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Double Marker Test

Also known as: Prega screen (Dual Marker) Reflex - NIPT or Karyotyping

51+ booked in last 3 days

Prega screen (Dual Marker) Reflex - NIPT or Karyotyping Details in Brief

Also Known As Pregascreen (Dual Marker) Reflex – NIPT or Karyotyping, Pregascreen Dual Marker Reflex Test, First Trimester Screening, Double Marker Test
Purpose Screens for chromosomal abnormalities during pregnancy; detects common conditions, such as Down syndrome and trisomy 18
Preparation A completely filled maternal TRF with barcode and the latest USG report is required. Medical history is mandatory.
Fasting Not Required
Reporting Time Same Day: 9:00 PM
Cost 3,600

What Is a Double Marker Test?

The Double Marker Test is a safe, non-invasive prenatal screening test that helps assess the risk of chromosomal abnormalities in your developing baby during the first trimester of pregnancy. This test uses a simple blood sample from the mother to evaluate the likelihood of conditions like Down syndrome (Trisomy 21), Edwards syndrome (Trisomy 18), and Patau syndrome (Trisomy 13).

It's important to understand that this is a screening test, not a diagnostic test, which means it indicates risk levels rather than providing a definitive diagnosis.

What Does the Double Marker Test Measure?

The double marker test evaluates specific substances in your blood to calculate risk factors for chromosomal conditions:

Free beta-human chorionic gonadotropin (Free β-hCG): A hormone produced by the placenta during early pregnancy. Abnormal levels may indicate increased risk for chromosomal abnormalities.
Pregnancy-Associated Plasma Protein-A (PAPP-A): A protein produced by the placenta. Lower than expected levels in the first trimester may suggest a higher risk for Down syndrome (Trisomy 21) and other chromosomal abnormalities.
Risk calculation: These measurements are combined with your age and ultrasound findings to provide a comprehensive risk assessment.

Double Marker Test: Who Needs It and Why It's Done

What Symptoms May Call for a Double Marker Test?

This screening test is not performed based on any symptoms you might experience. The double marker test is offered as part of routine prenatal care to proactively assess your baby's health:


• Recommended as standard first-trimester care for all pregnancies
• Part of comprehensive antenatal monitoring
• Provides early reassurance about your baby’s well-being

Who Should Get a Double Marker Test?

This screening test is particularly recommended for certain groups, though it can benefit all pregnant women:

Women over 35 years: Advanced maternal age increases the risk of chromosomal abnormalities.
Family history: Those with a family history of chromosomal disorders or genetic conditions.
Previous pregnancy concerns: Women who have previously had a child with chromosomal abnormalities.
Medical history: Individuals with diabetes or those taking certain medications during pregnancy.
Routine prenatal care: All pregnant women, as part of comprehensive first-trimester screening.

Why Is a Double Marker Test Done?

The double marker test provides crucial early information about your pregnancy, helping you and your doctor make informed decisions about further testing and prenatal care while ensuring the safety of both mother and baby.

Importance of a Double Marker Test

The double marker test serves as a vital first step in prenatal screening, offering you peace of mind during early pregnancy. This safe, non-invasive test identifies pregnancies that may need closer monitoring or additional testing. When performed between 11–14 weeks of pregnancy, it provides crucial information that enables timely genetic counselling and appropriate prenatal care planning.

The test doesn't diagnose conditions but guides you towards the right next steps, ensuring you receive personalised care throughout your pregnancy journey.

Double Marker Test Booking & Reports – Metropolis Healthcare India

How to Book a Double Marker Test?

  1. Simple Online Booking
    Select 'the Double Marker Test', choose a convenient time slot and provide your address for home sample collection. You can also visit the nearest Metropolis Lab if you prefer to give the sample directly at the lab.
  2. Safe Home Sample Collection
    Our trained phlebotomists ensure the timely collection of your sample while strictly following all safety and hygiene protocols.
  3. Sample Tracking Updates
    Stay informed at every step — from collection to testing — and track your sample directly through the Metropolis Healthcare website.
  4. Accurate Laboratory Testing
    Your sample is processed at our NABL- & CAP-accredited laboratories, where expert technicians ensure accurate results.
  5. Quick & Easy Reports
    Receive your test reports promptly via email, WhatsApp, or by downloading them directly from the Metropolis Healthcare website or app.

Is Home Sample Collection for the Double Marker Test Available Near You?

Yes, Metropolis Healthcare provides home sample collection for the double marker test, making prenatal screening stress-free during this important time. Our trained phlebotomists visit your home at your preferred time, following strict safety protocols to ensure accurate sample collection. This service eliminates the need for hospital visits.

How Long Does It Take to Get a Double Marker Test Report?

Reports are typically available the same day — by 9:00 PM — after the sample reaches the lab.

Where Can I See or Get the Double Marker Test Results?

You can access your Metropolis Healthcare test results easily through multiple channels — website, app, email, or WhatsApp. Log in using your credentials to view or download reports. Additionally, test reports are sent via email or WhatsApp, and you also have the option to collect a physical copy directly from the lab.

Interpreting Double Marker Test Results

The following table helps you understand what your double marker test results mean and the risk assessments provided:

Disorder

Screen Positive Cut Off (ACOG 2007)

MOM Cut off

(ACOG 2007)

Remarks

Trisomy-21

1:250

Free β-hCG: ≥ 1.98

PAPP-A: ≤ 0.43

Confirmatory diagnostic testing (such as NIPT, CVS, or amniocentesis) should be considered under your doctor’s advice.

Trisomy-18 / Trisomy-13

1:100

Free β-hCG: ≤ 0.5

PAPP-A: ≤ 0.4

A detailed Level III (targeted) ultrasound is recommended for confirmation and further evaluation.

 

Conditions that May Affect Double Marker Test Accuracy

Several factors can influence your double marker test results and should be discussed with your doctor:

Incorrect gestational age: Inaccurate dating of pregnancy can affect risk calculations significantly.
Multiple pregnancies: Twin or triplet pregnancies may alter hormone levels and affect interpretation.
Maternal weight: Very high or low body weight can influence hormone concentrations in the blood.
Smoking: Heavy smoking can lower PAPP-A levels, potentially affecting risk calculations.
Certain medications: Some medicines may interfere with hormone levels during pregnancy.
Previous pregnancy complications: A history of pregnancy-related conditions may influence results.
Maternal diabetes: Can affect protein and hormone levels measured in the test

How Is a Double Marker Test Done?

The double marker test follows a simple and safe procedure that takes just a few minutes:

• You'll be seated comfortably, and the phlebotomist will clean the area on your arm with an antiseptic.
• A trained professional will locate a suitable vein, typically in your arm.
• A sterile needle is inserted to draw approximately 3 ml of blood into a special tube.
• The blood sample is properly labelled with your details and stored at the correct temperature.
• The needle is removed, and a cotton ball or bandage is applied to prevent bleeding.
• Your sample is sent to the laboratory for analysis.

How Should You Prepare for a Double Marker Test?

Preparing for your double marker test is straightforward and requires minimal effort:

No fasting required: You can eat and drink normally before the test.
Bring required documents: Ensure you have your filled maternal TRF with barcode and latest ultrasound report.
Medication information: Inform your doctor about all medications and supplements you're taking.
Comfortable clothing: Wear clothes that allow easy access to your arm for blood collection.
Stay hydrated: Drink enough water to make blood collection easier.
Medical history: Be prepared to share accurate pregnancy history and gestational age details.

Diseases that a Double Marker Test Can Help Detect

The double marker test screens for several important chromosomal conditions that can affect your baby's development:

Down syndrome (Trisomy 21): The most common chromosomal condition causing intellectual disability and characteristic physical features.
Edwards Syndrome (Trisomy 18): A chromosomal condition that affects multiple organ systems.
Patau Syndrome (Trisomy 13): A rare but severe chromosomal disorder affecting brain and heart development.
Neural tube defects: These are not detected by the Double Marker Test alone but may be identified in second-trimester screening (triple or quadruple marker tests)

Growth-related complications: Low PAPP-A levels may suggest potential growth issues.

Double Marker Tests/Packages that You Can Book With Metropolis Healthcare

Metropolis Healthcare offers comprehensive prenatal screening options to support your pregnancy journey:

Test/Package Name

Purpose/Highlights

Maternal Screen (Triple Test) Second Trimester Test

Screens for chromosomal abnormalities and neural tube defects in the second trimester

First-Trimester Test-V, Serum Quad Test (Free β-hCG, PAPP-A, AFP, PLGF)

Comprehensive first-trimester screening, including Free Beta HCG, PAPP-A, AFP, and PLGF

Trisomy (Aneuploidy) Chromosomes 13, 18, 21, X, and Y by FISH

Diagnostic confirmation test for specific chromosomal conditions

 

Double Marker Test Prices in Different Cities

The cost of a double marker test may vary depending on your location. Here's a table showing the approximate prices in different cities:

City

Price (₹)

Mumbai

₹ 3500 to ₹4000

Delhi

₹ 3500 to ₹4000

Bangalore

₹ 3500 to ₹4000

Chennai

₹ 3500 to ₹4000

Pune

₹ 3500 to ₹4000

Ahmedabad

₹ 3500 to ₹4000

Read More

Prega screen (Dual Marker) Reflex - NIPT or Karyotyping Price

Metropolis Healthcare is a leading diagnostics centre and pathology lab in India equipped with the latest state-of-the-art technologies that provides the Prega screen (Dual Marker) Reflex - NIPT or Karyotyping with a clear pricing structure.

The Prega screen (Dual Marker) Reflex - NIPT or Karyotyping Price in Mumbai is ₹ 3,600 .

We are committed to deliver accurate and quality results from the best labs in India with complete transparency regarding test cost and turnaround time. No matter where you are, we strive to offer patients high-quality service that is affordable and accessible.

Frequently Asked Questions

The Double Marker Test measures hormones and proteins in your blood, while NIPT analyzes cell-free fetal DNA in your blood. NIPT offers higher accuracy with fewer false positives but costs significantly more than the double marker test screening. 

Missing this test means missing early detection of potential chromosomal abnormalities. Without screening, high-risk pregnancies might go unidentified, reducing time for genetic counselling, further testing, and informed decision-making about your pregnancy. 

Most lifestyle factors don't significantly impact results, but heavy smoking can lower PAPP-A levels, potentially affecting risk calculations. Maintaining healthy habits and being honest with your doctor about lifestyle choices ensures accurate interpretation. 

Inconclusive results require discussion with your doctor about next steps. Options may include repeating the test, advanced screening like NIPT, or diagnostic tests like amniocentesis for definitive answers about your baby's condition. 

The test involves a simple blood draw similar to any routine blood test. You may feel a slight needle prick, but discomfort is minimal and temporary. The procedure takes only a few minutes to complete. 

The optimal timing is between 11–14 weeks of pregnancy during the first trimester. Testing within this window ensures maximum accuracy of results and proper risk assessment for chromosomal abnormalities in your baby. 

No fasting is required for this test. You can eat and drink normally before your blood sample collection. This makes the test convenient and doesn't require any special dietary preparation beforehand. 

Severe dehydration might affect blood component concentrations, though it's unlikely to significantly alter double marker test results. However, staying well-hydrated before any blood test is always recommended for easier sample collection. 

No special dietary preparation is needed. Inform your doctor about all medications, supplements, and over-the-counter medicines you're taking. Never stop prescribed medications without consulting your doctor first. 

A healthcare professional cleans your arm with an antiseptic, inserts a sterile needle into a vein, and draws blood into a vial. After removal, a cotton ball or bandage is applied to prevent bleeding. 

Results are reported as risk ratios, like 1:1500. Low-risk results have larger denominators (1:1000 or more), while High-risk results typically show ratios of 1:250 or lower (e.g., 1:100 or 1:200). Your doctor interprets these considering your age and ultrasound findings. 

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Metropolis has a team of 200 senior pathologists and over 2000 technicians delivering diagnostic solutions in the areas of routine, semi specialty and super specialty domains like Oncology, Neurology, Gynaecology, Nephrology and many more.

We offer a comprehensive range of 4000+ clinical laboratory tests and profiles, which are used for prediction, early detection, diagnostic screening, confirmation and/or monitoring of the disease.

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