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- Publisher Website: 10.1046/j.1365-2362.2003.01132.x
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- PMID: 12662160
- WOS: WOS:000181861400005
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Article: Plasma phospholipid transfer protein activity and small, dense LDL in type 2 diabetes mellitus
Title | Plasma phospholipid transfer protein activity and small, dense LDL in type 2 diabetes mellitus |
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Authors | |
Keywords | Cholesteryl ester transfer protein Dense LDL Phospholipid transfer protein Small Type 2 diabetes mellitus |
Issue Date | 2003 |
Publisher | Blackwell Publishing Ltd. The Journal's web site is located at http://www.blackwellpublishing.com/journals/ECI |
Citation | European Journal Of Clinical Investigation, 2003, v. 33 n. 4, p. 301-306 How to Cite? |
Abstract | Background: Phospholipid transfer protein (PLTP) and cholesteryl ester transfer protein (CETP) remodel circulating lipoproteins and play a role in the antiatherogenic reverse cholesterol transport pathway. The present study determined whether abnormalities in the LDL subfraction pattern in type 2 diabetic patients were related to changes in lipid transfer proteins. Methods: Low-density lipoprotein (LDL) subfractions were measured by density gradient ultracentrifugation and plasma PLTP and CETP activities by radiometric assays in 240 diabetic patients and 136 controls. Results: The diabetic patients had lower LDL-I (P < 0.001) and higher LDL-III concentrations than the controls (P < 0.001). Plasma PLTP activity was increased (P < 0.001) whereas no significant differences were seen in CETP activity. In the diabetic patients, small, dense LDL-III correlated with plasma triglyceride (r = 0.18, P < 0.01), HDL (r = -0.14, P < 0.05), PLTP (r = 0.29, P < 0.001) and CETP activity (r = 0.15, P < 0.05). Linear regression analysis showed that plasma PLTP activity, triglyceride and age were the major determinants of LDL-III concentration (r2 = 28%, P < 0.001). The univariate relationship between CETP and LDL-III was no longer significant after adjusting for PLTP activity. Conclusions: The increase in plasma PLTP activity was independently associated with small, dense LDL concentrations in type 2 diabetes. Hence, elevated PLTP activity might have both antiatherogenic and pro-atherogenic potential in these patients. |
Persistent Identifier | http://hdl.handle.net/10722/76771 |
ISSN | 2023 Impact Factor: 4.4 2023 SCImago Journal Rankings: 1.270 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Tan, KCB | en_HK |
dc.contributor.author | Shiu, SWM | en_HK |
dc.contributor.author | Wong, Y | en_HK |
dc.date.accessioned | 2010-09-06T07:24:45Z | - |
dc.date.available | 2010-09-06T07:24:45Z | - |
dc.date.issued | 2003 | en_HK |
dc.identifier.citation | European Journal Of Clinical Investigation, 2003, v. 33 n. 4, p. 301-306 | en_HK |
dc.identifier.issn | 0014-2972 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/76771 | - |
dc.description.abstract | Background: Phospholipid transfer protein (PLTP) and cholesteryl ester transfer protein (CETP) remodel circulating lipoproteins and play a role in the antiatherogenic reverse cholesterol transport pathway. The present study determined whether abnormalities in the LDL subfraction pattern in type 2 diabetic patients were related to changes in lipid transfer proteins. Methods: Low-density lipoprotein (LDL) subfractions were measured by density gradient ultracentrifugation and plasma PLTP and CETP activities by radiometric assays in 240 diabetic patients and 136 controls. Results: The diabetic patients had lower LDL-I (P < 0.001) and higher LDL-III concentrations than the controls (P < 0.001). Plasma PLTP activity was increased (P < 0.001) whereas no significant differences were seen in CETP activity. In the diabetic patients, small, dense LDL-III correlated with plasma triglyceride (r = 0.18, P < 0.01), HDL (r = -0.14, P < 0.05), PLTP (r = 0.29, P < 0.001) and CETP activity (r = 0.15, P < 0.05). Linear regression analysis showed that plasma PLTP activity, triglyceride and age were the major determinants of LDL-III concentration (r2 = 28%, P < 0.001). The univariate relationship between CETP and LDL-III was no longer significant after adjusting for PLTP activity. Conclusions: The increase in plasma PLTP activity was independently associated with small, dense LDL concentrations in type 2 diabetes. Hence, elevated PLTP activity might have both antiatherogenic and pro-atherogenic potential in these patients. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Blackwell Publishing Ltd. The Journal's web site is located at http://www.blackwellpublishing.com/journals/ECI | en_HK |
dc.relation.ispartof | European Journal of Clinical Investigation | en_HK |
dc.rights | European Journal of Clinical Investigation. Copyright © Blackwell Publishing Ltd. | en_HK |
dc.subject | Cholesteryl ester transfer protein | - |
dc.subject | Dense LDL | - |
dc.subject | Phospholipid transfer protein | - |
dc.subject | Small | - |
dc.subject | Type 2 diabetes mellitus | - |
dc.subject.mesh | Carrier Proteins - blood | en_HK |
dc.subject.mesh | Cholesterol Ester Transfer Proteins | en_HK |
dc.subject.mesh | Diabetes Mellitus, Type 2 - blood | en_HK |
dc.subject.mesh | Glycoproteins | en_HK |
dc.subject.mesh | Humans | en_HK |
dc.subject.mesh | Lipoproteins, LDL - blood | en_HK |
dc.subject.mesh | Membrane Proteins - blood | en_HK |
dc.subject.mesh | Middle Aged | en_HK |
dc.subject.mesh | Phospholipid Transfer Proteins | en_HK |
dc.title | Plasma phospholipid transfer protein activity and small, dense LDL in type 2 diabetes mellitus | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0014-2972&volume=33&issue=4&spage=301&epage=6&date=2003&atitle=Plasma+Phospholipid+Transfer+Protein+Activity+And+Small,+Dense+Ldl+In+Type+2+Diabetes+Mellitus. | en_HK |
dc.identifier.email | Tan, KCB:kcbtan@hku.hk | en_HK |
dc.identifier.authority | Tan, KCB=rp00402 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1046/j.1365-2362.2003.01132.x | en_HK |
dc.identifier.pmid | 12662160 | en_HK |
dc.identifier.scopus | eid_2-s2.0-0037395622 | en_HK |
dc.identifier.hkuros | 78705 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-0037395622&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 33 | en_HK |
dc.identifier.issue | 4 | en_HK |
dc.identifier.spage | 301 | en_HK |
dc.identifier.epage | 306 | en_HK |
dc.identifier.isi | WOS:000181861400005 | - |
dc.publisher.place | United Kingdom | en_HK |
dc.identifier.scopusauthorid | Tan, KCB=8082703100 | en_HK |
dc.identifier.scopusauthorid | Shiu, SWM=7005550652 | en_HK |
dc.identifier.scopusauthorid | Wong, Y=24073787400 | en_HK |
dc.identifier.issnl | 0014-2972 | - |