Ionized and total magnesium levels in patients with chronic kidney disease: associated factors and outcomes.

cardiovascular disease chronic kidney disease magnesium mortality

Journal

Clinical kidney journal
ISSN: 2048-8505
Titre abrégé: Clin Kidney J
Pays: England
ID NLM: 101579321

Informations de publication

Date de publication:
Apr 2024
Historique:
received: 13 12 2023
medline: 4 4 2024
pubmed: 4 4 2024
entrez: 4 4 2024
Statut: epublish

Résumé

The association between hypo- and/or hypermagnesaemia and cardiovascular (CV) outcomes or mortality has shown conflicting results in chronic kidney disease (CKD) and has been conducted on total magnesium (tMg) levels. Thus, the objectives of the present study were to (i) describe the serum ionized Mg (iMg) concentration in patients at various CKD stages, (ii) measure the correlation between iMg and tMg concentrations, (iii) identify their associated factors and (iv) determine whether serum tMg and/or iMg concentrations are associated with major adverse cardiovascular events (MACE) and mortality before kidney replacement therapy in CKD patients. Chronic Kidney Disease-Renal Epidemiology and Information Network (CKD-REIN) is a prospective cohort of CKD patients with an estimated glomerular filtration rate (eGFR) <60 mL/min/1.73 m Of the 2419 included patients, median age was 68 years, and the mean eGFR was 34.8 mL/min/1.73 m Our analysis of a large cohort of patients with moderate-to-advanced CKD demonstrated that individuals with higher serum tMg concentrations, although still within the normal range, had a greater likelihood of MACE and mortality. However, serum iMg levels were not associated with these outcomes.

Sections du résumé

Background UNASSIGNED
The association between hypo- and/or hypermagnesaemia and cardiovascular (CV) outcomes or mortality has shown conflicting results in chronic kidney disease (CKD) and has been conducted on total magnesium (tMg) levels. Thus, the objectives of the present study were to (i) describe the serum ionized Mg (iMg) concentration in patients at various CKD stages, (ii) measure the correlation between iMg and tMg concentrations, (iii) identify their associated factors and (iv) determine whether serum tMg and/or iMg concentrations are associated with major adverse cardiovascular events (MACE) and mortality before kidney replacement therapy in CKD patients.
Methods UNASSIGNED
Chronic Kidney Disease-Renal Epidemiology and Information Network (CKD-REIN) is a prospective cohort of CKD patients with an estimated glomerular filtration rate (eGFR) <60 mL/min/1.73 m
Results UNASSIGNED
Of the 2419 included patients, median age was 68 years, and the mean eGFR was 34.8 mL/min/1.73 m
Conclusions UNASSIGNED
Our analysis of a large cohort of patients with moderate-to-advanced CKD demonstrated that individuals with higher serum tMg concentrations, although still within the normal range, had a greater likelihood of MACE and mortality. However, serum iMg levels were not associated with these outcomes.

Identifiants

pubmed: 38572502
doi: 10.1093/ckj/sfae046
pii: sfae046
pmc: PMC10986257
doi:

Types de publication

Journal Article

Langues

eng

Pagination

sfae046

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of the ERA.

Déclaration de conflit d'intérêts

M.P., S.M.L., S.L., S.K. and M.M. have nothing to declare. Z.A.M. reports having received grants for CKD-REIN and other research projects from Amgen, Baxter, Fresenius Medical Care, GlaxoSmithKline, Merrck Sharp & Dohme-Chibret, Sanofi-Genzyme, Lilly, Otsuka, AstraZeneca, Vifor and the French government, as well as fees and grants to charities from AstraZeneca, Boehringer Ingelheim and GlaxoSmithKline. N.A.P. declare financial support from pharmaceutical companies integrating the public–private partnership of the CKD-REIN cohort: Fresenius Medical Care, GlaxoSmithKline (GSK), Vifor France and Boeringher Ingelheim; all grants are made to Paris Saclay University.

Auteurs

Maxime Pluquet (M)

MP3CV Laboratory, Jules Verne University of Picardie, Amiens, France.

Said Kamel (S)

MP3CV Laboratory, Jules Verne University of Picardie, Amiens, France.
Department of Biochemistry, Amiens-Picardie University Medical Center, Amiens, France.

Natalia Alencar de Pinho (N)

Centre for Research in Epidemiology and Population Health (CESP), INSERM UMRS 1018, Université Paris-Saclay, Université Versailles Saint Quentin, Villejuif, France.

Nicolas Mansencal (N)

Centre for Research in Epidemiology and Population Health (CESP), INSERM UMRS 1018, Université Paris-Saclay, Université Versailles Saint Quentin, Villejuif, France.
Department of Cardiology, Ambroise Paré University Hospital, APHP, Boulogne-Billancourt, Paris, France.

Christian Combe (C)

Service de Néphrologie Transplantation Dialyse Aphérèse, Centre Hospitalier Universitaire de Bordeaux, Bordeaux, France.
INSERM, U1026, Univ Bordeaux Segalen, Bordeaux, France.

Marie Metzger (M)

Centre for Research in Epidemiology and Population Health (CESP), INSERM UMRS 1018, Université Paris-Saclay, Université Versailles Saint Quentin, Villejuif, France.

Ziad A Massy (ZA)

Centre for Research in Epidemiology and Population Health (CESP), INSERM UMRS 1018, Université Paris-Saclay, Université Versailles Saint Quentin, Villejuif, France.
Department of Nephrology, Ambroise Paré University Hospital, APHP, Boulogne-Billancourt, Paris, France.

Sophie Liabeuf (S)

MP3CV Laboratory, Jules Verne University of Picardie, Amiens, France.
Pharmacoepidemiology Unit, Department of Clinical Pharmacology, Amiens-Picardie University Medical Center, Amiens, France.

Solène M Laville (SM)

MP3CV Laboratory, Jules Verne University of Picardie, Amiens, France.
Pharmacoepidemiology Unit, Department of Clinical Pharmacology, Amiens-Picardie University Medical Center, Amiens, France.

Classifications MeSH