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Article: Inflammatory biomarkers associated with obesity and insulin resistance: A focus on lipocalin-2 and adipocyte fatty acid-binding protein
Title | Inflammatory biomarkers associated with obesity and insulin resistance: A focus on lipocalin-2 and adipocyte fatty acid-binding protein |
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Authors | |
Keywords | Adipocyte fatty acid-binding protein Adipokine Cardiovascular disease Diabetes Inflammation Lipocalin-2 Obesity |
Issue Date | 2008 |
Publisher | Expert Reviews Ltd. The Journal's web site is located at http://www.future-drugs.com/loi/eem |
Citation | Expert Review Of Endocrinology And Metabolism, 2008, v. 3 n. 1, p. 29-41 How to Cite? |
Abstract | Obesity is an important risk factor for a cluster of metabolic and cardiovascular diseases, oincluding insulin resistance, Type 2 diabetes, nonalcoholic fatty liver disease and atherosclerosis. Systemic low-grade inflammation, characterized by elevated circulating concentrations of proinflammatory factors, has recently been proposed to be a key mediator that links obesity with its medical complications. Adipose tissue is now recognized as the major contributor to systemic inflammation associated with obesity. As obesity develops, adipose tissue is infiltrated with activated macrophages. The 'inflamed' adipose tissue secretes a large number of proinflammatory adipokines and/or cytokines, which can act either in an autocrine manner to perpetuate local inflammation or in an endocrine manner to induce insulin resistance and endothelial dysfunction. In this review, we summarize recent advances in several newly identified adipose tissue-derived inflammatory factors, with the focus on lipocalin-2 and adipocyte fatty acid-binding protein (A-FABP). Both lipocalin-2 and A-FABP possess lipid-binding properties and are important integrators of metabolic and inflammatory pathways. A growing body of evidence from experimental, epidemiological and genetic studies suggests that both lipocalin-2 and A-FABP represent a novel class of serum biomarkers for risk prediction and therapeutic intervention of obesity-related medical complications. © 2008 Future Drugs Ltd. |
Persistent Identifier | http://hdl.handle.net/10722/91616 |
ISSN | 2023 Impact Factor: 2.7 2023 SCImago Journal Rankings: 0.904 |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Hoo, RLC | en_HK |
dc.contributor.author | Yeung, DCY | en_HK |
dc.contributor.author | Lam, KSL | en_HK |
dc.contributor.author | Xu, A | en_HK |
dc.date.accessioned | 2010-09-17T10:22:15Z | - |
dc.date.available | 2010-09-17T10:22:15Z | - |
dc.date.issued | 2008 | en_HK |
dc.identifier.citation | Expert Review Of Endocrinology And Metabolism, 2008, v. 3 n. 1, p. 29-41 | en_HK |
dc.identifier.issn | 1744-6651 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/91616 | - |
dc.description.abstract | Obesity is an important risk factor for a cluster of metabolic and cardiovascular diseases, oincluding insulin resistance, Type 2 diabetes, nonalcoholic fatty liver disease and atherosclerosis. Systemic low-grade inflammation, characterized by elevated circulating concentrations of proinflammatory factors, has recently been proposed to be a key mediator that links obesity with its medical complications. Adipose tissue is now recognized as the major contributor to systemic inflammation associated with obesity. As obesity develops, adipose tissue is infiltrated with activated macrophages. The 'inflamed' adipose tissue secretes a large number of proinflammatory adipokines and/or cytokines, which can act either in an autocrine manner to perpetuate local inflammation or in an endocrine manner to induce insulin resistance and endothelial dysfunction. In this review, we summarize recent advances in several newly identified adipose tissue-derived inflammatory factors, with the focus on lipocalin-2 and adipocyte fatty acid-binding protein (A-FABP). Both lipocalin-2 and A-FABP possess lipid-binding properties and are important integrators of metabolic and inflammatory pathways. A growing body of evidence from experimental, epidemiological and genetic studies suggests that both lipocalin-2 and A-FABP represent a novel class of serum biomarkers for risk prediction and therapeutic intervention of obesity-related medical complications. © 2008 Future Drugs Ltd. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Expert Reviews Ltd. The Journal's web site is located at http://www.future-drugs.com/loi/eem | en_HK |
dc.relation.ispartof | Expert Review of Endocrinology and Metabolism | en_HK |
dc.subject | Adipocyte fatty acid-binding protein | en_HK |
dc.subject | Adipokine | en_HK |
dc.subject | Cardiovascular disease | en_HK |
dc.subject | Diabetes | en_HK |
dc.subject | Inflammation | en_HK |
dc.subject | Lipocalin-2 | en_HK |
dc.subject | Obesity | en_HK |
dc.title | Inflammatory biomarkers associated with obesity and insulin resistance: A focus on lipocalin-2 and adipocyte fatty acid-binding protein | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Hoo, RLC:rubyhoo@hkucc.hku.hk | en_HK |
dc.identifier.email | Lam, KSL:ksllam@hku.hk | en_HK |
dc.identifier.email | Xu, A:amxu@hkucc.hku.hk | en_HK |
dc.identifier.authority | Hoo, RLC=rp01334 | en_HK |
dc.identifier.authority | Lam, KSL=rp00343 | en_HK |
dc.identifier.authority | Xu, A=rp00485 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1586/17446651.3.1.29 | en_HK |
dc.identifier.scopus | eid_2-s2.0-37549058420 | en_HK |
dc.identifier.hkuros | 140651 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-37549058420&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 3 | en_HK |
dc.identifier.issue | 1 | en_HK |
dc.identifier.spage | 29 | en_HK |
dc.identifier.epage | 41 | en_HK |
dc.publisher.place | United Kingdom | en_HK |
dc.identifier.scopusauthorid | Hoo, RLC=6602369766 | en_HK |
dc.identifier.scopusauthorid | Yeung, DCY=36869426200 | en_HK |
dc.identifier.scopusauthorid | Lam, KSL=8082870600 | en_HK |
dc.identifier.scopusauthorid | Xu, A=7202655409 | en_HK |
dc.identifier.citeulike | 2152684 | - |
dc.identifier.issnl | 1744-6651 | - |