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The effects of magnesium and vitamin E co-supplementation on parameters of glucose homeostasis and lipid profiles in patients with gestational diabetes.

Lipids in health and disease
January 1, 1970
Maryam Maktabi et al. (5 authors)
Journal ArticleRandomized Controlled TrialHuman StudyClinical
Extracted Claims (10)
InterventionDirectionEndpointPopulationDosageImpactClaim #
magnesium plus vitamin E supplements
decrease
fasting plasma glucose
women with gestational diabetes (GDM)
β - 5.20 mg/dL
significantly lower
#1
magnesium plus vitamin E supplements
decrease
serum insulin levels
women with gestational diabetes (GDM)
β - 2.93 μIU/mL
significantly lower
#2
magnesium plus vitamin E supplements
decrease
homeostasis model of assessment-insulin resistance
women with gestational diabetes (GDM)
β - 0.78
significantly lower
#3
magnesium plus vitamin E supplements
increase
quantitative insulin sensitivity check index
women with gestational diabetes (GDM)
β 0.01
higher
#4
magnesium plus vitamin E supplementation
decrease
serum triglycerides
women with gestational diabetes (GDM)
β - 50.31 mg/dL
significant reduction in
#5
magnesium plus vitamin E supplementation
decrease
VLDL-cholesterol
women with gestational diabetes (GDM)
β - 10.06 mg/dL
significant reduction in
#6
magnesium plus vitamin E supplementation
decrease
total-cholesterol
women with gestational diabetes (GDM)
β - 26.10 mg/dL
significant reduction in
#7
magnesium plus vitamin E supplementation
decrease
LDL-cholesterol
women with gestational diabetes (GDM)
β - 15.20 mg/dL
significant reduction in
#8
magnesium plus vitamin E supplementation
decrease
total-/HDL-cholesterol ratio
women with gestational diabetes (GDM)
β - 0.46
significant reduction in
#9
Magnesium and vitamin E co-supplementation
no change
HDL-cholesterol levels
women with gestational diabetes (GDM)
-
did not affect
#10
Abstract

BACKGROUND: Magnesium and vitamin E are known to exert multiple beneficial effects, such as anti-glycemic and anti-lipidemic properties. The aim of this study was to determine the effects of magnesium and vitamin E co-supplementation on metabolic status of women with gestational diabetes (GDM). METHODS: This randomized, double-blinded, placebo-controlled trial was conducted among 60 subjects diagnosed with GDM, aged 18-40 years. Subjects were randomly allocated into two groups to receive 250 mg/day magnesium oxide plus 400 IU/day vitamin E supplements or placebo (n = 30 each group) for 6 weeks. Participants' blood samples were taken to determine their metabolic profiles. RESULTS: Subjects who received magnesium plus vitamin E supplements had significantly lower fasting plasma glucose (β - 5.20 mg/dL; 95% CI, - 7.88, - 2.52; P = 0.002), serum insulin levels (β - 2.93 μIU/mL; 95% CI, - 5.68, - 0.18; P = 0.02) and homeostasis model of assessment-insulin resistance (β - 0.78; 95% CI, - 1.42, - 0.14; P = 0.01), and higher quantitative insulin sensitivity check index (β 0.01; 95% CI, 0.005, 0.02; P = 0.002) compared with placebo. In addition, magnesium plus vitamin E supplementation resulted in a significant reduction in serum triglycerides (β - 50.31 mg/dL; 95% CI, - 67.58, - 33.04; P < 0.001), VLDL- (β - 10.06 mg/dL; 95% CI, - 13.51, - 6.60; P < 0.001), total- (β - 26.10 mg/dL; 95% CI, - 41.88, - 10.33; P = 0.004), LDL- (β - 15.20 mg/dL; 95% CI, - 29.50, - 0.91; P = 0.03) and total-/HDL-cholesterol ratio (β - 0.46; 95% CI, - 0.72, - 0.19; P < 0.001) compared with placebo. Magnesium and vitamin E co-supplementation did not affect HDL-cholesterol levels. CONCLUSIONS: Overall, magnesium and vitamin E co-supplementation for 6 weeks in women with GDM significantly improved glycemic control and lipid profiles, except for HDL-cholesterol levels. CLINICAL TRIAL REGISTRATION NUMBER: http://www.irct.ir : IRCT20170513033941N24.

Medical Subject Headings (MeSH)
AdultCholesterol, HDLDiabetes, GestationalDietary SupplementsFemaleHomeostasisHumansLipidsLipoproteins, LDLLipoproteins, VLDLMagnesiumPregnancyTreatment OutcomeVitamin E
Study Links
Citation Metrics
Total Citations22
Citations/Year3.1
Relative Citation Ratio1.46
NIH Percentile64.1%
Research Impact Scores
APT Score0.75
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