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- Publisher Website: 10.1016/j.atherosclerosis.2011.07.097
- Scopus: eid_2-s2.0-81155159707
- PMID: 21840002
- WOS: WOS:000296587200035
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Article: Oral zinc supplementation does not improve oxidative stress or vascular function in patients with type 2 diabetes with normal zinc levels
Title | Oral zinc supplementation does not improve oxidative stress or vascular function in patients with type 2 diabetes with normal zinc levels | ||||||
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Authors | |||||||
Keywords | Oxidative damage Type 2 diabetes Vascular function Zinc | ||||||
Issue Date | 2011 | ||||||
Publisher | Elsevier Ireland Ltd. The Journal's web site is located at http://www.elsevier.com/locate/atherosclerosis | ||||||
Citation | Atherosclerosis, 2011, v. 219 n. 1, p. 231-239 How to Cite? | ||||||
Abstract | Objective: There is considerable controversy about what constitutes optimal zinc intakes in patients with type 2 diabetes mellitus. Several studies suggest that higher zinc intakes improve vascular function and decrease oxidative damage. We aimed to assess the effects of zinc supplementation using a range of reliable biomarkers of oxidative damage and vascular function in patients with type 2 diabetes. Methods: Forty male type 2 diabetic patients were supplemented either with 240mg/day of zinc as zinc gluconate (n=20) or with placebo (n=20) for 3 months. Blood and spot urine samples were taken at baseline, days 3 and 7, months 1, 2 and 3 during supplementation and 1 month after cessation. Serum zinc, reliable biomarkers of oxidative damage (F 2-isoprostanes, neuroprostanes, cholesterol oxidation products, allantoin) as well as hydroxyeicosatetraenoic acid products and vascular-related indices (augmentation index, pulse wave velocity and aortic pressure) were measured. Results: Despite significantly higher levels of serum zinc in the treatment group, markers of oxidative damage, levels of hydroxyeicosatetraenoic acid products and vascular indices were unchanged by zinc supplementation during the four-month study period. Conclusion: Improving the zinc status in patients with type 2 diabetes with normal zinc levels did not have any impact on oxidative damage and vascular function, and such supplementation may not be generally beneficial in these individuals. © 2011 Elsevier Ireland Ltd. | ||||||
Persistent Identifier | http://hdl.handle.net/10722/143937 | ||||||
ISSN | 2023 Impact Factor: 4.9 2023 SCImago Journal Rankings: 1.461 | ||||||
ISI Accession Number ID |
Funding Information: Funding: Supported by the Biomedical Research Council (Grant 03/1/21/18/213) and National Medical Research Council (Grant NMRC/1157/2008), Singapore. | ||||||
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Seet, RCS | en_HK |
dc.contributor.author | Lee, CYJ | en_HK |
dc.contributor.author | Lim, ECH | en_HK |
dc.contributor.author | Quek, AML | en_HK |
dc.contributor.author | Huang, H | en_HK |
dc.contributor.author | Huang, SH | en_HK |
dc.contributor.author | Looi, WF | en_HK |
dc.contributor.author | Long, LH | en_HK |
dc.contributor.author | Halliwell, B | en_HK |
dc.date.accessioned | 2011-12-21T08:59:39Z | - |
dc.date.available | 2011-12-21T08:59:39Z | - |
dc.date.issued | 2011 | en_HK |
dc.identifier.citation | Atherosclerosis, 2011, v. 219 n. 1, p. 231-239 | en_HK |
dc.identifier.issn | 0021-9150 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/143937 | - |
dc.description.abstract | Objective: There is considerable controversy about what constitutes optimal zinc intakes in patients with type 2 diabetes mellitus. Several studies suggest that higher zinc intakes improve vascular function and decrease oxidative damage. We aimed to assess the effects of zinc supplementation using a range of reliable biomarkers of oxidative damage and vascular function in patients with type 2 diabetes. Methods: Forty male type 2 diabetic patients were supplemented either with 240mg/day of zinc as zinc gluconate (n=20) or with placebo (n=20) for 3 months. Blood and spot urine samples were taken at baseline, days 3 and 7, months 1, 2 and 3 during supplementation and 1 month after cessation. Serum zinc, reliable biomarkers of oxidative damage (F 2-isoprostanes, neuroprostanes, cholesterol oxidation products, allantoin) as well as hydroxyeicosatetraenoic acid products and vascular-related indices (augmentation index, pulse wave velocity and aortic pressure) were measured. Results: Despite significantly higher levels of serum zinc in the treatment group, markers of oxidative damage, levels of hydroxyeicosatetraenoic acid products and vascular indices were unchanged by zinc supplementation during the four-month study period. Conclusion: Improving the zinc status in patients with type 2 diabetes with normal zinc levels did not have any impact on oxidative damage and vascular function, and such supplementation may not be generally beneficial in these individuals. © 2011 Elsevier Ireland Ltd. | en_HK |
dc.language | eng | en_US |
dc.publisher | Elsevier Ireland Ltd. The Journal's web site is located at http://www.elsevier.com/locate/atherosclerosis | en_HK |
dc.relation.ispartof | Atherosclerosis | en_HK |
dc.subject | Oxidative damage | en_HK |
dc.subject | Type 2 diabetes | en_HK |
dc.subject | Vascular function | en_HK |
dc.subject | Zinc | en_HK |
dc.subject.mesh | Cholesterol - blood | - |
dc.subject.mesh | Diabetes Mellitus, Type 2 - blood - drug therapy - physiopathology | - |
dc.subject.mesh | Dietary Supplements | - |
dc.subject.mesh | Oxidative Stress - drug effects | - |
dc.subject.mesh | Zinc - administration and dosage - blood | - |
dc.title | Oral zinc supplementation does not improve oxidative stress or vascular function in patients with type 2 diabetes with normal zinc levels | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Lee, CYJ: jettylee@hku.hk | en_HK |
dc.identifier.authority | Lee, CYJ=rp01511 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/j.atherosclerosis.2011.07.097 | en_HK |
dc.identifier.pmid | 21840002 | - |
dc.identifier.scopus | eid_2-s2.0-81155159707 | en_HK |
dc.identifier.hkuros | 197983 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-81155159707&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 219 | en_HK |
dc.identifier.issue | 1 | en_HK |
dc.identifier.spage | 231 | en_HK |
dc.identifier.epage | 239 | en_HK |
dc.identifier.eissn | 1879-1484 | - |
dc.identifier.isi | WOS:000296587200035 | - |
dc.publisher.place | Ireland | en_HK |
dc.identifier.scopusauthorid | Seet, RCS=10045357300 | en_HK |
dc.identifier.scopusauthorid | Lee, CYJ=13104265200 | en_HK |
dc.identifier.scopusauthorid | Lim, ECH=8945547100 | en_HK |
dc.identifier.scopusauthorid | Quek, AML=13605538000 | en_HK |
dc.identifier.scopusauthorid | Huang, H=7405614576 | en_HK |
dc.identifier.scopusauthorid | Huang, SH=8367750600 | en_HK |
dc.identifier.scopusauthorid | Looi, WF=36523459100 | en_HK |
dc.identifier.scopusauthorid | Long, LH=7201908252 | en_HK |
dc.identifier.scopusauthorid | Halliwell, B=7101878919 | en_HK |
dc.identifier.citeulike | 9620354 | - |
dc.identifier.issnl | 0021-9150 | - |