Chemical Pathology

Notes

  • The clinical indications for the measurement of DHT are: investigation of 5α reductase deficiency in infants with ambiguous genitalia and palpable gonads; males with delayed puberty and/or undescended testes; and to confirm the presence of active testicular tissue. Investigation is aided by the use of human chorionic gonadotrophin stimulation. Urine steroid profiling is now more often performed.
  • Measurement is rarely of use in women.
  • DHT is a current requirement for patients being referred to the London Gender Identity Clinic.

Sample requirements

For adults, 5 ml of blood taken into a narrow gold top tube

5ml gold tube






For children, 3.5 ml of blood taken into a rust top tube

3.5ml rust top tube





Storage/transport

Send at ambient temperature to the laboratory on day of sample collection.

Required information

Relevant clinical details.

Turnaround times

Samples are sent for analysis to St. Thomas' Hospital, London with results expected back within 28 days.

Reference ranges

Age Male Female Status
< 14 days <1.89 <0.1
2w - 6m 0.14 - 4.13 <0.1
6m - <9.8y <0.1 <0.1 Tanner stage 1
9.8y - 14.5y 0.10 - 0.59 0.17 - 0.42 Tanner stage 2
10.7 - 15.4y 0.28 - 1.14 0.24 - 0.66 Tanner stage 3
11.8y - 16.2y 0.76 - 1.79 0.14 - 0.45 Tanner stage 4
12.8y - 17.3y 0.83 - 2.24 0.10 - 0.62 Tanner stage 5
Adult males 0.86 - 3.40
Adult females <1.27 Pre-menopausal
Adult females <0.62 Post-menopausal

Please note that there is approximately 8.7% interference from testosterone and also interference with finasteride treatment – raised results may require follow up with tandem mass spectrometry

Further information

Adult Gender Dysphoria Guidelines (RcPsych)

NHS Gender Dysphoria


Page last updated 03/05/2017