This is a prospective biobank set up to collect serum from patients with disorders associated with changes in androgens, estrogens or sex hormone-binding globulin (SHBG), before and/or after treatment.
In vitro cell-based bioassays may be a technique to measure serum androgen or estrogen bioactivity. In this study investigators are collecting serum (and if possible, urine) samples from different cohorts of patients, before and/or after treatment. The aim is to measure androgens, estrogens and SHBG as well as in vitro bioactivity with newly developed cell-based bioassays, and to compare different techniques to each other as well as to clinical endpoints available in the patient's Electronic Health Record.
Study Type
OBSERVATIONAL
Enrollment
73
Testosterone bioequivalents (in nanomolar)
Time frame: second blood sample at time of clinical follow-up (between 3 weeks and 1 year interval)
Estradiol bioequivalents (in picomolar)
Time frame: second blood sample at time of clinical follow-up (between 3 weeks and 1 year interval)
Calculated free and bioavailable testosterone (in nanomolar)
Time frame: second blood sample at time of clinical follow-up (between 3 weeks and 1 year interval)
Calculated free and bioavailable estradiol (in picomolar)
Time frame: second blood sample at time of clinical follow-up (between 3 weeks and 1 year interval)
Total serum testosterone (in nanomolar)
Measured by immunoassay or liquid chromatography tandem mass spectrometry (LC-MS/MS)
Time frame: second blood sample at time of clinical follow-up (between 3 weeks and 1 year interval)
Total serum estradiol (in picomolar)
Measured by immunoassay or LC-MS/MS
Time frame: second blood sample at time of clinical follow-up (between 3 weeks and 1 year interval)
Total serum SHBG (in nanomolar)
Measured by immunoassay
Time frame: second blood sample at time of clinical follow-up (between 3 weeks and 1 year interval)
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