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The Biochemical Role of Macro and Micro-Minerals in the Management of Diabetes Mellitus and its Associated Complications: A Review.

International journal for vitamin and nutrition research. Internationale Zeitschrift fur Vitamin- und Ernahrungsforschung. Journal international de vitaminologie et de nutrition
January 1, 2015
Cromwell Mwiti Kibiti et al. (2 authors)
Journal ArticleResearch Support, Non-U.S. Gov'tReviewHuman Study
Study Details

Study Goal

The researchers aimed to review and classify the modes of action of molybdenum and other mineral elements in diabetes mellitus therapy.

Results Summary

The study found that molybdenum facilitates glucose catabolism, enhances insulin activity, and stimulates lipogenesis, with mechanisms similar to conventional anti-diabetic drugs. However, the safe doses and synergistic effects of molybdenum combinations remain unclear.

Population

Not specified (general diabetic population inferred from literature review).

Effective Dosage

Not specified

Duration

Not specified

Interactions

None mentioned

Extracted Claims (16)
InterventionDirectionEndpointPopulationDosageImpactClaim #
magnesium
increase
glucose catabolism
-
-
facilitate
#1
molybdenum
increase
glucose catabolism
-
-
facilitate
#2
zinc
increase
glucose catabolism
-
-
facilitate
#3
vanadium
increase
glucose catabolism
-
-
facilitate
#4
manganese
increase
glucose catabolism
-
-
facilitate
#5
chromium
increase
insulin activity
-
-
enhance
#6
vanadium
increase
insulin activity
-
-
enhance
#7
zinc
increase
insulin activity
-
-
enhance
#8
molybdenum
increase
insulin activity
-
-
enhance
#9
magnesium
increase
insulin activity
-
-
enhance
#10
molybdenum
increase
lipogenesis
-
-
stimulate
#11
manganese
increase
lipogenesis
-
-
stimulate
#12
zinc
increase
lipogenesis
-
-
stimulate
#13
zinc
increase
glucose, metabolizing enzymes in the gastrointestinal tract
-
-
modulate
#14
iron
decrease
oxidative stress
-
-
limit
#15
mineral supplements
increase
good health
diabetics
-
promote
#16
Abstract

UNLABELLED: Diabetes mellitus is a chronic physiological glucose metabolic disorder. Its high prevalence globally has a significant impact on the quality of life. The management of diabetes includes non-pharmacological and glucose lowering agents. Although these methods are effective, they have drawbacks. This has led to a search for alternative therapy in macro and micro-minerals from dietary foods and plants. There is therefore a need to review, identify and classify their modes of action in diabetes mellitus therapy. MATERIALS AND METHODS: This review was carried out using comprehensive literature reports on the use of mineral elements in the management of diabetes. Empirical online searches were conducted for different elements that have been studied for their anti-diabetic potentials both in vivo and in vitro. The University of Fort Hare's online database was also used. RESULTS AND DISCUSSION: The results indicate that magnesium, molybdenum, zinc, vanadium and manganese facilitate glucose catabolism. Chromium, vanadium, zinc, molybdenum and magnesium can enhance insulin activity while molybdenum, manganese and zinc stimulate lipogenesis. Zinc and iron can modulate glucose, metabolizing enzymes in the gastrointestinal tract and limit oxidative stress, respectively. These agents have similar mechanisms to conventional drugs in ameliorating diabetic status and other associated complications. CONCLUSION: The mechanisms of these elements are well known, however, the synergetic effects of their combinations are still obscure. Literature on their safe dose(s) is still scanty. Evaluation of other useful macro and micro-minerals should also be undertaken. It is envisaged that the use of mineral supplements will promote good health in diabetics.

Medical Subject Headings (MeSH)
ChromiumDiabetes ComplicationsDiabetes MellitusDrug SynergismGlucoseHumansIronMagnesiumManganeseMineralsMolybdenumOxidative StressVanadiumZinc
Study Links
Quality Scores
SafetyNot Assessed
Efficacy75/10
Quality65/10
Citation Metrics
Total Citations14
Citations/Year1.4
Relative Citation Ratio0.73
NIH Percentile39.1%
Research Impact Scores
APT Score0.75
Weight Score1.50
Normalized Score0.63
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