Where does your testosterone rank for your age?
Enter your most recent lab value and see where you sit in the age-adjusted distribution. The blanket 300 ng/dL cutoff most GPs use ignores age. This calculator does not.
Querying clinical reference…
How old is your body really?
Your biological age from health markers, often very different from your chronological age.
How testosterone percentiles are calculated
This calculator uses age-adjusted reference ranges from Travison et al. (2017), which harmonised testosterone measurement across four major US cohort studies (Framingham, BLSA, MMAS, EMAS) covering more than 9,000 men. Female reference ranges are derived from Rothman et al. (2011) and NHANES III. For each age group and sex, the percentile is calculated by interpolating between centile breakpoints (2.5th, 10th, 25th, 50th, 75th, 90th, 97.5th). Testosterone is closely linked to erectile function: see the erectile dysfunction prevalence calculator for population data by age.
A 50-year-old man with a reading of 500 ng/dL is in the 50th percentile for his age. The same reading in a 25-year-old is in the 25th percentile. Age matters.
Age-adjusted ranges, not blanket cutoffs
The most widely-cited "low testosterone" cutoff in primary care is 300 ng/dL, derived from Endocrine Society guidance for younger men. But applying this single number across all ages misses the point: testosterone declines roughly 1 to 2% per year after age 30. A reading of 350 ng/dL might be entirely normal for a 70-year-old yet flag as borderline-low for a 25-year-old.
Why the 300 ng/dL cutoff misleads
The blanket cutoff was originally a clinical convenience for treatment thresholds in younger symptomatic men, not a population norm. Subsequent harmonisation work showed that the lower limit of normal varies meaningfully with age. Men with readings below the age-adjusted 10th percentile may benefit from clinical evaluation regardless of where they sit relative to the 300 ng/dL line. Testosterone levels also interact with overall metabolic health: check your biological age estimate to see how lifestyle factors compound over time.
Reference ranges by age (men, ng/dL)
| Age | 10th | 50th (median) | 90th |
|---|---|---|---|
| 18 to 25 | 380 | 612 | 850 |
| 26 to 35 | 370 | 590 | 820 |
| 36 to 45 | 350 | 560 | 790 |
| 46 to 55 | 330 | 530 | 760 |
| 56 to 65 | 310 | 500 | 730 |
| 66 to 75 | 290 | 470 | 700 |
| 76+ | 270 | 440 | 670 |
Harmonised reference values from Travison et al. (2017), Journal of Clinical Endocrinology & Metabolism.
Frequently asked questions
The median for men aged 18 to 25 is approximately 612 ng/dL, falling to 440 ng/dL by age 76+. The "normal range" widens with age, but the centre of the distribution shifts down. A 50-year-old at 530 ng/dL is at the median for his age. The same value in a 25-year-old is at the 25th percentile.
Yes. Testosterone follows a diurnal rhythm and is highest between 7am and 10am. Afternoon readings can be 20 to 25% lower than morning peaks. The Endocrine Society recommends morning fasting draws for diagnostic accuracy.
Total testosterone measures all circulating testosterone, including the portion bound to sex hormone binding globulin (SHBG) and albumin. Free testosterone is the unbound, biologically active fraction (typically 1 to 3% of total). For most clinical decisions, total testosterone is the primary measurement, but free or bioavailable testosterone may be more informative when SHBG is abnormal.
Testosterone levels and symptoms correlate more loosely than many people assume. SHBG levels, individual androgen receptor sensitivity, and other hormones (oestradiol, cortisol, thyroid) all modulate the symptomatic experience. A symptom-driven evaluation matters as much as the lab number.
Female testosterone is approximately one-twentieth of male levels. The median for women aged 18 to 25 is around 35 ng/dL, declining gradually to about 20 ng/dL post-menopause. Female reference ranges are less well-established than male, with significant variation between labs. Menopausal status is more predictive than age alone.
Yes, modestly. Weight loss in obese men can raise testosterone by 50 to 100 ng/dL on average. Resistance training has small acute effects but no consistent long-term effect on baseline levels in well-trained men. Improved sleep (especially treating sleep apnoea), reducing chronic stress, and moderate alcohol intake all have measurable effects. Effect sizes are typically modest compared to age-related decline.
Testosterone replacement therapy is appropriate for men with confirmed clinically low levels (typically below the age-adjusted 10th percentile) plus consistent symptoms. It is not appropriate for cosmetic boost or for men with normal age-adjusted levels. Risks include polycythaemia, fertility suppression, cardiovascular concerns (debated), and dependence on continued therapy.
TRT safety depends on the individual and requires medical supervision. The TRAVERSE trial (2023, N=5,204 men, NEJM) was the first large randomised controlled trial powered for cardiovascular outcomes and found TRT did not increase the risk of major adverse cardiovascular events compared to placebo in men aged 45 to 80 with pre-existing or high cardiovascular risk. Known risks include erythrocytosis (elevated red blood cell count), acne, potential worsening of sleep apnoea, and suppression of natural testosterone production. TRT is contraindicated in men actively trying to conceive and those with untreated severe sleep apnoea. The benefits, when genuinely low testosterone is confirmed, can include improved energy, libido, mood, bone density, and body composition. The decision should always involve a clinician who reviews your full blood panel, symptoms, and medical history.
- Travison TG et al. Harmonized reference ranges for circulating testosterone levels in men of four cohort studies. Journal of Clinical Endocrinology & Metabolism. 2017;102(4):1161-1173. doi:10.1210/jc.2016-2935
- Rothman MS et al. Reexamination of testosterone, dihydrotestosterone, estradiol and estrone levels across the menstrual cycle. Steroids. 2011;76(1-2):177-182. doi:10.1016/j.steroids.2010.10.010
- Bhasin S et al. Testosterone Therapy in Men with Hypogonadism: An Endocrine Society Clinical Practice Guideline. Journal of Clinical Endocrinology & Metabolism. 2018;103(5):1715-1744. doi:10.1210/jc.2018-00229
- Lincoff AM et al. Cardiovascular Safety of Testosterone-Replacement Therapy (TRAVERSE). New England Journal of Medicine. 2023;389(2):107-117. doi:10.1056/NEJMoa2215025
- Kelsey TW et al. A validated age-related normative model for male total testosterone shows increasing variance but no decline after age 40 years. PLoS One. 2014;9(10):e109346. doi:10.1371/journal.pone.0109346