MTHFR (Methylenetetrahydrofolate Reductase) is an enzyme that plays a crucial role in the metabolism of folic acid, a B-vitamin that is important for DNA synthesis, cell division, and red blood cell production. Variants of the MTHFR gene can affect the activity of this enzyme and, as a result, influence a person's dietary needs.
Genes play a crucial role in determining an individual's testosterone levels, which can significantly impact athletic performance. Testosterone is the primary male sex hormone but also plays a vital role in muscle development, bone density, and red blood cell production. In athletes, testosterone levels can be a predictor of their physical performance.
Genes play a crucial role in determining various physiological processes in the human body, and growth hormone levels are no exception. Growth hormone (GH) is produced by the pituitary gland that stimulates the growth and reproduction of cells in the body. It is essential for the development of bones, muscles, and other tissues and plays a key role in athletic performance.
Osteoarthritis is a chronic joint disorder that affects millions of people worldwide. It is characterized by gradual wear and tear of the cartilage, the soft cushioning material between bones, leading to pain, stiffness, and reduced mobility. While age, obesity, injury, and repetitive joint use are some of the well-known risk factors for developing osteoarthritis, recent research has shown that genetics also play a significant role in the development of the disease.
Studies have shown that genetics significantly determines an individual's baseline CRP levels and susceptibility to systemic inflammation. Single nucleotide polymorphisms (SNPs) in genes related to the immune system and inflammation have been found to be associated with increased CRP levels. This genetic predisposition to higher CRP levels can put individuals at a higher risk of developing chronic health conditions, highlighting the importance of lifestyle modifications to manage inflammation.
Inflammation is critical to the body’s immune response, essential for fighting off infections and healing injuries. Interleukin-6 (IL-6) is a cytokine that plays a key role in regulating the body's inflammatory response. However, it is also well known that excessive inflammation can lead to various health problems, including heart disease, diabetes, and even cancer.
Thus, your genetic predisposition to a higher or lower body fat percentage may be important when considering which sporting activities to invest your time and effort into. However, it's also important to note that while genetics may impact body fat percentage, it is not a determining factor. With the right diet and exercise regimen, anyone can improve their body fat percentage and reach their fitness and health goals.
The ACTN3 gene, also known as the 'sprinter gene,' has been the subject of much research in the field of sports science. This gene is believed to play a key role in determining athletic power and sports performance potential.
Lean body mass is an important metric in the sports and fitness world. However, few realize it is also crucial for general health and well-being. Lean body mass refers to all your mass, excluding your fat mass. Thus, it includes the mass of your bones, organs, connective tissue, blood, muscles and other tissues. Your muscles make up most of your lean body mass and are responsible for most of the interpersonal variability.
Handgrip strength is an important predictor of athletic performance potential. While training and nutrition play a big role in handgrip strength, it's also influenced by our genes. Research has shown that there are specific genes that are associated with handgrip strength and muscle mass, both of which are important factors in athletic performance.
Do our genes determine our preferred meal portion size? In this blog post, we will explore the connection between genetics and preferred meal portion size and how it can impact weight gain.
Athletic performance is a complex and multi-faceted aspect influenced by various factors, including cardiovascular function. One important aspect of cardiovascular function is left ventricular (LV) stroke volume, which refers to the amount of blood the heart pumps out with each beat. This can greatly impact athletic performance, especially endurance performance.
The COVID-19 pandemic has affected millions of people worldwide, and while some have had mild symptoms, others have suffered severe illness or death. One question that many people have is whether genetics play a role in determining how likely someone is to have severe illness if they contract COVID-19. Recent research has shown that there are indeed genetic factors that can increase the risk of severe illness from COVID-19.
Insulin-like Growth Factor 1 (IGF-1) is a hormone that plays a vital role in the growth and development of the human body. It has a significant impact on athletic performance as it influences muscle growth and helps the body to recover from physical activity. In this blog post, we will explore how genes influence IGF-1 levels and how this affects athletic performance.
Omega-3 fatty acids have been widely researched and studied for their potential health benefits, including reducing triglyceride levels. However, the question remains, do genes play a role in determining how effective omega-3 supplementation is for lowering triglycerides? The answer is yes; genes can play a role.
Athletic performance is a complex and multi-faceted aspect that is influenced by various factors, including genetics. Hemoglobin, a protein found in red blood cells, is responsible for carrying oxygen from the lungs to the rest of the body. As such, a person's hemoglobin concentration can greatly impact their endurance performance.
Recently, we at BioCertica introduced a pharmacogenetics test as a new brand product. However, since it is a new product, it is natural to face doubts and questions about its quality, or if it is worth buying it. Whether or not someone thinks it is worth doing, a pharmacogenetics test is a personal decision that depends on individual circumstances. Therefore, we need to carefully consider all benefits and limitations that these tests may have. Here we will discuss some of them.
Genotypes can be homozygous or heterozygous. A homozygous genotype is when the two alleles are the same, for example TT or CC. A heterozygous genotype is when the who alleles are different, for example AT or CA. You may have noticed that in the case of heterozygous genotypes, the order in which they are written sometimes differs.
One of the main goals of World Cancer Day is to reduce the number of preventable cancer-related deaths and raise awareness. This can be achieved through a variety of means, such as promoting healthy lifestyles, increasing access to cancer screenings, and investing in cancer research.
Psychiatric disorders contribute to 14% of the global burden of disease and are estimated to affect nearly 450 million people, and approximately one-third of those affected are considered to have long-term disability and dependency. Sadly, about half of the patients with major psychiatric disorders are non-adherent to their treatments. Although other factors that affect medication non-adherence among them are medication side effects and efficacy [1]. So the question is: can pharmacogenetic testing impact treating psychiatric illness?
If you are genetically predisposed to low iron levels but would like to donate blood, you must ensure that you eat enough iron-rich foods. On the other hand - if you have the genetic condition that causes your boy to store too much iron (hemochromatosis, or iron overload), donating blood may save your life while saving the life of someone else.
The most common vitamin deficiencies are D, C, A, B12, B6, and folate (B9). Genes are most strongly linked to the metabolism and levels of vitamins D, C, and B12. The levels of vitamins in our bodies, of course, depend on how much we consume. However, other factors also influence our vitamin levels and subsequent intake needs. Amongst these factors is DNA. Common genetic variations are associated with our bodies’ vitamin levels.
Technological advances in recent years have made genetic testing much more affordable than it once was. Subsequently, DNA testing technology is busy revolutionizing nutrition and healthcare. Genetic testing is shifting the focus to personalized preventative care and away from retroactive generalized treatments.
Our genetic makeup influences how our bodies metabolize the different macro- and micronutrients. The macronutrients provide energy and building blocks to the body, while the micronutrients are needed for immunity and the proper functioning of the body's systems.
Genes are crucial in determining various aspects of our health, including our post-meal insulin response. Insulin is a hormone produced by the pancreas that regulates our blood sugar levels. After we eat a meal, our body releases insulin to help move glucose (sugar) from our bloodstream into our cells, where it can be used for energy.
Genetic factors can greatly impact fasting insulin levels and play a role in the development of insulin resistance. It is important for individuals to be aware of their genetic predisposition to insulin resistance and make the necessary changes to their diet and lifestyle to maintain optimal fasting insulin levels and overall health.
Insulin sensitivity is one of the aspects of health that our DNA influences. Insulin sensitivity refers to the body's ability to respond to insulin, the hormone responsible for regulating blood sugar levels. A person with high insulin sensitivity will require less insulin to control their blood sugar, while a person with low insulin sensitivity will require more insulin.
Genes play a crucial role in determining our resting metabolic rate (RMR), which is the amount of energy (in the form of calories) we burn at rest to maintain our basic physiological functions. RMR makes up most of the total calories we burn in a day, and variations in RMR can impact our weight gain or loss if we do not eat accordingly.
The production and regulation of leptin levels are controlled by a number of genes, which can affect an individual's susceptibility to weight gain and obesity. Variations in these genes can lead to alterations in the amount of leptin produced and the sensitivity of the brain to its signals.
Delve into the world of body type. Find out your unique body type - ectomorph, mesomorph, or endomorph - and customize your fitness routines for optimal results.
“I'm truly astonished to see how accurately the fitness traits reflect my situation. I now have in-depth knowledge of how my genetics affects my training and can identify areas of improvement. This is what athletics is all about, constant improvement.” - Taylon.
Training program errors, inadequate muscle strengthening, imbalanced biomechanics (ineffective movement patterns), and genetics are among the factors that contribute to the risk of chronic injuries.
One way to make exercise less torturous is to exercise according to your genetic preferences, i.e., do the types of training for which your body is naturally built. If your genes make you less likely to engage in spontaneous physical activity, exercise must be as enjoyable as possible. Otherwise, chances are you won’t increase your physical activity levels.
Unlock the power of your body with a DNA test! Discover how understanding your body type (ecto, meso, endo) can optimize your health, sports performance, and nutrition. Tailor your routine to maximize your potential!
If you are looking for a pharmacogenomics report, you may have noticed a few on the market. You may have already read about the benefits of BioCertica’s pharmacogenetic test, but here we will dive into the usability of our report compared to a competitor’s report.
Pharmacogenetic testing is still a relatively new field, so much progress still needs to be made for this type of testing. As you may have read, in pharmacogenomic testing, DNA is genotyped and matched to known gene-drug interactions; however, there is no standardized approach for reporting this testing. This leads to many differences in how these reports are compiled and presented. Therefore BioCertica’s approach to presenting pharmacogenetic results is different from other companies that offer this testing in South Africa. For the sake of transparency, we would like to explain the difference.
We will tell you more about the polygenic risk scoring methodology in a bit. Before that, to underline that most of today’s genetic risk scoring reporting is based on individual genetic variants that are found to be associated with a given trait. For example, let’s say a genetic variant associated with whether you can detect bitter taste or not or similar traits controlled by single genetic variants.
Multiple companies are offering genetic tests in the South African market - which should you choose? The table in this article gives you several factors to consider when purchasing a DNA kit, but one of the most important factors to draw to your attention is the approach: the polygenic risk scoring (PRS) approach or the single-gene approach.
Heritage Day on 24 September recognises and celebrates the cultural wealth of our nation. South Africans celebrate the day by remembering the cultural heritage of the many cultures that make up the population of South Africa. Various events are staged throughout the country to commemorate this day.
A polygenic risk score (PRS) is obtained from a comprehensive method used to estimate the relative genetic risks of being affected by a certain condition or inheriting a certain trait. Instead of giving the results of single genes which have been identified to contribute towards certain traits.
You may have seen the older version of this feature on your BioCertica App but it's out with the old and in with the new. We have updated the nutrition and meal plans feature to be more practical and useful. Here's a quick run-through of the new feature.
Genetic predisposition to long-term memory is a topic that has garnered significant attention in recent years as researchers have begun to uncover the genetic basis of this complex cognitive trait. Long-term memory is a type of memory that allows us to retain information over extended periods. It plays a crucial role in our ability to learn, adapt, and navigate the world around us.
While the exact cause of ADHD is not fully understood, research suggests that genetic and environmental factors influence the disorder. In particular, studies have shown that genetic variations can significantly affect a person's predisposition to ADHD.
Intelligence is a complex trait influenced by many factors, including genetics. While it is impossible to predict a person's intelligence with certainty based solely on their genetic makeup, research has shown that certain genetic variants are associated with a higher likelihood of having higher non-verbal intelligence.
Baldness, also known as alopecia, is a common condition that affects many men. While some men may experience baldness due to aging or other factors, others may be genetically predisposed to the condition.
Working memory is an essential cognitive function that temporarily allows us to store and manipulate information in our minds. The mental workspace will enable us to perform complex mental tasks such as problem-solving and decision-making. Working memory is a critical aspect of our daily lives and is closely linked to our ability to learn, reason, and pay attention.
Pair bonding and sociability are important aspects of human behavior and relationships. Research has shown that there is a genetic component to these traits, which means that some people may be more predisposed to forming strong bonds with others and being more sociable than others.
Vitamin A is a vital nutrient for overall health and wellness, but did you know genetics play a role in how your body responds to and utilizes this essential vitamin? A genetic predisposition to Vitamin A in skincare can impact how well your skin absorbs and benefits from skincare products containing this nutrient.
Vitamin B12 is an essential nutrient that plays a crucial role in maintaining good health. It is important for the proper functioning of the brain and nervous system, as well as the formation of red blood cells. A deficiency in vitamin B12 can lead to a number of health problems, including anemia, fatigue, weakness, and nerve damage.
Vitamin B6, also known as pyridoxine, is an essential nutrient that plays a crucial role in maintaining healthy skin. It is involved in the production of collagen, the main structural protein found in the skin, as well as in the metabolism of fatty acids, which are important for maintaining the integrity of the skin's protective barrier.
Thyrotoxicosis can develop due to a variety of reasons, including autoimmune diseases, such as Graves' disease or Hashimoto's thyroiditis, thyroid nodules or goiters, or side effects of certain medications. In some cases, genetics may also play a role in the development of thyrotoxicosis.
If you are experiencing symptoms of type 1 diabetes, it's crucial to seek medical attention promptly. Early diagnosis and treatment may be essential. Thus, knowing your or your child’s genetic predisposition can help you be aware of the symptoms and find help sooner.
Research has shown that genetics may play a role in the development of UC. Studies have identified several genetic variations that increase an individual's risk of developing the condition. These genetic variations affect the body's immune response and can contribute to the inflammation and ulcers in the lining of the colon.
In conclusion, GPA is a rare autoimmune disease that primarily affects the respiratory system but can also impact other organs and systems. While the exact cause is not fully understood, genetics are believed to play a role in its development. Early recognition and prompt treatment can help manage symptoms and prevent complications.
Although autoimmune diseases cannot be cured, they can be managed for a better and prolonged life. Early recognition is the most crucial aspect of the management of these diseases. The sooner they are diagnosed, the sooner treatment can be initiated for an improved prognosis. Diagnosing autoimmune diseases can be difficult. This is where BioCertica can help!
The burden of TB in South Africa and low- to middle-income countries is especially high, but it remains a major concern worldwide. Annually, 10 million people contract the disease across the globe, leading to 1.5 million deaths. Since this disease is preventable and highly treatable, heightened awareness will help in fighting its spread.
Interaction between genes and environmental factors triggers the development of Rheumatoid Arthritis. Therefore, testing your genes can tell you how susceptible you are to more severe joint damage if you have the condition. This may be very valuable to guide treatment options.
Atrial fibrillation, also known as AF or AFib, is a common type of heart rhythm disorder. It is characterized by rapid and irregular beating of the heart, which can lead to a variety of symptoms, such as dizziness, shortness of breath, chest pain, and fatigue. AF can increase the risk of heart failure, stroke, and other serious complications in severe cases.
High levels of good cholesterol, also known as high-density lipoprotein (HDL), are considered a sign of good health. This type of cholesterol helps to remove low-density lipoprotein (LDL), or "bad" cholesterol, from the blood and transport it to the liver, where it can be broken down and eliminated from the body.
High levels of low-density lipoprotein (LDL), also known as "bad" cholesterol, can increase a person's risk of developing heart disease. Sometimes, a person may be genetically predisposed to high LDL levels. This means that their genes make them more likely to have high LDL levels compared to others who do not have the same genetic makeup.
Triglycerides are a type of fat found in the bloodstream. High levels of triglycerides in the blood can increase a person's risk of developing heart disease, diabetes, and other health conditions.
Genetic predisposition to manage blood triglycerides, also known as omega-3 fatty acid metabolism, is a common genetic variation that affects a person's ability to regulate blood lipid levels. This genetic variation can significantly impact a person's risk for developing conditions like heart disease, diabetes, and stroke.
Genetic predisposition refers to a person's inherited genetic makeup that makes them more likely to develop certain health conditions. One such condition is an increased risk for a heart attack, a serious and potentially life-threatening medical event.
Omega-3 fatty acids are essential for maintaining good health and preventing various diseases. They are known to have anti-inflammatory effects, which can help reduce the risk of chronic conditions such as heart disease, cancer, and arthritis. However, not everyone's body absorbs Omega-3 as efficiently, and some people may have a genetic predisposition to poor absorption.
Peripheral arterial disease (PAD) is common in which the arteries that carry blood to the legs and feet become narrowed or blocked. This can lead to a range of symptoms, including leg pain, numbness, and weakness. PAD is often caused by a buildup of plaque in the arteries, but in some cases, it may be due to a person's genetic predisposition to the condition.