Personalized antiaging diagnostic program
None of us wants to grow old or experience the diseases and disabilities associated with aging in the first place. The personalized antiaging diagnostic program helps detect your predisposition to age-related diseases and make your life more comfortable despite the passing of time. The personalized antiaging diagnostic program offers genetic testing for, among other things: cancer risk, cardiovascular disease risk, food intolerances, thrombophilia (a test especially recommended for women before starting hormone therapies) and cancer marker testing, hormone status assessment, osteoporosis risk assessment and much more.
Personalized antiaging diagnostic program is a program designed so that the results of the examination entail appropriate clinical prophylaxis, developed individually on the basis of medical records, medical history and test results. Preventive recommendations include, among other things, the type and frequency of diagnostic tests. On the basis of a thorough history, the results of genetic tests, tumor markers and other necessary laboratory tests, we prepare an individually tailored panel of preventive examinations, specialized consultations and the implementation of appropriate treatment.
The personalized antiaging diagnostic program is a project created for people who care about their safety.
Modern diagnostic technologies provide us with many preventive health tools. It is only necessary to know how to use them. The checkups we undergo, even if only annually as part of workplace prevention, do not detect the threat of disease but only an already existing disease process. And we, after all, above all, do not want to get sick, and if it does happen to us, we want to detect the disease before the first symptoms appear.
Oncogenetic tests are performed once in a lifetime. They give us an answer as to whether our health is at risk. They indicate the path of the most appropriate preventive tests and the frequency of their performance. Awareness of being a carrier of certain gene mutations gives us the opportunity for preventive action, as well as knowledge of what, if any, risks we are passing on to our children. People who are carriers of certain genetic mutations have a risk of developing cancer many times greater than others. If a person undergoing a genetic test is found to have an increased genetic predisposition to the development of malignant tumors, he or she should receive special care and meticulous observation.
A genetic test is a test to check the accuracy of our genetic information. It is a test in which inherited changes in genes from parents can be detected using laboratory methods. The test involves analyzing DNA sequences to look for changes that may affect the development of genetic disorders, including cancer.Genetic material (DNA) is tested, which is obtained from an oral swab - the material is taken during a routine visit to the clinic.
Nutrigenetic tests focused on studying genes related to metabolism.
From the results of the metabolic test we can read the predisposition to overweight, diabetes, insulin resistance, avitaminosis, food intolerances and other metabolic diseases and also what is our metabolism of fats, carbohydrates and micronutrients. The test examines our body's natural detoxification abilities, hormone activity and also inflammatory profile. The test examines sensitivities to several hundred foods and assesses which foods are advisable for us and which should be restricted.
Tumor markers are substances whose increased concentration in the blood can be associated with an ongoing cancer process in the body. They are specific to specific cancers (e.g., lung, testicular, ovarian), although some can be secreted by several different ones. Determination of markers represents, an excellent method of rapid, non-invasive initial diagnosis and, above all, a modern preventive test. Levels of cancer markers are determined in the blood, the test can be performed up to twice a year.
Intestinal flora testing is a modern test aimed at diagnosing the condition of the intestinal mucosa. As a result of many factors (gastrointestinal infections, antibiotic therapy, etc.), the mucosa becomes damaged, causing Leaky Gut Syndrome ( we check this condition by monitoring the level of zonulin - a marker of "leaky gut"). LGS is one of the main causes of food intolerances.
A properly functioning intestinal barrier works on the principle of a filter, allowing only properly assembled food particles to pass into the blood. As a result of damage to the barrier, nutrients that have not been fully digested, penetrate through the intestinal wall into the blood and are recognized as foreign elements to the body (antigens). A food particle, which is harmless to the body and has no infectious properties, is treated by the body's immune system similar to a virus or bacteria. Immune activation then occurs, with the goal of "eliminating" the intruder. The immune system produces antibodies that bind to antigens ( proteins supplied with food). Then the "war" begins, the goal of which is to remove the antigens from the blood. Unfortunately, in this case, there is no complete elimination of the enemy, because this, is supplied with each, successive portion of the meal. Food antigen and antibody, combined into immune complexes, circulate throughout the body and can settle in organs and tissues. As a result, inflammation in the body develops and is sustained, which, depending on the location, can manifest itself in different symptoms.
For some patients, it is important to correlate this test with testing for Candida and Helicobacter pylori.
Neurohormone function testing is a set of tests for people under chronic stress. Symptoms such as; irritability, sleep problems, concentration problems, migraines, cravings for sweets are usually a natural reaction to stress. If these symptoms persist we are dealing with a chronic stress response and complex changes in hormone release. Diagnosis of stress-related neurotransmitters - serotonin, dopamine, cortisol, GABA and others - allows us to determine the cause of the disorder and select appropriate therapy.
