top of page
test
Testosterone + DHEA
ANALYTES
Analytes are the substances measured in this test, which include:
DHEA
Testosterone
E1 + E2 + Progesterone
If estrogen and progesterone testing has been suggested, this test panel allows for their inclusion, and separate testing is not required.
Further, this tests analytes are the same test as the Menopause Profile
rESULTS
sample Req.
DHEA and testosterone constitute the primary focus of this assessment. These androgens demonstrate relative stability across the menstrual cycle and may therefore be measured at any phase without significant compromise to interpretive accuracy.
However, DHEA and testosterone are interpreted in conjunction with estradiol (E2), estrone (E1), and progesterone to provide a comprehensive evaluation of overall hormonal balance. For enhanced contextual insight we recommend that salivary collection be performed approximately seven days post-ovulation, during the mid-luteal phase, or midway between ovulation and the anticipated onset of the next menstrual cycle.
For greater precision, urinary ovulation predictor kits are available through pharmacies to assist in confirming ovulation timing.
If accurate menstrual tracking is not feasible, testing may still proceed, with results interpreted accordingly, please advise by email if this is the case for you.
Saliva
cOST
The results of your health assessment have identified specific signs and symptoms that are clinically consistent with an increased risk of
Hyperandrogenism
Hyperandrogenism is associated with a range of signs and symptoms, which have been clinically verified to include
Male pattern hair growth distribution
Acne, particularly lower face distribution
Diffuse central hair thinning
Infertility + miscarriage
Infrequent menstrual cycles
Cycles longer than 35 days
Energy decline between meals
Cravings for sweet or starchy food
Abdominal weight gain
This investigation is optional and may be used to verify the need for therapeutic intervention for Hyperandrogenism
In the absence of testing, treatment is tailored to address suspected contributors based on the presence of specific signs and symptoms and their degree of correlation with those contributors. If testing is undertaken, the assessment will be re-evaluated in accordance with the test results. You will be updated with the test results alongside any treatment revisions necessary.
A salivary collection kit will be provided for the assessment of midnight cortisol and melatonin levels. The kit includes detailed instructions outlining the required collection protocol to ensure accurate timing and sample integrity.
A pre-addressed, secure return package is included to facilitate safe transport of the specimen to the laboratory, where quantitative analysis will be performed using validated analytical techniques.
Estimated turnaround time: 5 business days
bottom of page