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- Publisher Website: 10.2337/dc09-2124
- Scopus: eid_2-s2.0-77954921980
- PMID: 20185735
- WOS: WOS:000277631200038
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Article: Markers of oxidative damage are not elevated in otherwise healthy individuals with the metabolic syndrome
Title | Markers of oxidative damage are not elevated in otherwise healthy individuals with the metabolic syndrome |
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Authors | |
Issue Date | 2010 |
Publisher | American Diabetes Association. The Journal's web site is located at http://diabetes.diabetesjournals.org/ |
Citation | Diabetes Care, 2010, v. 33 n. 5, p. 1140-1142 How to Cite? |
Abstract | OBJECTIVE- The role of oxidative damage in the pathogenesis of metabolic syndrome is poorly understood. RESEARCH DESIGN AND METHODS- A detailed cross-sectional study was performed to assess the relationship between lipid oxidation products, γ-glutamyltransferase, highsensitivity C-reactive protein (hs-CRP), and phospholipase activities with respect to the metabolic status in a cohort of otherwise healthy individuals. RESULTS- A total of 179 individuals (87 men and 92 women) aged 43 ± 14 years (mean ± SD) participated in this study. There were no differences in the levels of plasma F 2-isoprostanes, hydroxyeicosatetraenoic acids, cholesterol oxidation products, and phospholipase activities in individuals with features of metabolic syndrome. In multivariate analyses, serum hs-CRP was a consistent independent predictor of metabolic syndrome. CONCLUSIONS- Minimal changes were observed in multiple markers of oxidative damage in a well-characterized cohort of individuals with features of metabolic syndrome. © 2010 by the American Diabetes Association. |
Persistent Identifier | http://hdl.handle.net/10722/179203 |
ISSN | 2023 Impact Factor: 14.8 2023 SCImago Journal Rankings: 5.694 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Seet, RCS | en_US |
dc.contributor.author | Lee, CYJ | en_US |
dc.contributor.author | Lim, ECH | en_US |
dc.contributor.author | Quek, AML | en_US |
dc.contributor.author | Huang, SH | en_US |
dc.contributor.author | Khoo, CM | en_US |
dc.contributor.author | Halliwell, B | en_US |
dc.date.accessioned | 2012-12-19T09:52:54Z | - |
dc.date.available | 2012-12-19T09:52:54Z | - |
dc.date.issued | 2010 | en_US |
dc.identifier.citation | Diabetes Care, 2010, v. 33 n. 5, p. 1140-1142 | en_US |
dc.identifier.issn | 0149-5992 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/179203 | - |
dc.description.abstract | OBJECTIVE- The role of oxidative damage in the pathogenesis of metabolic syndrome is poorly understood. RESEARCH DESIGN AND METHODS- A detailed cross-sectional study was performed to assess the relationship between lipid oxidation products, γ-glutamyltransferase, highsensitivity C-reactive protein (hs-CRP), and phospholipase activities with respect to the metabolic status in a cohort of otherwise healthy individuals. RESULTS- A total of 179 individuals (87 men and 92 women) aged 43 ± 14 years (mean ± SD) participated in this study. There were no differences in the levels of plasma F 2-isoprostanes, hydroxyeicosatetraenoic acids, cholesterol oxidation products, and phospholipase activities in individuals with features of metabolic syndrome. In multivariate analyses, serum hs-CRP was a consistent independent predictor of metabolic syndrome. CONCLUSIONS- Minimal changes were observed in multiple markers of oxidative damage in a well-characterized cohort of individuals with features of metabolic syndrome. © 2010 by the American Diabetes Association. | en_US |
dc.language | eng | en_US |
dc.publisher | American Diabetes Association. The Journal's web site is located at http://diabetes.diabetesjournals.org/ | en_US |
dc.relation.ispartof | Diabetes Care | en_US |
dc.title | Markers of oxidative damage are not elevated in otherwise healthy individuals with the metabolic syndrome | en_US |
dc.type | Article | en_US |
dc.identifier.email | Lee, CYJ: jettylee@hku.hk | en_US |
dc.identifier.authority | Lee, CYJ=rp01511 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.2337/dc09-2124 | en_US |
dc.identifier.pmid | 20185735 | - |
dc.identifier.scopus | eid_2-s2.0-77954921980 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-77954921980&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 33 | en_US |
dc.identifier.issue | 5 | en_US |
dc.identifier.spage | 1140 | en_US |
dc.identifier.epage | 1142 | en_US |
dc.identifier.eissn | 1935-5548 | - |
dc.identifier.isi | WOS:000277631200038 | - |
dc.publisher.place | United States | en_US |
dc.identifier.scopusauthorid | Seet, RCS=10045357300 | en_US |
dc.identifier.scopusauthorid | Lee, CYJ=13104265200 | en_US |
dc.identifier.scopusauthorid | Lim, ECH=8945547100 | en_US |
dc.identifier.scopusauthorid | Quek, AML=13605538000 | en_US |
dc.identifier.scopusauthorid | Huang, SH=8367750600 | en_US |
dc.identifier.scopusauthorid | Khoo, CM=15842051800 | en_US |
dc.identifier.scopusauthorid | Halliwell, B=7101878919 | en_US |
dc.identifier.issnl | 0149-5992 | - |