Can Genetic Testing be the Answer for Pain Relief?

Studies have shown that approximately $300 billion is wasted each year on drugs that do not work in people who carry certain genes.  

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While some people never receive the full benefit from these drugs, others experience dangerous side effects.

In order to treat individuals who have had many failures with drugs, some doctors are turning towards personalized medicine – which provides a method by which doctors can customize medication regimens so that they are effective from the start.

What role does genetics have in pain?
Research shows that  genetic factors account for a substantial proportion of all elements contributing to a patient’s response to drugs (others include age, sex, weight, general health and liver function).

Genes provide your body with instructions for making enzymes, which help break down drugs in your system, allowing your body to benefit from the medicine. Differences in your enzymes can affect how your body metabolizes a drug and how long the drug stays your body – and thus, how well drugs may work in an individual.

In particular, common pain medications require activation by an enzyme called CYP2D6 to become effective. Approximately half of patients have genes that alter the function of CYP2D6. Testing for these gene alterations allows for changes to dosage regimens in order to compensate for altered metabolisms –  and optimizes the safety and efficacy of pain medications.

Without knowing an individual’s specific genetic code, physicians may often need to go through months of trial-and-error prescribing to find the right drug and dose. Physicians are often baffled when a drug will work for one person but not for another with the same diagnosis. The fact of the matter is that physicians really do not know how to predict drug effectiveness or toxicity because everyone is different.  Genetic testing helps assess drug responsiveness. An individual’s genes can be a map that serves as a guide for physicians.

What is Pharmacogenetic Testing (PGT)?
A simple saliva test can evaluate an individual’s ability to metabolize or process drugs. Pain medications such as hydrocodone, oxycodone, diazepam and morphine utilize the CYP2D6 enzyme in order to metabolize the drug. As a drug gets metabolized, it is broken down into harmless pieces and eventually cleared. The activity of your clearance system is based on your genetic code. Once tested, this knowledge about an individual’s unique drug metabolizing system can help guide physicians.

What is the purpose of PGT?
Physicians would like to be able to anticipate how one may respond to a drug instead of relying on a trial-and-error process. By knowing the specific way one may break-down drugs, a physician can tailor treatment according to an individual’s unique metabolism and immediately find the right drug. Not only will this information help physicians predict which drug will best treat pain, a physician will also be able to predict the effective dose and potential for toxicity. In theory, this knowledge has the potential to save time, money and lives.

Pharmacogenetic testing (PGT), specifically, is exceedingly important for the proper management of pain because finding the precise drug and dose for each patient is so critically important. The groundbreaking development of PGT testing provides more individualized drug treatment for patients while also reducing adverse effects.

What if someone is an ultra-rapid metabolizer?
Ultra-rapid metabolizers break down medications really fast. Individuals who often receive medications that do not work or frequently need double doses of medication in order to relieve pain may be ultra-rapid metabolizers.

What if someone is a poor metabolizer?
Poor metabolizers tend to have severe side effects at low doses.  Instead of going through one medication trial after another only to get sick every time, this test allows physicians to determine whether or not someone is a poor metabolizer, and act accordingly.

When is testing appropriate?
Undergoing genetic testing is a once in-a-lifetime experience because your genes do not change over time.  Since many drugs are metabolized by one enzyme, you may only need one test. Once you are tested, you can keep your genetic test results for the rest of your life and share them with future care professionals. If one uses several medications (polypharmacy) and/or if several medications have failed to work properly, PGT may be appropriate to consider.

The Bottom Line:
Pharmacogenetic testing is now available with most physician pain specialists. The results of these genetic tests may help doctors: adjust the dose of medications more efficiently, prescribe medications that will work properly and give the patient the full benefit of the drug. It can also help people avoid medications that may be more likely to cause dangerous side effects and will often save money for patients in the long run. Drug responses don’t have to be a mystery now that treatments can be tailored to custom fit an individual’s specific genetic code.

By:  Dr. Anita Gupta is an Award Winning Johns Hopkins Trained Anesthesiologist, Pain Specialist, Pharmacist & Editor. She currently is Associate Professor & Medical Director at Drexel University-College of Medicine in Philadelphia, PA.  Read entire article at Foxnews.com 

For more information on how you can implement Genetic Testing in your company, clinic, pharmacy or home, contact:
PGx Medical
Individualized Care – Personalized Medicine
Info@pgxmed.com
405-509-5112

 

How would you explain Pharmacogenetics to a 4th Grade Science Class?

If you had to explain your fields of pharmacogenetics, pharmacogenomics and clinical evaluation to a 4th grade science class, what would you say?

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Dr. Wolfgang Sadee
The Ohio State University

In an article on the American Association of Pharmaceutical Scientists, read how Dr. Wolfgang Sadee explained pharmacogenetics to a 4th grade science class…

“We know that everyone is an individual and each one is different. These differences come about at least in part through genetics. The genetic information that is contained in the DNA in every cell determines how you look like, what you do, how you feel, and so on. The fields of pharmacogenetics and pharmacogenomics explore how this difference in genetics affects your risk of actually getting a disease later in life and how it affect your response to drugs. People respond differently to the drugs they take.  Take aspirin, for example. While it does its job well for most people, some cannot tolerate it and get stomach bleeding. We would like to find out why responses differ and utilize this information to optimize drug therapy for each patient individually. We think people all need to get somewhat different medication in order to be helped optimally.

Pharmacogenetics is a discipline that is already about 50 years old. Back then we usually looked at a single gene that could be defective in how it metabolizes a drug in the body. But now we know about all genes in the body and we understand that each drug interacts with numerous proteins in each gene. This means that genetic variations in a very large number of genes can affect the body’s response to the drug, so that is why we now look at all genes at the same time. This field of study is called genomics.”

Read more at the American Association of Pharmaceutical Scientists

 

To learn more about pharmacogenetics, contact:

PGx Medical
Individualized Care – Personalized Medicine
info@pgxmed.com
405-509-5112

Adverse Drug Events in Older Adults

Medicines cure infectious diseases, prevent problems from chronic diseases, and alleviate pain and suffering for millions of Americans every day. But medicines can also cause harm.

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Adverse drug events cause over 700,000 emergency department visits each year. Nearly 120,000 patients each year need to be hospitalized for further treatment after emergency visits for adverse drug events. As more and more people take more medicines, the risk of adverse events may increase.

As people age, they typically take more medicines. Older adults (65 years or older) are twice as likely as others to come to emergency departments for adverse drug events (over 177,000 emergency visits each year) and nearly seven times more likely to be hospitalized after an emergency visit.

Anti-psychotics are frequently prescribed when people have dementia. For some, a light dose may just be the right thing, but one medication doesn’t suit all elder issues.

One of the largest segments of the older population treated with antipsychotics is dementia patients with psychosis. One half of patients with dementia have comorbid psychosis. There are over 4 million people with Alzheimer disease in the United States today, and that number is expected to increase to 15 million in another 20 years. Just imagine one half of them having psychosis.

Wouldn’t it be helpful to know if the medications you are giving your patients are effective?  How do you know if their body metabolizes the medications or if there are adverse drug reactions with the combinations of medications?

Pharmacogenetic testing is a type of genetic test that assesses a patient’s risk of adverse response or likelihood to respond to a given drug, informing drug selection and dosing.  It is personalizing medicine for each patient.

If you would like more information regarding our Metabolic Validation Program through pharmacogenetic testing, contact:

PGx Medical
Empowerment at the Source of Treatment
info@pgxmed.com
405-509-5112

Individualized Care – Personalized Medicine

 

Reference:  cdcgov.comMedscape.com