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J Am Coll Cardiol, 2006; 47:764-768, doi:10.1016/j.jacc.2005.09.056 (Published online 6 February 2006).
© 2006 by the American College of Cardiology Foundation
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CLINICAL RESEARCH: HEART RHYTHM DISORDER

Effect of Clinical Phenotype on Yield of Long QT Syndrome Genetic Testing

David J. Tester, BS, Melissa L. Will, BS, Carla M. Haglund and Michael J. Ackerman, MD, PhD, FACC*

Divisions of Cardiovascular Diseases and Pediatric Cardiology and Departments of Internal Medicine, Pediatrics, and Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic College of Medicine, Rochester, Minnesota.

Manuscript received July 8, 2005; revised manuscript received August 23, 2005, accepted September 12, 2005.

* Reprint requests and correspondence: Dr. Michael J. Ackerman, Long QT Syndrome Clinic and Sudden Death Genomics Laboratory, Guggenheim 501, Mayo Clinic, Rochester, Minnesota 55905. (Email: ackerman.michael{at}mayo.edu).

OBJECTIVES: The purpose of this study was to examine the effect of clinical phenotype on the yield of genetic testing for congenital long QT syndrome (LQTS).

BACKGROUND: Since the discovery of the first LQTS susceptibility genes in 1995, numerous genotype-phenotype relationships have emerged during the past decade of research genetic testing. In May 2004, LQTS genetic testing became a clinically available molecular diagnostic test.

METHODS: Blinded to genetic test results, analysis of the clinical phenotype was performed in 541 consecutive unrelated patients referred to Mayo Clinic’s Sudden Death Genomics Laboratory for LQTS genetic testing from August 1997 to July 2004.

RESULTS: The yield of genetic testing correlated significantly with the corrected QT interval (QTc) and clinical diagnostic score ranging from 0% when QTc was <400 ms to 62% when QTc was >480 ms (p < 0.0001). Among those with the highest clinical probability, the yield was 72% (89 of 123). The yield fluctuated substantially depending on age at diagnosis in males. Among physicians who referred ≥5 patients, the yield ranged from 0% to 80% (p < 0.0001).

CONCLUSIONS: In this large cohort of unrelated patients referred for LQTS genetic testing, the clinical phenotype strongly correlated with the likelihood of elucidating a pathogenic mutation with the cardiac channel gene screen.

Abbreviations and Acronyms
  LQTS = long QT syndrome
  QTc = corrected QT interval




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