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      Betaine and Secondary Events in an Acute Coronary Syndrome Cohort

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          Abstract

          Background

          Betaine insufficiency is associated with unfavourable vascular risk profiles in metabolic syndrome patients. We investigated associations between betaine insufficiency and secondary events in acute coronary syndrome patients.

          Methods

          Plasma (531) and urine (415) samples were collected four months after discharge following an acute coronary event. Death (34), secondary acute myocardial infarction (MI) (70) and hospital admission for heart failure (45) events were recorded over a median follow-up of 832 days.

          Principal Findings

          The highest and lowest quintiles of urinary betaine excretion associated with risk of heart failure ( p = 0.0046, p = 0.013 compared with middle 60%) but not with subsequent acute MI. The lowest quintile of plasma betaine was associated with subsequent acute MI ( p = 0.014), and the top quintile plasma betaine with heart failure ( p = 0.043), especially in patients with diabetes ( p<0.001). Top quintile plasma concentrations of dimethylglycine (betaine metabolite) and top quintile plasma homocysteine both associated with all three outcomes, acute MI ( p = 0.004, <0.001), heart failure ( p = 0.027, p<0.001) and survival ( p<0.001, p<0.001). High homocysteine was associated with high or low betaine excretion in >60% of these subjects ( p = 0.017). Median NT-proBNP concentrations were lowest in the middle quintile of plasma betaine concentration ( p = 0.002).

          Conclusions

          Betaine insufficiency indicates increased risk of secondary heart failure and acute MI. Its association with elevated homocysteine may partly explain the disappointing results of folate supplementation. In some patients, especially with diabetes, elevated plasma betaine also indicates increased risk.

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          Most cited references58

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          Homocysteine lowering with folic acid and B vitamins in vascular disease.

          In observational studies, lower homocysteine levels are associated with lower rates of coronary heart disease and stroke. Folic acid and vitamins B6 and B12 lower homocysteine levels. We assessed whether supplementation reduced the risk of major cardiovascular events in patients with vascular disease. We randomly assigned 5522 patients 55 years of age or older who had vascular disease or diabetes to daily treatment either with the combination of 2.5 mg of folic acid, 50 mg of vitamin B6, and 1 mg of vitamin B12 or with placebo for an average of five years. The primary outcome was a composite of death from cardiovascular causes, myocardial infarction, and stroke. Mean plasma homocysteine levels decreased by 2.4 micromol per liter (0.3 mg per liter) in the active-treatment group and increased by 0.8 micromol per liter (0.1 mg per liter) in the placebo group. Primary outcome events occurred in 519 patients (18.8 percent) assigned to active therapy and 547 (19.8 percent) assigned to placebo (relative risk, 0.95; 95 percent confidence interval, 0.84 to 1.07; P=0.41). As compared with placebo, active treatment did not significantly decrease the risk of death from cardiovascular causes (relative risk, 0.96; 95 percent confidence interval, 0.81 to 1.13), myocardial infarction (relative risk, 0.98; 95 percent confidence interval, 0.85 to 1.14), or any of the secondary outcomes. Fewer patients assigned to active treatment than to placebo had a stroke (relative risk, 0.75; 95 percent confidence interval, 0.59 to 0.97). More patients in the active-treatment group were hospitalized for unstable angina (relative risk, 1.24; 95 percent confidence interval, 1.04 to 1.49). Supplements combining folic acid and vitamins B6 and B12 did not reduce the risk of major cardiovascular events in patients with vascular disease. (ClinicalTrials.gov number, NCT00106886; Current Controlled Trials number, ISRCTN14017017.). Copyright 2006 Massachusetts Medical Society.
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            Choline and betaine in health and disease.

            Choline is an essential nutrient, but is also formed by de novo synthesis. Choline and its derivatives serve as components of structural lipoproteins, blood and membrane lipids, and as a precursor of the neurotransmitter acetylcholine. Pre-and postnatal choline availability is important for neurodevelopment in rodents. Choline is oxidized to betaine that serves as an osmoregulator and is a substrate in the betaine-homocysteine methyltransferase reaction, which links choline and betaine to the folate-dependent one-carbon metabolism. Choline and betaine are important sources of one-carbon units, in particular, during folate deficiency. Choline or betaine supplementation in humans reduces concentration of total homocysteine (tHcy), and plasma betaine is a strong predictor of plasma tHcy in individuals with low plasma concentration of folate and other B vitamins (B₂, B₆, and B₁₂) in combination TT genotype of the methylenetetrahydrofolate reductase 677 C->T polymorphism. The link to one-carbon metabolism and the recent availability of food composition data have motivated studies on choline and betaine as risk factors of chronic diseases previously studied in relation to folate and homocysteine status. High intake and plasma level of choline in the mother seems to afford reduced risk of neural tube defects. Intake of choline and betaine shows no consistent relation to cancer or cardiovascular risk or risk factors, whereas an unfavorable cardiovascular risk factor profile was associated with high choline and low betaine concentrations in plasma. Thus, choline and betaine showed opposite relations with key components of metabolic syndrome, suggesting a disruption of mitochondrial choline oxidation to betaine as part of the mitochondrial dysfunction in metabolic syndrome.
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              Guidelines for the diagnosis and treatment of chronic heart failure.

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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2012
                23 May 2012
                : 7
                : 5
                : e37883
                Affiliations
                [1 ]Clinical Biochemistry Unit, Canterbury Health Laboratories, Christchurch, New Zealand
                [2 ]Department of Pathology, University of Otago (Christchurch), Christchurch, New Zealand
                [3 ]The Christchurch Cardioendocrine Research Group, Department of Medicine, University of Otago (Christchurch), Christchurch, New Zealand
                Virginia Commonwealth University, United States of America
                Author notes

                Conceived and designed the experiments: STC SS PMG ML AMR RWT. Performed the experiments: WA JLE SLM ML SS. Analyzed the data: ML CMF SS. Contributed reagents/materials/analysis tools: WA ML. Wrote the paper: ML CMF SS PMG STC AMR.

                Article
                PONE-D-11-25842
                10.1371/journal.pone.0037883
                3359285
                22649561
                f3b986ae-9f86-4695-9049-949a8c30a11b
                Lever et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
                History
                : 22 December 2011
                : 26 April 2012
                Page count
                Pages: 9
                Categories
                Research Article
                Biology
                Biochemistry
                Metabolism
                Metabolic Pathways
                Medicine
                Cardiovascular
                Atherosclerosis
                Coronary Artery Disease
                Heart Failure
                Myocardial Infarction
                Endocrinology
                Diabetic Endocrinology
                Diabetes Mellitus Type 2
                Nutrition
                Micronutrient Deficiencies
                Obesity

                Uncategorized
                Uncategorized

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