The effects of magnesium-zinc-calcium-vitamin D co-supplementation on biomarkers of inflammation, oxidative stress and pregnancy outcomes in gestational diabetes

This study was approved by the Ethics Committee of the Arak University of Medical Sciences (AUMS). It was conducted according to the principles explained in the Declaration of Helsinki. All participants provided written and informed consent. The present clinical trial was registered at the Iranian website for registration of clinical trials (www.​irct.​ir: IRCT201704225623N109).

This was a prospective, randomized, double-blind, placebo-controlled trial of women with GDM. This single-center study was conducted in Arak, Iran between March and November 2017. Participants were 60 women, aged 18 to 40 years, with GDM who were referred to the Kosar Clinic in Arak, Iran. Gestational diabetes was diagnosed using a “one-step” 2-h 75-g oral glucose tolerance test (OGTT) at 24–28 weeks’ gestation and was applied as the inclusion criteria for this trial. Diagnosis of GDM was based on the American Diabetes Association guidelines [16]: women whose plasma glucose level met one of the following criteria were considered as having GDM: fasting plasma glucose level (FPG) ≥ 92 mg/dL, 1 h OGTT≥180 mg/dL and 2 h OGTT≥153 mg/dL. Exclusion criteria included: history of placenta abruption, pre-eclampsia, eclampsia, hypo and hyperthyroidism, kidney or liver diseases, taking magnesium, zinc, calcium and vitamin D supplements prior to intervention, being smoker, and insulin therapy after GDM diagnosis.

In the present study, the primary outcomes were serum hs-CRP and plasma total nitrite levels. The secondary outcomes were the biomarkers of oxidative stress and pregnancy outcomes.

Anthropometric measurements were conducted by a trained midwife at baseline and the end of the intervention. Weight and height were measured using a Seca 713 scale without shoes and in light clothing to the nearest 0.1 kg and 0.1 cm, respectively. BMI was calculated as the ratio of the current body weight to height squared (kg/m²). After labor, all newborns’ weight and length were measured by a trained midwife using the standard methods (Seca 155 Scale, Hamburg; Germany). Infants’ head circumference was measured to the nearest 1 mm with a Seca girth measuring tape. Moreover, we determined infants’ 1- and 5-min Apgar scores as another measure of pregnancy outcome.

Polyhydramnios was diagnosed using the sonographic estimation method at the end of the trial. Applying sonography, polyhydramnios was detected when amniotic fluid index (AFI) exceeded 25 cm [17]. Preterm delivery was defined as delivery occurred at < 37 weeks of pregnancy and newborn’s macrosomia was defined as baby’s birth weight of > 4000 g. Large-for-gestational-age (LGA) newborns were live-born infants with their birth weight ≥ 90th percentile of birth weight according to the latest normograms based on gender and gestational age [18].

Ten milliliter fasting blood was collected for biomarkers measurements at weeks 0 and 6 of the intervention. Serum magnesium, zinc and calcium concentrations were measured using enzymatic kits (Pars Azmun, Tehran, Iran), with inter- and intra-assay coefficient variances (CVs) of less than 5%. To determine FPG, we used enzymatic kits (Pars Azmun, Tehran, Iran). Serum 25-hydroxyvitamin D concentrations were measured using a commercial ELISA kit (IDS, Boldon, UK) with inter- and intra-assay CVs of 4.6 and 6.4%, respectively. Serum hs-CRP levels were assessed using ELISA kit (LDN, Nordhorn, Germany) with intra- and inter-assay CVs of 4.0 and 6.1%, respectively. Part of blood samples were immediately centrifuged (3000×g, 10 min, 4^°C) after collection; the plasma was then separated and stored at -70^oC until the analysis for total nitrite, malondialdehyde (MDA), total antioxidant capacity (TAC), and GSH. The plasma total nitrite concentrations were measured using Griess method [19]; GSH concentrations by the method of Beutler et al. [20] and MDA levels using thiobarbituric acid reactive substance spectrophotometric test [21]. Plasma TAC concentrations were measured using the ferric reduction antioxidant power method developed by Benzie and Strain [22]. CVs for plasma total nitrite, TAC, GSH and MDA were lower than 5%. Newborns’ hyperbilirubinemia was determined by the total serum bilirubin levels above 15 mg/dL (257 μmol/L) among infants who were 25 to 48 h old, 18 mg/dL (308 μmol/L) in infants who were 49 to 72 h old, and above 20 mg/dL (342 μmol/L) in infants older than 72 h [23].

Applying hs-CRP as a primary outcome with a mean distinction of 3.2 mg/L and a SD of 4.0 mg/L, we used the standard formula for sample size calculation in clinical trials. Considering a type one error (α) of 0.05 and type two error (β) of 0.20 with the power of 80%, the calculated sample size was 25 subjects in each treatment group [24]. Assuming 5 dropouts in each group, the final sample size was determined to be 30 subjects in each group.

Kolmogorov-Smirnov test was used to check the normal distribution of data. General characteristics and dietary intakes were compared between two treatment groups using an independent-samples t-test. To determine the effects of magnesium-zinc-calcium-vitamin D on biomarkers of inflammation and oxidative stress, we used independent-samples t-test. To control confounding variables including; baseline values, maternal age and baseline BMI, we used ANCOVA test, using general linear models. Differences in proportions were assessed using Chi square test or Fisher’s exact tests. P < 0.05 was considered as statistically significant. All statistical analyses were conducted using the SPSS Software (version 18.0, SPSS Inc., Chicago, Illinois, USA).

Elevated hs-CRP is more common among women with GDM as compared to women with normal pregnancy. A reference value of hs-CRP levels below 3 mg/L is considered normal [29], and there are a few studies have reported circulating levels of hs-CRP higher than 3 mg/L in women with GDM [30, 31]. Our findings demonstrated that co-administering of magnesium-zinc-calcium-vitamin D for 6 weeks to women with GDM attenuated inflammation and oxidative stress, through decreasing serum hs-CRP, plasma total nitrite, and MDA levels, and increasing TAC levels. The impact of mono-nutrient therapy has been depicted in already published clinical trials. We have previously shown that magnesium oxide (250 mg/day) plus zinc sulfate (220 mg/day) co-supplementation for 12 weeks had beneficial effects on hs-CRP and TAC levels, and gene expression related to IL-1 and TNF-α in women diagnosed with PCOS [32]. Consistent with our results, co-administration of calcium (1000 mg/day) with vitamin D (50,000 IU/week) supplements for 12 weeks has been shown to significantly lessen systemic inflammation, through decreasing IL-6 and TNF-α levels in patients with T2DM [33]. Moreover, among young men with sedentary lifestyle, magnesium supplementation for 4 weeks had remarkable impacts on diminishing DNA oxidative damage [34]. In another study, taking zinc gluconate by obese individuals, at a dosage of 30 mg/day, for 8 weeks resulted in a significant reduction in serum hs-CRP concentrations [35]. Elevated inflammatory cytokines and oxidative stress during pregnancy contribute to increased cardiovascular risk [36] and insulin resistance post-partum [31, 37]. Anti-inflammatory effects of magnesium, vitamin D and zinc may be due to their antagonistic impact on serum calcium [31, 38] and their role in regulating nuclear factor-κB activity, and peroxisome proliferator activated receptor-α signaling pathway, which require zinc and magnesium for their anti-inflammatory effects [39]. In addition, less production of parathyroid hormone following the intake of calcium and vitamin D supplements may result in the reduced production of inflammatory factors [40]. Magnesium and zinc intake might reduce oxidative damage through decreasing ROS production [41] and decrease the formation of ^·OH from hydrogen peroxide by counteracting the redox-active transition metals [42]. Furthermore, antioxidant impact of vitamin D might be explained by a significant decrease in ROS and pro-inflammatory markers [43].

Additional demands associated with pregnancy and fetal growth, pose pregnant women at more risk for multiple nutrient deficiencies [44]. The results of current study revealed a decreasing trend in newborns’ weight and the rate of macrosomia in the magnesium-zinc-calcium-vitamin D co-supplemented group compared to the placebo group. Following supplementation, the difference between birth weights was large and non-significant between intervention groups (3089.8 vs. 3346.3, P = 0.05). This result has been presented as mean values, however when we assessed data of birth weight individually we did not see any birth weight below normal value. On the other hand, the reduction in macrosomia rate was one of the goals of this study. Overall, based on current findings we did not consider these reductions as negative effects. Same research group has already shown that magnesium supplementation might decrease the incidence of newborn hyperbilirubinemia and newborn hospitalization and was less associated with macrosomia [10]. Looking at the effect of zinc on pregnancy outcomes, the results are inconclusive, which might be related to high incidence of zinc deficiency in pregnancy and low doses of supplementation are usually used in different trials [45, 46]. The combination of vitamin D and calcium has been shown significant reduction in the rate of macrosomia and caesarean section in women with GDM [12]. The inconclusive results in the current trial, as a multi-nutrients supplementation approach might be related to the following parameters; supplementation strategies might be beneficial when a deficiency is observed, maternal weight gain during pregnancy is of major importance and is affected by different factors like woman’s age, environmental conditions, diet, socioeconomic status and psychological parameters, higher doses of nutrients might be required to see any effect on pregnancy outcomes [47].

The current study had a few limitations. The sample size was not large enough to detect more detailed outcomes changes following supplementation. Six weeks of intervention might not be long enough to determine any changes resulted from multi-nutrients supplementation. Therefore, future studies with longer duration of the intervention, and larger sample sizes are needed to confirm our findings. In addition, we did not determine the effects of magnesium-zinc-calcium-vitamin D co-supplementation on all of the pregnancy outcomes including the infant respiratory status and the duration of neonatal intensive care, as well as the gene expression related to inflammation and oxidative stress. We were not able to assess intracellular magnesium concentrations in the current study due to funding limitations. However, TAC levels are evaluated using FRAP assays. Since hemoglobin data were not available in this study, we were not able to adjust our results based on circulating hemoglobin levels. This should be considered in the interpretation of our findings. In addition, we did not evaluate the sensitivity of plasma total nitrite concentrations using Griess method.