NITROUS oxide inhibits vitamin B12
(cobalamin) by irreversibly oxidizing the cobalt atom of cobalamin.1,2
This leads to a subsequent inhibition of enzymes requiring cobalamin in its coenzyme form. Inhibition of vitamin B12
lasts several days because of the irreversible nature of the chemical reaction.3,4
Among the enzymes that require active vitamin B12
as a cofactor, methionine synthase (gene symbol MTR
, EC 184.108.40.206) is crucial because it is located at the juncture of two pathways: homocysteine remethylation and the folate cycle (fig. 1
). Therefore, inhibition of methionine synthase via
oxidized cobalamin results in a sustained increase of plasma homocysteine concentrations and lack of biologically active folate (“folate trapping”) that can be used for the conversion of homocysteine to methionine.5,6
In the methylenetetrahydrofolate reductase (MTHFR
) gene, which is operant in the folate cycle, two common single nucleotide polymorphisms have been described (MTHFR
1298A>C) that are associated with a reduced enzyme activity.7,8
Together, both polymorphisms have a combined prevalence of approximately 20% in the Western European population.9 MTHFR
677C>T results in decreased formation of active folate, methyltetrahydrofolate,10
which in turn leads to an increase in plasma total homocysteine concentrations.7
677C>T polymorphism is considered the single most important genetic determinant of plasma homocysteine.11
Recently, two reports describing children carrying several polymorphisms and mutations in the MTHFR
gene were published. The children developed catastrophic neurologic outcomes after being anesthetized with nitrous oxide.12,13
Based on these reports and the apparent importance of the MTHFR
genotype for plasma homocysteine, we hypothesized that patients carrying MTHFR
677C>T and/or 1298A>C mutations develop higher plasma homocysteine concentrations compared with noncarriers.
To test this hypothesis, we conducted a prospective cohort study in which all patients received 66% nitrous oxide. Patients were unaware of their MTHFR genotype before the study. We measured plasma total homocysteine concentrations as the main outcome variable before and after nitrous oxide anesthesia.
Materials and Methods
In this prospective, observational cohort study, all patients received nitrous oxide. Because genotyping was performed after completion of the study, patients and research staff were blinded to the MTHFR
genotype. Our research design used a population-based randomization of the two MTHFR
polymorphisms, which is also known as mendelian randomization (randomization according to the naturally occurring genotype frequencies).14
The study was approved by the Ethics Committee at the Medical University of Vienna, and every patient gave written, informed consent before participating.
Between November 2004 and March 2007, 140 healthy patients (American Society of Anesthesiologist status I or II) who were scheduled to undergo orthopedic surgery during general anesthesia were recruited to participate in this study. Surgical procedures included mostly arthroscopic surgery and some prosthetic procedures.
Inclusion criteria were American Society of Anesthesiology status I or II, age older than 18 yr, and surgery scheduled for 2 h or longer. Exclusion criteria were pregnancy, age younger than 18 yr, contraindication against the use of nitrous oxide (e.g., pneumothorax, mechanical bowel obstruction, middle ear occlusion, laparoscopic surgery, elevated intracranial pressure), and preoperative use of supplemental vitamin B12 or folate.
All patients received the same standardized general anesthetic regimen including 66% nitrous oxide. After premedication with 2 mg midazolam and application of standard monitoring (electrocardiogram, noninvasive blood pressure, pulse oximetry), general anesthesia was induced with fentanyl (1–3 μg/kg) and propofol (2–3 mg/kg). Muscle relaxation was achieved by administration of 0.6 mg/kg rocuronium, and all patients were orally intubated. For maintenance of anesthesia, patients received 1–2 vol% sevoflurane in a nitrous oxide:oxygen mixture of 66%:33%.
Blood samples for the main outcome variable total homocysteine were collected at three different time points: preoperatively (in the holding area), after 2 h of general anesthesia, and at the end of surgery. Homocysteine samples were immediately put on ice after drawing and then transported to the laboratory within 15 min and analyzed after the end of the study.
Vitamin B12, holotranscobalamin II, and folate samples were drawn before and at the end of surgery. In addition, plasma creatinine and albumin concentrations were tested because they influence total plasma homocysteine concentrations. Blood for MTHFR genotyping was drawn before surgery, but samples were not analyzed before the end of the study.
EDTA blood for homocysteine, folate, and holotranscobalamin II assays was immediately placed on ice and centrifuged at 2,000g
at 4°C (20 min) within 60 min. Plasma aliquots and 500 μl blood for isolation of DNA were snap-frozen and stored at −70°C. Plasma concentrations of total homocysteine (free plus protein-bound homocysteine)15
were determined by microparticle enzyme immunoassay (AxSYM homocysteine assay; Abbott GmbH & Co. KG, Wiesbaden, Germany). Holotranscobalamin II plasma concentration was measured by AxSYM HoloTC assay (Abbott). Folate and vitamin B12
plasma levels were analyzed with a radioassay (SimulTRAC-SNB; ICN Pharmaceuticals Inc., Costa Mesa, CA). Interassay variability was 4–5% for folate measurements and 4–6% for vitamin B12
Identification of the MTHFR
677C>T transition and the MTHFR
1298A>C transversion was conducted using restriction fragment length polymorphism analysis and the polymerase chain reaction primers and restriction enzymes Hinf
I and Fnu4
HI as previously described.7,16
Furthermore, we also calculated the allele frequencies for both mutations and tested for violations of the Hardy-Weinberg equilibrium assumption.
Sample Size Determination
On the basis of previous trials demonstrating (1) higher plasma total homocysteine concentrations in healthy individuals with the MTHFR 677TT genotype (approximately 11 vs. 9 μm in CC/CT genotype subjects) and (2) an increase of plasma total homocysteine concentrations of up to 76% during general anesthesia using nitrous oxide as compared with preoperative concentrations, we calculated that 16 patients with a MTHFR 677TT genotype would be required to give a statistical power of 80% at a two-sided α level of 5% to detect a mean difference in homocysteine plasma concentrations of 5 μm homocysteine (17 vs. 12 μm, SD of 5 μm) versus CC/CT genotype patients.
Because the frequency of the MTHFR 677TT genotype is approximately 12% in the Caucasian population of Austria, we included 140 patients in this study to expect a minimum of 16 MTHFR 677TT genotype patients.
Continuous variables are described as mean (± SD) for normally distributed data and with median (minimum–maximum or interquartile range) for skewed data. Binary variables are described as absolute frequencies and percentages. Two-sided t tests were used for group comparisons of normally distributed continuous variables, and the Wilcoxon rank sum test was used for not normally distributed continuous variables. For continuous paired observations, the paired t test was used for normally distributed differences, and the Wilcoxon signed rank test was used otherwise. The chi-square test was used for binary variables.
Changes over time from baseline to end of surgery, differences between the six combined genotypes, and their interaction were modeled by a linear mixed model accounting for the repeated measurements of the patients by a first-order autoregressive variance–covariance structure. Within this framework, several contrasts were calculated to test specific questions, such as the change from baseline to end of surgery for the six genotype groups. A second linear mixed model was used where the baseline measurements were included as independent factors to account for the differences at baseline to provide a better comparison of the 2-h and end-of-surgery measurements. For specific questions, contrasts were again calculated. The assumptions for both models (normally distributed residuals with equal variances) were checked visually by residual graphs. A logarithmic transformation was performed to homocysteine concentrations because of their skewed distributions.
All calculated P values are two-sided, and P ≤ 0.05 was considered significant. All calculations were performed with the statistical software SAS (version 9.1; SAS Institute Inc., Cary, NC).
Among the 140 patients in the study, the baseline characteristics between patients homozygous for MTHFR
677C>T or 1298A>C (n = 25) and heterozygous or wild type (n = 115) were similar except for baseline plasma total homocysteine concentrations, which were significantly higher among homozygotes. This is consistent with the underlying biologic role of the MTHFR
677C>T or 1298A>C polymorphism on homocysteine (table 1
Allele Frequency of MTHFR 677C>T or 1298A>C and Combined Genotype Distribution
After genotyping all patients, six combinations of MTHFR
677 and 1298 alleles were found (table 2
). In general, a patient could be homozygous (mutations in both copies of the gene), heterozygous (one mutant copy, one wild-type copy), or wild type (two wild-type copies) at either MTHFR
allele (677 or 1298). Theoretically, 3 × 3 combinations were possible, but in our patient population, we only observed six. No patient was found with homozygosity for both MTHFR
polymorphisms (677TT, 1298CC) or with a combination of a homozygous and a heterozygous mutation (table 2
). The allele frequency of MTHFR
677T was 0.34, and that of MTHFR
1298C was 0.31. The observed allele frequency of MTHFR
677C>T and 1298A>C in our study sample closely followed the Hardy-Weinberg equilibrium (chi-square test; based on published MTHFR
allele frequencies) and is comparable to previously published studies.17
Homocysteine Concentrations after Nitrous Oxide Anesthesia
Patients with homozygosity for MTHFR
677T or MTHFR
1298C developed significantly higher plasma total homocysteine concentrations after nitrous oxide anesthesia than wild-type patients (fig. 2
). The absolute increase in homocysteine concentrations was tripled in patients homozygous for either mutation compared with wild-type patients (5.6 vs.
1.8 μm; P
= 0.03). Only patients homozygous for either mutation reached median total homocysteine concentrations exceeding 15 μm, reflecting hyperhomocysteinemia. However, plasma total homocysteine concentrations increased after nitrous oxide anesthesia—not unexpectedly—among all MTHFR
677/1298 variants. This finding is consistent with the fact that nitrous oxide inhibits vitamin B12
in all patients irrespective of the underlying MTHFR
genotype (table 3
The effect of the homozygous genotypes (MTHFR 677TT, MTHFR 1298CC) on plasma total homocysteine concentrations after nitrous oxide anesthesia was not uniform: Patients with the 1298CC genotype experienced a 76% increase, whereas patients with the 677TT genotype had a 36% increase. Whether this disparity is due to a true biologic difference or due to random variation because of the small sample size in the subgroups (n = 8 and 17) remains to be determined.
Because inactivation rates of methionine synthase vary substantially in humans after exposure to nitrous oxide,18
we wanted to determine whether patients with a very long nitrous oxide exposure time exhibit a similar or greater effect on plasma total homocysteine concentrations. In total, 16 patients experienced nitrous oxide anesthesia times longer than 4 h. Plasma homocysteine concentrations increased significantly from 8.1 (7.3–10.0) to 14.6 (13.1–22.8) μm [median (interquartile range); P
< 0.001], a relative increase of approximately 80% (fig. 3
). This increase was substantially larger than during shorter nitrous oxide exposure times. Although four patients in this group were homozygous for one MTHFR
genotype, the effect of long nitrous oxide exposure time on plasma total homocysteine concentrations was independent of the MTHFR
Plasma Folate Concentrations after Nitrous Oxide Anesthesia
Plasma folate concentrations increased in all groups after nitrous oxide exposure, on average by 20%, except for double-wild-type patients. No difference between homozygous patients and others was found. Because the plasma folate assay measures predominantly 5-methyl-tetrahydrofolate, the folate substrate upstream of methionine synthase, the observed increase in folate indicates inhibition of methionine synthase and subsequent folate trapping.
Plasma Vitamin B12 and Holotranscobalamin II Concentrations after Nitrous Oxide Anesthesia
concentrations decreased uniformly across all groups; the effect was slightly more pronounced in homozygous patients (12% decrease vs.
4%). This effect of nitrous oxide on vitamin B12
was unexpected as endogenous vitamin B12
stores usually last several months. Therefore, we did not expect a priori
to find any changes in vitamin B12
plasma concentrations after nitrous oxide anesthesia. To corroborate these findings, we decided to additionally measure plasma holotranscobalamin II concentrations. Holotranscobalamin II is the fraction of cobalamin that is bound to transcobalamin II and represents the biologically active vitamin B12
that is available to DNA-synthesizing cells.19
The results show that holotranscobalamin II concentrations remained essentially unchanged after exposure to nitrous oxide (table 3
), indicating that in fact no actual change in blood vitamin B12
This study shows that patients who are homozygous for MTHFR 677C>T or 1298A>C develop significantly higher homocysteine concentrations after nitrous oxide anesthesia than noncarriers. This increase was nearly tripled in homozygous patients and reached concentrations defined as hyperhomocysteinemia (> 15 μm).
The inhibition of methionine synthase by nitrous oxide has two consequences because the enzyme is located at a critical juncture between two pathways (fig. 1
First, as clearly shown in this study as well as previous studies, inhibition of methionine synthase by nitrous oxide leads to an increase in homocysteine because it cannot be remethylated to methionine.5,21–23
Second, the inactivation causes a process called “folate trapping,” where the folate substrate upstream of the enzyme block, 5-methyl-tetrahydrofolate, accumulates and lack of biologically available methyl groups ensues.24
The lack of activated folate and methyl groups can ensue quickly and subsequently severely limits the de novo
synthesis of DNA resulting in apoptosis of rapidly dividing cells.25
This process is the cause for the megaloblastic changes observed in blood cells and bone marrow after nitrous oxide exposure. Therefore, the increase in serum folate concentrations after nitrous oxide anesthesia found in this study is not surprising and is consistent with trapping of methylated tetrahydrofolate.
The observed decrease of vitamin B12 concentrations after nitrous oxide exposure was unexpected because endogenous vitamin B12 stores usually last several months before being depleted. The results from our subsequent holotranscobalamin II tests showed that this was a spurious finding: Serum vitamin B12 concentrations apparently do not change after nitrous oxide exposure. A possible cause for this finding is that nitrous oxide might interfere with some commercial vitamin B12 assay, perhaps by altering binding of cobalamin substrates to intrinsic factor, the most commonly used method of vitamin B12 detection, and thus leading to falsely low vitamin B12 concentrations. However, there is currently no evidence, and this hypothesis should be studied formally in biochemical studies.
What are the clinical implications of our finding? To answer this question, two separate issues arise: (1) Is there evidence for nitrous oxide toxicity related to homocysteine and MTHFR genotype, and (2) is acute hyperhomocysteinemia associated with adverse outcomes?
Several lines of evidence support the hypothesis of homocysteine and MTHFR
genotype being associated with nitrous oxide toxicity. During the past 30 yr, more than a dozen case reports have been published where nitrous oxide anesthesia led to neurologic complications including myelopathy, peripheral neuropathy, and even hemiparesis.26–28
In most cases, nitrous oxide–induced folate trapping in conjunction with chronic vitamin B12
deficiency was responsible for the neurologic damage. How catastrophic nitrous oxide–induced hyperhomocysteinemia and folate trapping can be when they develop on top of an inherited MTHFR
enzyme defect was highlighted by two recent reports, one of which described the death of an infant after being anesthetized twice with nitrous oxide.12,13
In their report, Selzer et al.13
postulated a “double-hit” hypothesis to explain the pathophysiology of the fatal neurologic outcome. This hypothesis links nitrous oxide–induced hyperhomocysteinemia and inhibition of folate metabolism with an underlying MTHFR
gene defect. Our results are consistent with this “double-hit” hypothesis and might be applicable to other patients with a deficiency in vitamin B12
/folate metabolism who are exposed to nitrous oxide, e.g.
, patients with other common MTHFR
Polymorphisms in genes within the folate cycle or homocysteine–methionine pathway that go in hand with reduced enzyme activity are common and affect the population at large.9
As in our study, the cumulative prevalence of homozygous MTHFR
677C>T and 1298A>C mutations approaches 20%, rendering these patients susceptible for a “double hit” when they are exposed to nitrous oxide. Although evidence is currently lacking, these genetically “at-risk” patients might develop hypomethylation of DNA and defective DNA synthesis with apoptosis and megaloblastic anemia and sequelae related to hyperhomocysteinemia.
The neurologic damage caused by nitrous oxide occurs often in combination with hematologic changes such as megaloblastic anemia and bone marrow disorders.29,30
These toxic side effects of nitrous oxide have been recognized for decades and are directly associated with nitrous oxide’s inhibition of methionine synthase and folate metabolism.
Nitrous oxide has been linked in a recent study by Myles et al.31
to an increased risk for adverse postoperative outcomes, including a higher trend for adverse cardiovascular outcomes including myocardial infarction. In a smaller study, patients receiving nitrous oxide had higher rates of postoperative myocardial ischemia.32
Although the inhibition of vitamin B12
and the subsequent hyperhomocysteinemia due to nitrous oxide lasts for only a few days,33
this effect coincides with a period of increased vulnerability for the postoperative patient, highlighted by the fact that the highest risk for major cardiovascular complications after surgery occurs on the second and third postoperative day.34,35
For both studies, nitrous oxide–induced hyperhomocysteinemia and impaired folate metabolism could serve as a potential pharmacogenetic explanation to account for the increased risk.
The second question regarding the clinical implications of our findings, whether acute nitrous oxide–induced hyperhomocysteinemia is associated with adverse outcomes, is difficult to answer. Although homocysteine has emerged from numerous studies as an established risk factor for long-term cardiovascular morbidity and mortality,9,36,37
the clinical impact of an acute elevation of plasma homocysteine caused by nitrous oxide is currently unclear. Recent experimental studies, however, investigated the effects of acute hyperhomocysteinemia and showed that in humans and animals, acute hyperhomocysteinemia impairs myocardial substrate use and causes endothelial dysfunction in blood vessels indicating a profound effect on cardiovascular function.38–40
It also causes enhanced platelet aggregation, which might be causative for its procoagulatory effects.41
Our study was designed to measure biochemical markers after nitrous oxide anesthesia and not to detect clinical outcomes. Therefore, any inference about a possible link between nitrous oxide, elevated homocysteine, and adverse outcomes cannot be made. The sample size in our study was large enough to include a sufficient number of homozygous patients, although we did not observe double homozygous patients (MTHFR 677TT, 1298CC) or the combination of homozygous and heterozygous. In addition, because all patients in our study were exposed to nitrous oxide, we could not observe the effects of a nitrous oxide–free anesthetic regimen on homocysteine concentrations in the different MTHFR genotype populations. Although unlikely, there is a small chance that patients with homozygous MTHFR genotypes would develop higher homocysteine concentrations even without being exposed to nitrous oxide.
In summary, the results of our study show that patients with reduced 5,10-methylenetetrahydrofolate reductase enzyme activity caused by a homozygous MTHFR 677C>T or 1298A>C gene polymorphism are at higher risk to develop hyperhomocysteinemia after nitrous oxide anesthesia. It seems that this subgroup of patients with a combined prevalence in the general population of approximately 20% may be particularly susceptible to the toxic effects of nitrous oxide on vitamin B12 and folate metabolism. The question of whether this biochemical effect translates into a higher risk for adverse clinical outcomes requires large-scale clinical trials.
The authors thank Evan Kharasch, M.D., Ph.D. (Russell D. and Mary B. Shelden Professor of Anesthesiology and Director, Division of Clinical and Translational Research), and C. Michael Crowder, M.D., Ph.D. (Associate Professor; both Department of Anesthesiology, Washington University School of Medicine, St. Louis, Missouri), for their invaluable help in revising the manuscript. Furthermore, the authors acknowledge Gere Sunder-Plassmann, M.D. (Associate Professor, Department of Internal Medicine, Medical University of Vienna, Vienna, Austria), for his help in the sample size calculation.
1. Banks RGS, Henderson RJ, Pratt JM: Reactions of gases in solution, part III: Some reactions of nitrous oxide with transition-metal complexes. J Chem Soc A 1968; 2886–9
2. Deacon R, Lumb M, Perry J, Chanarin I, Minty B, Halsey MJ, Nunn JF: Selective inactivation of vitamin B12 in rats by nitrous oxide. Lancet 1978; 2:1023–4
3. Koblin DD, Watson JE, Deady JE, Stokstad EL, Eger EI III: Inactivation of methionine synthetase by nitrous oxide in mice. Anesthesiology 1981; 54:318–24
4. Kondo H, Osborne ML, Kolhouse JF, Binder MJ, Podell ER, Utley CS, Abrams RS, Allen RH: Nitrous oxide has multiple deleterious effects on cobalamin metabolism and causes decreases in activities of both mammalian cobalamin-dependent enzymes in rats. J Clin Invest 1981; 67:1270–83
5. Badner NH, Drader K, Freeman D, Spence JD: The use of intraoperative nitrous oxide leads to postoperative increases in plasma homocysteine. Anesth Analg 1998; 87:711–3
6. Christensen B, Guttormsen AB, Schneede J, Riedel B, Refsum H, Svardal A, Ueland PM: Preoperative methionine loading enhances restoration of the cobalamin-dependent enzyme methionine synthase after nitrous oxide anesthesia. Anesthesiology 1994; 80:1046–56
7. Frosst P, Blom HJ, Milos R, Goyette P, Sheppard CA, Matthews RG, Boers GJ, den Heijer M, Kluijtmans LA, van den Heuvel LP, Rozen R: A candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahydrofolate reductase. Nat Genet 1995; 10:111–3
8. van der Put NM, Gabreels F, Stevens EM, Smeitink JA, Trijbels FJ, Eskes TK, van den Heuvel LP, Blom HJ: A second common mutation in the methylenetetrahydrofolate reductase gene: An additional risk factor for neural-tube defects? Am J Hum Genet 1998; 62:1044–51
9. Ueland PM, Hustad S, Schneede J, Refsum H, Vollset SE: Biological and clinical implications of the MTHFR C677T polymorphism. Trends Pharmacol Sci 2001; 22:195–201
10. Molloy AM, Daly S, Mills JL, Kirke PN, Whitehead AS, Ramsbottom D, Conley MR, Weir DG, Scott JM: Thermolabile variant of 5,10-methylenetetrahydrofolate reductase associated with low red-cell folates: Implications for folate intake recommendations. Lancet 1997; 349:1591–3
11. Gellekink HMS, den Heijer MMD, Heil SPD, Blom HPD: Genetic determinants of plasma total homocysteine. Semin Vascul Med 2005; 5:98–109
12. Lacassie HJ, Nazar C, Yonish B, Sandoval P, Muir HA, Mellado P: Reversible nitrous oxide myelopathy and a polymorphism in the gene encoding 5,10-methylenetetrahydrofolate reductase. Br J Anaesth 2006; 96:222–5
13. Selzer RR, Rosenblatt DS, Laxova R, Hogan K: Adverse effect of nitrous oxide in a child with 5,10-methylenetetrahydrofolate reductase deficiency. N Engl J Med 2003; 349:45–50
14. Ebrahim S, Davey Smith G: Mendelian randomization: Can genetic epidemiology help redress the failures of observational epidemiology? Hum Genet 2008; 123:15–33
15. American Society of Human Genetics/American College of Medical Genetics Test and Transfer Committee Working Group. Measurement and use of total plasma homocysteine. Am J Hum Genet 1998; 63:1541–3
16. Weisberg I, Tran P, Christensen B, Sibani S, Rozen R: A second genetic polymorphism in methylenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity. Mol Genet Metab 1998; 64:169–72
17. Brown NM, Pratt VM, Buller A, Pike-Buchanan L, Redman JB, Sun W, Chen R, Crossley B, McGinniss MJ, Quan F, Strom CM: Detection of 677CT/1298AC “double variant” chromosomes: Implications for interpretation of MTHFR genotyping results. Genet Med 2005; 7:278–82
18. Royston BD, Nunn JF, Weinbren HK, Royston D, Cormack RS: Rate of inactivation of human and rodent hepatic methionine synthase by nitrous oxide. Anesthesiology 1988; 68:213–6
19. Ulleland M, Eilertsen I, Quadros EV, Rothenberg SP, Fedosov SN, Sundrehagen E, Orning L: Direct assay for cobalamin bound to transcobalamin (holo-transcobalamin) in serum. Clin Chem 2002; 48:526–32
20. Fowler BPD: Homocysteine: Overview of biochemistry, molecular biology, and role in disease processes. Semin Vascul Med 2005; 5:77–86
21. Christensen B, Ueland PM: Methionine synthase inactivation by nitrous oxide during methionine loading of normal human fibroblasts: Homocysteine remethylation as determinant of enzyme inactivation and homocysteine export. J Pharmacol Exp Ther 1993; 267:1298–303
22. Ermens AA, Refsum H, Rupreht J, Spijkers LJ, Guttormsen AB, Lindemans J, Ueland PM, Abels J: Monitoring cobalamin inactivation during nitrous oxide anesthesia by determination of homocysteine and folate in plasma and urine. Clin Pharmacol Ther 1991; 49:385–93
23. Foschi D, Rizzi A, Zighetti ML, Bissi M, Corsi F, Trabucchi E, Mezzetti M, Cattaneo M: Effects of surgical stress and nitrous oxide anaesthesia on peri-operative plasma levels of total homocysteine: A randomised, controlled study in general surgery. Anaesthesia 2001; 56:676–9
24. Smulders YM, Smith DEC, Kok RM, Teerlink T, Swinkels DW, Stehouwer CDA, Jakobs C: Cellular folate vitamer distribution during and after correction of vitamin B12 deficiency: A case for the methylfolate trap. Br J Haematol 2006; 132:623–9
25. Koury MJ, Price JO, Hicks GG: Apoptosis in megaloblastic anemia occurs during DNA synthesis by a p53-independent, nucleoside-reversible mechanism. Blood 2000; 96:3249–55
26. Felmet K, Robins B, Tilford D, Hayflick SJ: Acute neurologic decompensation in an infant with cobalamin deficiency exposed to nitrous oxide. J Pediatr 2000; 137:427–8
27. Flippo TS, Holder WD Jr: Neurologic degeneration associated with nitrous oxide anesthesia in patients with vitamin B12 deficiency. Arch Surg 1993; 128:1391–5
28. Hadzic A, Glab K, Sanborn KV, Thys DM: Severe neurologic deficit after nitrous oxide anesthesia. Anesthesiology 1995; 83:863–6
29. Amess JA, Burman JF, Rees GM, Nancekievill DG, Mollin DL: Megaloblastic haemopoiesis in patients receiving nitrous oxide. Lancet 1978; 2:339–42
30. Cullen MH, Rees GM, Nancekievill DG, Amess JA: The effect of nitrous oxide on the cell cycle in human bone marrow. Br J Haematol 1979; 42:527–34
31. Myles PS, Leslie K, Chan MT, Forbes A, Paech MJ, Peyton P, Silbert BS, Pascoe E: Avoidance of nitrous oxide for patients undergoing major surgery: A randomized controlled trial. Anesthesiology 2007; 107:221–31
32. Badner NH, Beattie WS, Freeman D, Spence JD: Nitrous oxide-induced increased homocysteine concentrations are associated with increased postoperative myocardial ischemia in patients undergoing carotid endarterectomy. Anesth Analg 2000; 91:1073–9
33. Koblin DD, Tomerson BW: Methionine synthase activities in mice following acute exposures to ethanol and nitrous oxide. Biochem Pharmacol 1989; 38:1353–8
34. Fleischmann KE, Goldman L, Young B, Lee TH: Association between cardiac and noncardiac complications in patients undergoing noncardiac surgery: Outcomes and effects on length of stay. Am J Med 2003; 115:515–20
35. Badner NH, Knill RL, Brown JE, Novick TV, Gelb AW: Myocardial infarction after noncardiac surgery. Anesthesiology 1998; 88:572–8
36. Lewis SJ, Ebrahim S, Davey Smith G: Meta-analysis of MTHFR 677C->T polymorphism and coronary heart disease: Does totality of evidence support causal role for homocysteine and preventive potential of folate? BMJ 2005; 331:1053
37. Wald DS, Wald NJ, Morris JK, Law M: Folic acid, homocysteine, and cardiovascular disease: Judging causality in the face of inconclusive trial evidence. BMJ 2006; 333:1114–7
38. Abahji TN, Nill L, Ide N, Keller C, Hoffmann U, Weiss N: Acute hyperhomocysteinemia induces microvascular and macrovascular endothelial dysfunction. Arch Med Res 2007; 38:411–6
39. Chambers JC, McGregor A, Jean-Marie J, Obeid OA, Kooner JS: Demonstration of rapid onset vascular endothelial dysfunction after hyperhomocysteinemia: An effect reversible with vitamin C therapy. Circulation 1999; 99:1156–60
40. Suematsu N, Ojaimi C, Kinugawa S, Wang Z, Xu X, Koller A, Recchia FA, Hintze TH: Hyperhomocysteinemia alters cardiac substrate metabolism by impairing nitric oxide bioavailability through oxidative stress. Circulation 2007; 115:255–62
41. Harpel PC, Zhang X, Borth W: Homocysteine and hemostasis: Pathogenetic mechanisms predisposing to thrombosis. J Nutr 1996; 126:1285S–9
© 2008 American Society of Anesthesiologists, Inc.