Adventia test

The Adventia test is a genetic test to check for the carriage of inherited diseases before planning a pregnancy. It is estimated that 1 in 4 people carry a genetic mutation, often without symptoms. The test analyses hundreds of genes at the same time, detecting changes that may affect the health of the baby. It uses advanced NGS technology, ensuring high accuracy of results. The test is painless, requiring only a saliva or blood sample. You receive the result in 2-3 weeks. The test helps you make informed parenting decisions and plan for appropriate medical care. Find out the details of the test and how it can support your family plans.

Highlights

  • 1 in 4 people are carriers of a genetic disease, often without any symptoms or family burden.
  • The Adventia test analyses hundreds of genes simultaneously using NGS technology with high accuracy and sensitivity.
  • The test requires only a blood or saliva sample and results are ready in 2-3 weeks.
  • Early detection of carriage enables informed family planning and the preparation of appropriate medical care for the child.

Test Adventia - what is the study?

Carrying genetic diseases often does not give any symptoms. Changes can occur in the genes which, if present in both parents, can increase the risk of serious diseases in the child.

It is estimated that up to 1 in 4 people are carriers of a genetic disease¹. Although many of these diseases are rare, they can have a serious impact on a child's health and development, and some can be life-threatening. Without screening, carriers of recessive mutations are often not detected until after the birth of the affected child.

In order to prevent such situations, it is recommended that a modern screening test for genetic diseases be carried out - the Adventia test. This test analyses a large number of genes for abnormalities that may be inherited, even if there are no previous conditions in the family.

Thanks to the Adventia test, parents-to-be can find out about possible genetic risks in advance and - if necessary - consult a geneticist, carry out additional tests (e.g. prenatal tests) and, above all, make informed and responsible decisions about planning their pregnancy.

Who is the Adventia test for?

The Adventia test is intended for anyone who wants to take an informed approach to family planning and take care of the health of their future child, it is particularly recommended in certain situations and can be performed by anyone interested in their genetic profile.

The Adventia study is worth considering if:

  • you are planning a pregnancy;

  • you use assisted reproduction techniques (e.g. in vitro),

  • you are a donor or recipient of reproductive cells (ova or sperm),

  • there is a history of genetic diseases in your family,

  • you want to know your genetic carrier profile, even if you have no symptoms or family history.

Taking the Adventia test is a responsible step - whether you are planning a pregnancy now, in the future or simply want to better understand your genetic health. Knowing early can help you make wise, calm decisions.

Why choose the Adventia test?

  • Early detection of risk. The test identifies gene alterations that do not produce symptoms in the parents, but can lead to serious diseases in the child.

  • Conscious family planning. The result of the test helps to make informed decisions about the way forward: from genetic consultation, to prenatal diagnosis, to the choice of form of treatment.

  • A chance for earlier treatment and care. In some cases, early diagnosis makes it possible to plan appropriate treatment or medical care as soon as the child is born.

  • Peace of mind and reassurance. For many couples, the test result is an important piece of information that provides a sense of security and better preparation for their role as parents.

Adventia is not just research - it is a conscious step towards a healthy and responsible future.

The Adventia test combines the latest advances in genetics with a practical concern for the health of future generations. Thanks to the use of modern technology, this test is not only extremely precise, but also completely safe and comfortable for the patient.

Advantages of the Adventia test

Key benefits of the Adventia study:

  • Advanced NGS technology (next generation sequencing) - enables the simultaneous analysis of hundreds of genes, making it possible to detect even very rare genetic mutations with high accuracy.

  • Target Capture Enrichment (DNA) - The test focuses on well-defined, clinically relevant fragments of the genome, which increases the efficiency and reliability of the analysis.

  • Modern bioinformatics methods - genetic data are interpreted using advanced algorithms, which minimises the risk of error and ensures the reliability of the result.

  • High sensitivity and specificity - the test has a very high accuracy, which means that false positives or false negatives are rare.

  • Full coverage of the genes analysed - This means that all regions of the genes included in the test are thoroughly checked, with no 'gaps' in the analysis.

The Adventia test is one of the most comprehensive and reliable carrier tests available on the market today. It provides reliable information that can be crucial to a child's health and parents' peace of mind.

Benefits of the Adventia test

The Adventia study is not only state-of-the-art technology, but above all real support in making informed and responsible decisions about a child's future.

What do you gain by choosing Adventia?

  • Wide range of diseases studied.

    The test involves the analysis of up to 231 genes, which allows the detection of a wide range of hereditary conditions - including those that are rare but serious in their consequences.

  • Full gene analysis.
    Thanks to the comprehensive coverage of all the gene fragments analysed, the test result is accurate and reliable - with no missed spots.

  • Sound knowledge - greater peace of mind.

    The test result not only informs, but also helps to make concrete decisions - from planning further diagnostics to choosing the best path of medical care.

  • Support every step of the way.

    If necessary, a consultation with a clinical geneticist is available to help understand the result and plan the next steps - calmly and in confidence.

How to conduct the Adventia test?

The Adventia test is completely safe, painless and very simple to perform. No special preparations are required and the whole procedure takes place in a few steps. Depending on the variant of the test, it can be carried out individually or as a couple with a partner.

What does it look like to carry out the Adventia test?

Shipping to the laboratory

The sample collected is sent to a laboratory, where it undergoes detailed genetic analysis using state-of-the-art technology.

Waiting for the result

The waiting time for the test result is usually around 2-3 weeks.

Once the analysis is completed, the patient receives a clear and understandable report, which they can consult with a geneticist to discuss the results and answer any questions.

How do I order an Adventia test?

The Adventia test is available at all Invimed clinics.

How do I sign up for research at Invimed?

  • Use the helpline: call 500 900 888.

  • Complete the online form: fill in the form on the clinic website.

  • Go in person to one of the Invimed clinics.

1 Lazarin, Gabriel A., et al. "An Empirical Estimate of Carrier Frequencies for 400+ Causal Mendelian Variants: Results from an Ethnically Diverse Clinical Sample of 23,453 Individuals." Genetics in Medicine, vol. 15, no. 3, 2012, pp. 178-186

Frequently asked questions - FAQ

Can the carrier test already be performed during pregnancy?

Yes, carrier testing can be done during pregnancy, but it is best to do it before becoming pregnant. Doing the test during pregnancy limits management options and can cause additional stress for parents-to-be.

How much does a genetic disease carrier test cost?

The cost of a carrier test ranges from several hundred to several thousand zloty, depending on the number of genes analysed.

What should be done when the result indicates carrier status in both partners?

If both partners are carriers of the same mutation, the risk of the disease in the child is 25% in each pregnancy. Genetic consultation and consideration of prenatal or preimplantation diagnosis for IVF procedures is then recommended.

Can the result of a carrier test change over time?

No, the result of a carrier test does not change throughout life as it relates to congenital DNA changes. The test only needs to be carried out once and the information obtained will be valid for the planning of each subsequent pregnancy.

Can all genetic diseases be detected by a carrier test?

The test detects only selected recessive and X-chromosome coupled diseases, not all genetic conditions. It does not cover chromosomal diseases or dominant mutations, which require other types of genetic testing.

The medical information presented should be considered as general guidelines and does not replace the individual judgement of the doctor regarding the medical management of each patient. The doctor, after a thorough examination of the patient's condition, determines the extent and frequency of diagnostic tests and/or therapeutic procedures, taking into account specific medical indications. All medical decisions are made in full consultation with the patient.

Author of the article

Invimed editorial team - we serve patients by solving their fertility problems. We use world medical knowledge, state-of-the-art technology and treatment methods. We are here to make dreams of parenthood come true. The smiles on the faces of happy parents give meaning to our work.

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