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450 AED

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Androstenedione Serum Test in UAE | 450 AED | 2026 DHA Guidelines

تحليل الأندروستينيديون في الإمارات | 450 درهم | معتمد من هيئة الصحة بدبي

Clinical Executive Summary

ملخص تنفيذي سريري: اختبار الأندروستينيديون في المصل هو فحص مخبري كمي معتمد من هيئة الصحة بدبي لتقييم وظيفة الغدة الكظرية وإنتاج الأندروجين التناسلي، ويُجرى وفق بروتوكولات الجمع الصباحي الباكر مع مراعاة توقيت الدورة الشهرية لدى الإناث، وتبلغ مدة إصدار النتيجة في نفس اليوم للعينات المسحوبة يومي الاثنين أو الخميس قبل الساعة 11 صباحاً.

  • Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing (Cert: INT/EGQ/2509DA/3139).
  • Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection and VIP Mobile Phlebotomy — covering all seven Emirates, 8:00 AM to 11:00 PM daily.
  • Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation by DHA-licensed endocrine specialists.
  • Insurance: Direct Billing Verification via WhatsApp at +971 54 548 8731.

Test Overview

The Androstenedione Serum Test is a quantitative hormonal assay 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.
يقيس اختبار الأندروستينيديون في المصل مستوى هذا الهرمون الستيرويدي الذي تنتجه الغدد الكظرية والغدد التناسلية، ويُستخدم في تشخيص اضطرابات الغدة الكظرية وفرط الأندروجين.

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 9834453 Variable / Unverified

Physician Insight & Safety Protocol

A Note from Dr. Prabhakar Reddy, DHA License No. 61713011

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 endocrinologist, 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. Please rest assured that 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.

⚠ Medication Warning

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 — CDS Law 2026): Patients under 18 years require documented parental or legal guardian consent per UAE Federal Decree-Law No. 41 of 2024, Article 87.
  • 🚨 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.

يقيس اختبار الأندروستينيديون إنتاج الأندروجين من الغدد الكظرية والتناسلية لتقييم الاختلالات الهرمونية وتشخيص فرط تنسج الغدة الكظرية الخلقي ومتلازمة المبيض متعدد الكيسات. يُطلب هذا التحليل عند وجود أعراض فرط الأندروجين مثل نمو الشعر الزائد واضطرابات الدورة الشهرية والبلوغ المبكر أو المتأخر، ويُفسر بالاشتراك مع فحوصات هرمونية أخرى للحصول على صورة سريرية متكاملة.

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.

يجب سحب عينة الدم في الصباح الباكر بين الساعة 7 و9 صباحاً بعد صيام 8-10 ساعات، مع مراعاة أن يكون التوقيت قبل الدورة الشهرية بأسبوع أو بعدها بأسبوع لدى الإناث. يُنصح بتجنب التمارين الشاقة والكحول قبل الفحص، والإبلاغ عن جميع الأدوية والمكملات الهرمونية لضمان دقة النتيجة وتجنب التداخلات التحليلية.

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- clinical guidance line is available to discuss preliminary findings via WhatsApp at +971 54 548 8731.

تُصدر النتائج في نفس اليوم للعينات المسحوبة يومي الاثنين أو الخميس قبل الساعة 11 صباحاً، مع توفر استشارة سريرية هاتفية من أطباء مرخصين من هيئة الصحة بدبي. تختلف النطاقات المرجعية حسب العمر والجنس ومرحلة تانر لدى الأطفال، وتُفسر النتائج غير الطبيعية بناءً على السياق السريري الكامل وقد تستدعي فحوصات إضافية أو تصويراً أو اختبارات جينية.

DHA-Certified Diagnostic Excellence | ISO 9001:2015 | UAE PDPL Compliant

WhatsApp: +971 54 548 8731 | Facility License: 9834453 | Home Collection: 8 AM – 11 PM Daily

مختبر معتمد من هيئة الصحة بدبي | شهادة الأيزو 9001:2015 | امتثال كامل لقانون حماية البيانات الشخصية الإماراتي

Regulatory Compliance: This service complies with UAE Federal Decree-Law No. 41 of 2024 (Article 87 — Minor Consent Requirements), UAE Communicable Disease Surveillance Law 2026 (Minors provision), and UAE PDPL (Federal Decree-Law No. 45 of 2021). All laboratory processing adheres to DHA/MOHAP 2026 endocrine testing standards.

ICD-10-CM 2026 Codes: E27.8 (Other specified disorders of adrenal gland) | E25.0 (Congenital adrenogenital disorders associated with enzyme deficiency) | Z13.29 (Encounter for screening for other suspected endocrine disorder). LOINC: 1854-9 — Androstenedione [Mass/volume] in Serum or Plasma (loinc.org/1854-9).

Methodology Update: Chemiluminescent Immunoassay (CLIA) performed on ISO-calibrated automated platforms with inter-laboratory proficiency testing per DHA External Quality Assurance Scheme (EQAS) 2026 standards.

Disclaimer: This content is for informational purposes only and does not constitute medical advice. Always consult a DHA-licensed physician for diagnosis and treatment decisions.

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