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Anesthesiology:
doi: 10.1097/ALN.0b013e31829761e3
Perioperative Medicine

Influence of Nitrous Oxide Anesthesia, B-Vitamins, and MTHFR Gene Polymorphisms on Perioperative Cardiac Events: The Vitamins in Nitrous Oxide (VINO) Randomized Trial

Nagele, Peter M.D., M.Sc.*; Brown, Frank B.Sc.; Francis, Amber B.S.N, R.N.; Scott, Mitchell G. Ph.D.; Gage, Brian F. M.D., M.Sc.§; Miller, J. Philip A.B.; for the VINO Study Team

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Abstract

Background: Nitrous oxide causes an acute increase in plasma homocysteine that is more pronounced in patients with the methylenetetrahydrofolate reductase (MTHFR) C677T or A1298C gene variant. In this randomized controlled trial, the authors sought to determine whether patients carrying the MTHFR C677T or A1298C variant had a higher risk for perioperative cardiac events after nitrous oxide anesthesia and whether this risk could be mitigated by B-vitamins.
Methods: The authors randomized adult patients with cardiac risk factors undergoing noncardiac surgery, to receive nitrous oxide plus intravenous B-vitamins before and after surgery, or to nitrous oxide and placebo. Serial cardiac biomarkers and 12-lead electrocardiograms were obtained. The primary study endpoint was the incidence of myocardial injury, as defined by cardiac troponin I increase within the first 72 h after surgery.
Results: A total of 500 patients completed the trial. Patients who were homozygous for either MTHFR C677T, or A1298C gene variant (n = 98; 19.6%) had no increased rate of postoperative cardiac troponin I increase compared with wild-type and heterozygous patients (11.2 vs. 14.0%; relative risk 0.96; 95% CI, 0.85–1.07; P = 0.48). B-vitamins blunted the rise in homocysteine, but had no effect on cardiac troponin I increase compared with patients receiving placebo (13.2 vs. 13.6%; relative risk 1.02; 95% CI 0.78 to 1.32; P = 0.91).
Conclusions: Neither MTHFR C677T and A1298C gene variant, nor acute homocysteine increase are associated with perioperative cardiac troponin increase after nitrous oxide anesthesia. B-vitamins blunt nitrous oxide-induced homocysteine increase but have no effect on cardiac troponin I increase.
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What We Already Know about This Topic

* Nitrous oxide increases circulating homocysteine concentration, and may do so more in patients with variants of the methylenetetrahydrofolate reductase gene
* Whether patients with these variants have increased cardiac risk from nitrous oxide exposure and whether this can be mitigated by vitamin B12 administration are not known
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What This Article Tells Us That Is New

* In 500 patients with cardiac risk factors undergoing noncardiac surgery with nitrous oxide, methylenetetrahydrofolate reductase gene variant did not alter homocysteine concentration or the incidence of cardiac injury
* Vitamin B12, although decreasing homocysteine concentration, did not alter the incidence of cardiac injury
IN use for more than 150 yr, nitrous oxide (laughing gas) is not only the oldest, but also one of the most widely used general anesthetics, worldwide. Because of its weak potency, nitrous oxide is typically used as an adjunct during general anesthesia, at a concentration of 50–70%. Its use during general anesthesia, particularly among patients with cardiac risk factors, has been associated with an increased risk for perioperative myocardial ischemia and infarction in some studies,1–3 but not others.4–8
Nitrous oxide causes an acute increase in plasma homocysteine by irreversible inactivation of vitamin B12,9–11 a side effect unrelated to its anesthetic action.12,13 The acute increase in homocysteine has been proposed as the cause for the increased perioperative myocardial infarction risk.14 Previously, we showed that patients homozygous for the C677T or A1298C variant in the methylenetetrahydrofolate reductase (MTHFR) gene, which is the most important genetic determinant of plasma homocysteine,15–19 developed higher plasma homocysteine concentrations after nitrous oxide anesthesia.20
The purpose of the present investigation was to determine whether patients who were homozygous for the MTHFR C677T or A1298C variant had an increased risk for perioperative cardiac events after nitrous oxide anesthesia, and whether this risk could be mitigated by B-vitamins, which reliably lowers plasma homocysteine.21–23 To answer this question, we conducted a double-blind, randomized placebo-controlled trial. In the trial, patients scheduled for nitrous oxide anesthesia were randomly allocated to receive B-vitamins or placebo.
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Materials and Methods

Study Design and Oversight
The Vitamins in Nitrous Oxide trial was a single-center randomized, double-blind placebo-controlled trial of nitrous oxide and B-vitamins in patients with or at risk for coronary artery disease, undergoing noncardiac surgery at Barnes-Jewish-Hospital, St. Louis. The investigators were responsible for all aspects of the trial, including design, protocol, data collection, and analyses. The study was conducted in accordance to the protocol. A data and safety monitoring board monitored the trial. The study was approved by the Washington University institutional review board (St. Louis, Missouri), and all patients provided written, informed consent. The trial was registered at clinicaltrials.gov with the identifier NCT00655980.
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Patients
Adult patients diagnosed with or at risk for coronary artery disease (combination of at least two risk factors, such as smoking history, hypertension, hypercholesterolemia, peripheral vascular disease, diabetes, stroke/transient ischemic attack), who were scheduled for elective noncardiac surgery under general anesthesia lasting more than 2 h, were assessed for eligibility. Patients were ineligible: if they had a contraindication to the use of nitrous oxide (e.g., pneumothorax, bowel obstruction, laparoscopic surgery, increased intracranial pressure, middle-ear occlusion); clinically significant pulmonary disease requiring supplemental oxygen; patients not expected to survive 24 h; patients taking supplemental vitamin B12 or folic acid; allergy or hypersensitivity to cobalamins; Leber disease or a seizure disorder.
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Randomization and Intervention
The Vitamins in Nitrous Oxide trial consisted of two randomized arms, with a total sample size of 500 patients, all of whom received nitrous oxide throughout surgery at a concentration of 60%. Patients were randomized to receive either 1 mg vitamin B12 and 5 mg folic acid (in 100 ml of normal saline) before and after surgery (nitrous oxide/B-vitamin group; n = 250), or a placebo infusion (100 ml normal saline; nitrous oxide/placebo group; n = 250). After initiation of the trial, the addition of a nitrous oxide-free nonrandomized reference group (n = 125) was recommended during scientific review at the National Institutes of Health, to determine if nitrous oxide had an effect on perioperative cardiac events independent of homocysteine increase. Patients in this reference cohort were drawn from the same population, had identical inclusion and exclusion criteria, but received nitrous oxide-free anesthesia and no B-vitamins. The protocol was amended, and the first patient in the reference group was enrolled in May 2010 (around study midpoint). No changes to the primary and secondary study outcomes were made. Patients in the reference group received an identical intraoperative oxygen concentration (40% oxygen; 60% nitrogen). All other aspects of intraoperative management were at the discretion of the anesthesia team.
The B-vitamin/placebo-infusion was covered with aluminum foil by an independent clinical pharmacist to prevent unblinding. Randomization was performed by our clinical pharmacy service as well and was in blocks of random sizes, using the Moses–Oakford algorithm24; no member of the study team had access to the randomization sequence until study enrolment finished. Patients, all members of the clinical care team (anesthesia team, surgeons, nurses), all members of the study team, and outcome assessors were blinded to the group assignment and genotype, which was determined after the patient had completed the study. The administration of nitrous oxide was open label due to practical reasons.
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Outcomes
For outcome assessments, patients had five serial blood collections and electrocardiograms at the following time points: preoperative (baseline), end of surgery, and postoperative days 1, 2, and 3. Plasma total homocysteine (tHcy), serum troponin I (TnI; Siemens Dimension RxL; Siemens, Tarrytown, NY), and high-sensitivity troponin T (hs-cTnT; Roche Elycsys 2010; Roche Diagnostics, Indianapolis, IN) were measured at all time points; serum folate and vitamin B12 were measured at baseline and on postoperative day 1. MTHFR genotypes (rs1801131, rs1801133) were determined by the Sequenom MassARRAY (Sequenom, San Diego, CA) system.
The primary study endpoint was the incidence of myocardial injury, as defined by cardiac troponin I (cTnI) increase within the first 72 h after surgery. Secondary endpoints were the incidence of myocardial infarction within the first 72 h after surgery, and a composite of 30-day mortality and nonfatal myocardial infarction, which were assessed by a 30-day follow-up interview and medical records review. For the assessment of the primary study outcome, a Food and Drug Administration-cleared troponin I assay was used (Siemens Dimension RxL; limit of detection: 0.04 μg/l; 99th percentile: 0.07 μg/l; 10% coefficient of variation: 0.14 μg/l).25 During the course of the trial, a novel high-sensitivity troponin T assay became available (Roche Elecsys; limit of detection: 5.0 ng/l; 99th percentile: 14 ng/l; 10% coefficient of variation: 13 ng/l),25 which we additionally used due to its markedly increased sensitivity in the detection of circulating troponins (currently not cleared by the U.S. Food and Drug Administration). Cardiac troponin increase was defined as a peak postoperative cardiac troponin I concentration more than 99th percentile (>0.07 μg/l). Myocardial infarction was defined according to the universal definition (troponin I increase >99th percentile plus electrocardiogram changes indicative of myocardial ischemia and/or clinical symptoms).26 Electrocardiograms were read and analyzed by an expert assessor blinded to the group assignment. Adverse events were assessed by the study team from patient medical records.
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Statistical Analysis
Patients were grouped according to their MTHFR genotype in homozygotes (MTHFR 677TT and 1298CC) and wild-type or heterozygotes (MTHFR 677CC and CT, and 1298AA and AC) on the basis of our previous observation, suggesting a significantly higher homocysteine increase after nitrous oxide anesthesia among MTHFR homozygous patients.20 The sample size determination was planned for the two randomized trial arms and did not include the reference group. Extrapolated from incidences observed in patients undergoing vascular surgery and our previous study,20 we expected an incidence rate of cardiac troponin increase among MTHFR homozygous patients (expected proportion 20% of the study population) of 24% (with B-vitamins) and 47% (placebo), and at 20% for nonhomozygous patients (B-vitamins) and 32% (placebo).
On the basis of these assumptions, a sample size of n equals to 500 was sufficient to detect a statistically significant difference between MTHFR homozygotes with an α = 0.05 and β = 0.30, and between MTHFR nonhomozygotes with an α = 0.05 and β = 0.22. Using continuous data, we could detect at a power of 0.7, a difference of 0.5 of a SD between MTHFR homozygotes, and a difference of 0.28 SDs between nonhomozygotes. All power calculations are based on two-tail tests, with a 0.05 significance level, using the program STPLAN (M.D. Anderson Cancer Center, University of Texas, Houston, TX).
Data were entered into a Research Electronic Data Capture (REDCap) database27 and exported into SAS (Cary, NC). Descriptive statistics for each group were computed, including the calculation of the median and 25th and 75th percentiles because many of the distributions were skewed or means ± SD. When analyzing dichotomous outcomes, chi-square tests and logistic regression were used. For continuous values, which were obtained at multiple time points, a repeated measures ANOVA was computed, and appropriate contrasts from the time*group effect constructed to compare changes from baseline to peak values between groups. Analyses were also repeated using stratification by MTHFR genotype. Where regression diagnostics raised concerns, results were confirmed using transformations (e.g., logarithmic) or rank order transformations. Significance level was set at 0.05, two-tailed.
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Results

Patients
Table 1
Table 1
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Fig. 1
Fig. 1
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From March 2008 to December 2011, we enrolled 687 patients into the study; sixty-two patients were withdrawn after randomization but before surgery, resulting in a final intention-to-treat sample of 625 patients. The most common causes for withdrawal were cancelled surgeries or refusal by the anesthesia team (fig. 1). Of the final study sample, 250 patients were randomly assigned to the nitrous oxide/B-vitamin group (5 patients did not receive nitrous oxide), and 250 to the nitrous oxide group/placebo (3 patients did not receive nitrous oxide). One hundred twenty-five patients were assigned to the nonrandomized reference group. Baseline characteristics between the two randomized study arms were well balanced (table 1). The MTHFR A1298C allele (minor allele frequency 0.29) was in Hardy–Weinberg equilibrium, but the C677T allele (minor allele frequency 0.28) was not. The TT variant had an observed prevalence of: 10.6% (expected: 7.8%; P < 0.001).
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Study Outcomes—Homocysteine
Table 2
Table 2
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Fig. 2
Fig. 2
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Patients in the nitrous oxide/B-vitamin group and nitrous oxide/placebo group had similar median exposures to nitrous oxide (measured as the product of duration of nitrous oxide anesthesia in hours and fraction of inspiratory nitrous oxide concentration: 1.7 ± 1.0 percent*hours vs. 1.7 ± 1.0 percent*hours (P = 0.62). Patients in the nitrous oxide/B-vitamin group had significantly higher postoperative vitamin B12 and folate concentrations compared with baseline and to both the other groups (see table, Supplemental Digital Content 1, http://links.lww.com/ALN/A937). Plasma total homocysteine concentrations rose in all patients who received nitrous oxide, regardless of MTHFR genotype. The increase was significantly blunted in patients receiving B-vitamins (fig. 2 and table 2). The MTHFR C677T and A1298C allele status did not influence the extent of plasma total homocysteine increase. In the B-vitamin group, homozygous patients had a median increase of 2.1 μM [interquartile range, 0–5.3] and wild-type/heterozygous patients had 2.1 μM [−0.2 to 5.5]; in the placebo group, homozygous patients had a 3.1-μM increase [interquartile range, 1.4–7.3] compared with 3.8 μM [interquartile range, 0.6–6.8] for wild-type/heterozygous patients.
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Influence of MTHFR Genotype on Perioperative Cardiac Events
Table 3
Table 3
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Among the 500 patients within the randomized trial, neither the MTHFR genotype, nor the B-vitamin treatment had an effect on cardiac study outcomes. Patients who were homozygous for the MTHFR C677T or A1298C gene variant (n= 98; 19.6%) had an 11.2% incidence rate of postoperative cTnI increase compared with 14.0% for wild-type and heterozygous patients (relative risk, 0.96; 95% CI, 0.85–1.07; P = 0.48; table 3). B-vitamins had no effect on cTnI increase compared with patients receiving placebo (13.2 vs. 13.6%; relative risk, 1.02; 95% CI, 0.78–1.32; P = 0.91), regardless of MTHFR genotype.
Patients who were homozygous for the MTHFR C677T or A1298C gene variant had a 3.1% incidence rate of perioperative myocardial infarction (within 3 days after surgery) compared with 4.7% for wild-type and heterozygous patients (relative risk, 0.93; 95% CI, 0.78–1.10; P = 0.48). The incidence of postoperative myocardial infarction was 6.0% in the nitrous oxide/placebo group and 2.8% in the nitrous oxide/B-vitamin group (relative risk, 1.60; 95% CI, 0.87–2.98; P = 0.09).
Fig. 3
Fig. 3
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The extent of myocardial injury or necrosis, as indicated by the rise in high-sensitivity troponin T (Δhs-cTnT), was not different among MTHFR homozygous and wild-type/heterozygous patients and patients who received B-vitamins or placebo (table 2 and fig. 3).
Acute homocysteine increase was not correlated with cardiac troponin release, as indicated by the rise in hs-cTnT (Δhs-cTnT; Spearman correlation coefficient = 0.003; P = 0.94). At 30 days, three patients (1.2%) had died in the nitrous oxide group and none in the B-vitamin group.
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Nonrandomized Nitrous Oxide-free Reference Group
In addition to the randomized trial cohort, an additional, nonrandomized reference group (n = 125) of patients, receiving nitrous oxide-free anesthesia, were enrolled. Nine patients inadvertently received nitrous oxide during emergence from anesthesia and four patients for the duration of the case. The baseline characteristics of the nitrous oxide-free reference group were very similar to the randomized cohort (see table, Supplemental Digital Content 2, http://links.lww.com/ALN/A938). Patients in the nitrous oxide-free reference group had similar incidence rates of cardiac troponin I increase (13.6 vs. 13.4%) and a slightly increased rate of myocardial infarction (6.4 vs. 4.4%). The median Δhs-cTnT was similar to the randomized cohort, indicative of a similar magnitude of perioperative myocardial injury between patients receiving nitrous oxide and nitrous oxide-free anesthesia (see tables, Supplemental Digital Content 3, http://links.lww.com/ALN/A939, and Supplemental Digital Content 4, http://links.lww.com/ALN/A940).
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Safety
Table 4
Table 4
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No adverse events were related to the administration of intravenous B-vitamins (table 4). Within the first 3 postoperative days, 16 patients (6.4%) in the nitrous oxide/B-vitamin group had a cardiovascular event compared with 25 (10.0%) in the nitrous oxide/placebo group (table 4; see table, Supplemental Digital Content 5, http://links.lww.com/ALN/A941).
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Discussion

This trial resulted in several findings: First, the prophylactic use of vitamin B12 and folic acid successfully blunted the nitrous oxide-induced increase in plasma homocysteine but had no effect on perioperative cardiac outcomes. Second, patients who are homozygous for the MTHFR C677T and A1298C gene variants had no increased risk for perioperative cardiac events after nitrous oxide anesthesia. Third, the acute increase in plasma homocysteine caused by nitrous oxide was not associated with perioperative cardiac troponin increases.
Several points deserve comment. Consistent with earlier evidence,9 our study showed that nitrous oxide causes an acute increase in plasma homocysteine, which lasts several days. Contrary to previous suggestions, however, the observed plasma homocysteine increase was not associated with troponin increases or myocardial infarction. The administration of B-vitamins before and after nitrous oxide anesthesia clearly lowered plasma homocysteine levels, but did not decrease the rate and magnitude of postoperative cardiac troponin increase, or myocardial infarction. We therefore, question the notion that acute nitrous oxide-induced hyperhomocysteinemia has a causal effect on perioperative myocardial ischemia and infarction. There is now an emerging consensus that homocysteine may be a marker, rather than a cause of atherosclerotic disease and increased cardiovascular risk,23,28,29 despite impressive associations between chronically increased homocysteine and coronary artery disease.30,31
To our surprise, and contrary to our previous work, the MTHFR C677T and A1298C genotype had no influence on nitrous oxide-induced homocysteine increase.20 A likely explanation for this lack of influence lies in the mandatory dietary folate fortification of all grain products in the United States, which has increased folate levels throughout the population.32 Dietary folate fortification also reduces the effects of the MTHFR polymorphisms.19,33 Our previous study was conducted in Austria, a country without mandatory folate fortification, which may explain why we previously observed a significant effect of MTHFR polymorphisms on nitrous oxide-induced homocysteine concentrations.
Previous research provides conflicting evidence regarding nitrous oxide and perioperative myocardial ischemia and infarction. Several smaller studies in high-risk patients observed no effect of nitrous oxide on myocardial ischemia,4–6 whereas, a recent study showed an increased risk for ischemic electrocardiogram changes;1 however, in this latter study, no cardiac biomarkers or clinical outcomes were reported. The only large clinical trial investigating nitrous oxide and cardiovascular outcomes, the ENIGMA trial, reported an inconclusive, statistically nonsignificant increase in the incidence of myocardial infarction from 0.7% (n = 7 of 997) to 1.3% (n = 13 of 1,015; odds ratio, 0.54; 95% CI, 0.22–1.37; P = 0.2), in patients receiving nitrous oxide.2 Nevertheless, since the publication of these studies, many practitioners have abandoned the use of nitrous oxide for patients with cardiac risk factors. Our study suggests that there is no increased cardiac risk from acute nitrous oxide-induced hyperhomocysteinemia. The ongoing ENIGMA-II trial, a large-scale multicenter clinical trial, will provide robust and definitive evidence to the question of the association between nitrous oxide and perioperative myocardial infarction.34
In addition to a standard Food and Drug Administration-cleared troponin I assay, our study used a novel high-sensitivity troponin T assay, to detect myocardial necrosis and infarction. High-sensitivity troponin assays allow the detection of circulating cardiac troponins at extremely low levels (nanogram/liter), allowing for the calculation of a relative change Δhs-cTnT compared with baseline within each patient.35 In our study, more than 80% of patients had a measurable rise in postoperative high-sensitivity troponin T compared with baseline. Our data suggest that high-sensitivity troponin assays may be the most sensitive method for the detection of perioperative myocardial injury and infarction.
The study has several limitations. First, the observed event rate of cardiac troponin I increases was substantially lower than expected. In hindsight, expecting an event rate of 47% among patients homozygous for either of the MTHFR variant who received nitrous oxide, was probably overly optimistic and resulted in a lower than expected study power. Given the remarkably negative results, both in the incidence rates between the groups, and the extent of myocardial injury as indicated by the nearly identical change in high-sensitivity troponin T, we doubt that a larger sample size would have resulted in a different study outcome.
Second, because our study was conducted in a country with dietary folate fortification, it is possible that its findings may not be generalizable to regions that do not have dietary folate fortification. Third, in the United States, many adults use over-the counter multivitamins, and we cannot rule out the possibility that some of the patients self-medicated multivitamins within the first days after surgery, which could have affected plasma homocysteine concentration and theoretically, study outcomes.
In summary, the findings of this trial suggest that neither nitrous oxide-induced acute hyperhomocysteinemia, nor MTHFR genotype is associated with perioperative cardiac troponin increase after nitrous oxide anesthesia. The prophylactic use of B-vitamins is efficacious in blunting nitrous oxide-induced homocysteine increase but has no effect on perioperative cardiac events. We therefore, believe that based on current evidence, practitioners who feel that nitrous oxide could be beneficial for their patients should not refrain from administering it because of concern for acute homocysteine increase or MTHFR gene variant.
The authors thank all faculty members, residents, and CRNAs at Barnes-Jewish Hospital (St. Louis, Missouri) who supported the Vitamins in Nitrous Oxide (VINO) trial, most importantly to Alex S. Evers, M.D., Henry Mallinckrodt Professor of Anesthesiology and Chairman, Department of Anesthesiology, Washington University, St. Louis, Missouri, without whose support the VINO trial would have been impossible to conduct. The authors give special thanks to Kathryn Vehe, Pharm.D., from the Investigational Pharmacy, Barnes-Jewish Hospital, for her strong support. The authors also thank Ningying Wu, Ph.D. (Division of Biostatistics, Washington University School of Medicine, St. Louis, Missouri), for her help during the statistical analysis and Barbara Zehnbauer, Ph.D., Professor of Pathology and Immunology and Medical Director, Molecular Diagnostics Laboratory, Washington University School of Medicine, (now as Branch Chief and Senior Service Fellow, Centers for Disease Control and Prevention, Atlanta, Georgia) for her help in planning the genetic analysis. Most important, the authors thank Evan D. Kharasch, M.D., Ph.D., Russell D. and Mary B. Shelden Professor of Anesthesiology, Director of the Division of Clinical and Translational Research in the Department of Anesthesiology, and Vice Chancellor for Research at Washington University in St. Louis, for his outstanding mentorship and his invaluable advice and support in planning, execution, and publication of the VINO trial.
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References

1. 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

2. Myles PS, Leslie K, Chan MT, Forbes A, Paech MJ, Peyton P, Silbert BS, Pascoe EENIGMA Trial Group. . Avoidance of nitrous oxide for patients undergoing major surgery: A randomized controlled trial. ANESTHESIOLOGY. 2007;107:221–31

3. Leslie K, Myles PS, Chan MT, Forbes A, Paech MJ, Peyton P, Silbert BS, Williamson E. Nitrous oxide and long-term morbidity and mortality in the ENIGMA trial. Anesth Analg. 2011;112:387–93

4. Cahalan MK, Prakash O, Rulf EN, Cahalan MT, Mayala AP, Lurz FC, Rosseel P, Lachitjaran E, Siphanto K, Gussenhoven EJ. Addition of nitrous oxide to fentanyl anesthesia does not induce myocardial ischemia in patients with ischemic heart disease. ANESTHESIOLOGY. 1987;67:925–9

5. Kozmary SV, Lampe GH, Benefiel D, Cahalan MK, Wauk LZ, Whitendale P, Schiller NB, Eger EI II. No finding of increased myocardial ischemia during or after carotid endarterectomy under anesthesia with nitrous oxide. Anesth Analg. 1990;71:591–6

6. Mitchell MM, Prakash O, Rulf EN, van Daele ME, Cahalan MK, Roelandt JR. Nitrous oxide does not induce myocardial ischemia in patients with ischemic heart disease and poor ventricular function. ANESTHESIOLOGY. 1989;71:526–34

7. Sanders RD, Graham C, Lewis SC, Bodenham A, Gough MJ, Warlow CGALA Trial Investigators. . Nitrous oxide exposure does not seem to be associated with increased mortality, stroke, and myocardial infarction: A non-randomized subgroup analysis of the General Anaesthesia compared with Local Anaesthesia for carotid surgery (GALA) trial. Br J Anaesth. 2012;109:361–7

8. Turan A, Mascha EJ, You J, Kurz A, Shiba A, Saager L, Sessler DI. The association between nitrous oxide and postoperative mortality and morbidity after noncardiac surgery. Anesth Analg. 2012;116:1026–33

9. 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

10. 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

11. Amess JA, Burman JF, Rees GM, Nancekievill DG, Mollin DL. Megaloblastic haemopoiesis in patients receiving nitrous oxide. Lancet. 1978;2:339–42

12. Jevtović-Todorović V, Todorović SM, Mennerick S, Powell S, Dikranian K, Benshoff N, Zorumski CF, Olney JW. Nitrous oxide (laughing gas) is an NMDA antagonist, neuroprotectant and neurotoxin. Nat Med. 1998;4:460–3

13. Nagele P, Metz LB, Crowder CM. Nitrous oxide (N(2)O) requires the N-methyl-D-aspartate receptor for its action in Caenorhabditis elegans. Proc Natl Acad Sci U S A. 2004;101:8791–6

14. Myles PS, Leslie K, Silbert B, Paech MJ, Peyton P. A review of the risks and benefits of nitrous oxide in current anaesthetic practice. Anaesth Intensive Care. 2004;32:165–72

15. Kang SS, Passen EL, Ruggie N, Wong PW, Sora H. Thermolabile defect of methylenetetrahydrofolate reductase in coronary artery disease. Circulation. 1993;88(4 Pt 1):1463–9

16. Frosst P, Blom HJ, Milos R, Goyette P, Sheppard CA, Matthews RG, Boers GJ, den Heijer M, Kluijtmans LA, van den Heuvel LP. A candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahydrofolate reductase. Nat Genet. 1995;10:111–3

17. 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

18. Bathum L, Petersen I, Christiansen L, Konieczna A, Sørensen TI, Kyvik KO. Genetic and environmental influences on plasma homocysteine: Results from a Danish twin study. Clin Chem. 2007;53:971–9

19. Nagele P, Meissner K, Francis A, Födinger M, Saccone NL. Genetic and environmental determinants of plasma total homocysteine levels: Impact of population-wide folate fortification. Pharmacogenet Genomics. 2011;21:426–31

20. Nagele P, Zeugswetter B, Wiener C, Burger H, Hüpfl M, Mittlböck M, Födinger M. Influence of methylenetetrahydrofolate reductase gene polymorphisms on homocysteine concentrations after nitrous oxide anesthesia. ANESTHESIOLOGY. 2008;109:36–43

21. Albert CM, Cook NR, Gaziano JM, Zaharris E, MacFadyen J, Danielson E, Buring JE, Manson JE. Effect of folic acid and B vitamins on risk of cardiovascular events and total mortality among women at high risk for cardiovascular disease: A randomized trial. JAMA. 2008;299:2027–36

22. Armitage JM, Bowman L, Clarke RJ, Wallendszus K, Bulbulia R, Rahimi K, Haynes R, Parish S, Sleight P, Peto R, Collins R. Effects of homocysteine-lowering with folic acid plus vitamin B12 vs placebo on mortality and major morbidity in myocardial infarction survivors: A randomized trial. JAMA. 2010;303:2486–94

23. Lonn E, Yusuf S, Arnold MJ, Sheridan P, Pogue J, Micks M, McQueen MJ, Probstfield J, Fodor G, Held C, Genest J JrHeart Outcomes Prevention Evaluation (HOPE) 2 Investigators. . Homocysteine lowering with folic acid and B vitamins in vascular disease. N Engl J Med. 2006;354:1567–77

24. Meinert CL Clinical Trials: Design, Conduct, and Analysis. 1986 New York Oxford University Press

25. Apple FS, Collinson POIFCC Task Force on Clinical Applications of Cardiac Biomarkers. . Analytical characteristics of high-sensitivity cardiac troponin assays. Clin Chem. 2012;58:54–61

26. Thygesen K, Alpert JS, White HD, Jaffe AS, Apple FS, Galvani M, Katus HA, Newby LK, Ravkilde J, Chaitman B, Clemmensen PM, Dellborg M, Hod H, Porela P, Underwood R, Bax JJ, Beller GA, Bonow R, Van der Wall EE, Bassand JP, Wijns W, Ferguson TB, Steg PG, Uretsky BF, Williams DO, Armstrong PW, Antman EM, Fox KA, Hamm CW, Ohman EM, Simoons ML, Poole-Wilson PA, Gurfinkel EP, Lopez-Sendon JL, Pais P, Mendis S, Zhu JR, Wallentin LC, Fernández-Avilés F, Fox KM, Parkhomenko AN, Priori SG, Tendera M, Voipio-Pulkki LM, Vahanian A, Camm AJ, De Caterina R, Dean V, Dickstein K, Filippatos G, Funck-Brentano C, Hellemans I, Kristensen SD, McGregor K, Sechtem U, Silber S, Tendera M, Widimsky P, Zamorano JL, Morais J, Brener S, Harrington R, Morrow D, Lim M, Martinez-Rios MA, Steinhubl S, Levine GN, Gibler WB, Goff D, Tubaro M, Dudek D, Al-Attar NJoint ESC/ACCF/AHA/WHF Task Force for the Redefinition of Myocardial Infarction. . Universal definition of myocardial infarction. Circulation. 2007;116:2634–53

27. Harris PA, Taylor R, Thielke R, Payne J, Gonzalez N, Conde JG. Research electronic data capture (REDCap)—A metadata-driven methodology and workflow process for providing translational research informatics support. J Biomed Inform. 2009;42:377–81

28. Bønaa KH, Njølstad I, Ueland PM, Schirmer H, Tverdal A, Steigen T, Wang H, Nordrehaug JE, Arnesen E, Rasmussen KNORVIT Trial Investigators. . Homocysteine lowering and cardiovascular events after acute myocardial infarction. N Engl J Med. 2006;354:1578–88

29. Clarke R, Halsey J, Lewington S, Lonn E, Armitage J, Manson JE, Bønaa KH, Spence JD, Nygård O, Jamison R, Gaziano JM, Guarino P, Bennett D, Mir F, Peto R, Collins RB-Vitamin Treatment Trialists’ Collaboration. . Effects of lowering homocysteine levels with B vitamins on cardiovascular disease, cancer, and cause-specific mortality: Meta-analysis of 8 randomized trials involving 37,485 individuals. Arch Intern Med. 2010;170:1622–31

30. Chambers JC, Obeid OA, Refsum H, Ueland P, Hackett D, Hooper J, Turner RM, Thompson SG, Kooner JS. Plasma homocysteine concentrations and risk of coronary heart disease in UK Indian Asian and European men. Lancet. 2000;355:523–7

31. Nygård O, Nordrehaug JE, Refsum H, Ueland PM, Farstad M, Vollset SE. Plasma homocysteine levels and mortality in patients with coronary artery disease. N Engl J Med. 1997;337:230–6

32. Jacques PF, Selhub J, Bostom AG, Wilson PW, Rosenberg IH. The effect of folic acid fortification on plasma folate and total homocysteine concentrations. N Engl J Med. 1999;340:1449–54

33. Holmes MV, Newcombe P, Hubacek JA, Sofat R, Ricketts SL, Cooper J, Breteler MM, Bautista LE, Sharma P, Whittaker JC, Smeeth L, Fowkes FG, Algra A, Shmeleva V, Szolnoki Z, Roest M, Linnebank M, Zacho J, Nalls MA, Singleton AB, Ferrucci L, Hardy J, Worrall BB, Rich SS, Matarin M, Norman PE, Flicker L, Almeida OP, van Bockxmeer FM, Shimokata H, Khaw KT, Wareham NJ, Bobak M, Sterne JA, Smith GD, Talmud PJ, van Duijn C, Humphries SE, Price JF, Ebrahim S, Lawlor DA, Hankey GJ, Meschia JF, Sandhu MS, Hingorani AD, Casas JP. Effect modification by population dietary folate on the association between MTHFR genotype, homocysteine, and stroke risk: A meta-analysis of genetic studies and randomised trials. Lancet. 2011;378:584–94

34. Myles PS, Leslie K, Peyton P, Paech M, Forbes A, Chan MT, Sessler D, Devereaux PJ, Silbert BS, Jamrozik K, Beattie S, Badner N, Tomlinson J, Wallace SANZCA Trials Group. . Nitrous oxide and perioperative cardiac morbidity (ENIGMA-II) Trial: Rationale and design. Am Heart J. 2009;157:488–494.e1

35. Kavsak PA, Walsh M, Srinathan S, Thorlacius L, Buse GL, Botto F, Pettit S, McQueen MJ, Hill SA, Thomas S, Mrkobrada M, Alonso-Coello P, Berwanger O, Biccard BM, Cembrowski G, Chan MT, Chow CK, de Miguel A, Garcia M, Graham MM, Jacka MJ, Kueh JH, Li SC, Lit LC, Martínez-Brú C, Naidoo P, Nagele P, Pearse RM, Rodseth RN, Sessler DI, Sigamani A, Szczeklik W, Tiboni M, Villar JC, Wang CY, Xavier D, Devereaux PJ. High sensitivity troponin T concentrations in patients undergoing noncardiac surgery: A prospective cohort study. Clin Biochem. 2011;44:1021–4

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Appendix
Vitamins in Nitrous Oxide (VINO) Study Team: Peter Nagele, M.D., M.Sc., Assistant Professor; Frank Brown, B.Sc., Research Coordinator; Amber Francis, B.S.N, R.N., Research Coordinator; Joshua Johnston, M.D., Resident; Lesley K. Rao, M.D., Instructor; Jane Blood, R.N., Research Nurse Supervisor; Konrad Meissner, M.D., Instructor; Anson Liu, B.Sc., Graduate Research Assistant; Olumuyiwa Idowu, Undergraduate Research Assistant; Samantha Morley, B.Sc., Undergraduate Research Assistant; Kenji Kobayashi, Undergraduate Research Assistant (All from the Division of Clinical and Translational Research, Department of Anesthesiology).
Mitchell Scott, Ph.D., Professor, Department of Pathology and Immunology; Brian F. Gage, M.D., M.Sc., Professor, Division of General Medical Sciences, Department of Internal Medicine; Lisa de las Fuentes, M.D., Assistant Professor, Cardiovascular Division, Department of Internal Medicine; J. Philip Miller, A.B., Professor, Division of Biostatistics.
All from the Washington University School of Medicine, St.Louis, Missouri.

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