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Plasma methylmalonic acid predicts risk of acute myocardial infarction and mortality in patients with coronary heart disease: A prospective 2‐cohort study

Background Elevated plasma methylmalonic acid (MMA) is reported in patients with established coronary heart disease (CHD) and is considered a marker of vitamin B12 deficiency. Moreover, MMA‐dependent reactions have been linked to alterations in mitochondrial energy metabolism and oxidative stress, k...

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Published in:Journal of internal medicine 2023-04, Vol.293 (4), p.508-519
Main Authors: Dhar, Indu, Lysne, Vegard, Ulvik, Arve, Svingen, Gard F. T., Pedersen, Eva R., Bjørnestad, Espen Ø., Olsen, Thomas, Borsholm, Robert, Laupsa‐Borge, Johnny, Ueland, Per M., Tell, Grethe S., Berge, Rolf K., Mellgren, Gunnar, Bønaa, Kaare H., Nygård, Ottar K
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container_issue 4
container_start_page 508
container_title Journal of internal medicine
container_volume 293
creator Dhar, Indu
Lysne, Vegard
Ulvik, Arve
Svingen, Gard F. T.
Pedersen, Eva R.
Bjørnestad, Espen Ø.
Olsen, Thomas
Borsholm, Robert
Laupsa‐Borge, Johnny
Ueland, Per M.
Tell, Grethe S.
Berge, Rolf K.
Mellgren, Gunnar
Bønaa, Kaare H.
Nygård, Ottar K
description Background Elevated plasma methylmalonic acid (MMA) is reported in patients with established coronary heart disease (CHD) and is considered a marker of vitamin B12 deficiency. Moreover, MMA‐dependent reactions have been linked to alterations in mitochondrial energy metabolism and oxidative stress, key features in the pathophysiology of cardiovascular diseases (CVDs). Objectives We examined whether plasma MMA prospectively predicted the long‐term risk of acute myocardial infarction (AMI) and mortality. Methods and results Using Cox modeling, we estimated hazard ratios (HRs) for endpoints according to per 1‐SD increment of log‐transformed plasma MMA in two independent populations: the Western Norway Coronary Angiography Cohort (WECAC) (patients evaluated for CHD; n = 4137) and the Norwegian Vitamin Trial (NORVIT) (patients hospitalized with AMI; n = 3525). In WECAC and NORVIT, 12.8% and 18.0% experienced an AMI, whereas 21.8% and 19.9% died, of whom 45.5% and 60.3% from CVD‐related causes during follow‐up (range 3–11 years), respectively. In WECAC, age‐ and gender‐adjusted HRs (95% confidence interval) were 1.18 (1.09–1.28), 1.25 (1.18–1.33), and 1.28 (1.17–1.40) for future AMI, total mortality, and CVD mortality, respectively. Corresponding risk estimates were 1.19 (1.10–1.28), 1.22 (1.14–1.31), and 1.30 (1.19–1.42) in NORVIT. These estimates were only slightly attenuated after multivariable adjustments. Across both cohorts, the MMA‐risk association was stronger in older adults, women, and non‐smokers. Conclusions Elevated MMA was associated with an increased risk of AMI and mortality in patients with suspected or verified CHD.
doi_str_mv 10.1111/joim.13610
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T. ; Pedersen, Eva R. ; Bjørnestad, Espen Ø. ; Olsen, Thomas ; Borsholm, Robert ; Laupsa‐Borge, Johnny ; Ueland, Per M. ; Tell, Grethe S. ; Berge, Rolf K. ; Mellgren, Gunnar ; Bønaa, Kaare H. ; Nygård, Ottar K</creator><creatorcontrib>Dhar, Indu ; Lysne, Vegard ; Ulvik, Arve ; Svingen, Gard F. T. ; Pedersen, Eva R. ; Bjørnestad, Espen Ø. ; Olsen, Thomas ; Borsholm, Robert ; Laupsa‐Borge, Johnny ; Ueland, Per M. ; Tell, Grethe S. ; Berge, Rolf K. ; Mellgren, Gunnar ; Bønaa, Kaare H. ; Nygård, Ottar K</creatorcontrib><description>Background Elevated plasma methylmalonic acid (MMA) is reported in patients with established coronary heart disease (CHD) and is considered a marker of vitamin B12 deficiency. Moreover, MMA‐dependent reactions have been linked to alterations in mitochondrial energy metabolism and oxidative stress, key features in the pathophysiology of cardiovascular diseases (CVDs). Objectives We examined whether plasma MMA prospectively predicted the long‐term risk of acute myocardial infarction (AMI) and mortality. Methods and results Using Cox modeling, we estimated hazard ratios (HRs) for endpoints according to per 1‐SD increment of log‐transformed plasma MMA in two independent populations: the Western Norway Coronary Angiography Cohort (WECAC) (patients evaluated for CHD; n = 4137) and the Norwegian Vitamin Trial (NORVIT) (patients hospitalized with AMI; n = 3525). In WECAC and NORVIT, 12.8% and 18.0% experienced an AMI, whereas 21.8% and 19.9% died, of whom 45.5% and 60.3% from CVD‐related causes during follow‐up (range 3–11 years), respectively. In WECAC, age‐ and gender‐adjusted HRs (95% confidence interval) were 1.18 (1.09–1.28), 1.25 (1.18–1.33), and 1.28 (1.17–1.40) for future AMI, total mortality, and CVD mortality, respectively. Corresponding risk estimates were 1.19 (1.10–1.28), 1.22 (1.14–1.31), and 1.30 (1.19–1.42) in NORVIT. These estimates were only slightly attenuated after multivariable adjustments. Across both cohorts, the MMA‐risk association was stronger in older adults, women, and non‐smokers. Conclusions Elevated MMA was associated with an increased risk of AMI and mortality in patients with suspected or verified CHD.</description><identifier>ISSN: 0954-6820</identifier><identifier>EISSN: 1365-2796</identifier><identifier>DOI: 10.1111/joim.13610</identifier><identifier>PMID: 36682040</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Aged ; Angiography ; biological markers ; Biomarkers ; Cardiovascular disease ; Cardiovascular diseases ; Cohort analysis ; Cohort Studies ; Confidence intervals ; Coronary artery disease ; Coronary Disease ; coronary heart disease ; Energy metabolism ; Estimates ; Female ; Heart attacks ; Heart diseases ; Humans ; Methylmalonic Acid ; Mitochondria ; Mortality ; Myocardial Infarction ; Older people ; Oxidative metabolism ; Oxidative stress ; Plasma ; Prospective Studies ; Risk ; Risk Factors ; Vitamin B12 ; Vitamin deficiency</subject><ispartof>Journal of internal medicine, 2023-04, Vol.293 (4), p.508-519</ispartof><rights>2023 The Association for the Publication of the Journal of Internal Medicine.</rights><rights>2023. This article is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). 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T.</creatorcontrib><creatorcontrib>Pedersen, Eva R.</creatorcontrib><creatorcontrib>Bjørnestad, Espen Ø.</creatorcontrib><creatorcontrib>Olsen, Thomas</creatorcontrib><creatorcontrib>Borsholm, Robert</creatorcontrib><creatorcontrib>Laupsa‐Borge, Johnny</creatorcontrib><creatorcontrib>Ueland, Per M.</creatorcontrib><creatorcontrib>Tell, Grethe S.</creatorcontrib><creatorcontrib>Berge, Rolf K.</creatorcontrib><creatorcontrib>Mellgren, Gunnar</creatorcontrib><creatorcontrib>Bønaa, Kaare H.</creatorcontrib><creatorcontrib>Nygård, Ottar K</creatorcontrib><title>Plasma methylmalonic acid predicts risk of acute myocardial infarction and mortality in patients with coronary heart disease: A prospective 2‐cohort study</title><title>Journal of internal medicine</title><addtitle>J Intern Med</addtitle><description>Background Elevated plasma methylmalonic acid (MMA) is reported in patients with established coronary heart disease (CHD) and is considered a marker of vitamin B12 deficiency. Moreover, MMA‐dependent reactions have been linked to alterations in mitochondrial energy metabolism and oxidative stress, key features in the pathophysiology of cardiovascular diseases (CVDs). Objectives We examined whether plasma MMA prospectively predicted the long‐term risk of acute myocardial infarction (AMI) and mortality. Methods and results Using Cox modeling, we estimated hazard ratios (HRs) for endpoints according to per 1‐SD increment of log‐transformed plasma MMA in two independent populations: the Western Norway Coronary Angiography Cohort (WECAC) (patients evaluated for CHD; n = 4137) and the Norwegian Vitamin Trial (NORVIT) (patients hospitalized with AMI; n = 3525). In WECAC and NORVIT, 12.8% and 18.0% experienced an AMI, whereas 21.8% and 19.9% died, of whom 45.5% and 60.3% from CVD‐related causes during follow‐up (range 3–11 years), respectively. In WECAC, age‐ and gender‐adjusted HRs (95% confidence interval) were 1.18 (1.09–1.28), 1.25 (1.18–1.33), and 1.28 (1.17–1.40) for future AMI, total mortality, and CVD mortality, respectively. Corresponding risk estimates were 1.19 (1.10–1.28), 1.22 (1.14–1.31), and 1.30 (1.19–1.42) in NORVIT. These estimates were only slightly attenuated after multivariable adjustments. Across both cohorts, the MMA‐risk association was stronger in older adults, women, and non‐smokers. 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T.</au><au>Pedersen, Eva R.</au><au>Bjørnestad, Espen Ø.</au><au>Olsen, Thomas</au><au>Borsholm, Robert</au><au>Laupsa‐Borge, Johnny</au><au>Ueland, Per M.</au><au>Tell, Grethe S.</au><au>Berge, Rolf K.</au><au>Mellgren, Gunnar</au><au>Bønaa, Kaare H.</au><au>Nygård, Ottar K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Plasma methylmalonic acid predicts risk of acute myocardial infarction and mortality in patients with coronary heart disease: A prospective 2‐cohort study</atitle><jtitle>Journal of internal medicine</jtitle><addtitle>J Intern Med</addtitle><date>2023-04</date><risdate>2023</risdate><volume>293</volume><issue>4</issue><spage>508</spage><epage>519</epage><pages>508-519</pages><issn>0954-6820</issn><eissn>1365-2796</eissn><abstract>Background Elevated plasma methylmalonic acid (MMA) is reported in patients with established coronary heart disease (CHD) and is considered a marker of vitamin B12 deficiency. Moreover, MMA‐dependent reactions have been linked to alterations in mitochondrial energy metabolism and oxidative stress, key features in the pathophysiology of cardiovascular diseases (CVDs). Objectives We examined whether plasma MMA prospectively predicted the long‐term risk of acute myocardial infarction (AMI) and mortality. Methods and results Using Cox modeling, we estimated hazard ratios (HRs) for endpoints according to per 1‐SD increment of log‐transformed plasma MMA in two independent populations: the Western Norway Coronary Angiography Cohort (WECAC) (patients evaluated for CHD; n = 4137) and the Norwegian Vitamin Trial (NORVIT) (patients hospitalized with AMI; n = 3525). In WECAC and NORVIT, 12.8% and 18.0% experienced an AMI, whereas 21.8% and 19.9% died, of whom 45.5% and 60.3% from CVD‐related causes during follow‐up (range 3–11 years), respectively. In WECAC, age‐ and gender‐adjusted HRs (95% confidence interval) were 1.18 (1.09–1.28), 1.25 (1.18–1.33), and 1.28 (1.17–1.40) for future AMI, total mortality, and CVD mortality, respectively. Corresponding risk estimates were 1.19 (1.10–1.28), 1.22 (1.14–1.31), and 1.30 (1.19–1.42) in NORVIT. These estimates were only slightly attenuated after multivariable adjustments. Across both cohorts, the MMA‐risk association was stronger in older adults, women, and non‐smokers. Conclusions Elevated MMA was associated with an increased risk of AMI and mortality in patients with suspected or verified CHD.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>36682040</pmid><doi>10.1111/joim.13610</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0001-9594-1855</orcidid><orcidid>https://orcid.org/0000-0002-3096-8165</orcidid><oa>free_for_read</oa></addata></record>
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source NORA - Norwegian Open Research Archives; Wiley-Blackwell Read & Publish Collection
subjects Aged
Angiography
biological markers
Biomarkers
Cardiovascular disease
Cardiovascular diseases
Cohort analysis
Cohort Studies
Confidence intervals
Coronary artery disease
Coronary Disease
coronary heart disease
Energy metabolism
Estimates
Female
Heart attacks
Heart diseases
Humans
Methylmalonic Acid
Mitochondria
Mortality
Myocardial Infarction
Older people
Oxidative metabolism
Oxidative stress
Plasma
Prospective Studies
Risk
Risk Factors
Vitamin B12
Vitamin deficiency
title Plasma methylmalonic acid predicts risk of acute myocardial infarction and mortality in patients with coronary heart disease: A prospective 2‐cohort study
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