24
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Serum Magnesium and Sudden Death in European Hemodialysis Patients

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Despite suggestions that higher serum magnesium (Mg) levels are associated with improved outcome, the association with mortality in European hemodialysis (HD) patients has only scarcely been investigated. Furthermore, data on the association between serum Mg and sudden death in this patient group is limited. Therefore, we evaluated Mg in a post-hoc analysis using pooled data from the CONvective TRAnsport STudy (CONTRAST, NCT00205556), a randomized controlled trial (RCT) evaluating the survival risk in dialysis patients on hemodiafiltration (HDF) compared to HD with a mean follow-up of 3.1 years. Serum Mg was measured at baseline and 6, 12, 24 and 36 months thereafter. Cox proportional hazards models, adjusted for confounders using inverse probability weighting, were used to estimate hazard ratios (HRs) of baseline serum Mg on all-cause mortality, cardiovascular mortality, non-cardiovascular mortality and sudden death. A generalized linear mixed model was used to investigate Mg levels over time. Out of 714 randomized patients, a representative subset of 365 (51%) were analyzed in the present study. For every increase in baseline serum Mg of 0.1 mmol/L, the HR for all-cause mortality was 0.85 (95% CI 0.77–94), the HR for cardiovascular mortality 0.73 (95% CI 0.62–0.85) and for sudden death 0.76 (95% CI 0.62–0.93). These findings did not alter after extensive correction for potential confounders, including treatment modality. Importantly, no interaction was found between serum phosphate and serum Mg. Baseline serum Mg was not related to non-cardiovascular mortality. Mg decreased slightly but statistically significant over time (Δ -0.011 mmol/L/year, 95% CI -0.017 to -0.009, p = 0.03). In short, serum Mg has a strong, independent association with all-cause mortality, cardiovascular mortality and sudden death in European HD patients. Serum Mg levels decrease slightly over time.

          Related collections

          Most cited references25

          • Record: found
          • Abstract: not found
          • Article: not found

          The clinical epidemiology of cardiac disease in chronic renal failure.

            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Hypomagnesemia is a significant predictor of cardiovascular and non-cardiovascular mortality in patients undergoing hemodialysis.

            Although previous studies in the general population showed that hypomagnesemia is a risk for cardiovascular diseases (CVD), the impact of magnesium on the prognosis of patients on hemodialysis has been poorly investigated. To gain information on this we conducted a nationwide registry-based cohort study of 142,555 hemodialysis patients to determine whether hypomagnesemia is an independent risk for increased mortality in this population. Study outcomes were 1-year all-cause and cause-specific mortality with baseline serum magnesium levels categorized into sextiles. During follow-up, a total of 11,454 deaths occurred, of which 4774 had a CVD cause. In a fully adjusted model, there was a J-shaped association between serum magnesium and the odds ratio of all-cause mortality from the lowest to highest sextile, with significantly higher mortality in sextiles 1-3 and 6. Similar associations were found between magnesium and both CVD and non-CVD mortality. The proportion of patients with a baseline intact parathyroid hormone level under 50 pg/ml was significantly higher in the highest sextile; however, after excluding these patients, the CVD mortality risk in the highest sextile was attenuated. Thus, hypomagnesemia was significantly associated with an increased risk of mortality in hemodialysis patients. Interventional studies are needed to clarify whether magnesium supplementation is beneficial for improving patient prognosis.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Progressive vascular calcification over 2 years is associated with arterial stiffening and increased mortality in patients with stages 4 and 5 chronic kidney disease.

              Vascular calcification is increasingly recognized as an important component of cardiovascular disease in chronic kidney disease. The objective of this study was to investigate prospectively the determinants, cardiovascular functional consequences, and survival associated with vascular calcification over 24 mo. A total of 134 patients (60 on hemodialysis, 28 on peritoneal dialysis, and 46 with stage 4 chronic kidney disease) were studied. Vascular calcification of the superficial femoral artery was assessed using multislice spiral computed tomography; pulse wave velocity; all medications and time-averaged biochemical parameters were recorded at baseline and 12 and 24 mo. A total of 101 patients remained at 24 mo. Progressive calcification was seen in 58 of 101 patients. Most (31 of 46) patients with an initial calcification score of zero did not develop calcification. The hemodialysis group demonstrated a greater degree of progression than patients who were on peritoneal dialysis or had stage 4 chronic kidney disease. Progressive calcification was associated with age, male gender, serum alkaline phosphatase, beta blockers, and lipid-lowering agents. Increases in vascular calcification correlated with increased arterial stiffness. Vascular calcification was present in 20 of 21 patients who died. Cox proportional hazard analysis identified change in calcification score, calcium intake from phosphate binders, and low albumin as risk factors for death. Patients with stages 4 and 5 chronic kidney disease and preexisting vascular calcification exhibit significantly increased calcification over 24 mo. Rapid progression of calcification is associated with arterial stiffness and mortality.
                Bookmark

                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, CA USA )
                1932-6203
                23 November 2015
                2015
                : 10
                : 11
                : e0143104
                Affiliations
                [1 ]Department of Nephrology, VU University Medical Center, Amsterdam, the Netherlands
                [2 ]Institute for Cardiovascular Research, VU University Medical Center (ICaR-VU), VU University Medical Center, Amsterdam, the Netherlands
                [3 ]Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht, the Netherlands
                [4 ]Department of Nephrology, University Medical Center Utrecht, Utrecht, the Netherlands
                [5 ]Fresenius Medical Care Deutschland GmbH, Bad Homburg, Germany
                [6 ]Department of Cardiology and Vascular Medicine, University Hospital Aachen, Aachen, Germany
                [7 ]Department of Internal Medicine, Maasstad Hospital, Rotterdam, the Netherlands
                University of São Paulo School of Medicine, BRAZIL
                Author notes

                Competing Interests: Muriel P.C. Grooteman reports research funded by Fresenius Medical Care and Gambro/Baxter and honoraria received from Fresenius Medical Care. Peter J. Blankestijn reports research funded by Fresenius Medical Care and Gambro/Baxter and honoraria received from Fresenius Medical Care. Sonja Steppan and Janine Büchel are fulltime employees of Fresenius Medical Care Deutschland GmbH. Vincent Brandenburg reports research/honoria or scientific advisory board membership from/at Abbvie, Amgen, Bayer, Fresenius Medical Care, Novartis, Sanofi, Servier, and Synlab. The membership of the scientific advisory board of Fresenius Medical Care did not have any influence on the present manuscript. Marc G. Vervloet reports research or fees from Abbie Inc, Fresenius Medical Care, Amgen, Baxter, and Shire. There are no patents, products in development, or marketed products to declare. This does not alter the authors’ adherence to all the PLOS ONE policies on sharing data and materials, as detailed online in the guide for authors.

                Conceived and designed the experiments: CdRvZ MG MB PB MvdD PtW MN MV. Performed the experiments: CdRvZ MG MB PB MvdD PtW MN MV. Analyzed the data: CdRvZ MG SS JB RG VB MN MV. Wrote the paper: CdRvZ MG MB PB SS JB RG VB MvdD PtW MN MV.

                Article
                PONE-D-15-36751
                10.1371/journal.pone.0143104
                4658157
                26600017
                19fc4efe-55ee-49e0-a3fb-f9f9e29b0c68
                Copyright @ 2015

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited

                History
                : 21 August 2015
                : 30 October 2015
                Page count
                Figures: 3, Tables: 2, Pages: 13
                Funding
                CONTRAST was financially supported by a grant from the Dutch Kidney Foundation (Nierstichting Nederland, grant C02.2019) and unrestricted grants from Fresenius Medical Care (The Netherlands) and Gambro Lundia AB (Sweden). Additional support was received from the Dr E.E. Twiss Fund, Roche Netherlands, the International Society of Nephrology/Baxter Extramural Grant Program, and the Dutch Organization for Health Research and Development (ZonMW, grant 17088.2802). The funders had no role in study design, data collection, analysis, or the decision to publish. The present project was additionally funded by a grant from Fresenius Medical Care Deutschland GmbH, Bad Homburg, Germany. Fresenius Medical Care Deutschland GmbH did not have any additional role in the study design, data collection, and analysis of the manuscript, but provided support in the form of salaries for authors (SS, JB) and intellectual content, and consented to publish the manuscript. The specific roles of the authors related to Fresenius Medical Care are articulated in the ‘author contributions’ section.
                Categories
                Research Article
                Custom metadata
                Due to ethical restrictions as a consequence of the multicentre character of the CONTRAST study, the data cannot be made publicly available online. However, the data set underlying the findings of the present study is available to all interested researchers upon request. The CONTRAST investigators can be reached by contacting professor M.L. Bots, epidemiologist, at M.L.Bots@ 123456umcutrecht.nl .

                Uncategorized
                Uncategorized

                Comments

                Comment on this article