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PPARG Gene Carotid intimal medial thickness type 1 NGS Genetic Test

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PPARG Gene Carotid intimal medial thickness type 1 NGS Genetic Test

Short Name: PPARG CIMT Type 1 NGS Test

Also known as: PPARG Gene Test, CIMT Type 1 Genetic Test, Carotid Intimal Medial Thickness Genetic Test

PPARG Gene Carotid intimal medial thickness type 1 NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses Next-Generation Sequencing (NGS) on Blood or Extracted DNA or One drop Blood on FTA Card samples. Results in 3 to 4 Weeks. Free home collection in 300+ cities across India.

Next-Generation Sequencing (NGS)🏠 Home Collection

✍️ Written By

🩺 Medically Reviewed By

Dr SULOCHANA HEMCHANDRA HOLLA

Dr SULOCHANA HEMCHANDRA HOLLA

Consultant Medical Geneticist · Reg: 8532

Last reviewed: September 7, 2026

Overview

The purpose of this test is to identify genetic variations in the PPARG gene that are associated with an increased risk of carotid intimal medial thickness type 1, which serves as an early indicator of atherosclerosis. This information helps in assessing cardiovascular risk, guiding preventive measures, and informing personalized treatment plans.

Test Code
5315
Price
₹20,000
Sample Type
Blood or Extracted DNA or One drop Blood on FTA Card
Result Time
3 to 4 Weeks
Fasting Required
No
Method
Next-Generation Sequencing (NGS)
Step 1

Sample Collection

No specific preparation required. Provide clinical history and undergo genetic counseling as recommended.

Method: Venipuncture

Step 2

Laboratory Analysis

A blood sample will be drawn from a vein in your arm by a trained phlebotomist. The process is quick and minimally invasive.

Step 3

Report Delivery

Apply pressure to the puncture site to prevent bruising. Resume normal activities immediately.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Genetic counseling session to discuss family history and test implications. Provide informed consent.
2
During the Test:Blood sample collection followed by NGS analysis in the laboratory.
3
After the Test:Receive results via online portal, email, or WhatsApp. Schedule follow-up counseling if needed.

About This Test

Who Should Get This Test

The purpose of this test is to identify genetic variations in the PPARG gene that are associated with an increased risk of carotid intimal medial thickness type 1, which serves as an early indicator of atherosclerosis. This information helps in assessing cardiovascular risk, guiding preventive measures, and informing personalized treatment plans.

How to Prepare

  • Ensure proper identification
  • Avoid strenuous activity post-collection
  • Store sample at ambient temperature if using FTA card

Doctor's Notes

Reviewed by — MBBS, MD (Medical Genetics) · Reg. No. 8532

"This genetic test is crucial for identifying individuals at risk of cardiovascular diseases early, allowing for preventive measures and personalized healthcare plans."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample Volume3-5 mL of blood
ContainerEDTA tube or FTA card
Collection MethodVenipuncture

Sample Stability

Blood sample: 24 hours at room temperature
Extracted DNA: Stable for years if stored properly
Sample Rejection Criteria:
  • Hemolyzed or clotted samples
  • Insufficient sample volume
  • Improper labeling or documentation

Understanding Your Results

Results indicate the presence or absence of genetic variants in the PPARG gene associated with increased CIMT type 1 risk. Consult a genetic counselor for detailed interpretation.
📊

No pathogenic variants

Low genetic risk for CIMT type 1; maintain healthy lifestyle

📊

Pathogenic variant detected

Increased risk; recommend cardiovascular monitoring and preventive measures

📊

Variant of uncertain significance

Further testing or family studies may be needed

⚠️ When to Consult a Doctor:

Consult a doctor if you have a family history of heart disease, experience symptoms like chest pain, or receive abnormal test results for personalized advice.

Limitations

  • ⚠Test may not detect all genetic variants
  • ⚠Results do not guarantee disease development
  • ⚠Limited to PPARG gene analysis only
  • ⚠Environmental factors not assessed

Risks & Considerations

  • ●Minor bruising at puncture site
  • ●Rare infection risk
  • ●Emotional impact of genetic results

Interfering Factors

  • ●Sample contamination
  • ●Degraded DNA quality
  • ●Recent blood transfusions
  • ●Use of certain medications affecting lipid metabolism

Frequently Asked Questions

What is the PPARG Gene Carotid Intimal Medial Thickness Type 1 NGS Genetic Test?
It is a genetic test that analyzes the PPARG gene for variations linked to increased risk of carotid artery thickening, an early sign of atherosclerosis.
Who should consider this test?
Individuals with a family history of cardiovascular disease, personal history of heart issues, or those seeking early detection of vascular risks.
How is the test performed?
A blood sample is collected and analyzed using next-generation sequencing technology to examine the PPARG gene.
What does the test cost?
The test costs INR 20000, which includes sample collection, analysis, and reporting.
Is fasting required before the test?
No, fasting is not required for this genetic test.
How long does it take to get results?
Results are typically available within 3 to 4 weeks after sample collection.
What do the results indicate?
Results show if you have genetic variants in the PPARG gene that may increase your risk of carotid intimal medial thickness type 1 and atherosclerosis.
Is the test painful?
The test involves a standard blood draw, which may cause minor discomfort but is generally painless.
Can this test diagnose heart disease?
No, it assesses genetic risk factors; a diagnosis requires clinical evaluation and other tests.
What should I do after receiving results?
Consult a genetic counselor or doctor to understand the implications and plan preventive measures.
Is home sample collection available?
Yes, DNA Labs India offers free home sample collection across India for online bookings.
Are there any risks associated with the test?
Risks are minimal, such as bruising from blood draw, but genetic results may have emotional impacts.
Worried about the process? Our certified phlebotomists collect thousands of samples every month across India. The process takes under 5 minutes and is virtually painless. Questions? Message us on WhatsApp — we're here 7 days a week.

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For Hospitals & Clinics

Reference Laboratory Services

We serve as a reference laboratory for hospitals and clinics across India. Send samples from your facility with same-day pickup, priority processing, and results delivered through our online portal. Competitive institutional pricing available.

LIMS Integration

Your Data Privacy

Your medical data is protected under Indian law.

✓ Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.

✓ DPDP Act Compliant: Under the Digital Personal Data Protection Act 2023, you can request deletion of your records at any time by contacting support.

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