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Anesth Analg 2005;101:1401-1406
© 2005 International Anesthesia Research Society
doi: 10.1213/01.ANE.0000180214.74580.39


TECHNOLOGY, COMPUTING, AND SIMULATION

Denaturing High Performance Liquid Chromatography Screening of Ryanodine Receptor Type 1 Gene in Patients with Malignant Hyperthermia in Taiwan and Identification of a Novel Mutation (Y522C)

Huei-Ming Yeh, MD*, Mei-Chuan Tsai, BS§, Yi-Ning Su, MD{dagger}, Rong-Ching Shen§, Jeuy-Jen Hwang, MD{ddagger}, Wei-Zen Sun, MD*, and Ling-Ping Lai, MD, PhD{ddagger}§

Departments of *Anesthesiology, {dagger}Medical Genetics, and {ddagger}Internal Medicine, National Taiwan University Hospital; and §Institute of Pharmacology, National Taiwan University, Taipei, Taiwan

Address correspondence and reprint requests to Dr. Ling-Ping Lai, No. 1, Jen-Ai Rd., Section 1, Institute of Pharmacology, National Taiwan University, Taipei, Taiwan, 100. Address e-mail to lai{at}ha.mc.ntu.edu.tw.

We performed the present study to identify the mutation in patients in Taiwan with malignant hyperthermia (MH). We also test the hypothesis that a denaturing high-performance liquid chromatography (DHPLC) protocol can be used for mutation detection in these patients. We identified five Taiwanese patients with typical clinical presentations of MH after general anesthesia. We also enrolled 50 healthy volunteers. Polymerase chain reaction was used to amplify the ryanodine receptor (RYR1) gene mutation hot spots and DHPLC techniques were used to screen for mutations. Upon detection of a heterozygous elution pattern in DHPLC analysis, DNA sequencing reaction was performed to identify the nucleotide variations. We identified a RYR1 mutation in all 5 patients with MH. There were 4 different mutations in the 5 patients: Tyr522Cys, Arg552Trp, Val2168Met, and Thr2206Arg. Among the 5 patients, 2 unrelated patients had the same Thr2206Arg mutation. Three of the mutations had been reported before, but the Tyr522Cys mutation was novel. None of the MH-related mutations were found in the control group. In conclusion, we identified RYR1 mutations in 5 Taiwanese patients with MH using a DHPLC-based approach. A DHPLC-based genetic test may be developed as a noninvasive and convenient test for MH.




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P.-L. Chen, Y.-W. Chang, C.-Y. Chen, Y.-C. Hsiang, and Y.-J. Day
Novel Variants Near the Central Domain of RYR1 in Two Malignant Hyperthermia-Susceptible Families from Taiwan
Anesth. Analg., October 1, 2009; 109(4): 1273 - 1277.
[Abstract] [Full Text] [PDF]




Lippincott, Williams & Wilkins Anesthesia & Analgesia® is published for the International Anesthesia Research Society® by Lippincott Williams & Wilkins and Stanford University Libraries' HighWire Press®. Copyright 2005 by the International Anesthesia Research Society. Online ISSN: 1526-7598   Print ISSN: 0003-2999 HighWire Press
Copyright © 2005 by the International Anesthesia Research Society.