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- Publisher Website: 10.1513/pats.200708-139MG
- Scopus: eid_2-s2.0-39049145641
- PMID: 18250214
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Conference Paper: Obstructive sleep apnea and metabolic syndrome: Alterations in glucose metabolism and inflammation
Title | Obstructive sleep apnea and metabolic syndrome: Alterations in glucose metabolism and inflammation |
---|---|
Authors | |
Keywords | Glucose metabolism Inflammation Metabolic syndrome Sleep apnea |
Issue Date | 2008 |
Publisher | American Thoracic Society. The Journal's web site is located at http://www.thoracic.org/publications/pats/pats.asp |
Citation | The 104th International Conference of the American Thoracic Society (ATS 2008), Toronto, ON., Canada, 16-21 May 2008. In
Proceedings of The American Thoracic Society, 2008, v. 5 n. 2, p. 207-217 How to Cite? |
Abstract | Metabolic syndrome (MS), the commonly used term for the clustering of obesity, insulin resistance, hypertension, and dyslipidemia, affects millions of people worldwide, and is associated with an increased risk of cardiovascular disease and type 2 diabetes. Recently, it has been suggested that obstructive sleep apnea (OSA), an increasingly prevalent condition, may contribute to the development of MS and diabetes. Despite substantial evidence from both clinical and population studies to suggest an independent link between OSA and metabolic abnormalities, the issue still remains controversial. Obesity, particularly visceral obesity, is an important factor in the assessment of adverse metabolic outcome in OSA. Further prospective and interventional studies, with adequate sample sizes and longer follow-up, rigorous control for adiposity, and, ideally, randomization and control for any therapeutic intervention, are clearly needed to address the direction of causality. There are multiple mechanistic pathways involved in the interaction between OSA, obesity, and metabolic derangements. Chronic intermittent hypoxia and sleep fragmentation with sleep loss in OSA are likely key triggers that initiate or contribute to the sustenance of inflammation as a prominent phenomenon, but their complex interplay remains to be elucidated. In summary, OSA may represent a novel risk factor for MS and diabetes, and thus clinicians should be encouraged to systematically evaluate the presence of metabolic abnormalities in OSA and vice versa. |
Persistent Identifier | http://hdl.handle.net/10722/77976 |
ISSN | 2023 Impact Factor: 6.8 |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Tasali, E | en_HK |
dc.contributor.author | Ip, MSM | en_HK |
dc.date.accessioned | 2010-09-06T07:37:48Z | - |
dc.date.available | 2010-09-06T07:37:48Z | - |
dc.date.issued | 2008 | en_HK |
dc.identifier.citation | The 104th International Conference of the American Thoracic Society (ATS 2008), Toronto, ON., Canada, 16-21 May 2008. In Proceedings of The American Thoracic Society, 2008, v. 5 n. 2, p. 207-217 | en_HK |
dc.identifier.issn | 1546-3222 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/77976 | - |
dc.description.abstract | Metabolic syndrome (MS), the commonly used term for the clustering of obesity, insulin resistance, hypertension, and dyslipidemia, affects millions of people worldwide, and is associated with an increased risk of cardiovascular disease and type 2 diabetes. Recently, it has been suggested that obstructive sleep apnea (OSA), an increasingly prevalent condition, may contribute to the development of MS and diabetes. Despite substantial evidence from both clinical and population studies to suggest an independent link between OSA and metabolic abnormalities, the issue still remains controversial. Obesity, particularly visceral obesity, is an important factor in the assessment of adverse metabolic outcome in OSA. Further prospective and interventional studies, with adequate sample sizes and longer follow-up, rigorous control for adiposity, and, ideally, randomization and control for any therapeutic intervention, are clearly needed to address the direction of causality. There are multiple mechanistic pathways involved in the interaction between OSA, obesity, and metabolic derangements. Chronic intermittent hypoxia and sleep fragmentation with sleep loss in OSA are likely key triggers that initiate or contribute to the sustenance of inflammation as a prominent phenomenon, but their complex interplay remains to be elucidated. In summary, OSA may represent a novel risk factor for MS and diabetes, and thus clinicians should be encouraged to systematically evaluate the presence of metabolic abnormalities in OSA and vice versa. | en_HK |
dc.language | eng | en_HK |
dc.publisher | American Thoracic Society. The Journal's web site is located at http://www.thoracic.org/publications/pats/pats.asp | en_HK |
dc.relation.ispartof | Proceedings of the American Thoracic Society | en_HK |
dc.subject | Glucose metabolism | - |
dc.subject | Inflammation | - |
dc.subject | Metabolic syndrome | - |
dc.subject | Sleep apnea | - |
dc.subject.mesh | Adult | en_HK |
dc.subject.mesh | Blood Glucose - metabolism | en_HK |
dc.subject.mesh | Humans | en_HK |
dc.subject.mesh | Inflammation - etiology - physiopathology | en_HK |
dc.subject.mesh | Metabolic Syndrome X - etiology - metabolism - physiopathology | en_HK |
dc.subject.mesh | Risk Factors | en_HK |
dc.subject.mesh | Sleep Apnea, Obstructive - complications - metabolism - physiopathology | en_HK |
dc.title | Obstructive sleep apnea and metabolic syndrome: Alterations in glucose metabolism and inflammation | en_HK |
dc.type | Conference_Paper | en_HK |
dc.identifier.email | Ip, MSM:msmip@hku.hk | en_HK |
dc.identifier.authority | Ip, MSM=rp00347 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1513/pats.200708-139MG | en_HK |
dc.identifier.pmid | 18250214 | - |
dc.identifier.scopus | eid_2-s2.0-39049145641 | en_HK |
dc.identifier.hkuros | 149908 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-39049145641&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 5 | en_HK |
dc.identifier.issue | 2 | en_HK |
dc.identifier.spage | 207 | en_HK |
dc.identifier.epage | 217 | en_HK |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Tasali, E=6505939327 | en_HK |
dc.identifier.scopusauthorid | Ip, MSM=7102423259 | en_HK |
dc.customcontrol.immutable | sml 170609 amended | - |
dc.identifier.issnl | 1546-3222 | - |