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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 |
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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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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”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>info:eu-repo/semantics/openAccess</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4180-532ca5624d62db7d2f070af299f9f18202c1e3560701f8dceda2b753cb796ef33</citedby><cites>FETCH-LOGICAL-c4180-532ca5624d62db7d2f070af299f9f18202c1e3560701f8dceda2b753cb796ef33</cites><orcidid>0000-0001-9594-1855 ; 0000-0002-3096-8165</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,26567,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36682040$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dhar, Indu</creatorcontrib><creatorcontrib>Lysne, Vegard</creatorcontrib><creatorcontrib>Ulvik, Arve</creatorcontrib><creatorcontrib>Svingen, Gard F. 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.
Conclusions
Elevated MMA was associated with an increased risk of AMI and mortality in patients with suspected or verified CHD.</description><subject>Aged</subject><subject>Angiography</subject><subject>biological markers</subject><subject>Biomarkers</subject><subject>Cardiovascular disease</subject><subject>Cardiovascular diseases</subject><subject>Cohort analysis</subject><subject>Cohort Studies</subject><subject>Confidence intervals</subject><subject>Coronary artery disease</subject><subject>Coronary Disease</subject><subject>coronary heart disease</subject><subject>Energy metabolism</subject><subject>Estimates</subject><subject>Female</subject><subject>Heart attacks</subject><subject>Heart diseases</subject><subject>Humans</subject><subject>Methylmalonic Acid</subject><subject>Mitochondria</subject><subject>Mortality</subject><subject>Myocardial Infarction</subject><subject>Older people</subject><subject>Oxidative metabolism</subject><subject>Oxidative stress</subject><subject>Plasma</subject><subject>Prospective Studies</subject><subject>Risk</subject><subject>Risk Factors</subject><subject>Vitamin B12</subject><subject>Vitamin deficiency</subject><issn>0954-6820</issn><issn>1365-2796</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>3HK</sourceid><recordid>eNp9kctu1DAUhi0EotPChgdAltigSim-JE7Crqq4FBWVBawjj32s8ZDYg-20yo5H4AF4Op6EM0zLggVe-EjHn_9z-Ql5xtkZx_NqG_10xqXi7AFZYWwq0fbqIVmxvqkr1Ql2RI5z3jLGJVPsMTmSap-t2Yr8_DTqPGk6Qdks46THGLyh2nhLdwmsNyXT5PNXGh1m5wJ0WqLRyXo9Uh-cTqb4GKgOlk4xFT36suAD3eniIeDvW1821MQUg04L3YBOhVqfQWd4Tc-xSsw7QJEboOLX9x8mblCG5jLb5Ql55PSY4eldPCFf3r75fPG-urp-d3lxflWZmnesaqQwulGitkrYdWuFYy3TTvS96x3HQYXhIBuFWe46a8BqsW4bada4JnBSnhB60DU4avFhCDHpgbOuEXiruuaIvDwg2O-3GXIZJp8NjKMOEOc8iBY3KjkTNaIv_kG3cU4BB0CqU7IRqm6ROr2vGXNO4IZd8hOuCCsOe1uHva3DH1sRfn4nOa8nsH_Rex8R4Afg1o-w_Edq-HB9-fEg-hvRwa8H</recordid><startdate>202304</startdate><enddate>202304</enddate><creator>Dhar, Indu</creator><creator>Lysne, Vegard</creator><creator>Ulvik, Arve</creator><creator>Svingen, Gard F. T.</creator><creator>Pedersen, Eva R.</creator><creator>Bjørnestad, Espen Ø.</creator><creator>Olsen, Thomas</creator><creator>Borsholm, Robert</creator><creator>Laupsa‐Borge, Johnny</creator><creator>Ueland, Per M.</creator><creator>Tell, Grethe S.</creator><creator>Berge, Rolf K.</creator><creator>Mellgren, Gunnar</creator><creator>Bønaa, Kaare H.</creator><creator>Nygård, Ottar K</creator><general>Blackwell Publishing Ltd</general><general>Blackwell Science Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>C1K</scope><scope>K9.</scope><scope>7X8</scope><scope>3HK</scope><orcidid>https://orcid.org/0000-0001-9594-1855</orcidid><orcidid>https://orcid.org/0000-0002-3096-8165</orcidid></search><sort><creationdate>202304</creationdate><title>Plasma methylmalonic acid predicts risk of acute myocardial infarction and mortality in patients with coronary heart disease: A prospective 2‐cohort study</title><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4180-532ca5624d62db7d2f070af299f9f18202c1e3560701f8dceda2b753cb796ef33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Aged</topic><topic>Angiography</topic><topic>biological markers</topic><topic>Biomarkers</topic><topic>Cardiovascular disease</topic><topic>Cardiovascular diseases</topic><topic>Cohort analysis</topic><topic>Cohort Studies</topic><topic>Confidence intervals</topic><topic>Coronary artery disease</topic><topic>Coronary Disease</topic><topic>coronary heart disease</topic><topic>Energy metabolism</topic><topic>Estimates</topic><topic>Female</topic><topic>Heart attacks</topic><topic>Heart diseases</topic><topic>Humans</topic><topic>Methylmalonic Acid</topic><topic>Mitochondria</topic><topic>Mortality</topic><topic>Myocardial Infarction</topic><topic>Older people</topic><topic>Oxidative metabolism</topic><topic>Oxidative stress</topic><topic>Plasma</topic><topic>Prospective Studies</topic><topic>Risk</topic><topic>Risk Factors</topic><topic>Vitamin B12</topic><topic>Vitamin deficiency</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dhar, Indu</creatorcontrib><creatorcontrib>Lysne, Vegard</creatorcontrib><creatorcontrib>Ulvik, Arve</creatorcontrib><creatorcontrib>Svingen, Gard F. 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><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>NORA - Norwegian Open Research Archives</collection><jtitle>Journal of internal medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dhar, Indu</au><au>Lysne, Vegard</au><au>Ulvik, Arve</au><au>Svingen, Gard F. 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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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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