Study Identifies Genetic Mutation That May Cause Malignant Hyperthermia
Main Category: Pain / AnestheticsAlso Included In: Genetics
Article Date: 23 Aug 2008 - 2:00 PDT
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After a surgical procedure, an 18-year old cheerleader from Florida died as a result of malignant hyperthermia, a condition triggered by certain anesthetics where the body heats up to dangerous levels. A study published in the September issue of Anesthesiology has identified a genetic mutation that could cause malignant hyperthermia (MH), this rare but potentially deadly condition. The goal of this research is to develop methods to identify patients with this disease so that these disastrous, rare consequences of certain anesthetics can be avoided.
Lukas Georg Weigl, Ph.D., and his research group from the Medical University of Vienna found the MH-associated mutation in the ryanodine receptor 1 (RYR1) gene, which is located in the body's skeletal muscles. Although the mutation was found only in a single Austrian family, its identification could help others in the future.
MH is an inherited condition and one that is notoriously difficult to identify prior to actual clinical exposure to a triggering anesthetic. Since clinical MH episodes typically first appear when patients are given an anesthetic for surgery, anesthesiologists are particularly interested in identifying the mutations that can cause the condition.
The effects of MH can be devastating. "When a triggering agent, such as a volatile anesthetic, is introduced into an MH-susceptible person's body, increased temperature and muscle rigidity can occur, leading to muscle damage and release of ions and proteins into the blood," said Dr. Weigl. "This can result in the death of the patient due to an irregular heart beat or kidney failure after the surgical procedure."
Unfortunately, doctors may not know a patient is susceptible to MH until an episode occurs. And, currently, testing for MH involves a highly invasive diagnostic surgical procedure that requires removing muscle tissue from the individual's thigh and checking it for sensitivity to triggering substances.
Researchers have long desired to replace this invasive test with a much simpler and cheaper genetic test. But each potential genetic mutation needs to be identified before a genetic test can be given to test for MH susceptibility with high predictability. There are currently around 170 identified variations in the RYR1 gene that are linked to MH.
"Proving the causative role of a new mutation enables researchers to include it in the list of MH mutations and makes the genetic test more reliable," said Dr. Weigl. "This is an important step toward establishing an inexpensive and minimally invasive genetic test for diagnosing MH. This new mutation should, therefore, be included in the current list of MH-causing mutations."
For more information visit the Anesthesiology Web site at http://www.anesthesiology.org and the American Society of Anesthesiologists Web site at http://www.asahq.org.
Founded in 1905, the American Society of Anesthesiologists is an educational, research and scientific association with 43,000 members organized to raise and maintain the standards of the medical practice of anesthesiology and improve the care of the patient.
American Society of Anesthesiologists (ASA)
520 N Northwest Hwy.
Park Ridge, IL 60068-2573
United States
http://www.ASAhq.org
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MLA
13 Feb. 2012. <http://www.medicalnewstoday.com/releases/119117.php>
APA
http://www.medicalnewstoday.com/releases/119117.php.
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Visitor Opinions In Chronological Order (1)
Malignant Hyperthermia
posted by Anon on 23 Aug 2008 at 1:55 pmIt is welcoming to read any information regarding malignant hyperthermia - we have at least seven family members, myself included, who have proved positive to this susceptibility. It is only in the last 15 years that it was diagnosed in our family, mainly because a relative in Australia developed complications under surgery, but fortunately the medical staff realised in time what was happening.
In our instance it has been discovered that the relative in Australia had a completely different strain, through his father's side - no blood relation to our family. The first one diagnosed on our side of the family was through a niece, and brought about by extreme physical stress. The coincidence of one of her cousins having been diagnosed possibly saved her.
I live in New Zealand, and tests here are undertaken in Palmerston North. Even should one should prove negative, if there is an incidence of malignant hyperthermia in a family, it is wise to be cautious.
Much more publicity should be given to the possibility of malignant hyperthermia, the more research into it the better.
To be able to take a blood test instead of undergoing a biopsy to see if one is positive would be a lifesaver in itself, a biopsy is not usually done until a child is over ten years old.
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