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dc.contributor.author
Miksztowicz, Veronica Julieta
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McCoy, Mary G.
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Schreier, Laura Ester
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Cacciagiú, Leonardo Damian
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Elbert, Alicia
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González, Ana Inés
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Billheimer, Jeffrey
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Eacho, Patrick
dc.contributor.author
Rader, Daniel J.
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Berg, Gabriela Alicia
dc.date.available
2025-10-03T10:22:01Z
dc.date.issued
2012-12
dc.identifier.citation
Miksztowicz, Veronica Julieta; McCoy, Mary G.; Schreier, Laura Ester; Cacciagiú, Leonardo Damian; Elbert, Alicia; et al.; Endothelial Lipase Activity Predicts High-Density Lipoprotein Catabolism in Hemodialysis; Lippincott Williams; Arteriosclerosis, Thrombosis, and Vascular Biology; 32; 12; 12-2012; 3033-3040
dc.identifier.issn
1079-5642
dc.identifier.uri
http://hdl.handle.net/11336/272669
dc.description.abstract
Objective: A novel phospholipase assay was used to measure for the first time the behavior of endothelial and hepatic phospholipase activities in postheparin human plasma of hemodialyzed patients and its relationship with atherogenic and antiatherogenic lipoprotein levels.Methods and Results:Endothelial and hepatic phospholipase activity was assessed in a total SN1-specific phospholipase assay, using (1-decanoylthio-1-deoxy-2-decanoyl-sn-glycero-3-phosphoryl) ethylene glycol as the substrate. Hemodialyzed patients presented lower values of total and hepatic phospholipase activity than controls: 4.4 (1.9?9.0) versus 7.5 (3.6-18.0) and 2.6 (0.7-6.2) versus 6.6 (1.3-15.2) μmol of fatty acid released per milliliter of postheparin plasma per hour, respectively (P<0.001); however, endothelial lipase (EL) phospholipase activity was increased in patients: 1.7 (0.8-3.0) versus 1.1 (0.1-2.7) μmol of fatty acid released per milliliter of postheparin plasma per hour (P=0.008). EL was negatively associated with high-density lipoprotein (HDL)-cholesterol (r=-0.427; P=0.001), and apolipoprotein A-I levels, total phospholipase, and hepatic lipase activity were directly associated with low-density lipoprotein-cholesterol and apolipoprotein B. The association of EL and HDL-cholesterol remained significant when adjusting for waist circumference (β=-0.26; P=0.05), and the effect of hepatic lipase on low-density lipoprotein-cholesterol continued after adjusting for age (β=0.46; P= 0.001).Conclusion: Our results support the hypothesis that EL is the predominant enzyme responsible for lipolytic catabolism of HDLs in hemodialyzed patients and resolve the apparent paradox observed between low hepatic lipase activity and decreased HDL-cholesterol levels observed in these patients. In addition, the ability to assess total hepatic lipase and EL phospholipase activity in plasma will increase our knowledge of the mechanisms involved in controlling HDL levels and cardiovascular risk in hemodialyzed patients, as well as other populations with low levels of HDL-cholesterol.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
Lippincott Williams
dc.rights
info:eu-repo/semantics/openAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
Chronic kidney disease
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Endothelial lipase
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Hepatic lipase
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High-density lipoprotein-cholesterol
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Otras Ciencias de la Salud
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Ciencias de la Salud
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CIENCIAS MÉDICAS Y DE LA SALUD
dc.title
Endothelial Lipase Activity Predicts High-Density Lipoprotein Catabolism in Hemodialysis
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2025-10-02T11:58:34Z
dc.journal.volume
32
dc.journal.number
12
dc.journal.pagination
3033-3040
dc.journal.pais
Estados Unidos
dc.journal.ciudad
Philadelphia
dc.description.fil
Fil: Miksztowicz, Veronica Julieta. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Bioquímica Clínica; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
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Fil: McCoy, Mary G.. Institute For Translational Medicine And Therapeutics; Estados Unidos
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Fil: Schreier, Laura Ester. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Bioquímica Clínica; Argentina
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Fil: Cacciagiú, Leonardo Damian. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Bioquímica Clínica; Argentina
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Fil: Elbert, Alicia. No especifíca;
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Fil: González, Ana Inés. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Bioquímica Clínica; Argentina
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Fil: Billheimer, Jeffrey. Institute For Translational Medicine And Therapeutics; Estados Unidos
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Fil: Eacho, Patrick. Lilly Research Laboratories, Eli Lilly And Company; Estados Unidos
dc.description.fil
Fil: Rader, Daniel J.. Institute For Translational Medicine And Therapeutics; Estados Unidos
dc.description.fil
Fil: Berg, Gabriela Alicia. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Bioquímica Clínica; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
dc.journal.title
Arteriosclerosis, Thrombosis, and Vascular Biology
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.ahajournals.org/doi/10.1161/atvbaha.112.300110
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1161/ATVBAHA.112.300110
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