In vitro contracture test and gene typing in diagnosing malignant hyperthermia

Background: Malignant hyperthermia (MH) is an autosomal dominantly inherite d disorder,triggered in susceptible individuals by inhalation anesthetics a nd depolarizing muscle relaxants such as succinylcholine. Because of its hi gh sensitivity (97-99%) and specificity (93,6%) as well as the genetic hete rogeneity of MH disorder, the in vitro contracture test (IVCT) following th e European-MH-Group is considered to be the "Gold Standard" for phenotypica l determination of predisposed patients. On the other hand mutations in the skeletal muscle ryanodine receptor gene (RYR1) are tightly linked with MH susceptibility. After detecting a C1840T-mutation (Arg614Cys) in the RYR1 g ene in one individual of a large MH family, we searched far this mutation i n the remaining family members and determined the concordance with IVCT. Methods: According to the European standard protocol for MH, 43 individuals of a large MH pedigree were assigned the status of MH susceptible (MHS), - negative (MHN) or - equivocal (MHE). The genetic investigation of 44 famil y members for the Arg614Cys-mutation was carried out by restriction fragmen t analysis:Genomic DNA was prepared from EDTA whole blood followed by ampli fication of a 918 bp RYR1 gene fragment by polymerase chain reaction. In pr esence of the Arg614Cys-mutation digestion with the restriction endonucleas e RsaI would result in different DNA fragments of the amplified sequence th an in absence of mutation. Results: According to the response to IVCT, 25 individuals phenotypically r evealed MHS, 7 MHE and 11 MHN status. Out of the 44 family members screened genetically for the Arg614Cys-mutation, the mutation was detected in 23 in dividuals. Out of them 19 were MHS and one was MHEc. The mutation was absen t in 9 predisposed individuals, but six of them were MHE and three MHS. The mutation was also present in three individuals who had no MH screening (IV CT) before. For these last mentioned individuals the diagnosis MHS was dedu ced from genetic results. Conclusion: Based on results of IVCT the identification of a MH associated mutation in a MH-family can make and support a correct MH diagnosis and can resolve MHE findings.