Test Price
450 AED✅ Home Collection Available
Androstenedione Serum Test in UAE | 450 AED | DHA Certified
Executive Summary & Core Metrics
Clinical Executive Summary
- ◆ Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing (Cert: INT/EGQ/2509DA/3139).
- ◆ Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection — available daily from 8:00 AM to 11:00 PM across all seven Emirates.
- ◆ Clinical Guidance: Telephonic post-test interpretation by DHA-licensed general practitioners.
- ◆ Insurance: Direct Billing Verification via WhatsApp at +971 54 548 8731.
Test Overview & Methodology
The Androstenedione Serum Test is a quantitative chemiluminescent immunoassay (CLIA) that measures circulating androstenedione — a key androgen precursor produced by the adrenal glands and gonads — to aid in diagnosing adrenal disorders, congenital adrenal hyperplasia (CAH), polycystic ovary syndrome (PCOS), and androgen-secreting tumors. This test is clinically indicated when evaluating hyperandrogenism, precocious puberty, delayed puberty, or suspected enzymatic deficiencies in steroidogenesis pathways.
| Parameter | Our Test (DHA-Certified) | Closest Alternative |
|---|---|---|
| Precision (CV%) | ≤ 3.5% Intra-Assay (CLIA, ISO-Calibrated) | 5–8% (Standard Immunoassay, Non-ISO) |
| Methodology | Chemiluminescent Immunoassay (CLIA) — 2026 Standardized | ELISA / RIA (Legacy Platforms) |
| Turnaround | Same Day (Mon/Thu before 11 AM) | 48–72 Hours (Routine Lab) |
| Pre-Analytical Protocol | Circadian & Menstrual-Phase Optimized | Non-Specific / Non-Standardized |
| Accreditation | ISO 9001:2015 + DHA Facility License 1143 | Variable / Unverified |
Physician Insight & Safety Protocols
A Note from Dr. Ajay Singh, DHA License No. 36234132
Understanding your androstenedione levels requires careful clinical correlation with your symptoms, medical history, and other hormonal assays including DHEA-S, testosterone, and 17-hydroxyprogesterone. As your consulting general practitioner, I emphasize that this test is one piece of a comprehensive diagnostic puzzle, and results must be interpreted within the full context of your endocrine health — never in isolation. Our team is committed to guiding you through every step of your diagnostic journey with precision, empathy, and the highest standards of UAE healthcare excellence.
Advisory & Medication Warning
⚠ Important Safety Notice
Do not discontinue any prescribed medication, including corticosteroids, oral contraceptives, anti-androgens, or hormone replacement therapy, without consulting your treating physician. Abrupt cessation of adrenal-suppressive medications may precipitate acute adrenal crisis, a life-threatening emergency. Inform your phlebotomist of all medications, supplements, and herbal preparations prior to sample collection.
Exclusion Criteria & Emergency Red Flags
- 🚨 Exclusion: Active febrile illness, acute infection, or hospitalization within 72 hours — reschedule collection.
- 🚨 Exclusion: Recent administration of radio-contrast agents or nuclear medicine isotopes (within 7 days).
- 🚨 Exclusion (Minors): Patients under 18 years require documented parental or legal guardian consent per UAE Federal Decree-Law No. 4 of 2016 on Medical Liability.
- 🚨 ER Red Flag: If you experience severe abdominal pain, hypotension, altered consciousness, or signs of acute adrenal insufficiency post-collection, proceed to the nearest emergency department immediately.
- 🚨 Data Privacy: All patient data is protected under UAE PDPL (Federal Decree-Law No. 45 of 2021). Results are encrypted and accessible only to the ordering physician and authorized patient portal.
Patient FAQ & Clinical Guidance
1. What is the Androstenedione test used for, and why has my doctor ordered it?
The Androstenedione test measures adrenal and gonadal androgen production to evaluate hormonal imbalances, congenital adrenal hyperplasia, polycystic ovary syndrome, and androgen-secreting neoplasms. Your endocrinologist or functional medicine practitioner has ordered this test to investigate symptoms such as hirsutism, menstrual irregularity, precocious or delayed puberty, or unexplained hyperandrogenism. Elevated levels may indicate 21-hydroxylase deficiency (the most common form of CAH), adrenal tumors, or PCOS-related ovarian overproduction, while low levels can suggest adrenal insufficiency or hypogonadism. The test is most informative when interpreted alongside DHEA-S, total and free testosterone, 17-hydroxyprogesterone, and cortisol in a comprehensive adrenal panel.
2. How should I prepare for the Androstenedione blood test in the UAE?
An early morning fasting blood sample collected between 7:00 AM and 9:00 AM is required because androstenedione follows a pronounced circadian rhythm. For female patients, the optimal collection window is one week before or one week after the menstrual period to avoid mid-cycle physiological fluctuations that may confound interpretation. You should fast for 8–10 hours prior to collection (water is permitted), avoid strenuous exercise for 24 hours, and refrain from alcohol consumption for 48 hours. Inform the phlebotomist of all medications — particularly corticosteroids, oral contraceptives, anti-androgens, and any over-the-counter hormonal supplements — as these may interfere with assay accuracy. Our ISO-certified home collection team will arrive with pre-chilled SST vacutainers and cold-chain transport containers to ensure specimen integrity from collection to laboratory analysis.
3. When will I receive my Androstenedione test results, and how are they interpreted?
Results are reported the same day for samples collected on Monday or Thursday before 11:00 AM, with telephonic clinical guidance available from DHA-licensed specialists. Androstenedione reference ranges vary by age, sex, and Tanner stage (in pediatric patients), and your result will be interpreted against validated UAE population reference intervals. Typical adult male values range from 0.6–3.1 ng/mL, while premenopausal females range from 0.3–3.3 ng/mL with mid-cycle peaks. Postmenopausal values decline to 0.2–1.7 ng/mL. Abnormal results require correlation with clinical findings and may necessitate repeat testing, imaging studies (adrenal CT/MRI), or genetic testing for CAH (CYP21A2 gene sequencing). Your ordering physician will receive a comprehensive interpretive report, and our post-test clinical guidance line is available to discuss preliminary findings via WhatsApp at +971 54 548 8731.
UAE Regulatory & Data Privacy Adherence
Data Protection: All personal data is processed in strict compliance with UAE Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) and Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields. Patient health information is encrypted, access-controlled, and disclosed only to the ordering physician and authorized personnel.
Clinical Safety & Consent: The collection and handling of all specimens adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability, ensuring informed consent and patient safety at every step. The laboratory holds DHA Facility License No. 1143 and operates under ISO 9001:2015 certified quality management systems.
Clinical & Logistical Metadata
| Test Name | Androstenedione Serum Test |
| Price (AED) | 450 AED |
| Turnaround Time | Same Day (Mon/Thu before 11 AM) |
| Sample Type / Matrix | Serum (peripheral whole blood) |
| Methodology Used | Chemiluminescent Immunoassay (CLIA) |
| ICD-10-CM Code | E27.8, E25.0, Z13.29 |
| LOINC Code | 1854-9 |
| DHA Facility License & Address | License No. 1143 — Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
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