Muniz Viviane P, Silva Helga C A, Tsanaclis Ana Maria C, Vainzof Mariz
Human Genome Research Center, Department of Biology, IB, University of Sao Paulo, Sao Paulo, Brazil.
J Mol Neurosci. 2003;21(1):35-42. doi: 10.1385/JMN:21:1:35.
Malignant hyperthermia (MH) is a potentially lethal pharmacogenetic predisposition associated with a susceptibility to volatile anesthetics and depolarizing muscle relaxants that lead to a fulminant anesthetic crisis with hyperthermia, skeletal muscle rigidity, respiratory and metabolic acidosis, and muscle rhabdomyolysis. Malignant hyperthermia crises are caused by an abnormal regulation of the calcium release mechanism, which reflects the consequences of disturbed skeletal muscle calcium homeostasis. We screened 64 individuals of 27 unrelated families for the most frequently described mutations associated with MH in the genes RYR1 and CACNL1A3. We identified only one family with the Arg614Cys mutation but with a discordant segregating pattern to the in vitro contracture test (IVCT). To elucidate which other mechanism could lead to susceptibility in the members of this family, we tested it for further MH susceptibility loci. The same haplotype was shown to segregate with the individuals carrying the Arg614Cys mutation in chromosome 19; however, the other susceptible and equivocal individuals do not share this haplotype. Markers for the susceptible locus in chromosome regions 17q, 7q, 3q, and 5p did not segregate with the IVCT phenotype in the susceptible individuals, suggesting that the positivity of the IVCT could be attributable to other ambient factors.
恶性高热(MH)是一种潜在致命的药物遗传学易感性疾病,与对挥发性麻醉剂和去极化肌肉松弛剂的易感性相关,可导致高热、骨骼肌强直、呼吸和代谢性酸中毒以及肌肉横纹肌溶解的暴发性麻醉危机。恶性高热危机是由钙释放机制的异常调节引起的,这反映了骨骼肌钙稳态紊乱的后果。我们对27个无亲缘关系家庭的64名个体进行了筛查,以寻找RYR1和CACNL1A3基因中最常描述的与MH相关的突变。我们仅发现一个家庭存在Arg614Cys突变,但与体外挛缩试验(IVCT)的分离模式不一致。为了阐明该家庭其他成员可能导致易感性的机制,我们对其进行了进一步的MH易感位点检测。结果显示,相同的单倍型与19号染色体上携带Arg614Cys突变的个体分离;然而,其他易感和疑似个体并不共享此单倍型。17q、7q、3q和5p染色体区域易感位点的标记物在易感个体中与IVCT表型不分离,这表明IVCT的阳性结果可能归因于其他环境因素。