Literature DB >> 14500992

Screening for mutations in the RYR1 gene in families with malignant hyperthermia.

Viviane P Muniz1, Helga C A Silva, Ana Maria C Tsanaclis, Mariz Vainzof.   

Abstract

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.

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Year:  2003        PMID: 14500992     DOI: 10.1385/JMN:21:1:35

Source DB:  PubMed          Journal:  J Mol Neurosci        ISSN: 0895-8696            Impact factor:   3.444


  37 in total

1.  Malignant hyperthermia in infancy and identification of novel RYR1 mutation.

Authors:  D Chamley; N A Pollock; K M Stowell; R L Brown
Journal:  Br J Anaesth       Date:  2000-04       Impact factor: 9.166

2.  A genome wide search for susceptibility loci in three European malignant hyperthermia pedigrees.

Authors:  R L Robinson; N Monnier; W Wolz; M Jung; A Reis; G Nuernberg; J L Curran; K Monsieurs; P Stieglitz; L Heytens; R Fricker; C van Broeckhoven; T Deufel; P M Hopkins; J Lunardi; C R Mueller
Journal:  Hum Mol Genet       Date:  1997-06       Impact factor: 6.150

3.  A mutation in the transmembrane/luminal domain of the ryanodine receptor is associated with abnormal Ca2+ release channel function and severe central core disease.

Authors:  P J Lynch; J Tong; M Lehane; A Mallet; L Giblin; J J Heffron; P Vaughan; G Zafra; D H MacLennan; T V McCarthy
Journal:  Proc Natl Acad Sci U S A       Date:  1999-03-30       Impact factor: 11.205

4.  A search for three known RYR1 gene mutations in 41 Swedish families with predisposition to malignant hyperthermia.

Authors:  T H Fagerlund; G Islander; E R Twetman; K Berg
Journal:  Clin Genet       Date:  1995-07       Impact factor: 4.438

5.  Identification and functional characterization of a novel ryanodine receptor mutation causing malignant hyperthermia in North American and South American families.

Authors:  N Sambuughin; T E Nelson; J Jankovic; C Xin; G Meissner; M Mullakandov; J Ji; H Rosenberg; K Sivakumar; L G Goldfarb
Journal:  Neuromuscul Disord       Date:  2001-09       Impact factor: 4.296

6.  Identification of heterozygous and homozygous individuals with the novel RYR1 mutation Cys35Arg in a large kindred.

Authors:  P J Lynch; R Krivosic-Horber; H Reyford; N Monnier; K Quane; P Adnet; G Haudecoeur; I Krivosic; T McCarthy; J Lunardi
Journal:  Anesthesiology       Date:  1997-03       Impact factor: 7.892

7.  Linkage of malignant hyperthermia and hyperkalemic periodic paralysis to the adult skeletal muscle sodium channel (SCN4A) gene in a large pedigree.

Authors:  R Moslehi; S Langlois; I Yam; J M Friedman
Journal:  Am J Med Genet       Date:  1998-02-26

8.  A mutation in the human ryanodine receptor gene associated with central core disease.

Authors:  Y Zhang; H S Chen; V K Khanna; S De Leon; M S Phillips; K Schappert; B A Britt; A K Browell; D H MacLennan
Journal:  Nat Genet       Date:  1993-09       Impact factor: 38.330

9.  Discordance, in a malignant hyperthermia pedigree, between in vitro contracture-test phenotypes and haplotypes for the MHS1 region on chromosome 19q12-13.2, comprising the C1840T transition in the RYR1 gene.

Authors:  T Deufel; R Sudbrak; Y Feist; B Rübsam; I Du Chesne; K L Schäfer; N Roewer; T Grimm; F Lehmann-Horn; E J Hartung
Journal:  Am J Hum Genet       Date:  1995-06       Impact factor: 11.025

Review 10.  Recent developments in the molecular genetics of malignant hyperthermia: implications for future diagnosis at the DNA level.

Authors:  T V McCarthy; J M Healy; M Lehane; J J Heffron
Journal:  Acta Anaesthesiol Belg       Date:  1990
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  3 in total

1.  PharmGKB summary: very important pharmacogene information for CACNA1S.

Authors:  Katrin Sangkuhl; Robert T Dirksen; Maria L Alvarellos; Russ B Altman; Teri E Klein
Journal:  Pharmacogenet Genomics       Date:  2020-02       Impact factor: 2.000

2.  Life-threatening Episodes of Malignant Hyperthermia Following Halothane Anesthesia in Three Children: A Case Series and Review of Literature.

Authors:  Somrita Laha; Prabhas P Giri; Agnisekhar Saha; Partha P Gupta; Anisha De
Journal:  Indian J Crit Care Med       Date:  2019-01

3.  [Profile of malignant hyperthermia susceptibility reports confirmed with muscular contracture test in Brazil].

Authors:  Helga Cristina Almeida da Silva; Gisele Ferreira; Gislene Rodrigues; Joilson Moura Dos Santos; Pamela Vieira Andrade; Alexandre Hortense; Marcelo Vaz Perez; José Luiz Gomes do Amaral
Journal:  Braz J Anesthesiol       Date:  2018-10-26
  3 in total

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