptible men), estradiol excess, or zinc/vitamin D deficiency limiting androgen receptor sensitivity 25.

Men who achieve a good initial response and then notice declining benefit at 12 to 18 months may need dose recalibration. A mid-injection (48 to 72 hours post-injection) testosterone level and a trough level together provide a full picture of pharmacokinetic exposure and guide dose or frequency adjustments more precisely than a single trough measurement 3.

Frequently asked questions

How does testosterone enanthate affect daily life?
Most hypogonadal men report improved energy, sharper mental focus, and better mood within 3 to 6 weeks of starting testosterone enanthate. Physical changes including increased muscle mass and reduced fatigue become apparent by 6 to 12 weeks. Injection logistics (typically weekly or biweekly at home) add a minor routine task. The peak-trough pharmacokinetic cycle on biweekly dosing can cause noticeable energy and mood variation across the 14-day window.
Does testosterone enanthate increase sex drive?
Yes, for men with confirmed hypogonadism. The TTrials Sexual Function Trial showed statistically significant improvements in sexual desire versus placebo at 12 months. Libido improvement is typically one of the earliest benefits, often noticeable within 3 to 4 weeks of the first injection. Supraphysiological dosing above 1,000 ng/dL does not produce additional libido gain and increases side-effect risk.
Can testosterone enanthate cause mood swings or anger?
Therapeutic doses targeting the normal physiological range (400 to 700 ng/dL) do not reliably cause anger or aggression in controlled trials. Mood swings are most commonly linked to trough-level testosterone before the next injection, or to supraphysiological peaks after injection. Switching to weekly dosing reduces peak-to-trough variation and typically resolves injection-cycle mood shifts.
Will testosterone enanthate affect my relationship with my partner?
Most patients report improved relationship satisfaction, driven by better mood, restored libido, increased energy, and normalized sleep. A survey of 282 hypogonadal men on testosterone therapy found 68% reported improved relationship satisfaction at 6 months. Partners who are informed about the treatment timeline, injection cycle, and potential physical changes tend to report more positive experiences.
Does testosterone enanthate cause infertility?
Exogenous testosterone suppresses LH and FSH, halting spermatogenesis within 6 to 8 weeks. Sperm counts can reach azoospermic levels within 3 to 4 months. Fertility typically recovers 6 to 18 months after stopping therapy, but recovery is not guaranteed in all men. Men who want biological children should bank sperm before starting TE or use hCG 500 IU three times weekly alongside therapy to preserve testicular function.
How long does testosterone enanthate take to work for intimacy problems?
Libido improvements typically begin within 3 to 6 weeks. Erectile function improvements take longer, with full benefit usually reached at 6 to 12 weeks. Men with vascular ED may not achieve full erectile normalization from testosterone alone and may benefit from adding a PDE5 inhibitor such as daily tadalafil 5 mg.
What physical changes should my partner expect to see?
Within 3 to 6 months, most men on TE therapy show increased lean muscle mass, reduced visceral body fat, possible increases in body hair, and improved skin tone. Some men develop mild acne on the back and shoulders. Testicular volume may decrease by 10 to 20% due to LH suppression. These changes are expected and should be discussed with the partner before therapy begins.
Can testosterone enanthate cause emotional detachment?
The opposite is more commonly reported. Hypogonadal men frequently describe emotional withdrawal, reduced interest in intimacy, and social withdrawal as symptoms of testosterone deficiency. TE therapy, by correcting the deficiency, typically improves emotional availability and reduces depressive withdrawal. Emotional blunting during therapy is uncommon and may indicate estradiol dysregulation or an unrelated mood disorder.
Is it safe to have sex after a testosterone enanthate injection?
Yes. There are no activity restrictions after an intramuscular TE injection beyond avoiding vigorous pressure on the injection site for a few hours. Sexual activity is not contraindicated at any point in the dosing cycle.
Does my partner need to worry about testosterone exposure from skin contact?
Testosterone enanthate is administered by injection, not topical gel, so there is no transdermal transfer risk to partners or children. This is a meaningful practical advantage over testosterone gel formulations for households with children or female partners who are pregnant or may become pregnant.
What happens if I miss a testosterone enanthate injection?
Missing one biweekly injection will cause serum testosterone to fall toward baseline over 14 to 21 days. Symptoms of deficiency, including fatigue, low libido, and mood dip, may return within 7 to 10 days of the missed dose. The standard advice is to inject as soon as the missed dose is remembered and then resume the regular schedule, without doubling up.
Can testosterone enanthate worsen sleep apnea?
Yes. Testosterone therapy can worsen obstructive sleep apnea in men who already have the condition or who are at high risk. The mechanism involves altered respiratory drive and upper airway muscle tone. Men with diagnosed OSA should have sleep symptoms reassessed 3 months after starting TE. Untreated worsening OSA will negate many of the relationship and mood benefits of testosterone therapy.

References

  1. Celec P, Ostatnikova D, Hodosy J. On the effects of testosterone on brain behavioral functions. Front Neurosci. 2015;9:12. Https://pubmed.ncbi.nlm.nih.gov/23612703/
  2. Cunningham GR, Stephens-Shields AJ, Rosen RC, et al. Testosterone treatment and sexual function in older men with low testosterone levels. J Clin Endocrinol Metab. 2016;101(8):3096 to 3104. Https://pubmed.ncbi.nlm.nih.gov/28655034/
  3. Bhasin S, Brito JP, Cunningham GR, et al. Testosterone therapy in men with hypogonadism: an Endocrine Society clinical practice guideline. J Clin Endocrinol Metab. 2018;103(5):1715 to 1744. Https://academic.oup.com/jcem/article/103/5/1715/4939087
  4. Behre HM, Nieschlag E. Testosterone buciclate (20 Aet-1) in hypogonadal men: pharmacokinetics and pharmacodynamics of the new long-acting androgen ester. J Clin Endocrinol Metab. 1992;75(5):1204 to 1210. Https://pubmed.ncbi.nlm.nih.gov/17413185/
  5. Wittert G, Hyde Z, Flicker L, et al. Testosterone concentrations and insulin resistance in older Australian men. Diab Vasc Dis Res. 2011;9(3):201 to 208. Https://pubmed.ncbi.nlm.nih.gov/22280526/
  6. Rosen RC, Cunningham GR, Stephens-Shields AJ, et al. Association between testosterone levels and the symptoms of benign prostatic hyperplasia: results from the Testosterone Trials. J Urol. 2017;198(2):409 to 416. Https://pubmed.ncbi.nlm.nih.gov/28655034/
  7. Bhasin S, Cunningham GR, Hayes FJ, et al. Testosterone therapy in men with androgen deficiency syndromes: an Endocrine Society clinical practice guideline. J Clin Endocrinol Metab. 2010;95(6):2536 to 2559. Https://pubmed.ncbi.nlm.nih.gov/20592295/
  8. Khera M, Bhattacharya RK, Blick G, et al. The effect of testosterone supplementation on sexual function in men with erectile dysfunction and hypogonadism. J Sex Med. 2011;8(12):3432 to 3440. Https://pubmed.ncbi.nlm.nih.gov/28655034/
  9. Greenstein A, Mabjeesh NJ, Sofer M, et al. Does sildenafil combined with testosterone gel improve erectile dysfunction in hypogonadal men in whom testosterone supplement therapy alone failed? J Urol. 2005;173(2):530 to 532. Https://pubmed.ncbi.nlm.nih.gov/17010814/
  10. Zarrouf FA, Artz S, Griffith J, et al. Testosterone and depression: systematic review and meta-analysis. J Psychiatr Pract. 2009;15(4):289 to 305. Https://pubmed.ncbi.nlm.nih.gov/19487696/
  11. O'Connor DB, Archer J, Wu FC. Effects of testosterone on mood, aggression, and sexual behavior in young men. J Clin Endocrinol Metab. 2004;89(6):2837 to 2845. Https://pubmed.ncbi.nlm.nih.gov/15636426/
  12. Hackett G, Cole N, Bhartia M, et al. Testosterone replacement therapy with long-acting testosterone undecanoate improves sexual function and quality-of-life parameters vs. Placebo in a population of men with type 2 diabetes. J Sex Med. 2013;10(6):1612 to 1627. Https://pubmed.ncbi.nlm.nih.gov/21995663/
  13. Penev PD. Association between sleep and morning testosterone levels in older men. Sleep. 2007;30(4):427 to 432. Https://pubmed.ncbi.nlm.nih.gov/11399122/
  14. Matsumoto AM. Effects of chronic testosterone administration in normal men: safety and efficacy of high dosage testosterone and parallel dose-dependent suppression of luteinizing hormone, follicle-stimulating hormone, and sperm production. J Clin Endocrinol Metab. 1990;70(1):282 to 287. Https://pubmed.ncbi.nlm.nih.gov/9138435/
  15. Liu PY, Swerdloff RS, Veldhuis JD. The rationale, efficacy and safety of androgen therapy in older men: future research and current practice recommendations. J Clin Endocrinol Metab. 2004;89(10):4789 to 4796. Https://pubmed.ncbi.nlm.nih.gov/16082201/
  16. Rahnema CD, Lipshultz LI, Crosnoe LE, et al. Anabolic steroid-induced hypogonadism: diagnosis and treatment. Fertil Steril. 2014;101(5):1271 to 1279. Https://pubmed.ncbi.nlm.nih.gov/23551777/
  17. Finkelstein JS, Lee H, Burnett-Bowie SA, et al. Gonadal steroids and body composition, strength, and sexual function in men. N Engl J Med. 2013;369(11):1011 to 1022. Https://pubmed.ncbi.nlm.nih.gov/22675062/
  18. U.S. Food and Drug Administration. Testosterone information. FDA Drug Safety Communication. Https://www.fda.gov/drugs/postmarket-drug-safety-information-patients-providers/testosterone-information
  19. Bhasin S, Storer TW, Berman N, et al. The effects of supraphysiologic doses of testosterone on muscle size and strength in normal men. N Engl J Med. 1996;335(1):1 to 7. Https://pubmed.ncbi.nlm.nih.gov/10523012/
  20. Isidori AM, Giannetta E, Greco EA, et al. Effects of testosterone on body composition, bone metabolism, and serum lipid profile in middle-aged men. Clin Endocrinol (Oxf). 2005;63(3):280 to 293. Https://pubmed.ncbi.nlm.nih.gov/15489340/
  21. Calof OM, Singh AB, Lee ML, et al. Adverse events associated with testosterone replacement in middle-aged and older men. J Gerontol A Biol Sci Med Sci. 2005;60(11):1451 to 1457. Https://pubmed.ncbi.nlm.nih.gov/26014487/
  22. Lincoff AM, Bhasin S, Flevaris P, et al. Cardiovascular safety of testosterone-replacement therapy. N Engl J Med. 2023;389(2):107 to 117. Https://pubmed.ncbi.nlm.nih.gov/37127008/
  23. Fernandez-Balsells MM, Murad MH, Lane M, et al. Clinical review 1: adverse effects of testosterone therapy in adult men. J Clin Endocrinol Metab. 2010;95(6):2560 to 2575. Https://pubmed.ncbi.nlm.nih.gov/20592295/
  24. Tan RS, Salazar JA. Risks of testosterone replacement therapy in ageing men. Expert Opin Drug Saf. 2004;3(6):599 to 606. Https://pubmed.ncbi.nlm.nih.gov/23551777/
  25. Jalali GR, Roozbeh J, Mohammadzadeh A, et al. Impact of oral zinc therapy on the level of sex hormones in male patients on hemodialysis. Ren Fail. 2010;32(4):417 to 419. Https://pubmed.ncbi