Test Price
160 AED✅ Home Collection Available
Anti‑dsDNA Antibody EIA Test in UAE | 160 AED | DHA‑Licensed Precision Serology
Executive Summary & Core Metrics
Executive Summary: The Anti‑dsDNA Antibody EIA Test provides quantitative measurement of IgG autoantibodies against double‑stranded DNA using high‑specificity enzyme immunoassay (ELISA) technology. This serological marker is essential for diagnosing and monitoring systemic lupus erythematosus (SLE) activity. The test is performed under DHA Facility License No. 1143 at DNA Labs UAE, Dubai Healthcare City, with same‑day reporting, temperature‑controlled specimen logistics, and post‑test telephonic clinical guidance from a DHA‑licensed physician.
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 (Daily 8 AM–11 PM).
Clinical Guidance
Telephonic Post‑Test Clinical Guidance for result interpretation by a DHA‑licensed physician.
Insurance
Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
The Anti‑dsDNA Antibody EIA Test quantifies circulating IgG autoantibodies targeting native double‑stranded DNA, a highly specific seromarker for systemic lupus erythematosus (SLE). The enzyme immunoassay (ELISA) method provides quantitative results with superior specificity compared to indirect immunofluorescence (IIF) techniques, enabling accurate differentiation between active SLE and other autoimmune conditions. This test is a cornerstone for initial diagnosis, disease activity monitoring, and therapeutic response assessment in accordance with international rheumatology guidelines.
| Feature | Our Test (Anti‑dsDNA EIA) | Closest Alternative |
|---|---|---|
| Precision | Quantitative EIA with high specificity >95% | Immunofluorescence (IIF) – semi‑quantitative |
| Methodology | Enzyme Immunoassay (ELISA) | Crithidia luciliae IFA |
| TAT | Same‑day (Sample by 9 AM) | 24–48 hours |
Physician Insight & Safety Protocols
“The Anti‑dsDNA antibody test is a clinically valuable tool when integrated with a thorough history and physical examination. A positive result supports the diagnosis of SLE but should never be interpreted in isolation. Correlation with complement levels, urinary sediment, and clinical symptoms is essential for accurate disease staging and management decisions.”
— Dr. Ajay Singh, General Practitioner, DHA Registration ID: 36234132, Medical Content Supervisor
Medical Advisory – Medication Continuity
Do not discontinue any prescribed immunosuppressants, corticosteroids, or antimalarial agents without direct consultation with your treating rheumatologist. Abrupt cessation of therapy may precipitate a severe disease flare or organ-threatening complication. Always inform your physician of all current medications before the blood draw.
Exclusion Criteria & Emergency Red Flags
- Active severe infection or acute febrile illness may produce false‑positive antibody elevation.
- Recent vaccination (within 4 weeks) can transiently increase autoantibody levels.
- Known primary immunodeficiency or recent biologic therapy (e.g., rituximab, belimumab) may alter serological results.
- Seek emergency care immediately if you experience new‑onset chest pain, severe dyspnoea, facial swelling, sudden vision loss, or acute neurological deficit.
Patient FAQ & Clinical Guidance
1. Why is the Anti‑dsDNA test important for lupus diagnosis?
This test directly detects autoantibodies targeting native double‑stranded DNA, which is a highly specific seromarker for systemic lupus erythematosus. When positive alongside clinical criteria defined by the American College of Rheumatology, it confirms SLE with over 95% specificity and helps differentiate lupus from other connective tissue diseases. Serial measurements also guide disease activity monitoring and treatment adjustment.
2. Do I need to fast before the test?
Overnight fasting (8–12 hours) is preferred to minimize lipaemia interference in the serum sample, but it is not mandatory. If fasting is not possible, a light meal low in fat is acceptable. Always follow the specific pre‑test instructions provided during appointment confirmation. Staying well‑hydrated with water is recommended.
3. How quickly will I receive the results, and who interprets them?
When your blood sample reaches our laboratory before 9 AM, the quantitative EIA result is issued the same day. A secure digital report is made available through your patient portal, and a DHA‑licensed physician provides telephonic clinical guidance to help you understand the implications. We strongly recommend reviewing the results with your specialist rheumatologist for comprehensive care planning.
UAE Regulatory & Data Privacy Adherence
Regulatory Compliance: This diagnostic service operates under DHA Facility License No. 1143 and complies with Federal Decree‑Law No. 45 of 2021 on Personal Data Protection (PDPL) for all patient data processing, storage, and transfer. All health information is handled in accordance with Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields, ensuring secure electronic health records and telemedicine frameworks. Clinical safety and patient consent protocols adhere to Federal Decree‑Law No. 4 of 2016 on Medical Liability. Laboratory quality management is certified under ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139).
Clinical & Logistical Metadata
| Test Name | Anti‑dsDNA Antibody EIA Test |
| Price (AED) | 160 AED |
| Turnaround Time | Same‑day (Sample by 9 AM) |
| Sample Type / Matrix | Blood (Serum or Plasma) |
| Methodology Used | Enzyme Immunoassay (ELISA) |
| ICD-10-CM Code | M32.9, M32.0, Z15.89 |
| LOINC Code | 3403-7 |
| DHA Facility License & Laboratory Address | DHA License No. 1143 — Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE |
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