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Medical information Clinical review pending

Immunology Testing

Mitochondrial Antibody AMA IFA in Dilutions Test

The Mitochondrial Antibody AMA IFA in Dilutions Test helps diagnose autoimmune liver diseases by detecting specific antibodies in the blood. It is important for patients with symptoms or abnormal liver function tests.

General information only: This page is not a diagnosis or personal medical advice. A qualified clinician should decide whether testing is appropriate and interpret results in context.

Review status: No completed medical review is recorded for this page.

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Counselor guidance included Confidential handling Kenya-wide coordination

At a glance

Plan your test

Sample
3 mL (1.5 mL minimum) serum collected in an SST tube.
Results
Confirm with the laboratory before booking.
Preparation
Overnight fasting is preferred before sample collection. Confirm specific preparation requirements with the laboratory before booking.
Test priceKSh 9,000

Payment: M-Pesa and card options can be confirmed during booking.

Insurance & government schemes

Is this test covered for you?

We help you verify whether the Mitochondrial Antibody AMA IFA in Dilutions Test test can be claimed against your insurer, employer scheme or a Kenyan government health scheme — before you book. Coverage depends on your plan, clinical indication and your provider's rules; final approval always rests with them.

Talk to a claims advisor

Providers & schemes we can help you check

Government & public schemes

SHIF — Social Health Insurance Fund Linda Mama EduAfya NHIF (legacy cards)

Eligibility and benefits follow the current rules of the Social Health Authority (SHA) and applicable government programmes.

Private insurers & employer schemes

Jubilee Health AAR APA Britam CIC Madison Resolution Pioneer Minet Old Mutual GA Life Heritage + other licensed insurers

Names shown for identification only — listing does not imply partnership or guarantee of coverage.

Have these ready when we check

  • Insurer or scheme name & policy / member number
  • A clinician's request / prescription for the test
  • Pre-authorisation letter, if your plan requires one

Free coverage check

Ask us to verify your cover

Send your details and our claims team confirms what documents you need and whether pre-authorisation applies — usually the same working day.

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Used only to process your coverage check — see our Privacy Policy. Verification support is free and does not guarantee your provider will pay.

01

Start with fit

Is this the right test for you?

The best test starts with a clear clinical question. These are common reasons a clinician or family may consider this test.

  • ✓Symptoms suggestive of liver disease (e.g., fatigue, jaundice, abdominal pain)
  • ✓Abnormal liver function tests
  • ✓Family history of autoimmune diseases
  • ✓Suspected autoimmune hepatitis
  • ✓Suspected primary biliary cholangitis
  • ✓Monitoring known autoimmune liver disease
02

In plain language

What this test helps you understand

This test is used to aid in the diagnosis of autoimmune liver diseases, such as primary biliary cholangitis (PBC) and autoimmune hepatitis (AIH). It helps identify the presence of specific antibodies associated with these conditions.
The Mitochondrial Antibody AMA IFA in Dilutions Test is a diagnostic tool used to identify autoimmune disorders, particularly those affecting the liver. This test detects the presence of mitochondrial antibodies (AMA) in your blood, which can indicate conditions like autoimmune hepatitis or primary biliary cholangitis. Early and accurate diagnosis is crucial for managing these liver diseases effectively.

This test measures the levels of AMA in your serum. A positive result suggests the possibility of an autoimmune liver condition, prompting further investigation.

Individuals experiencing symptoms like fatigue, jaundice, or abdominal pain, those with a family history of autoimmune diseases, or people with abnormal liver function tests may benefit from this test.

Taking this test allows for early detection of autoimmune liver diseases, helps guide treatment decisions, and aids in monitoring the progression of the disease and response to therapy.

Your results will indicate the presence or absence of mitochondrial antibodies. A positive result usually requires consultation with a gastroenterologist for further evaluation and management. Discuss your results thoroughly with your healthcare provider.
03

Medical review status

Clinical review pending

A completed medical review is not recorded for this page. No clinician has endorsed the information shown here. Please discuss testing decisions with a qualified healthcare professional.

Meet the DNA Labs Kenya medical team →
04

A simple process

What happens next?

You do not have to navigate the test alone. We help you move from question to next step.

1

Speak with us

We check the test and answer your questions before collection.

2

Give your sample

Choose home collection or a coordinated hub visit in Kenya. We explain whether this test uses a cheek swab or blood draw.

3

Understand your report

A counselor helps you understand the result and the next steps.

05

Choose your collection

Home collection or a lab visit

We will explain the sample, preparation, and next steps before anything is collected.

Home collection

Choose a coordinated visit at home or another convenient location. Our team confirms the appointment and sample requirements in advance.

Lab or hub visit

Prefer to visit a coordinated location? We can guide you to the right hub and explain what to expect when you arrive.

Ask about locations →
PreparationOvernight fasting is preferred before sample collection. Confirm specific preparation requirements with the laboratory before booking.
Sample3 mL (1.5 mL minimum) serum collected in an SST tube.
MethodologyImmunofluorescence Assay (IFA) in dilutions.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This test detects the presence of AMA but does not confirm a specific diagnosis on its own. Other tests and clinical evaluation are necessary. False positive or negative results can occur. Confirm with the laboratory before booking.
06

Read your report

What common result terms mean

PositiveA finding was identified. Your clinician or counselor will explain what it means for your care.
NegativeThe specific finding tested for was not identified. It does not rule out every possible cause.
VUSA variant was found, but current evidence is not enough to classify it. Your counselor can explain follow-up.
07

Questions people ask

Frequently asked questions

This test detects the presence of mitochondrial antibodies (AMA) in your blood, which are often associated with autoimmune liver diseases.
Individuals with symptoms of liver disease, abnormal liver function tests, or a family history of autoimmune conditions may need this test.
A positive result indicates the presence of mitochondrial antibodies and may suggest an autoimmune liver disease. Further evaluation by a doctor is necessary.
Overnight fasting is preferred. Please confirm specific preparation instructions with the laboratory before your appointment.
Turnaround time varies. Please confirm the expected turnaround time with the laboratory before booking.
08

Collaboration

Open for partnership with hospitals, clinics, doctors & researchers

Whether you are referring patients, building a research programme or supporting students, we work as an extension of your team — with responsive communication and clear scientific standards.

Hospitals & clinics

Referral pathways, coordinated sample logistics and shared reporting that fits your clinical workflow.

Doctors & specialists

LOINC-coded reports, ACMG-based variant classification and a direct scientific line for complex cases.

Research institutions

Sanger sequencing, NGS panels and custom assays — with project design support, batch pricing and agreed turnaround commitments.

Students & academic projects

Discounted laboratory services for college, master's and PhD research projects — including proposal guidance and cost-effective batch testing.

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09

Trust & transparency

Sources, standards & how this page is maintained

Standards & references

  • ACMG/AMP technical standards for sequence variant interpretation
  • ClinGen curation and gene–disease validity frameworks where applicable
  • LOINC-coded reporting for interoperable results
  • ISO 9001:2015 quality management; ISO 15189 accreditation in progress

Page provenance

  • Last updated: September 27, 2026
  • Medical review: not yet completed
  • Written for patients & clinicians in Kenya; reviewed periodically against current guidance

Medical disclaimer: this page is general information, not a diagnosis or personal medical advice. Testing decisions and result interpretation should be made with a qualified healthcare professional.

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