Hypomagnesemia associates with inflammation and risk of diabetes and hypertension, which may contribute to kidney function decline. We hypothesized that low serum magnesium (SMg) levels independently associate with a significant decline in estimated glomerular filtration rate (eGFR). We analyzed SMg levels in 2056 participants from the Dallas Heart Study, a longitudinal, population‐based, multiethnic, cohort study involving residents of Dallas County, Texas, USA. The primary study outcome was the change in eGFR using multivariable linear regression models adjusted for demographics, anthropometric and biochemical parameters, medications, C reactive protein levels, prevalent hypertension and diabetes. During a median follow-up of 7.0 years (25th, 75th percentile: 6.5, 7.6), the median decrease in eGFR was −0.71 (25th, 75th percentile: −2.43, +0.68) mL/min/1.73 m2 per year in the entire cohort. In a fully adjusted model, the lowest SMg quintile (≤1.9 mg/dL or ≤0.8 mM) was associated with a −0.50 mL/min/1.73 m2 per year drop in eGFR (95% CI −0.95 to –0.05; p=0.028) compared with the highest SMg quintile (≥2.3 mg/dL or ≥1.0 mM). Every 0.2 mg/dL (0.08 mM) decrease in SMg was associated with an eGFR decline of −0.23 mL/min/1.73 m2 per year (95% CI −0.38 to –0.08; p=0.003), a decline that was more pronounced in participants with prevalent diabetes compared with patients without diabetes (−0.51 vs −0.18 mL/min/1.73 m2 per year, respectively). In conclusion, low SMg was independently associated with eGFR decline. Further studies are needed to determine whether Mg repletion can ameliorate inflammation, lower blood pressure and serum glucose and ultimately prevent or retard kidney function decline.
- chronic kidney disease
- diabetes mellitus
Statistics from Altmetric.com
Significance of this study
What is already known about this subject?
Both low magnesium (Mg) intake and low serum Mg (SMg) levels are associated with an increased incidence of diabetes and hypertension, two major risk factors for the development of chronic kidney disease (CKD).
Low SMg levels independently associate with incidence and progression of CKD after controlling for potential socioeconomic and clinical confounders of kidney function decline.
Mg supplementation inhibits the expression of profibrotic and proinflammatory cytokines in endothelial and renal tubular cells in vitro.
What are the new findings?
This is the first study to show that every 0.2 mg/dL (0.08 mM) decrease in SMg was independently associated with an estimated glomerular filtration rate (eGFR) decline of −0.23 mL/min/1.73 m2 per year (95% CI −0.38 to –0.08; p=0.003) in a multiethnic cohort with approximately 50% African-Americans.
The lowest SMg quintile (≤1.9 mg/dL or ≤0.8 mM) was associated with a −0.50 mL/min/1.73 m2 per year drop in eGFR (95% CI −0.95 to –0.05; p=0.028) compared with the highest SMg quintile (≥2.3 mg/dL or ≥1.0 mM).
The eGFR decline was more pronounced in participants with prevalent diabetes compared with patients without diabetes (−0.51 vs −0.18 mL/min/1.73 m2 per year, respectively).
How might these results change the focus of research or clinical practice?
The modulation of SMg levels through Mg supplementation could represent a novel therapeutic target for the prevention of kidney function decline in patients with and without diabetes, who are at high risk of developing CKD.
Chronic kidney disease (CKD) is a global public health problem with an overall prevalence in the general population of approximately 14%–20%.1 2 Diabetes and hypertension are major risk factors for the development of CKD and nearly two-thirds of cases of end-stage renal disease (ESRD) in the USA are attributed to these underlying prevalent conditions.3 The mechanisms governing CKD onset and progression are only partially understood. Besides early detection by biomarkers of kidney dysfunction or injury, the identification of novel risk factors for incidence or progression of CKD may improve our understanding of the pathogenesis of CKD, allow more accurate risk stratification and lead to the development of new therapies.
Magnesium (Mg) is essential for human health, being the second most abundant intracellular cation after potassium, and is involved in virtually every biologic process in the cell.4 In the general population, both low Mg intake and low serum Mg (SMg) levels are associated with an increased incidence of diabetes,5 hypertension,6 metabolic syndrome,7 inflammation8 9 and cardiovascular disease (CVD).10–13 Hypomagnesemia is postulated to contribute to the development of diabetes by impairing the insulin receptor downstream signaling and increasing inflammation,14–16 which further increases insulin resistance. In addition, both in vivo and in vitro studies showed that hypomagnesemia may increase blood pressure and promote CVD by enhancing the production of vasoconstrictor agents and cytokines (eg, endothelin-1 and interleukin-8),17 18 decreasing the production of endothelial-derived vasodilators (eg, prostacyclin and nitric oxide)19 20 and increasing oxidative stress.21 Observational studies have shown that low SMg levels independently associate with incidence and progression of CKD in patients with or without diabetes,22–26 as well as cardiovascular events and mortality in patients with CKD or undergoing hemodialysis.27–32 The molecular mechanisms underlying possible deleterious effects of low SMg on renal function are largely unknown.
In this study, we tested the hypothesis that low SMg levels are independently associated with kidney function decline in the Dallas Heart Study (DHS) cohort participants who did not have CKD at baseline. The DHS is a large multiethnic population characterized by standardized longitudinal data collection methodology with a comprehensive biochemical phenotype assessment, and the availability of biomarkers of inflammation, blood pressure and glycemic parameters.
Materials and methods
The DHS is a multiethnic, population-based, cohort study of Dallas County adults aged 30–65 years in which deliberate oversampling of African-Americans was performed. Written informed consent was provided by all participants. Baseline data collection during DHS phase 1 (DHS-1) was conducted in three visits between 2000 and 2002. The design and detailed methods of DHS-1 have been previously described.33 In DHS phase 2 (DHS-2), participants who already completed DHS-1 underwent follow-up testing in a single visit to UT Southwestern Medical Center between 2007 and 2009. Participants were followed for predefined clinical events and death. For this study, the observation period was 7.0 years (25th, 75th percentile: 6.5, 7.6). We excluded participants with prevalent CKD (n=244) to avoid confounding effects from comorbidity, those with missing SMg measurements at DHS-1 (n=6) and/or with missing serum creatinine levels at either DHS-1 or DHS-2 (n=1382), resulting in a final cohort of 2056 participants. According to the latest Kidney Disease Improving Global Outcomes (KDIGO) guidelines, prevalent CKD at DHS-1 was defined as an microalbumin/creatinine ratio ≥30 mg/g and/or an eGFR <60 mL/min/1.73 m2.3 The number of deaths that occurred during the follow-up period was limited to 241 and baseline SMg levels were clinically comparable in those excluded because of death and all survivors at DHS-2 included in the study. Moreover, there were no major differences in medical history, demographics or biomarker data between eligible DHS-1 participants who did and did not complete DHS-2 (follow-up).34
The exposure of interest was SMg at DHS-1 analyzed according to statistical quintiles or as a continuous variable per 0.2 mg/dL decline. SMg was measured in the UT Southwestern General Clinical Research Center laboratory using a SYNCHRON CX9 ALX system (Beckman Coulter, Fullerton, California, USA) (normal SMg range: 1.7–2.8 mg/dL or 0.69–1.15 mM).
Primary study outcome
The primary study outcome was the change in eGFR (ΔeGFR) during the observation period calculated as the values at DHS-2 minus the values at DHS-1. eGFR was estimated using the four-variable Modification of Diet in Renal Disease equation (p. 63).35
Variable definitions and measurements
Race/ethnicity and medication usage were self-reported. Prevalent hypertension (n=764) at DHS-1 was defined by need for pharmacological treatment for hypertension, or a systolic blood pressure (SBP) of ≥140 mm Hg or a diastolic blood pressure (DBP) of ≥90 mm Hg. Prevalent diabetes (n=187) was defined by pharmacological treatment for diabetes, fasting blood glucose ≥126 mg/dL (7 mM) or non-fasting blood glucose level ≥200 mg/dL (11.1 mM). All baseline laboratory parameters were measured from the fasting blood samples obtained at a second in-home visit during DHS-1 with the exception of n=45 samples that were obtained non-fasting. High-sensitive C reactive protein (CRP) measurements were performed using the Roche/Hitachi 912 System, Tina-quant assay (Roche Diagnostics, Indianapolis, Indiana, USA), a latex-enhanced immunoturbidimetric method.36 Diuretic use included thiazide-like diuretics, loop diuretics, potassium-sparing diuretics and/or aldosterone antagonists. Dietary supplements consisted of any combination or single treatment with Mg, calcium, vitamin D and/or multivitamins.
Baseline characteristics at DHS-1 in the entire cohort stratified by SMg quintiles were analyzed by Jonckheere-Terpstra and Cochran-Armitage for continuous and dichotomous categorical variables, respectively. Data are presented as the mean±SD or median (25th, 75th percentile) for continuous variables and as the number (%) for categorical variables, respectively. To investigate the relationship between SBP, DBP, serum glucose (SGlu), ΔeGFR, CRP and SMg levels, Spearman’s correlation analysis was performed. Multivariable linear regression models were constructed to examine the association between baseline SMg and the study outcome of ΔeGFR. Model 1 was adjusted for age, gender, race/ethnicity and body mass index (BMI). Model 2 was adjusted for variables in model 1 plus serum phosphorus, calcium, bicarbonate, albumin, intact parathyroid hormone, total cholesterol and high-density lipoprotein. Model 3 was adjusted for variables in model 2 plus use of diuretics, dietary supplements, ACE inhibitors (ACEI) and angiotensin II receptor blockers (ARB). Model 4 was adjusted for variables in model 3 plus prevalent hypertension and CRP at DHS-1. Model 5 was adjusted for variables in model 4 plus prevalent diabetes at DHS-1. For interaction analyses, a p value of <0.10 was considered to be statistically significant. All other statistical analyses used two-sided α-values at the significance level of 0.05. Analyses were performed using SAS V.9.4 (Cary, North Carolina, USA).
Of the 2056 participants without pre-existing CKD who had SMg measurements at DHS-1 (baseline) and serum creatinine measurements available both at DHS-1 and DHS-2 (follow-up visit), 41.9% were male, 48.9% were black, 35.1% were white and 14% were Hispanic (table 1). Mean baseline eGFR±SD in the entire cohort was 99.9±20.7 mL/min/1.73 m2 at DHS-1 (table 1), and 93.5±22.7 mL/min/1.73 m2 at DHS-2 (data not shown). The prevalence of diabetes and hypertension were 9.1% and 37.3%, respectively. SMg was normally distributed with a mean±SD value of 2.10±0.20 mg/dL (0.86±0.08 mM) in the entire cohort. The comparison of baseline characteristics according to SMg quintiles revealed that patients in the lowest SMg quintile were mostly female (73.5%), included a greater proportion of non-Hispanic black (65.9%), and had a higher prevalence of diabetes (18.5%) and hypertension (42.8%; table 1). Consequently, the use of diuretics, ACEI inhibitors or ARB was significantly higher in the lowest SMg quintile. Lower serum bicarbonate and albumin levels and higher BMI and CRP levels were also observed in the lowest SMg quintile (table 1).
Univariable association of SMg levels with kidney function decline
During a median follow-up of 7.0 years (25th, 75th percentile: 6.5, 7.6), the median eGFR change (ΔeGFR) was −0.71 (25th, 75th percentile: −2.43, +0.68) mL/min/1.73 m2 per year in the entire cohort. When analyzing ΔeGFR across SMg quintiles, the group with the lowest SMg quintile had a greater decline in eGFR compared with the highest SMg quintile during follow-up (−1.08 [25th, 75th percentile: −3.06, 0.46] vs −0.53 [25th, 75th percentile: −1.96, 0.97] mL/min/1.73 m2 per year, respectively; p<0.001; table 1).
There was a significant positive correlation between SMg levels and ΔeGFR (table 2). Moreover, there was an inverse relationship between baseline SMg levels and CRP, DBP and SGlu levels (table 2). We also found that SBP and SGlu levels inversely correlated with ΔeGFR, and positively correlated with CRP (table 2).
Multivariable association of SMg levels and decline in eGFR
The lowest SMg quintile (≤1.9 mg/dL, or ≤0.8 mM) was associated with a −0.50 mL/min/1.73 m2 per year decline in eGFR (95% CI −0.95 to –0.05; p=0.028 for lowest vs highest quintile) after adjustment for the major traditional risk factors for kidney function decline, including demographics, anthropometric and biochemical parameters, medications, CRP and prevalent hypertension and diabetes (table 3). In the same fully adjusted model, every 0.2 mg/dL (0.08 mM) decrease in SMg was associated with an eGFR decline of −0.23 mL/min/1.73 m2 per year (95% CI −0.38 to –0.08; p=0.003; table 6).
Sensitivity analysis examining the association of SMg levels and decline in eGFR in study participants with and without prevalent diabetes
Although the association remained significant after the inclusion of prevalent diabetes, a significant interaction between SMg and prevalent diabetes on the association between SMg levels and eGFR decline was observed (p=0.02). Therefore, we stratified the study cohort based on prevalent diabetes at DHS-1. Participants with prevalent diabetes were older, mostly female (59.4%), and a greater proportion was non-Hispanic black (65.2%; table 4). They had higher BMI, SGlu, HDL, CRP; higher prevalence of comorbidities, including prevalent hypertension, and higher use of diuretics, ACEI and ARB. Mean SMg levels were significantly lower in participants with and without diabetes (1.96±0.20 vs 2.08±0.17 mg/dL, or 0.81±0.08 vs 0.86±0.07 mM, p<0.001, respectively), whereas serum calcium and phosphate were similar. There was a significant positive correlation between SMg levels and ΔeGFR in both subgroups, which was stronger in patients with diabetes than in patients without diabetes (r=0.25 vs 0.06, respectively; table 5). CRP was inversely correlated with SMg, and positively correlated with SBP, DBP and SGlu in both subgroups. SGlu was inversely correlated with ΔeGFR and SMg only in patients with diabetes.
During follow-up, the decline in eGFR in participants with prevalent diabetes was higher than in participants without prevalent diabetes (−1.97 [25th, 75th percentile: −3.79, –0.13] vs −0.64 [25th, 75th percentile: −2.28, +0.71] mL/min/1.73 m2 per year, respectively, p<0.001; table 4). Every 0.2 mg/dL (0.08 mM) decrease in SMg was associated with a greater eGFR decline in participants with prevalent diabetes (−0.51 mL/min/1.73 m2 per year [95% CI −1.09 to +0.08; p=0.09]) vs those without prevalent diabetes (−0.18 mL/min/1.73 m2 per year [95% CI −0.34, to –0.02; p=0.02]) in fully adjusted models (table 6).
The principal finding of this study is that, in a large multiethnic population-based cohort, low SMg levels were associated with a greater decline in eGFR even after adjustment for the major traditional risk factors for kidney function decline, suggesting that low SMg may contribute to the pathogenesis of kidney disease and loss of renal function in a direct independent manner. Specifically, every 0.2 mg/dL (0.08 mM) decrease in SMg was independently associated with an eGFR decline of −0.23 mL/min/1.73 m2 per year during a median follow-up of 7.0 years in the entire cohort of DHS participants who did not have CKD at baseline. Moreover, the lowest SMg quintile (≤1.9 mg/dL or ≤0.8 mM) was associated with a −0.50 mL/min/1.73 m2 per year drop in eGFR (95% CI −0.95 to –0.05; p=0.028) compared with the highest SMg quintile (≥2.3 mg/dL or ≥1.0 mM) despite the lowest SMg quintile had the highest eGFR at baseline. Of note, the variations in SMg being evaluated in this study are within normal values (1.6–2.6 mg/dL). Only 16 out of 460 participants (3.5%) in the lowest quintile had SMg ≤1.6 mg/dL, and 4 out of 460 participants (0.9%) had SMg <1.6 mg/dL. Thus, it is unlikely that study participants with SMg below the normal limit may drive the results observed in this study.
This eGFR decline was greater in participants with prevalent diabetes compared with those without prevalent diabetes (−0.51 vs −0.18 mL/min/1.73 m2 per year, respectively). However, the adjusted association in participants with prevalent diabetes was borderline significant (p=0.09) probably due to the small number of subjects (n=187 subjects with prevalent diabetes vs n=1869 subjects without prevalent diabetes), which may have limited statistical power.
Other studies showed the association of SMg with markers of kidney function decline after controlling for diabetes.22 25 26 Tin et al identified a large number of incident CKD cases (n=1965) in the Atherosclerosis Risk in Communities (ARIC) study.22 They found that low SMg associated with incident CKD over a median follow-up of 21 years and after stratification by diabetes and hypertension.22 Compared with DHS, participants in the ARIC study were older (45–64 years in ARIC vs 30–65 years in DHS) and had longer follow-up (21 years in ARIC vs 7 years in DHS). In a multivariable regression analysis, Pham et al showed that in a small cohort of patients with diabetes (n=550), low SMg associated with a faster rate of kidney function deterioration, as determined by the slope of serum creatinine over a mean follow-up of 5.2±1.9 years.25 In an adjusted analysis, Sakaguchi et al found that in a cohort of 455 patients with CKD those with diabetic CKD (n=144) and low SMg levels had a significant higher risk of progression to renal replacement therapy compared with those with high SMg levels over a median follow-up of 1.9 years.26 In subjects with CKD and without diabetes, there was no significant difference in outcome between the low and high SMg groups.26
In our study, the decline in eGFR during follow-up was greater in participants with prevalent diabetes compared with subjects without prevalent diabetes as expected due to the underlying comorbidity. The positive correlation between SMg levels and ΔeGFR was stronger in patients with diabetes than in patients without diabetes, which supports the observation of a greater eGFR decline for every 0.2 mg/dL (0.08 mM) decrease in SMg in patients with diabetes than in patients without diabetes, even in a fully adjusted model. Of note, SMg levels were lower in participants with diabetes compared with participants without diabetes, a finding that has been previously shown in this patient population.37 38 Whether low SMg is causative or a consequence of diabetes cannot be determined from this study, but epidemiological studies support a potential causal role of Mg in the development of diabetes possibly though hyperglycemia and/or inflammation.39 40
Overall, the independent association of lower SMg levels with kidney function decline observed in the DHS cohort and in other cohorts may be explained at the molecular level by direct effects of Mg on renal and/or vascular cells.17 24 41 Sakaguchi et al reported that, in a small group of non-diabetic CKD patients, subjects with high serum phosphate had a higher risk of ESRD when they had concomitant low SMg levels at baseline.24 They demonstrated that Mg suppresses phosphate-induced apoptosis of renal tubular cells in vitro experiments by inhibiting the expression of profibrotic and proinflammatory cytokines, and by inhibiting mitochondria-mediated cell death.24 In our study, the association of low SMg with eGFR decline was independent of serum phosphate, which was included as a confounding variable in our models. Besides a direct nephrotoxic effect, low extracellular Mg induces production of inflammatory and proatherogenic cytokines in endothelial cells,17 and promote vascular calcification in both in vitro and in vivo studies.41–43 Together these multiple molecular pathways can contribute to intrarenal chronic inflammation and impaired hemostasis that have been previously linked to kidney function decline.44–48
Some limitations of our study warrant mention. First, the number of patients with prevalent diabetes in our cohort is small. This may have limited statistical power after stratification for prevalent diabetes status. Second, this study is observational and thus cannot provide evidence of a causal relationship between SMg and kidney function decline. Our study has also several strengths. First, we used a large multiethnic population-based cohort with approximately 50% African- Americans, a population at high risk of CKD. Second, our cohort has an adequate median follow-up of 7.0 years for the observation of the outcome of eGFR decline, and is characterized by standardized longitudinal data collection methodology with a comprehensive biochemical phenotype assessment. Third, the availability of biomarkers of inflammation, BP and glycemic parameters underpinned important observations to construct plausible biological hypotheses that can guide further bench and clinical research.
In summary, we identified that low SMg is independently associated with eGFR decline in a large multiethnic cohort, and that the eGFR decline was greater in subjects with prevalent diabetes. Future studies are required to determine whether the modulation of SMg levels could represent a novel therapeutic target for the prevention of CKD in patients with and without diabetes who are at high risk of developing CKD.
Contributors Study concept and design: SF and JN. Acquisition, analysis or interpretation of data: SF, XL, BAH and JN. Drafting of the manuscript: SF and JN. Critical revision of the manuscript for intellectual content: NMM, KS, RT and OM. Statistical analysis: SF, XL, BAH and JN. Obtained funding: RT and OM. Study supervision: NMM, KS, RT, OM and JN.
Funding The Dallas Heart Study is supported by grant UL1TR001105 from the National Center for Advancing Translational Science of the National Institutes of Health. This work was also supported by the University of Texas Southwestern Medical Center O’Brien Kidney Research Center (P30-DK079328). Dr Ferrè was supported by the Charles and Jane Pak Center Innovative Research Support Award. Dr Neyra is currently supported by an Early Career Pilot Grant from the National Center for Advancing Translational Sciences, National Institutes of Health, through Grant UL1TR001998.
Competing interests None declared.
Ethics approval The UT Southwestern Institutional Review Board approved the study.
Provenance and peer review Not commissioned; externally peer reviewed.
Patient consent for publication Obtained.
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.