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Effects of zinc and multimineral vitamin supplementation on glycemic and lipid control in adult diabetes
AIMS: To evaluate the effects of zinc with or without other antioxidants on blood glucose, lipid profile, and serum creatinine in adult diabetics on long-term follow-up. MATERIALS AND METHODS: Patients (n = 96) were randomly allocated to three groups: group A (n = 29) was supplemented with oral zinc...
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Formato: | Texto |
Lenguaje: | English |
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Dove Medical Press
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3064411/ https://www.ncbi.nlm.nih.gov/pubmed/21448322 http://dx.doi.org/10.2147/DMSO.S16691 |
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author | Gunasekara, Priyanka Hettiarachchi, Manjula Liyanage, Chandrani Lekamwasam, Sarath |
author_facet | Gunasekara, Priyanka Hettiarachchi, Manjula Liyanage, Chandrani Lekamwasam, Sarath |
author_sort | Gunasekara, Priyanka |
collection | PubMed |
description | AIMS: To evaluate the effects of zinc with or without other antioxidants on blood glucose, lipid profile, and serum creatinine in adult diabetics on long-term follow-up. MATERIALS AND METHODS: Patients (n = 96) were randomly allocated to three groups: group A (n = 29) was supplemented with oral zinc sulfate (22 mg/day) and multivitamin/mineral (zinc+MVM) preparation; group B (n = 31) was given the same preparation without zinc (MVM); and group C (n = 36) was given a matching placebo for a period of 4 months in a single-blinded study. Blood samples were taken at baseline and after 4 months of supplementation to assess blood glucose (fasting and postprandial) and glycosylated hemoglobin (Hb(A1C)%) and serum levels of zinc, creatinine, and lipids. RESULTS: The zinc+MVM group had a mean change of fasting blood sugar −0.33 mmol/L (standard error of the mean 0.21 mmol/L) and was significant (P = 0.05) when compared with the other two groups (mean change in the MVM group +0.19 (0.31) mmol/L and +0.43 (0.23) mmol/L in the control group, respectively). The Hb(A1C)% level reduced significantly, irrespective of the baseline level, in zinc+MVM-supplemented individuals. In the other two groups, the change of Hb(A1C)% level was not significant. Serum lipid levels reduced significantly in the zinc+MVM and MVM groups. CONCLUSIONS: Zinc+MVM supplementation showed beneficial effects in the metabolic control of adult diabetics in addition to elevating their serum zinc level. Zinc supplementation improved glycemic control measured by Hb(A1C)% and fasting and postprandial glucose. Furthermore, zinc supplementation lowered serum cholesterol and cholesterol/high-density lipoprotein ratio. |
format | Text |
id | pubmed-3064411 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-30644112011-03-29 Effects of zinc and multimineral vitamin supplementation on glycemic and lipid control in adult diabetes Gunasekara, Priyanka Hettiarachchi, Manjula Liyanage, Chandrani Lekamwasam, Sarath Diabetes Metab Syndr Obes Original Research AIMS: To evaluate the effects of zinc with or without other antioxidants on blood glucose, lipid profile, and serum creatinine in adult diabetics on long-term follow-up. MATERIALS AND METHODS: Patients (n = 96) were randomly allocated to three groups: group A (n = 29) was supplemented with oral zinc sulfate (22 mg/day) and multivitamin/mineral (zinc+MVM) preparation; group B (n = 31) was given the same preparation without zinc (MVM); and group C (n = 36) was given a matching placebo for a period of 4 months in a single-blinded study. Blood samples were taken at baseline and after 4 months of supplementation to assess blood glucose (fasting and postprandial) and glycosylated hemoglobin (Hb(A1C)%) and serum levels of zinc, creatinine, and lipids. RESULTS: The zinc+MVM group had a mean change of fasting blood sugar −0.33 mmol/L (standard error of the mean 0.21 mmol/L) and was significant (P = 0.05) when compared with the other two groups (mean change in the MVM group +0.19 (0.31) mmol/L and +0.43 (0.23) mmol/L in the control group, respectively). The Hb(A1C)% level reduced significantly, irrespective of the baseline level, in zinc+MVM-supplemented individuals. In the other two groups, the change of Hb(A1C)% level was not significant. Serum lipid levels reduced significantly in the zinc+MVM and MVM groups. CONCLUSIONS: Zinc+MVM supplementation showed beneficial effects in the metabolic control of adult diabetics in addition to elevating their serum zinc level. Zinc supplementation improved glycemic control measured by Hb(A1C)% and fasting and postprandial glucose. Furthermore, zinc supplementation lowered serum cholesterol and cholesterol/high-density lipoprotein ratio. Dove Medical Press 2011-01-26 /pmc/articles/PMC3064411/ /pubmed/21448322 http://dx.doi.org/10.2147/DMSO.S16691 Text en © 2011 Gunasekara et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited. |
spellingShingle | Original Research Gunasekara, Priyanka Hettiarachchi, Manjula Liyanage, Chandrani Lekamwasam, Sarath Effects of zinc and multimineral vitamin supplementation on glycemic and lipid control in adult diabetes |
title | Effects of zinc and multimineral vitamin supplementation on glycemic and lipid control in adult diabetes |
title_full | Effects of zinc and multimineral vitamin supplementation on glycemic and lipid control in adult diabetes |
title_fullStr | Effects of zinc and multimineral vitamin supplementation on glycemic and lipid control in adult diabetes |
title_full_unstemmed | Effects of zinc and multimineral vitamin supplementation on glycemic and lipid control in adult diabetes |
title_short | Effects of zinc and multimineral vitamin supplementation on glycemic and lipid control in adult diabetes |
title_sort | effects of zinc and multimineral vitamin supplementation on glycemic and lipid control in adult diabetes |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3064411/ https://www.ncbi.nlm.nih.gov/pubmed/21448322 http://dx.doi.org/10.2147/DMSO.S16691 |
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