(Circulation. 2000;101:e36.)
© 2000 American Heart Association, Inc.
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1 Circulation Newswriter
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Approximately 50% of LQTS is associated with mutations in 5 known genes that encode cardiac ion channels or auxiliary ion-channel subunits, according to Michael Ackerman, MD, who led the research team. In their report, the group described a new mutation in the KVLQT1 gene of a 19-year-old woman who was found face down in 4 feet of water in her health club swimming pool. Although she was resuscitated, she died 12 days later. Researchers conducted the genetic testing because of the unexplained death in the strong swimmer, the fact that she had a prolonged QT interval in an electrocardiogram test done during her hospitalization after her electrolyte balances were normal, and the signs of moderate myocardial ischemia at autopsy.
Researchers were able to use the information derived from studies of her DNA to find the same syndrome in her maternal grandfather, her mother, and her 18-year-old sister. Her sister is now receiving treatment to prevent a similar problem. After investigating this case, researchers reviewed 35 cases of LQTS seen at the Mayo Clinic and identified 6 patients who had a person or family history of drowning or near-drowning. They found mutations of the KVLQT1 gene in all 6 of the patients with such a history but in only 3 of the 29 patients with no family history.
"Swimming appears to be a gene-specific (KVLQT1) arrhythmogenic trigger for LQTS," they concluded in a report published in Mayo Clinic Proceedings (Ackerman MJ, Tester DJ, Porter CJ. Swimming, a gene-specific arrhythmogenic trigger for inherited long QT syndrome. Mayo Clin Proc. 1999;74:10881094). "This study provides proof of principle that an unexplained drowning or near-drowning may have a genetic basis."
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