• Barbara W Brandom, Saiid Bina, Cynthia A Wong, Tarina Wallace, Mihaela Visoiu, Paul J Isackson, Georgirene D Vladutiu, Nyamkhishig Sambuughin, and Sheila M Muldoon.
• From the Department of Anesthesiology, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania; Department of Anesthesiology, Uniformed Services University of the Health Sciences, Bethesda, Maryland; Department of Anesthesiology, Northwestern University, Chicago, Illinois; Children's Hospital, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania; and Departments of Pediatrics, Neurology, Pathology and Anatomical Sciences, School of Medicine and Biomedical Sciences, State University of New York at Buffalo, Buffalo, New York.
• Anesth. Analg. 2013 May 1; 116 (5): 107810861078-1086.

BackgroundMutations in the ryanodine receptor type 1 gene (RYR1) that encodes the skeletal muscle-specific intracellular calcium (Ca(2+)) release channel are a cause of malignant hyperthermia (MH). In this study, we examined RYR1 mutations in a large number of North American MH-susceptible (MHS) subjects without prior genetic diagnosis.MethodsRYR1 was examined in 120 unrelated MHS subjects from the United States in a tiered manner. The α-1 subunit of the dihydropyridine receptor gene (CACNA1S) was screened for 4 variants in subjects in whom no abnormality was found in ≥ 100 exons of RYR1.ResultsTen known causative MH mutations were found in 26 subjects. Variants of uncertain significance in RYR1 were found in 36 subjects, 16 of which are novel. Novel variants in both RYR1 and CACNA1S were found in the 1 subject who died of MH. Two RYR1 variants were found in 4 subjects. Variants of uncertain significance were found outside and inside the hotspots of RYR1. Maximal contractures in the caffeine-halothane contracture test were greater in those who had a known MH mutation or variant of uncertain significance in RYR1 than in those who did not.ConclusionsThe identification of novel RYR1 variants and previously observed RYR1 variants of uncertain significance in independent MHS families is necessary for demonstrating the significance of these variants for MH susceptibility and supports the need for functional studies of these variants. Continued reporting of the clinical phenotypes of MH is necessary for interpretation of genetic findings, especially because the pathogenicity of most of these genetic variants associated with MHS remains to be elucidated.

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