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 in | Journal of the American Society of Nephrology Vol. 34; no. 5; pp. 886 - 894 |
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Main Authors | , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
American Society of Nephrology
01.05.2023
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Online Access | Get full text |
ISSN | 1046-6673 1533-3450 1533-3450 |
DOI | 10.1681/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). |
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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 |
Author_xml | – sequence: 1 givenname: Iain orcidid: 0000-0003-2711-4799 surname: Bressendorff fullname: Bressendorff, Iain organization: Department of Nephrology, Herlev and Gentofte Hospital, Herlev, Denmark – sequence: 2 givenname: Ditte orcidid: 0000-0003-4929-7901 surname: Hansen fullname: Hansen, Ditte organization: Department of Nephrology, Herlev and Gentofte Hospital, Herlev, Denmark – sequence: 3 givenname: Morten surname: Schou fullname: Schou, Morten organization: Department of Cardiology, Herlev and Gentofte Hospital, Herlev, Denmark – sequence: 4 givenname: Charlotte surname: Kragelund fullname: Kragelund, Charlotte organization: Department of Cardiology, Nordsjællands Hospital, Hillerød, Denmark – sequence: 5 givenname: My surname: Svensson fullname: Svensson, My organization: Department of Nephrology, Akershus University Hospital, Lørenskog, Norway – sequence: 6 givenname: Bahram surname: Hashemi fullname: Hashemi, Bahram organization: Department of Nephrology, Aalborg University Hospital, Aalborg, Denmark – sequence: 7 givenname: Tilde surname: Kristensen fullname: Kristensen, Tilde organization: Division of Nephrology, Department of Medicine, Hospitalsenheden Midt, Viborg, Denmark – sequence: 8 givenname: Marie Houmaa surname: Vrist fullname: Vrist, Marie Houmaa organization: Department of Nephrology, Gødstrup Hospital, Herning, Denmark – sequence: 9 givenname: Rikke surname: Borg fullname: Borg, Rikke organization: Department of Medicine, Division of Nephrology, Zealand University Hospital, Roskilde, Denmark – sequence: 10 givenname: Birgitte surname: Tougaard fullname: Tougaard, Birgitte organization: Department of Nephrology, Aarhus University Hospital, Aarhus, Denmark – sequence: 11 givenname: Kristine surname: Borg fullname: Borg, Kristine organization: Hans Christian Andersen Children's Hospital, Odense University Hospital, Odense, Denmark – sequence: 12 givenname: Henrik Øder orcidid: 0000-0001-5786-4561 surname: Hjortkjær fullname: Hjortkjær, Henrik Øder organization: Department of Cardiology, Rigshospitalet, Copenhagen, Denmark – sequence: 13 givenname: Cathrine Helgestad surname: Kristiansen fullname: Kristiansen, Cathrine Helgestad organization: Department of Imaging, Akershus University Hospital, Lørenskog, Norway – sequence: 14 givenname: Nicholas surname: Carlson fullname: Carlson, Nicholas organization: Department of Nephrology, Rigshospitalet, Copenhagen, Denmark – sequence: 15 givenname: Mohammad orcidid: 0000-0003-1306-0013 surname: Nasiri fullname: Nasiri, Mohammad organization: Department of Cardiology, Sygehus Lillebælt, Vejle, Denmark – sequence: 16 givenname: Haseem surname: Ashraf fullname: Ashraf, Haseem organization: Department of Pulmonary Medicine, Herlev and Gentofte Hospital, Gentofte, Denmark – sequence: 17 givenname: Andreas surname: Pasch fullname: Pasch, Andreas organization: Department of Physiology and Pathophysiology, Johannes Kepler University Linz, Linz, Austria – sequence: 18 givenname: Lisbet surname: Brandi fullname: Brandi, Lisbet organization: Department of Endocrinology and Nephrology, Nordsjællands Hospital, Hillerød, Denmark |
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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 ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Undefined-1 ObjectType-Feature-3 content type line 23 |
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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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