Category: Lab Tests & Results

  • Are You Worried About Statin Side Effects? Why 47% of Patients Stop Their Medication

    Are You Worried About Statin Side Effects? Why 47% of Patients Stop Their Medication

    Have you been prescribed a medication, like a statin, and worried about side effects? Did you stop your medication? Or maybe you never even started it.

    Traditionally doctors have relied on a ‘trial and error’ approach to medication.

    The “Trial-and-Error” Gamble with Statin Prescriptions

    Over 5 million people in the UK are prescribed statin medication every year. But we know that approaching 50% of patients stop them in the first year, or never even get their tablets.

    Either experiencing side effects or worry about them are two of the biggest reasons for this. This is a big problem for your health. Cardiovascular disease is the leading cause of death, but a massive 80% of cardiovascular disease is preventable. Controlling lipids with medications like statins is a key weapon to prevent deaths from cardiovascular disease.

    What is Pharmacogenomics (PGx)? The End of “One-Size-Fits-All” Medicine

    Pharmacogenomics analyses your DNA, looking at specific genes which dictate how your body responds to medicines. We have excellent detailed data that can predict how your body will metabolise drugs. This impacts not just whether the drug is effective, but also the risk of nasty side effects.

    In the clinic we take a simple blood sample which is analysed in a specialist genetic laboratory in Germany. The result gives us a detailed profile of your pharmacogenomics.

    How a Simple Genetic Test Can Predict Your Body’s Response to Statins

    The SLCO1B1 gene in your DNA codes for making a protein that is vital in controlling the metabolism of statins by your liver. We all have slightly different copies of this gene, called polymorphisms.

    Up to 36% of people tested have a copy of SLCO1B1 with decreased function. This means that the body has trouble clearing statins from the bloodstream to be metabolised by the liver. This means levels of the statin drug can build up in the blood stream, and cause side effects such as muscle pain and inflammation.

    A Patient Story: Replacing Statin Fear with Confidence

    In the clinic we can check your pharmacogenomic profile before starting medication. This means we can then choose a statin or other cholesterol lowering medicine which is much safer for you. You will be less likely to experience side effects and the drug is also more likely to be effective.

    We had a patient recently who wanted to start a statin to reduce their long-term risk of heart disease, they had read a lot about people experiencing muscle pain. As a really fit and active person they didn’t want anything which would impact their busy lifestyle. Their pharmacogenomic profile showed they have decreased SLCO1B1 function and were at high risk of side effects with the most commonly prescribed statins, atorvastatin and simvastatin. We were able to choose a low dose of rosuvastatin for them, this is the most effective and safest choice for them.

    Take the Guesswork Out of Your Heart Health

    We are incredibly lucky to be alive in a time where medical advances give us the chance for preventative healthcare. This chance was denied to many generations before us.

    We know though that many patients worry about taking medications, especially about unwanted side effects. Pharmacogenomics is a key tool we can use make sure you get the right medication. We can go from ‘trial and error’ to a truly personalised cardiovascular disease prevention plan.

    Interested in finding out your pharmacogenomic profile and what real-life personalised medicine means? We’d love to help you, so book today or get in touch.

    British Society for Genetic Medicine  ·  European Atherosclerosis Society  · 
    Independent Doctors Federation

    As seen in BBC, The Guardian, Women’s Health, The Times and Tatler

    For educational purposes. This article is written by a practising GP and is intended to inform, not replace a consultation with your own doctor. It does not constitute medical advice. A note on clinical guidelines: Coyne Medical is an independent private clinic. Our approach is guided by the best available evidence, tailored to each individual. This may go beyond standard NHS or NICE guidance, which is designed for population-level care and weighted by resource constraints.

  • Using Your DNA To Personalise Your Medication

    Using Your DNA To Personalise Your Medication

    Treat. Better.

    What is pharmacogenomics? It is the idea that a person’s genes influence their response to medicinal drugs. This means that by knowing and understanding your genes we can discover the right medication for you at the optimum dose.

    Personalised Medicine

    Many patients do not benefit from the first medication they are prescribed. Some will have side effects. Pharmacogenomics has the ability to make the medicines you are prescribed personalised to you.

    The Benefits of Pharmacogenomics

    The idea of pharmacogenetics is not a new one. As early as 1953 University of Washington geneticist Arno Motulski had established that gene variants affect the metabolism of certain drugs. Our Pharmacogenomics testing examines 50 well-established genes with over 200 gene-varients to establish:

    • What medication is right for you.
    • What is the best medication dose for you.
    • Whether you may experience side effects.

    Getting the Most out of Pharmacogenomics

    The people who benefit most from pharmacogenomic testing are those who require a long-term medication. This is particularly the case when there is more than one potential medication to choose from when the medication carries with it a high risk or side effects, when the starting dosage is undecided, or when patients are on more than one medication.

    Accurate Results

    Once your saliva sample is taken it is sent to the laboratory to undergo cutting edge, next-generation sequencing. The testing has demonstrated 100% sensitivity (true positive detection rate) and 100% specificity (true negative detection rate).

    Contact us to arrange your pharmacogenetics test or find out more here.

    British Association of Sports and Exercise Medicine  ·  European Atherosclerosis Society  · 
    Independent Doctors Federation

    As seen in The Independent, The Daily Mail and Tatler

    For educational purposes. This article is written by a practising GP and is intended to inform, not replace a consultation with your own doctor. It does not constitute medical advice. A note on clinical guidelines: Coyne Medical is an independent private clinic. Our approach is guided by the best available evidence, tailored to each individual. This may go beyond standard NHS or NICE guidance, which is designed for population-level care and weighted by resource constraints.