Genetics and diabetes
Learn about your genetic predisposition to developing diabetes
MyPrevention Diabetes analyzes genetic variants in more than one hundred genes with scientific evidence in characterizing diabetes and its treatment, making it possible to personalize prevention and the therapeutic approach.
Non-invasive
Saliva sample, painless and suitable for anyone of any age
Once in a lifetime
Your genetics don’t change: the analysis is performed only once
20 days
Results available within 20 business days after the sample is received
Diabetes prevention
A genetic test to get ahead of diabetes
Diabetes affects approximately 10.5% of the world’s adult population, of whom between 85% and 95% are diagnosed as type 2. Knowing the genetics related to this disease makes it possible to personalize prevention guidelines and treatment.
MyPrevention Diabetes determines the presence or absence of genetic variants associated with the different types of diabetes, providing the medical specialist with high-value genetic information.
What is MyPrevention Diabetes for?
- Identify the genetic predisposition to developing type 2 diabetes and MODY diabetes
- Distinguish between the different types of diabetes analyzed
- Learn the pharmacogenetic compatibility with the medications most commonly used in treatment
- Personalize habits and treatment based on each individual’s genetic needs
Types of diabetes analyzed
Type 2 diabetes and MODY diabetes
One in every two adults with diabetes has not been diagnosed. Early detection through genetics makes it possible to act before symptoms appear.
Type 2
Type 2 diabetes
Characterized by a slow disease progression, which is why it is usually diagnosed in adults. Its origin is multifactorial: both genetics and environment play an important role.
Type 2 diabetes can be caused by alterations in three processes: reduced insulin sensitivity, reduced insulin production and increased insulin breakdown.
MODY
MODY diabetes
MODY diabetes (Maturity Onset Diabetes of the Young) presents characteristics similar to type 2 but has a purely genetic origin. It is estimated that 1 in every 1,000 people with diabetes has it.
The test analyzes the 9 most frequent subtypes, each characterized by a mutation in one gene: HNF4A, GCK, HNF1A, PDX1, HNF1B, KLF11, BLK, ABCC8 and KCNJ11.
MyPrevention Diabetes Report
Genetic predisposition and pharmacogenetics in a single test
In addition to assessing the predisposition to diabetes, the test includes a pharmacogenetic analysis that makes it possible to learn the compatibility with the medications most commonly used in its treatment.
- Genetic predisposition to type 2 diabetes and the 9 MODY subtypes
- Pharmacogenetic compatibility with the most common treatments
- Information to personalize the medication and dosage based on the genetic profile
- Analysis of more than 100 genes with scientific evidence
Process
How the diabetes genetic test works
A simple, non-invasive process designed to fit into clinical practice.
Receive the test
The user receives instructions to correctly collect the sample.
Collect the sample
DNA is obtained through a saliva sample, painlessly and non-invasively.
Genetic analysis
The sample is processed to analyze genetic variants related to diabetes and its treatment.
Results
The report details the genetic predisposition, the diabetes classification and the pharmacogenetic compatibility.
Target population
Who is MyPrevention Diabetes aimed at?
Designed for medical specialists in the prevention, diagnosis and treatment of diabetes: primary care physicians, endocrinologists and pediatricians. It is recommended for people with diabetes, clinical suspicion or a family history.
Primary care
A genetic screening tool to identify predisposed patients before symptoms appear.
Endocrinology
Genetic discrimination between type 2 diabetes and MODY for a specific, personalized therapeutic approach.
Family history
People with diabetic family members who want to know their genetic predisposition in order to act preventively.
Frequently asked questions
Frequently asked questions about MyPrevention Diabetes
What is MyPrevention Diabetes?
It is a genetic test that analyzes variants in more than one hundred genes with scientific evidence in characterizing type 2 diabetes and MODY diabetes, as well as the pharmacogenetic compatibility with the most commonly used treatments.
What’s the difference between type 2 diabetes and MODY diabetes?
Type 2 diabetes has a multifactorial origin (genetics + environment) and develops slowly, usually being diagnosed in adults. MODY diabetes has a purely genetic origin, is associated with a mutation in a single gene, and can appear at an early age. Distinguishing between the two is key for appropriate treatment.
Does it include pharmacogenetics?
Yes. In addition to assessing the predisposition to diabetes, the test analyzes the genetic compatibility with the most common medications for its treatment, making it possible to personalize the drug and the dosage.
How is the sample collected?
The sample is obtained non-invasively through saliva. It is painless and suitable for anyone of any age.
Does the test need to be repeated?
No. Genetics doesn’t change throughout life. The analysis is performed only once and the results remain valid permanently.
How long do results take?
Once the sample is received at the lab, results are available within a maximum of 20 business days.
Who is this test recommended for?
For people with diabetes or clinical suspicion, with a family history of diabetes, or as a prevention tool for specialists in primary care, endocrinology and pediatrics.
Take the step
Interested in the diabetes genetic test?
Contact our team for more information about MyPrevention Diabetes or to request a genetic study.