The Effect of Magnesium Supplementation on Vascular Calcification in CKD: A Randomized Clinical Trial (MAGiCAL-CKD)

Significance StatementMagnesium prevents vascular calcification in animals with CKD. In addition, lower serum magnesium is associated with higher risk of cardiovascular events in CKD. In a randomized, double-blinded, placebo-controlled trial, the authors investigated the effects of magnesium supplem...

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Published inJournal of the American Society of Nephrology Vol. 34; no. 5; pp. 886 - 894
Main Authors Bressendorff, Iain, Hansen, Ditte, Schou, Morten, Kragelund, Charlotte, Svensson, My, Hashemi, Bahram, Kristensen, Tilde, Vrist, Marie Houmaa, Borg, Rikke, Tougaard, Birgitte, Borg, Kristine, Hjortkjær, Henrik Øder, Kristiansen, Cathrine Helgestad, Carlson, Nicholas, Nasiri, Mohammad, Ashraf, Haseem, Pasch, Andreas, Brandi, Lisbet
Format Journal Article
LanguageEnglish
Published United States American Society of Nephrology 01.05.2023
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Online AccessGet full text
ISSN1046-6673
1533-3450
1533-3450
DOI10.1681/ASN.0000000000000092

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Abstract Significance StatementMagnesium prevents vascular calcification in animals with CKD. In addition, lower serum magnesium is associated with higher risk of cardiovascular events in CKD. In a randomized, double-blinded, placebo-controlled trial, the authors investigated the effects of magnesium supplementation versus placebo on vascular calcification in patients with predialysis CKD. Despite significant increases in plasma magnesium among study participants who received magnesium compared with those who received placebo, magnesium supplementation did not slow the progression of vascular calcification in study participants. In addition, the findings showed a higher incidence of serious adverse events in the group treated with magnesium. Magnesium supplementation alone was not sufficient to delay progression of vascular calcification, and other therapeutic strategies might be necessary to reduce the risk of cardiovascular disease in CKD.BackgroundElevated levels of serum magnesium are associated with lower risk of cardiovascular events in patients with CKD. Magnesium also prevents vascular calcification in animal models of CKD.MethodsTo investigate whether oral magnesium supplementation would slow the progression of vascular calcification in CKD, we conducted a randomized, double-blinded, placebo-controlled, parallel-group, clinical trial. We enrolled 148 subjects with an eGFR between 15 and 45 ml/min and randomly assigned them to receive oral magnesium hydroxide 15 mmol twice daily or matching placebo for 12 months. The primary end point was the between-groups difference in coronary artery calcification (CAC) score after 12 months adjusted for baseline CAC score, age, and diabetes mellitus.ResultsA total of 75 subjects received magnesium and 73 received placebo. Median eGFR was 25 ml/min at baseline, and median baseline CAC scores were 413 and 274 in the magnesium and placebo groups, respectively. Despite plasma magnesium increasing significantly during the trial in the magnesium group, the baseline-adjusted CAC scores did not differ significantly between the two groups after 12 months. Prespecified subgroup analyses according to CAC>0 at baseline, diabetes mellitus, or tertiles of serum calcification propensity did not significantly alter the main results. Among subjects who experienced gastrointestinal adverse effects, 35 were in the group receiving magnesium treatment versus nine in the placebo group. Five deaths and six cardiovascular events occurred in the magnesium group compared with two deaths and no cardiovascular events in the placebo group.ConclusionsMagnesium supplementation for 12 months did not slow the progression of vascular calcification in CKD, despite a significant increase in plasma magnesium.Clinical Trials Registrationwww.clinicaltrials.gov (NCT02542319).
AbstractList Significance StatementMagnesium prevents vascular calcification in animals with CKD. In addition, lower serum magnesium is associated with higher risk of cardiovascular events in CKD. In a randomized, double-blinded, placebo-controlled trial, the authors investigated the effects of magnesium supplementation versus placebo on vascular calcification in patients with predialysis CKD. Despite significant increases in plasma magnesium among study participants who received magnesium compared with those who received placebo, magnesium supplementation did not slow the progression of vascular calcification in study participants. In addition, the findings showed a higher incidence of serious adverse events in the group treated with magnesium. Magnesium supplementation alone was not sufficient to delay progression of vascular calcification, and other therapeutic strategies might be necessary to reduce the risk of cardiovascular disease in CKD.BackgroundElevated levels of serum magnesium are associated with lower risk of cardiovascular events in patients with CKD. Magnesium also prevents vascular calcification in animal models of CKD.MethodsTo investigate whether oral magnesium supplementation would slow the progression of vascular calcification in CKD, we conducted a randomized, double-blinded, placebo-controlled, parallel-group, clinical trial. We enrolled 148 subjects with an eGFR between 15 and 45 ml/min and randomly assigned them to receive oral magnesium hydroxide 15 mmol twice daily or matching placebo for 12 months. The primary end point was the between-groups difference in coronary artery calcification (CAC) score after 12 months adjusted for baseline CAC score, age, and diabetes mellitus.ResultsA total of 75 subjects received magnesium and 73 received placebo. Median eGFR was 25 ml/min at baseline, and median baseline CAC scores were 413 and 274 in the magnesium and placebo groups, respectively. Despite plasma magnesium increasing significantly during the trial in the magnesium group, the baseline-adjusted CAC scores did not differ significantly between the two groups after 12 months. Prespecified subgroup analyses according to CAC>0 at baseline, diabetes mellitus, or tertiles of serum calcification propensity did not significantly alter the main results. Among subjects who experienced gastrointestinal adverse effects, 35 were in the group receiving magnesium treatment versus nine in the placebo group. Five deaths and six cardiovascular events occurred in the magnesium group compared with two deaths and no cardiovascular events in the placebo group.ConclusionsMagnesium supplementation for 12 months did not slow the progression of vascular calcification in CKD, despite a significant increase in plasma magnesium.Clinical Trials Registrationwww.clinicaltrials.gov (NCT02542319).
Magnesium prevents vascular calcification in animals with CKD. In addition, lower serum magnesium is associated with higher risk of cardiovascular events in CKD. In a randomized, double-blinded, placebo-controlled trial, the authors investigated the effects of magnesium supplementation versus placebo on vascular calcification in patients with predialysis CKD. Despite significant increases in plasma magnesium among study participants who received magnesium compared with those who received placebo, magnesium supplementation did not slow the progression of vascular calcification in study participants. In addition, the findings showed a higher incidence of serious adverse events in the group treated with magnesium. Magnesium supplementation alone was not sufficient to delay progression of vascular calcification, and other therapeutic strategies might be necessary to reduce the risk of cardiovascular disease in CKD. Elevated levels of serum magnesium are associated with lower risk of cardiovascular events in patients with CKD. Magnesium also prevents vascular calcification in animal models of CKD. To investigate whether oral magnesium supplementation would slow the progression of vascular calcification in CKD, we conducted a randomized, double-blinded, placebo-controlled, parallel-group, clinical trial. We enrolled 148 subjects with an eGFR between 15 and 45 ml/min and randomly assigned them to receive oral magnesium hydroxide 15 mmol twice daily or matching placebo for 12 months. The primary end point was the between-groups difference in coronary artery calcification (CAC) score after 12 months adjusted for baseline CAC score, age, and diabetes mellitus. A total of 75 subjects received magnesium and 73 received placebo. Median eGFR was 25 ml/min at baseline, and median baseline CAC scores were 413 and 274 in the magnesium and placebo groups, respectively. Despite plasma magnesium increasing significantly during the trial in the magnesium group, the baseline-adjusted CAC scores did not differ significantly between the two groups after 12 months. Prespecified subgroup analyses according to CAC>0 at baseline, diabetes mellitus, or tertiles of serum calcification propensity did not significantly alter the main results. Among subjects who experienced gastrointestinal adverse effects, 35 were in the group receiving magnesium treatment versus nine in the placebo group. Five deaths and six cardiovascular events occurred in the magnesium group compared with two deaths and no cardiovascular events in the placebo group. Magnesium supplementation for 12 months did not slow the progression of vascular calcification in CKD, despite a significant increase in plasma magnesium. www.clinicaltrials.gov ( NCT02542319 ).
Magnesium prevents vascular calcification in animals with CKD. In addition, lower serum magnesium is associated with higher risk of cardiovascular events in CKD. In a randomized, double-blinded, placebo-controlled trial, the authors investigated the effects of magnesium supplementation versus placebo on vascular calcification in patients with predialysis CKD. Despite significant increases in plasma magnesium among study participants who received magnesium compared with those who received placebo, magnesium supplementation did not slow the progression of vascular calcification in study participants. In addition, the findings showed a higher incidence of serious adverse events in the group treated with magnesium. Magnesium supplementation alone was not sufficient to delay progression of vascular calcification, and other therapeutic strategies might be necessary to reduce the risk of cardiovascular disease in CKD.SIGNIFICANCE STATEMENTMagnesium prevents vascular calcification in animals with CKD. In addition, lower serum magnesium is associated with higher risk of cardiovascular events in CKD. In a randomized, double-blinded, placebo-controlled trial, the authors investigated the effects of magnesium supplementation versus placebo on vascular calcification in patients with predialysis CKD. Despite significant increases in plasma magnesium among study participants who received magnesium compared with those who received placebo, magnesium supplementation did not slow the progression of vascular calcification in study participants. In addition, the findings showed a higher incidence of serious adverse events in the group treated with magnesium. Magnesium supplementation alone was not sufficient to delay progression of vascular calcification, and other therapeutic strategies might be necessary to reduce the risk of cardiovascular disease in CKD.Elevated levels of serum magnesium are associated with lower risk of cardiovascular events in patients with CKD. Magnesium also prevents vascular calcification in animal models of CKD.BACKGROUNDElevated levels of serum magnesium are associated with lower risk of cardiovascular events in patients with CKD. Magnesium also prevents vascular calcification in animal models of CKD.To investigate whether oral magnesium supplementation would slow the progression of vascular calcification in CKD, we conducted a randomized, double-blinded, placebo-controlled, parallel-group, clinical trial. We enrolled 148 subjects with an eGFR between 15 and 45 ml/min and randomly assigned them to receive oral magnesium hydroxide 15 mmol twice daily or matching placebo for 12 months. The primary end point was the between-groups difference in coronary artery calcification (CAC) score after 12 months adjusted for baseline CAC score, age, and diabetes mellitus.METHODSTo investigate whether oral magnesium supplementation would slow the progression of vascular calcification in CKD, we conducted a randomized, double-blinded, placebo-controlled, parallel-group, clinical trial. We enrolled 148 subjects with an eGFR between 15 and 45 ml/min and randomly assigned them to receive oral magnesium hydroxide 15 mmol twice daily or matching placebo for 12 months. The primary end point was the between-groups difference in coronary artery calcification (CAC) score after 12 months adjusted for baseline CAC score, age, and diabetes mellitus.A total of 75 subjects received magnesium and 73 received placebo. Median eGFR was 25 ml/min at baseline, and median baseline CAC scores were 413 and 274 in the magnesium and placebo groups, respectively. Despite plasma magnesium increasing significantly during the trial in the magnesium group, the baseline-adjusted CAC scores did not differ significantly between the two groups after 12 months. Prespecified subgroup analyses according to CAC>0 at baseline, diabetes mellitus, or tertiles of serum calcification propensity did not significantly alter the main results. Among subjects who experienced gastrointestinal adverse effects, 35 were in the group receiving magnesium treatment versus nine in the placebo group. Five deaths and six cardiovascular events occurred in the magnesium group compared with two deaths and no cardiovascular events in the placebo group.RESULTSA total of 75 subjects received magnesium and 73 received placebo. Median eGFR was 25 ml/min at baseline, and median baseline CAC scores were 413 and 274 in the magnesium and placebo groups, respectively. Despite plasma magnesium increasing significantly during the trial in the magnesium group, the baseline-adjusted CAC scores did not differ significantly between the two groups after 12 months. Prespecified subgroup analyses according to CAC>0 at baseline, diabetes mellitus, or tertiles of serum calcification propensity did not significantly alter the main results. Among subjects who experienced gastrointestinal adverse effects, 35 were in the group receiving magnesium treatment versus nine in the placebo group. Five deaths and six cardiovascular events occurred in the magnesium group compared with two deaths and no cardiovascular events in the placebo group.Magnesium supplementation for 12 months did not slow the progression of vascular calcification in CKD, despite a significant increase in plasma magnesium.CONCLUSIONSMagnesium supplementation for 12 months did not slow the progression of vascular calcification in CKD, despite a significant increase in plasma magnesium.www.clinicaltrials.gov ( NCT02542319 ).CLINICAL TRIALS REGISTRATIONwww.clinicaltrials.gov ( NCT02542319 ).
Author Carlson, Nicholas
Ashraf, Haseem
Kristensen, Tilde
Bressendorff, Iain
Hashemi, Bahram
Nasiri, Mohammad
Hjortkjær, Henrik Øder
Tougaard, Birgitte
Hansen, Ditte
Svensson, My
Kristiansen, Cathrine Helgestad
Borg, Kristine
Pasch, Andreas
Brandi, Lisbet
Schou, Morten
Borg, Rikke
Vrist, Marie Houmaa
Kragelund, Charlotte
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  surname: Hansen
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  givenname: Morten
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  organization: Department of Cardiology, Herlev and Gentofte Hospital, Herlev, Denmark
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  givenname: Charlotte
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  organization: Department of Nephrology, Gødstrup Hospital, Herning, Denmark
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  organization: Department of Medicine, Division of Nephrology, Zealand University Hospital, Roskilde, Denmark
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  organization: Department of Nephrology, Aarhus University Hospital, Aarhus, Denmark
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  givenname: Kristine
  surname: Borg
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  organization: Hans Christian Andersen Children's Hospital, Odense University Hospital, Odense, Denmark
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  givenname: Henrik Øder
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  surname: Hjortkjær
  fullname: Hjortkjær, Henrik Øder
  organization: Department of Cardiology, Rigshospitalet, Copenhagen, Denmark
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  givenname: Cathrine Helgestad
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  organization: Department of Imaging, Akershus University Hospital, Lørenskog, Norway
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  fullname: Brandi, Lisbet
  organization: Department of Endocrinology and Nephrology, Nordsjællands Hospital, Hillerød, Denmark
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Cites_doi 10.1161/01.ATV.0000127024.40516.ef
10.1159/000100044
10.1016/j.atherosclerosis.2016.05.044
10.1681/ASN.2018111150
10.1681/ASN.2012030240
10.1016/j.kint.2017.04.011
10.1016/0735-1097(90)90282-T
10.1093/ndtplus/sfr163
10.1038/ki.2013.327
10.1053/j.ajkd.2011.04.024
10.1007/s10157-022-02182-4
10.1001/jamacardio.2017.0363
10.2215/CJN.13921217
10.1093/ndt/gfaa222
10.1056/NEJMoa041031
10.1093/ndt/gfz190
10.1093/ndtplus/sfr165
10.1136/bmjopen-2017-016795
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Issue 5
Keywords clinical trial
cardiovascular disease
coronary calcification
vascular calcification
magnesium
randomized controlled trials
CKD
Language English
License Copyright © 2023 by the American Society of Nephrology.
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Notes Correspondence: Dr. Iain Bressendorff, Department of Nephrology, Herlev and Gentofte Hospital, Borgmester Ib Juuls Vej 1, 2730 Herlev, Denmark. Email: iain@bressendorff.com
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References Go, Chertow, Fan, McCulloch, Hsu (B1) 2004; 351
Ter Braake, Eelderink, Zeper (B6) 2020; 35
Russo, Corrao, Miranda (B12) 2007; 27
Pasch, Farese, Graber (B11) 2012; 23
Bressendorff, Hansen, Schou, Kragelund, Brandi (B9) 2017; 7
Budoff, Rader, Reilly (B2) 2011; 58
Chen, Budoff, Reilly (B3) 2017; 2
Raggi, Callister, Shaw (B17) 2004; 24
Sakaguchi, Fujii, Shoji, Hayashi, Rakugi, Isaka (B5) 2014; 85
Agatston, Janowitz, Hildner, Zusmer, Viamonte, Detrano (B10) 1990; 15
Sakaguchi, Hamano, Obi (B13) 2019; 30
Sakaguchi (B15) 2022; 26
Jahnen-Dechent, Ketteler (B16) 2012; 5
Aghagolzadeh, Bachtler, Bijarnia (B7) 2016; 251
ter Braake, Vervloet, de Baaij, Hoenderop (B8) 2020; 37
Diaz-Tocados, Peralta-Ramirez, Rodriguez-Ortiz (B4) 2017; 92
Geiger, Wanner (B14) 2012; 5
Bressendorff, Hansen, Schou, Pasch, Brandi (B18) 2018; 13
Bressendorff (B9-20250823) 2017; 7
Sakaguchi (B13-20250823) 2019; 30
Aghagolzadeh (B7-20250823) 2016; 251
Go (B1-20250823) 2004; 351
Geiger (B14-20250823) 2012; 5
Jahnen-Dechent (B16-20250823) 2012; 5
Chen (B3-20250823) 2017; 2
Ter Braake (B6-20250823) 2020; 35
Sakaguchi (B15-20250823) 2022; 26
Agatston (B10-20250823) 1990; 15
Russo (B12-20250823) 2007; 27
Sakaguchi (B5-20250823) 2014; 85
ter Braake (B8-20250823) 2020; 37
Diaz-Tocados (B4-20250823) 2017; 92
Pasch (B11-20250823) 2012; 23
Bressendorff (B18-20250823) 2018; 13
Budoff (B2-20250823) 2011; 58
Raggi (B17-20250823) 2004; 24
References_xml – volume: 37
  start-page: 421
  issue: 3
  year: 2020
  end-page: 429
  ident: B8
  article-title: Magnesium to prevent kidney disease-associated vascular calcification: crystal clear?
  publication-title: Nephrol Dial Transplant.
– volume: 13
  start-page: 1373
  issue: 9
  year: 2018
  end-page: 1380
  ident: B18
  article-title: The effect of increasing dialysate magnesium on serum calcification propensity in subjects with end stage kidney disease: a randomized, controlled clinical trial
  publication-title: Clin J Am Soc Nephrol.
– volume: 58
  start-page: 519
  issue: 4
  year: 2011
  end-page: 526
  ident: B2
  article-title: Relationship of estimated GFR and coronary artery calcification in the CRIC (chronic renal insufficiency cohort) study
  publication-title: Am J Kidney Dis.
– volume: 26
  start-page: 379
  issue: 5
  year: 2022
  end-page: 384
  ident: B15
  article-title: The emerging role of magnesium in CKD
  publication-title: Clin Exp Nephrol.
– volume: 23
  start-page: 1744
  issue: 10
  year: 2012
  end-page: 1752
  ident: B11
  article-title: Nanoparticle-based test measures overall propensity for calcification in serum
  publication-title: J Am Soc Nephrol.
– volume: 351
  start-page: 1296
  issue: 13
  year: 2004
  end-page: 1305
  ident: B1
  article-title: Chronic kidney disease and the risks of death, cardiovascular events, and hospitalization
  publication-title: N Engl J Med.
– volume: 35
  start-page: 765
  issue: 5
  year: 2020
  end-page: 773
  ident: B6
  article-title: Calciprotein particle inhibition explains magnesium-mediated protection against vascular calcification
  publication-title: Nephrol Dial Transplant.
– volume: 27
  start-page: 152
  issue: 2
  year: 2007
  end-page: 158
  ident: B12
  article-title: Progression of coronary artery calcification in predialysis patients
  publication-title: Am J Nephrol.
– volume: 2
  start-page: 635
  issue: 6
  year: 2017
  end-page: 643
  ident: B3
  article-title: Coronary artery calcification and risk of cardiovascular disease and death among patients with chronic kidney disease
  publication-title: JAMA Cardiol.
– volume: 85
  start-page: 174
  issue: 1
  year: 2014
  end-page: 181
  ident: B5
  article-title: Hypomagnesemia is a significant predictor of cardiovascular and non-cardiovascular mortality in patients undergoing hemodialysis
  publication-title: Kidney Int.
– volume: 24
  start-page: 1272
  issue: 7
  year: 2004
  end-page: 1277
  ident: B17
  article-title: Progression of coronary artery calcium and risk of first myocardial infarction in patients receiving cholesterol-lowering therapy
  publication-title: Arterioscler Thromb Vasc Biol.
– volume: 251
  start-page: 404
  year: 2016
  end-page: 414
  ident: B7
  article-title: Calcification of vascular smooth muscle cells is induced by secondary calciprotein particles and enhanced by tumor necrosis factor-α
  publication-title: Atherosclerosis.
– volume: 30
  start-page: 1073
  issue: 6
  year: 2019
  end-page: 1085
  ident: B13
  article-title: A randomized trial of magnesium oxide and oral carbon adsorbent for coronary artery calcification in predialysis CKD
  publication-title: J Am Soc Nephrol.
– volume: 5
  start-page: i25
  year: 2012
  end-page: i38
  ident: B14
  article-title: Magnesium in disease
  publication-title: Clin Kidney J.
– volume: 7
  start-page: e016795
  issue: 6
  year: 2017
  ident: B9
  article-title: The effect of magnesium supplementation on vascular calcification in chronic kidney disease - a randomised clinical trial (MAGiCAL-CKD): essential study design and rationale
  publication-title: BMJ Open.
– volume: 5
  start-page: i3
  year: 2012
  end-page: i14
  ident: B16
  article-title: Magnesium basics
  publication-title: Clin Kidney J.
– volume: 92
  start-page: 1084
  issue: 5
  year: 2017
  end-page: 1099
  ident: B4
  article-title: Dietary magnesium supplementation prevents and reverses vascular and soft tissue calcifications in uremic rats
  publication-title: Kidney Int.
– volume: 15
  start-page: 827
  issue: 4
  year: 1990
  end-page: 832
  ident: B10
  article-title: Quantification of coronary artery calcium using ultrafast computed tomography
  publication-title: J Am Coll Cardiol.
– volume: 24
  start-page: 1272
  issue: 7
  year: 2004
  ident: B17-20250823
  article-title: Progression of coronary artery calcium and risk of first myocardial infarction in patients receiving cholesterol-lowering therapy
  publication-title: Arterioscler Thromb Vasc Biol.
  doi: 10.1161/01.ATV.0000127024.40516.ef
– volume: 27
  start-page: 152
  issue: 2
  year: 2007
  ident: B12-20250823
  article-title: Progression of coronary artery calcification in predialysis patients
  publication-title: Am J Nephrol.
  doi: 10.1159/000100044
– volume: 251
  start-page: 404
  year: 2016
  ident: B7-20250823
  article-title: Calcification of vascular smooth muscle cells is induced by secondary calciprotein particles and enhanced by tumor necrosis factor-α
  publication-title: Atherosclerosis.
  doi: 10.1016/j.atherosclerosis.2016.05.044
– volume: 30
  start-page: 1073
  issue: 6
  year: 2019
  ident: B13-20250823
  article-title: A randomized trial of magnesium oxide and oral carbon adsorbent for coronary artery calcification in predialysis CKD
  publication-title: J Am Soc Nephrol.
  doi: 10.1681/ASN.2018111150
– volume: 23
  start-page: 1744
  issue: 10
  year: 2012
  ident: B11-20250823
  article-title: Nanoparticle-based test measures overall propensity for calcification in serum
  publication-title: J Am Soc Nephrol.
  doi: 10.1681/ASN.2012030240
– volume: 92
  start-page: 1084
  issue: 5
  year: 2017
  ident: B4-20250823
  article-title: Dietary magnesium supplementation prevents and reverses vascular and soft tissue calcifications in uremic rats
  publication-title: Kidney Int.
  doi: 10.1016/j.kint.2017.04.011
– volume: 15
  start-page: 827
  issue: 4
  year: 1990
  ident: B10-20250823
  article-title: Quantification of coronary artery calcium using ultrafast computed tomography
  publication-title: J Am Coll Cardiol.
  doi: 10.1016/0735-1097(90)90282-T
– volume: 5
  start-page: i3
  issue: suppl 1
  year: 2012
  ident: B16-20250823
  article-title: Magnesium basics
  publication-title: Clin Kidney J.
  doi: 10.1093/ndtplus/sfr163
– volume: 85
  start-page: 174
  issue: 1
  year: 2014
  ident: B5-20250823
  article-title: Hypomagnesemia is a significant predictor of cardiovascular and non-cardiovascular mortality in patients undergoing hemodialysis
  publication-title: Kidney Int.
  doi: 10.1038/ki.2013.327
– volume: 58
  start-page: 519
  issue: 4
  year: 2011
  ident: B2-20250823
  article-title: Relationship of estimated GFR and coronary artery calcification in the CRIC (chronic renal insufficiency cohort) study
  publication-title: Am J Kidney Dis.
  doi: 10.1053/j.ajkd.2011.04.024
– volume: 26
  start-page: 379
  issue: 5
  year: 2022
  ident: B15-20250823
  article-title: The emerging role of magnesium in CKD
  publication-title: Clin Exp Nephrol.
  doi: 10.1007/s10157-022-02182-4
– volume: 2
  start-page: 635
  issue: 6
  year: 2017
  ident: B3-20250823
  article-title: Coronary artery calcification and risk of cardiovascular disease and death among patients with chronic kidney disease
  publication-title: JAMA Cardiol.
  doi: 10.1001/jamacardio.2017.0363
– volume: 13
  start-page: 1373
  issue: 9
  year: 2018
  ident: B18-20250823
  article-title: The effect of increasing dialysate magnesium on serum calcification propensity in subjects with end stage kidney disease: a randomized, controlled clinical trial
  publication-title: Clin J Am Soc Nephrol.
  doi: 10.2215/CJN.13921217
– volume: 37
  start-page: 421
  issue: 3
  year: 2020
  ident: B8-20250823
  article-title: Magnesium to prevent kidney disease–associated vascular calcification: crystal clear?
  publication-title: Nephrol Dial Transplant.
  doi: 10.1093/ndt/gfaa222
– volume: 351
  start-page: 1296
  issue: 13
  year: 2004
  ident: B1-20250823
  article-title: Chronic kidney disease and the risks of death, cardiovascular events, and hospitalization
  publication-title: N Engl J Med.
  doi: 10.1056/NEJMoa041031
– volume: 35
  start-page: 765
  issue: 5
  year: 2020
  ident: B6-20250823
  article-title: Calciprotein particle inhibition explains magnesium-mediated protection against vascular calcification
  publication-title: Nephrol Dial Transplant.
  doi: 10.1093/ndt/gfz190
– volume: 5
  start-page: i25
  issue: suppl 1
  year: 2012
  ident: B14-20250823
  article-title: Magnesium in disease
  publication-title: Clin Kidney J.
  doi: 10.1093/ndtplus/sfr165
– volume: 7
  start-page: e016795
  issue: 6
  year: 2017
  ident: B9-20250823
  article-title: The effect of magnesium supplementation on vascular calcification in chronic kidney disease - a randomised clinical trial (MAGiCAL-CKD): essential study design and rationale
  publication-title: BMJ Open.
  doi: 10.1136/bmjopen-2017-016795
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Snippet Significance StatementMagnesium prevents vascular calcification in animals with CKD. In addition, lower serum magnesium is associated with higher risk of...
Magnesium prevents vascular calcification in animals with CKD. In addition, lower serum magnesium is associated with higher risk of cardiovascular events in...
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SubjectTerms Chronic Kidney Disease
Clinical Research
Coronary Artery Disease - prevention & control
Dietary Supplements
Humans
Magnesium
Renal Insufficiency, Chronic - therapy
Vascular Calcification - prevention & control
Title The Effect of Magnesium Supplementation on Vascular Calcification in CKD: A Randomized Clinical Trial (MAGiCAL-CKD)
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https://www.ncbi.nlm.nih.gov/pubmed/36749131
https://www.proquest.com/docview/2774268677
https://pubmed.ncbi.nlm.nih.gov/PMC10125639
Volume 34
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