Reversible nitrous oxide myelopathy and a polymorphism in the gene encoding 5,10-methylenetetrahydrofolate reductase

Br J Anaesth. 2006 Feb;96(2):222-5. doi: 10.1093/bja/aei300. Epub 2005 Dec 16.

Abstract

We present a case of a patient who received nitrous oxide on two occasions within a period of 8 weeks and who subsequently developed a diffuse myelopathy, characterized by upper extremity paresis, lower extremity paraplegia and neurogenic bladder. Laboratory testing revealed hyperhomocysteinaemia and low levels of vitamin B(12). Because of this uncommon clinical presentation, we analysed the patient's DNA, and found a polymorphism in the MTHFR gene that is associated with the thermolabile isoform of the 5,10-methylenetetrahydrofolate reductase enzyme, which explained the myelopathy experienced by the patient after being exposed to nitrous oxide. Soon after initiating supplementary therapy with folic acid and vitamin B(12), the neurological symptoms subsided.

Publication types

  • Case Reports

MeSH terms

  • Anesthetics, Inhalation / adverse effects*
  • Folic Acid / therapeutic use
  • Genetic Predisposition to Disease
  • Humans
  • Hyperhomocysteinemia / complications
  • Male
  • Methylenetetrahydrofolate Reductase (NADPH2) / genetics*
  • Middle Aged
  • Nitrous Oxide / adverse effects*
  • Paralysis / chemically induced
  • Polymorphism, Genetic*
  • Postoperative Complications
  • Spinal Cord Diseases / chemically induced*
  • Spinal Cord Diseases / drug therapy
  • Spinal Cord Diseases / genetics
  • Vitamin B 12 / therapeutic use

Substances

  • Anesthetics, Inhalation
  • Folic Acid
  • Methylenetetrahydrofolate Reductase (NADPH2)
  • Nitrous Oxide
  • Vitamin B 12